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WO2008123756A1 - A pharmaceutical compositions containing lacton type pyridine derivatives as an effective ingredient for the prevention and treatment of ischemia - Google Patents

A pharmaceutical compositions containing lacton type pyridine derivatives as an effective ingredient for the prevention and treatment of ischemia Download PDF

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Publication number
WO2008123756A1
WO2008123756A1 PCT/KR2008/002030 KR2008002030W WO2008123756A1 WO 2008123756 A1 WO2008123756 A1 WO 2008123756A1 KR 2008002030 W KR2008002030 W KR 2008002030W WO 2008123756 A1 WO2008123756 A1 WO 2008123756A1
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WO
WIPO (PCT)
Prior art keywords
compound
dihydro
pyrano
pyridine
ridine
Prior art date
Application number
PCT/KR2008/002030
Other languages
French (fr)
Inventor
Yong-Baik Cho
Junwon Lee
Jung Bum Yi
Nam Kyu Lee
Bong-Yong Lee
Ki-Chul Hwang
Soyeon Lim
Woochul Chang
Ji Hyung Chung
Byung Ho Lee
Ho Won Seo
Original Assignee
Sk Chemicals Co., Ltd.
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Filing date
Publication date
Application filed by Sk Chemicals Co., Ltd. filed Critical Sk Chemicals Co., Ltd.
Publication of WO2008123756A1 publication Critical patent/WO2008123756A1/en

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/436—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • the present invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising a lactone type pyridine derivative effective in treating ischemic diseases.
  • Ischemic diseases including ischemic stroke and ischemic heart disease are caused by ischemia, which refers to the decrease in blood supply below a threshold value caused by the blocking of the cerebral artery or the coronary artery due to thrombosis or arteriosclerosis.
  • ischemia refers to the decrease in blood supply below a threshold value caused by the blocking of the cerebral artery or the coronary artery due to thrombosis or arteriosclerosis.
  • brain and heart cells are damaged and die, resulting in brain infarction and myocardial infarction.
  • drugs that prevent the damage of cells caused by ischemia or facilitate regeneration thereof can be an ultimate treatment for ischemic brain disease or heart disease.
  • Ischemic heart diseases and cerebrovascular diseases represented by myocardial infarction and stroke, are the first cause of death inside and outside Korea.
  • the drugs currently used for preventing and treating ischemic diseases include beta blockers, nitrates, calcium channel blockers, etc., which prevent the outbreak of ischemic diseases by reducing oxygen demand in the ischemic area or sustain a therapeutic effect after the outbreak, thrombolytic agents, antithrombotic agents, anti-platelet agents, etc., which are used for reperfusion to the ischemic area after the ischemic outbreak, and the like.
  • HSP heat shock proteins
  • adenosine receptor Al adenosine receptor Al
  • the present invention is directed to the control of homeostasis of calcium, which is excessively released from the cytoplasm under ischemic condition and leads to cell death.
  • HSP plays an important role in the control of calcium homeostasis. It is known that calcium is excessively released under ischemic condition. Also, the level of expression of HSP increases under ischemic condition to provide cell-protecting effect. According to a recent report, the excessive release of calcium induces the expression of the HSP27 protein, and the increased expression of HSP70 suppresses the excessive release of calcium. Therefore, it is probable that the exploration of a drug based on the relationship between calcium homeostasis and HSP expression may lead to the development of an ischemic disease treatment of new-concept.
  • an object of the present invention is to provide a new medicinal use of the lactone type pyridine derivatives disclosed in Korean Patent Publication Nos. 2005-69910, 2006-70945 and 2006-110764 and Korean Patent Application No. 2005-127801 and pharmaceutically acceptable salts thereof for preventing and treating ischemic diseases.
  • FIG. 1 shows the confocal microscopic images for evaluating myocardial protecting effect through control of intracellular calcium homeostasis in Example 3;
  • FIG. 2 and FIG. 3 show the photographs illustrating the change of the thickness of ventricular walls in an ischemic animal model in which rats underwent ligation of the distal left anterior descending coronary artery (Example 5) through TTC staining; and FIG. 4 shows the photographs illustrating the change of the thickness of ventricular walls in an ischemic animal model in which rats underwent ligation of the distal left anterior descending coronary artery (Example 5) through H&E staining.
  • the present invention is characterized by a pharmaceutical composition for treating and preventing ischemic disease comprising a lactone type pyridine derivative represented by the following Chemical Formula 1 or a pharmaceutically acceptable salt thereof or a drug prepared therefrom: [Chemical Formula 1 ]
  • miL j mmm represents a single or double bond
  • X is an oxygen or sulfur atom
  • each of R 1 , R 2 , R3, R4 / R5, Re and R7 is independently selected from hydrogen, halo, cyano, nitro, C2-C7 acyl, hydroxy, amino, C 1 -CO alkyl, C3-C9 cycloalkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxyalkyl, C 1 -C 6 alkylthio, C 1 -C 6 alkylamino, C 1 -C 6 alkoxyalkylamino, Q-C9 cycloalkylamino, C4-C9 heterocycloalkylamino, aryl Ci-C 6 alkylamino, arylamino, heteroaryl Ci-C 6 alkylamino, C2-C7 acylamino, saturated heterocycle, C2-C7 acyloxy
  • X is an oxygen or sulfur atom; and each of Ri, R 2 , R3, R 4 , Rs, R ⁇ , and R7 is independently selected from hydrogen, halo, hydroxy, amino, C 2 -C7 acyl, Q-C7 acyloxy, Ci-C 6 alkyl, C 2 -C 6 alkenyl, Ci-C 6 alkoxy, Ci-C 6 alkoxyalkyl, C3-C9 cycloalkyl, aryl Ci-C 6 alkyl, heteroaryl Ci-C 6 alkyl, saturated heterocyclo Ci-C 6 alkyl, mono(Ci-C 6 alkyl)amino, di(Ci-C 6 alkyl)amino, C 4 -C 9 cycloalkylamino, C 1 -C 6 alkoxyalkylamino, C 4 -C 9 heterocycloalkylamino, aryl Ci-C 6 alkylamino, heteroaryl Ci-C 6 alkylamino, ary
  • Ci-C 6 hydroxyalkyl amino, mono(Ci-C 6 alkyl)amino, di(Ci-Q alkyl)amino and aryl
  • Ci-C 6 alkylamino the aryl is phenyl; and each of the saturated heterocycle and heteroaryl is selected from furan, tetrahydrofuran, pyrrolidine, pyridine, morpholine, oxolane, benzodioxolane, thiophene, thiomorpholine, dioxothiomorpholine, piperidine and piperazine.
  • lactone type pyridine derivative represented by Chemical Formula 1 include:
  • the lactone type pyridine derivative represented by Chemical Formula 1 may form a pharmaceutically acceptable salt with an acid, for example, hydrochloric acid, bromic acid, sulfuric acid, phosphoric acid, methanesulfonic acid, acetic acid, citric acid, fumaric acid, lactic acid, maleic acid, succinic acid and tartaric acid.
  • the lactone type pyridine derivative represented by Chemical Formula l may form a pharmaceutically acceptable salt by reacting with an alkali metal ion such as sodium, potassium, etc., or an ammonium ion.
  • the pharmaceutical composition of the present invention may comprise, in addition to the lactone type pyridine derivative as an active ingredient, a commonly used nontoxic pharmaceutically acceptable vehicle, adjuvant, excipient, or the like so as to be prepared into preparation forms for oral or parenteral administration common in the pharmaceutical field, for example, tablet, capsule, troche, liquid, suspension, etc.
  • a commonly used nontoxic pharmaceutically acceptable vehicle, adjuvant, excipient, or the like so as to be prepared into preparation forms for oral or parenteral administration common in the pharmaceutical field, for example, tablet, capsule, troche, liquid, suspension, etc.
  • the composition may be prepared into tablet, capsule, solution, syrup, suspension, and the like.
  • parenteral administration it may be prepared into abdominal, subcutaneous, intramuscular or transdermal injection form.
  • the present invention encompasses a method for treating or preventing ischemic diseases comprising administering the compound represented by Chemical Formula 1 to a patient with a therapeutical dose capable of reducing cell death under ischemic condition.
  • the patient refers to a warm-blooded animal or mammal including human suffering from ischemic heart diseases and/ or ischemic cerebrovascular diseases represented by angina pectoris, myocardial infarction, stroke and cerebrovascular dementia.
  • Treatment of a ischemic disease patient means protection of cells and reduction of cell death of the patient.
  • Diagnosis of a patient with an ischemic disease is within the ability and knowledge of those skilled in the art.
  • a clinical doctor skilled in the related art can easily diagnose the disease based on clinical trials, medical checkup, health examination, family history, and the like.
  • the effective dose of the compound represented by Chemical Formula 1 can be easily determined based on the observation of results under similar conditions using common techniques.
  • the effective dose various factors, including but not limited to, constitution, age and general health condition of the patient, degree or severity of the disease, response of the patient, the particular compound to be administered, mode of administration, bioavailability of the administered drug, selected route of administration and presence of jointly administered drug.
  • a general dose for an adult patient whose body weight is 70 kg is 0.01 to 1000 mg/day. Based on the judgment of a doctor or a pharmacist, the dose may be administered once to several times a day at predetermined intervals.
  • the compound represented by Chemical Formula 1 may be administered by any mode or method, including oral and parenteral administration, that makes the compound biologically available at the effective dose.
  • the compound may be administered orally, subcutaneously, intramuscularly, intravenously, transdermally, intranasally or rectally.
  • oral administration is preferred.
  • Those skilled in preparing medical preparations can easily select the adequate form and mode of administration, considering the severity of disease or other situations.
  • the compound of the present invention may be administered in the form of a pharmaceutical composition or drug, which is prepared by mixing with a pharmaceutically acceptable vehicle or excipient.
  • a pharmaceutically acceptable vehicle or excipient The mixing ratio and kind of the vehicle or excipient are determined depending on the selected route of administration and in accordance with the general standard pharmaceutical guidance.
  • the pharmaceutical composition or drug is prepared by the methods known to those skilled in the pharmaceutical industry. [Mode for Invention]
  • a 78-mer nucleotide sequence containing three repeating heat shock response elements (HSRE; GAANNTTC), an Nhel site at the 5' end of the DNA sequence and a BgIII site at the 3' end (see the sequence below) and its complementary sequence were prepared.
  • a double helical DNA was prepared by heating at 80 °C for 5 minutes and then annealing at room temperature.
  • the DNA sequence was introduced to a pLUC vector (BD Biosciences, San Jose, CA, USA). After transfection in E. coli DH5 ⁇ and its culture thereof in a liquid medium (LB broth) containing ampicillin, the vector was isolated using a plasmid DNA prep kit (Qiagen, Hilden, Germany). The DNA sequence was identified by sequencing and the resultant vector was named as pHSR3.
  • a 1.5 kb DNA containing neomycin resistance gene ORF, SV40 early promoter, origin and polyA signal was produced by PCR using pcDNA3.1 plasmid (Invitrogen, Carlsbad, CA, USA) as template, and introduced into pHSR3 after BamHI single digestion. After transfection in E. coli DH5 ⁇ and its culture thereof, a new plasmid vector pHSR3-neo was obtained. To prepare an established cell line therefrom, HeLa cells were transfected with lipofectamine (Invitrogen) when they were grown in a Petri dish to 60% to 80% confluent growth.
  • lipofectamine Invitrogen
  • the cells were diluted along with the medium. After transferring to a new Petri dish, the medium was replaced by a medium containing G418. The cells were observed for 3 weeks, while exchanging the medium once in two days. Colonies exhibiting resistance to G418 were observed. The formed colonies were covered with a colony isolator, treated with trypsin and transferred to a 96-well plate, one per each. The cells were cultured using a medium containing G418 for 2 months, gradually transferring to a 24-well plate, to a 6-well plate, and finally to a Petri dish. Each prepared cell line was treated with each compound and was cultured in a CO2 incubator. 24 hours later, luciferase activity was measured using a luciferase activity assay kit (BD Biosciences). The result is given in the following Table 1. [Table 1]
  • cardiac myocytes were isolated from the heart of a newborn rat and then cultured. Experiment was carried out as follows. The ventricular portion was taken from the heart and the red blood cells were removed in PBS (Dulbecco's phosphate-buffered saline solution) (pH 7.4, Gibco BRL). Using micro-dissecting scissors, the heart was minced in 10 mL of collagenase I (0.8 mg/mL, 262 units/ mg, Gibco BRL) solution until the pieces were approximately 1 mm 3 and treated at 37 0 C for 15 minutes.
  • PBS Dulbecco's phosphate-buffered saline solution
  • the supernatant (collagenase I solution) was collected and the remaining tissues were treated with fresh collagenase I solution and left alone at 37 0 C for 15 minutes.
  • the collected supernatant was diluted in ⁇ -MEM (Gibco BRL) containing 10% FBS (fetal bovine serum).
  • FBS fetal bovine serum
  • the diluted supernatant was centrifuged at 1200 rpm, for 4 minutes at room temperature.
  • the precipitated cell pellets were resuspended in ⁇ -MEM medium containing 5 mL of 10% FBS.
  • the above procedure was repeated for about 10 to 15 times until the tissue morphology was changed.
  • the suspended cells were collected and cultured in a 100 mm tissue culture dish for 2 hours at 37 0 C.
  • the cells not adhering to the tissue culture dish were collected again and cultured after being distributed to a 96-well plate at IxIO 4 cells/ well. After culturing for 4 to 6 hours and washing twice with culture medium, 0.1 ⁇ M bromodeoxyuridine (BrdU) was added thereto. The cells were cultured at 37 0 C in a
  • MTT bromide solution 3-(4,5-dimethylthiazol-2- yl)-2,5-diphenyltetrazolium bromide solution (Sigma, St. Louis, MO) was added to each well until the final concentration was 0.5 mg/mL. Then, it was cultured at 37 0 C for 2 hours so as the MTT reaction to occur. The formazan crystal produced in each well was dissolved by adding dimethyl sulfoxide (DMSO) and absorbance was measured at 570 nm using a spectrophotometer. The result is given in the following Table 2. [Table 2]
  • Example 3 Evaluation of effect of myocardial protection through control of calcium homeostasis The level of cytosolic free Ca 2+ was measured by confocal microscopic analysis. Cardiac myocytes of newborn white rats were cultured for 24 hours in a 4- well plate (IxIO 5 cells/ well) coated with 1.5% gelatin, using 10% FBS ⁇ -MEM containing 0.1 ⁇ M BrdU. 24 hours later, the cells were washed twice with serum-free medium, and treated at room temperature with fluo-4 with a final concentration of 2 ⁇ M along with 500 ⁇ L of medium per well. Then, after treating in a 37 0 C incubator for 20 minutes, the cells were washed with PBS and covered with a cover slide after adding PBS to prevent them from drying.
  • Fluorescence images were taken from the light emitted through a 510 to 560 nm bandpass filter, upon activated at 488 nm by argon laser. The relative change of free intracellular Ca 2+ was determined based on the fluorescence intensity. The result is shown in FIG. 1.
  • Example 4 Evaluation of heart protecting effect In order to find out how the test compounds protect the heart from ischemia, anti-ischemic effects were investigated in white rats as follows.
  • mice Male white rats (300 to 450 g, Orient, Seoul, Korea) were anesthetized by injecting sodium pentobarbital (100 mg/kg) intra-abdominally. After intravenous injection of heparin (1000 U/ kg), the heart was collected by ablation. Specifically, a cannula (PE 240) was inserted and artificial respiration was performed using a rodent ventilator. Under that condition, an aortic cannula was inserted in the aorta and the heart was ablated under retrograde perfusion. The extracted heart was hung on Langendorff apparatus quickly and unnecessary tissues on the heart were removed.
  • PE 240 a cannula
  • the left ventricular pressure transmitted through the balloon was transduced by using a pressure transducer, and amplified by using an isovolumetric amplifier (Plugsys bridge amplifier). Then, the pressure was recorded in a recorder (Linearcorder mark 8 WR 3500). Thereafter, the heart was stabilized for 15 minutes. Then, left ventricular end-diastolic pressure (LVEDP) was given by 5 mmHg and such volume of the balloon was kept through the experiments.
  • LVEDP left ventricular end-diastolic pressure
  • LVSP left ventricular peak systolic pressure
  • LVEDP left ventricular end diastolic pressure
  • LVDP left ventricular developed pressure
  • Double product RPP rate-pressure product
  • Total coronary blood flow was measured by the use of a coronary flow probe (diameter: 1.0 mm) installed in the aortic cannula with an electromagnetic flowmeter.
  • Example 5 Activity analysis in an ischemic animal model under ligation of distal left anterior descending coronary artery
  • Myocardial infarction was induced in white rats through ligation of the distal left anterior descending coronary artery.
  • a cannula was inserted into an 8-week-old male Sprague Dawley rat (weighing about 250 g) anesthetized with ketamine (1 mL/rat).
  • Positive pressure circulation 180 mL/min was maintained using a
  • lactone type pyridine derivative represented by Chemical Formula 1 according to the present invention showed excellent HSP expression controlling and cardiac myocyte protecting activities, excellent myocardial protection activity through control of intracellular calcium homeostasis,

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Abstract

The present invention relates to a pharmaceutical composition comprising a lactone type pyridine derivative for the prevention and treatment of ischemic diseases, more particularly to a pharmaceutical composition for preventing and treating ischemic diseases comprising a lactone type pyridine derivative or a pharmaceutically acceptable salt thereof as an active ingredient, which provides superior cell-protecting effect and calcium homeostasis and HSP (heat shock protein) expression controlling effect.

Description

[DESCRIPTION] [Invention Title]
A PHARMACEUTICAL COMPOSITIONS CONTAINING LACTON TYPE PYRIDINE DERIVATIVES AS AN EFFECTIVE INGREDIENT FOR THE PREVENTION AND TREATMENT OF ISCHEMIA
[Technical Field]
The present invention relates to a pharmaceutical composition comprising a lactone type pyridine derivative effective in treating ischemic diseases.
[Background Art]
Ischemic diseases including ischemic stroke and ischemic heart disease are caused by ischemia, which refers to the decrease in blood supply below a threshold value caused by the blocking of the cerebral artery or the coronary artery due to thrombosis or arteriosclerosis. As a result, brain and heart cells are damaged and die, resulting in brain infarction and myocardial infarction.
Thus, drugs that prevent the damage of cells caused by ischemia or facilitate regeneration thereof can be an ultimate treatment for ischemic brain disease or heart disease. Ischemic heart diseases and cerebrovascular diseases, represented by myocardial infarction and stroke, are the first cause of death inside and outside Korea.
The drugs currently used for preventing and treating ischemic diseases include beta blockers, nitrates, calcium channel blockers, etc., which prevent the outbreak of ischemic diseases by reducing oxygen demand in the ischemic area or sustain a therapeutic effect after the outbreak, thrombolytic agents, antithrombotic agents, anti-platelet agents, etc., which are used for reperfusion to the ischemic area after the ischemic outbreak, and the like.
Because these drugs are not satisfactory either in efficiency or safety, there has been a continued need for the development of new drugs for the treatment of ischemic disease with new mechanisms.
Recent studies on ischemic diseases focus on the development of a drug that can prevent or treat damaged cells and tissues following ischemia better than clotblusters or coagulation inhibitors, which are problematic in safety and acceptability.
At present, efforts are made with respect to the drugs that can protect death of cardiac myocytes from ischemia and reperfusion by acting on the Na+/ H+- exchanger (NHE-I) and the K+-channel, which may be administered in combination with various ischemic drugs in order to inhibit the damage of cells and tissues in the ischemic area. With regard to stroke, developments of neuron-protecting agents that act on NMDA receptors, glycine receptors, and the like are carried out actively.
As heat shock proteins (HSP), adenosine receptor Al, etc., are known as possible targets in inhibiting cell death, researches on the above have been carried out recently. The present invention is directed to the control of homeostasis of calcium, which is excessively released from the cytoplasm under ischemic condition and leads to cell death. HSP plays an important role in the control of calcium homeostasis. It is known that calcium is excessively released under ischemic condition. Also, the level of expression of HSP increases under ischemic condition to provide cell-protecting effect. According to a recent report, the excessive release of calcium induces the expression of the HSP27 protein, and the increased expression of HSP70 suppresses the excessive release of calcium. Therefore, it is probable that the exploration of a drug based on the relationship between calcium homeostasis and HSP expression may lead to the development of an ischemic disease treatment of new-concept.
However, there are few reports about the substance for treating ischemic disease, which provides cell-protecting effect through controlling the intracellular expression and action of HSP under ischemic condition, controlling calcium homeostasis and improving cell viability. The inventors of the present invention found out that the lactone type pyridine derivatives (Korean Patent Publication Nos. 2005-69910, 2006-70945 and 2006-110764; Korean Patent Application No. 2005-127801) synthesized by them have an excellent effect of preventing and treating ischemic diseases through control of HSP expression and calcium homeostasis.
[Disclosure]
Therefore, an object of the present invention is to provide a new medicinal use of the lactone type pyridine derivatives disclosed in Korean Patent Publication Nos. 2005-69910, 2006-70945 and 2006-110764 and Korean Patent Application No. 2005-127801 and pharmaceutically acceptable salts thereof for preventing and treating ischemic diseases.
[Description of Drawings] The above and other objects, features and other advantages of the present invention will be more clearly understood from the following detailed description taken in conjunction with the accompanying drawings, in which:
FIG. 1 shows the confocal microscopic images for evaluating myocardial protecting effect through control of intracellular calcium homeostasis in Example 3;
FIG. 2 and FIG. 3 show the photographs illustrating the change of the thickness of ventricular walls in an ischemic animal model in which rats underwent ligation of the distal left anterior descending coronary artery (Example 5) through TTC staining; and FIG. 4 shows the photographs illustrating the change of the thickness of ventricular walls in an ischemic animal model in which rats underwent ligation of the distal left anterior descending coronary artery (Example 5) through H&E staining.
[Best Mode]
The present invention is characterized by a pharmaceutical composition for treating and preventing ischemic disease comprising a lactone type pyridine derivative represented by the following Chemical Formula 1 or a pharmaceutically acceptable salt thereof or a drug prepared therefrom: [Chemical Formula 1 ]
Figure imgf000005_0001
miLjmmm represents a single or double bond; X is an oxygen or sulfur atom; and each of R1, R2, R3, R4/ R5, Re and R7 is independently selected from hydrogen, halo, cyano, nitro, C2-C7 acyl, hydroxy, amino, C1-CO alkyl, C3-C9 cycloalkyl, C2-C6 alkenyl, C1-C6 alkoxy, C1-C6 alkoxyalkyl, C1-C6 alkylthio, C1-C6 alkylamino, C1-C6 alkoxyalkylamino, Q-C9 cycloalkylamino, C4-C9 heterocycloalkylamino, aryl Ci-C6 alkylamino, arylamino, heteroaryl Ci-C6 alkylamino, C2-C7 acylamino, saturated heterocycle, C2-C7 acyloxy, Ci-C6 alkylsulfinyl, Ci-C6 alkylsulfonyl, Ci-C6 alkylsulfonylamino, arylsulfinyl, arylsulfonyl, arylsulfonylamino, aryl, heteroaryl, aryl Ci-C6 alkyl, heteroaryl Ci-C6 alkyl, aryloxy and heteroaryl oxy, or each of them may form a ring by bonding with a neighboring substituent, wherein the aryl is selected from phenyl, naphthyl and fused phenyl; and each of the saturated heterocycle, aryl and heteroaryl may be substituted with 1 to 4 substituents selected from halo, hydroxy, Ci-C6 alkyl, Ci-C6 alkoxy, Ci-C6 haloalkyl, Ci-C6 hydroxyalkyl, aryl C2-C6 alkenyl, aryl C2-C6 acyl, amino, Ci-C6 alkylamino, aryl Ci-C6 alkylamino, heteroaryl, aminocarbonyl, C1-C6 alkoxycarbonyl, cyano, nitro, carbonyl and carboxyl; and each of the heteroaryl and saturated heterocycle may be a pentagonal or hexagonal heterocyclic ring or a fused heterocyclic ring containing 1 to 3 hetero atoms selected from oxygen, nitrogen and sulfur.
Preferably, in the lactone type pyridine derivative represented by Chemical Formula 1,
X is an oxygen or sulfur atom; and each of Ri, R2, R3, R4, Rs, Rδ, and R7 is independently selected from hydrogen, halo, hydroxy, amino, C2-C7 acyl, Q-C7 acyloxy, Ci-C6 alkyl, C2-C6 alkenyl, Ci-C6 alkoxy, Ci-C6 alkoxyalkyl, C3-C9 cycloalkyl, aryl Ci-C6 alkyl, heteroaryl Ci-C6 alkyl, saturated heterocyclo Ci-C6 alkyl, mono(Ci-C6 alkyl)amino, di(Ci-C6 alkyl)amino, C4-C9 cycloalkylamino, C1-C6 alkoxyalkylamino, C4-C9 heterocycloalkylamino, aryl Ci-C6 alkylamino, heteroaryl Ci-C6 alkylamino, arylamino, C2-C7 acylamino, Ci-C6 alkylsulfonylamino, arylsulfonylami.no, aryl, aryloxy, heteroaryl and saturated heterocycle, or each of them may form a phenyl ring by bonding with a neighboring substituent, wherein the saturated heterocycle may be substituted with 1 to 4 substituents selected from Ci-Q alkyl, C1-C6 alkoxy, Ci-C6 alkoxycarbonyl, aryl, aryl C2-C6 alkyl, aryl C2-C6 alkenyl, aryl C2-C6 acyl, amino, aminocarbonyl, Ci-C6 alkoxycarbonyl and heteroaryl; each of the aryl and heteroaryl may be substituted with 1 to 4 substituents selected from halo, hydroxy, Ci-C6 alkyl, Ci-C6 alkoxy, Ci-C6 haloalkyl,
Ci-C6 hydroxyalkyl, amino, mono(Ci-C6 alkyl)amino, di(Ci-Q alkyl)amino and aryl
Ci-C6 alkylamino; the aryl is phenyl; and each of the saturated heterocycle and heteroaryl is selected from furan, tetrahydrofuran, pyrrolidine, pyridine, morpholine, oxolane, benzodioxolane, thiophene, thiomorpholine, dioxothiomorpholine, piperidine and piperazine.
Specific examples of the lactone type pyridine derivative represented by Chemical Formula 1 according to the present invention include:
Compound 1. acetic acid l-oxo-6-phenyl-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester, Compound 2. 6-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 3. 6-methyl-8-phenethylamino-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 4. 6-methyl-8-phenylamino-3,4-dihydro-pyrano[3,4-c]pyridine-l- one, Compound 5. 6-methyl-8-(4-trifluoromethyl-phenylamino)-3,4-dihydro- pyrano[3,4-c]pyridine-l-one,
Compound 6. δ-chloro-ό-propyl-S^-dihydro-pyranoP^-cJpyridine-l-one,
Compound 7. 8-hydroxy-6-isopropyl-3,4-dihydro-pyrano [3,4-c] py ridine-1 - one,
Compound 8. 6-chloro-8-propyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 9. 8-[(benzo[l,3]dioxol-5-ylmethyl)-amino]-6-methyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 10. 8-methylamino-6-phenyl-3,4-dihydro-pyrano [3,4-c] pyridine- 1-one,
Compound 11. 8-dimethylamino-6-phenyl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 12. 8-(4-fluoro-phenylamino)-6-phenyl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one, Compound 13. 6-phenyl-8-pyrrolidine-l-yl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 14. 6-phenyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 15. 8-morpholine-4-yl-6-phenyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 16. acetic acid 6-cyclohexyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 17. 8-amino-6-cy clohexy 1-3,4-dihy dr o-py r ano [3,4-c] py ridine-1 - one, Compound 18. 6-ethyl-8-hydroxy-3,4-dihydro-pyrano [3,4-c] py ridine-1 -one, Compound 19. 6-cyclohexyl-8-(4-methoxy-benzylamino)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one,
Compound 20. 6-cyclohexyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 21. 6-chloro-8-cyclohexyl-3,4-dihydro-pyrano[3,4-c]pyridine-l- one,
Compound 22. δ-chloro-ό-ethyl-S/l-dihydro-pyranoP^-clpyridine-l-one,
Compound 23. 6-ethyl-8-(4-methoxy-benzylamino)-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 24. 8-amino-6-ethyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 25. acetic acid 6-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 26. 6-isopropyl-8-piperidine-l-yl~3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 27. 6-isopropyl-8-(4-methoxy-benzylamino)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 28. 8-amino-6-isopropyl-3,4-dihydro-pyrano [3,4-c] pyridine-1 -one,
Compound 29. 8-chloro-6-isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 30. 8-amino-6-propyl-3,4-dihydro-py rano [3,4-c] pyridine-1 -one, Compound 31. 8-morpholine-4-yl-6-propyl-3,4-dihydro-pyrano[3,4- c] pyridine-1 -one,
Compound 32. acetic acid l-oxo-6~thiophene-2-yl-3,4-dihydro-lH- py r ano [3,4-c] py ridine-8-y 1 ester,
Compound 33. 6-ethyl-8-piperidine-l-yl-3,4-dihydro-py rano [3,4-c] pyridine- 1-one, Compound 34. 3-phenyl-3,4-dihydro-pyrano [3,4-c] py ridine-1 -one, Compound 35. 3,4-dihydro-2-oxa-9-aza-phenanthrene-l-one, Compound 36. 6,8-dimethyl-3,4-dihydro-pyrano [3,4-c] py ridine-1 -one, Compound 37. 8-benzylamino-6-methy 1-3,4-dihy dro-pyrano [3,4-c] py ridine- 1-one,
Compound 38. 8-chloro-6-methy l-5-phenyl-3,4-dihy dro-pyrano [3,4- c] py ridine-1 -one,
Compound 39. 8-hydroxy-6-methyl-5-phenyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 40. 8-f uran-2-yl-6-methy 1-3,4-dihy dro-pyrano [3,4-c] pyridine-1- one,
Compound 41. 3,4-dihy dro-pyrano [3,4-c] py ridine-1 -one, Compound 42. 6-methyl-3,4-dihydro-pyrano[3,4-c]py ridine-1 -one, Compound 43. 8-methy 1-6-pheny 1-3,4-dihy dro-pyrano [3,4-c] py ridine-1 -one, Compound 44. 8-chloro-6-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 45. 8-methoxy-6-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 46. 8-chlor o-6-methy 1-3,4-dihy dro-pyrano [3,4-c] py ridine-1 -one, Compound 47. acetic acid 6-methyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester, Compound 48. 6-methyl-8-pheny 1-3,4-dihy dro-pyrano [3,4-c] py ridine-1 -one,
Compound 49. 6-methyl-8-phenoxy-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 50. 3,4-dihy dro-pyrano [3,4-c] py ridine-1 -thione, Compound 51. 6-methyl-5-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 52. 8-(4-fluoro-phenylamino)-6-methyl-3,4-dihy dro-pyrano [3,4- c]py ridine-1 -one, Compound 53. 6-chloro-8-methyl-3,4-dihydro-py rano [3,4-c] pyr idine-1 -one,
Compound 54. 8-amino-6-methy 1-3,4-dihy dr o-py rano [3,4-c] py r idine-1 -one,
Compound 55. 6~methyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one, Compound 56. 6-methyl-8-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 57. 6-methyl-8-(4-methyl-piperazine-l-yl)-3,4-dihydro- py rano [3,4-c] pyridine-1-one,
Compound 58. 8-(4-chloro-phenylamino)-6-methyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 59. 6-methyl-8-p-tolylamino-3,4-dihydro-py rano [3,4-c] pyridine- 1-one,
Compound 60. 6-methyl-8-thiophene-2-yl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one, Compound 61. 6~methyl-8-pyridine-2-yl-3,4-dihydro-py rano [3,4-c] pyridine-
1-one,
Compound 62. 6-furan-2-yl-8-methy 1-3,4-dihy dr o-py rano [3,4-c] pyridine-1- one,
Compound 63. 8-methy l-6-thiophene-2-yl-3,4-dihydro-py rano [3,4- c]pyridine-l-one,
Compound 64. 6-benzo[l,3]dioxol-5-yl-8-methyl-3,4-dihydro-pyrano[3,4- c] pyridine-1-one,
Compound 65. 6-(4-dimethylamino-phenyl)-8-methyl-3,4-dihydro- py rano [3,4-c] py ridine-1 -one, Compound 66. acetic acid l-oxo-6-propyl-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 67. N-(6-methyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine~8- yl)-acetamide, Compound 68. N-(6-methyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-benzamide,
Compound 69. 8-amino-6-phenyl-3/4-dihydro-pyrano[3/4-c]pyridine-l-one,
Compound 70. 8-(4-methoxy-benzylamino)-6-phenyl-3,4-dihydro- py rano [3,4-c] py r idine-1 -one, Compound 71. N-(l-oxo-6-pheny 1-3,4-dihy dro-lH-pyrano [3,4-c] pyridine-8- yl)-acetamide,
Compound 72. N-(l-oxo-6-phenyl-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-benzamide,
Compound 73. 8-chlor o-6-cy clohexy 1-3,4-dihy dr o-py r ano [3,4-c] py r idine-1 - one,
Compound 74. acetic acid 6-ethyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 75. 8-f uran-2-yl-6-pheny 1-3,4-dihy dr o-py rano [3,4-c] py ridine-1 - one, Compound 76. 6-phenyl-8-thiophene-2-yl-3,4-dihydro-pyrano [3,4-c] pyridine-
1-one,
Compound 77. 8-(4-f luoro-pheny l)-6-pheny 1-3,4-dihy dro-py rano [3,4- c] py ridine-1 -one,
Compound 78. 8-(4-fluoro-pheny l)-6-isopr opy 1-3,4-dihy dro-py rano [3,4- c]pyridine-l-one, Compound 79. 6-chloro-8-isopropy 1-3,4-dihy dr o-py r ano [3,4-c] pyridine-1-one,
Compound 80. 8-isopropyl-6-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 81. 8-isopropyl-6-(4-methoxy-benzylamino)-3,4-dihydro- pyrano [3,4-c] pyridine-1-one,
Compound 82. 6-chloro-8-cyclohexyl-3,4-dihydro-pyrano[3,4-c]pyridine-l- one,
Compound 83. 8-cy clohexyl-6-piperidine~l-y 1-3,4-dihy dro-pyrano [3,4- c] py ridine-1 -one, Compound 84. 8-cyclohexy l-6-morpholine-4-y 1-3,4-dihy dro-pyrano [3,4- c] pyridine-1-one,
Compound 85. 8-cyclohexyl-6-(4-methoxy-benzylamino)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 86. 8-pr opy 1-6-py rr olidine-1 -y 1-3,4-dihy dr o-py r ano [3,4- c] py ridine-1 -one,
Compound 87. 6-piperidine-l-yl-8-propyl-3,4-dihydro-pyrano[3,4- c] pyridine-1-one,
Compound 88. 6-morpholine-4-yl-8-propyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 89. 6-amino-8-propyl-3,4-dihydro-pyrano [3,4-c] pyridine-1-one,
Compound 90. 6-(4-methoxy-benzylamino)-8-propyl-3,4-dihydro- pyrano [3,4-c] pyridine-1-one,
Compound 91. 6-hydroxy-8-propy 1-3,4-dihy dr o-py r ano [3,4-c] pyridine-1-one,
Compound 92. 4-(2-hydroxy-ethyl)-6-methoxy-2-propyl-nicotinonitrile, Compound 93. 6-amino-8-isopropyl-3,4-dihydro-pyrano [3,4-c] pyridine-1-one, Compound 94. ό-amino-δ-cyclohexyl-S^-dihydro-pyranoP/i-clpyridine-l- one,
Compound 95. 4-fluoro-N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-6-yl)-benzenesulfonamide, Compound 96. 4-chloro-N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-6-yl)-benzenesulfonamide,
Compound 97. N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 6-yl)-benzenesulfonamide,
Compound 98. N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 6-y l)-4-methoxy-benzenesulf onamide,
Compound 99. N-(8-isoρropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 6-yl)-4-methyl-benzenesulfonamide,
Compound 100. δ-vinyl-S/l-dihydro-pyranop^-clpyridine-l-one,
Compound 101. 8-[4-(2-hydroxy-ethyl)-piperazine-l-yl]-6-isopropyl-3/4- dihy dr o-py r ano [3,4-c] py ridine-1 -one,
Compound 102. 8-(4-benzyl-piperazine-l-yl)-6-isopropyl-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 103. 6-isopropyl-8-(4-phenyl-piperazine-l-yl)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one, Compound 104. 8-[4-(2-ethoxy-phenyl)-piperazine-l-yl]-6-isopropyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 105. 8-[4-(2-chloro-phenyl)-piperazine-l-yl]-6-isopropyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 106. 6-isopropyl-8-(4-pyridine-2-yl-piperazine-l-yl)-3,4-dihydro- pyrano [3,4-c] py ridine-1 -one, Compound 107. 6-isopropyl-8-(4-methyl~piperazine-l-yl)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one,
Compound 108. 6-isopropyl-8-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 109. 6-isopropyl-8-pyrrolidine-l-yl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 110. 6-isopropyl-8-(methyl-phenethyl-amino)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 111. 8-(4-benzyl-piperidine-l-yl)-6-isopropyl-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 112. l-(6-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 8-yl)-piperidine-3-carboxylic acid amide,
Compound 113. 6-isopropyl-8-thiomorpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 114. 6-fer£-butyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 115. 8-(l,l-dioxo-lλ6-thiomorpholine-4-yl)-6-isopropyl-3,4- dihy dr o-py rano [3,4-c] py ridine-1 -one,
Compound 116. 6-fert-butyl-8-chloro-3,4-dihydr o-py rano [3,4-c] py ridine-1 - one,
Compound 117. 6-methoxy-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 118. 6-chloro-8-ethyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 119. 8-ethyl-6-(4-methoxy-benzylamino)-3,4-dihydro-pyrano[3,4- c]py ridine-1 -one, Compound 120. 6-amino-8-ethy 1-3,4-dihy dr o-py rano [3,4-c] py r idine-1 -one,
Compound 121. N-(8-ethyl-l-oxo-3,4-dihydro-lH-pyrano [3,4-c] pyridine-6- yl)-4-fluoro-benzenesulfonamide,
Compound 122. N-(8-ethyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-6- yl)-3-fluoro-benzenesulfonamide,
Compound 123. 6-(2-methoxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 124. 6-(2-hydroxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 125. 6-(4-methoxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 126. 6-(3-methoxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 127. 6-(3-hy droxy-phenyl)-8-methy 1-3,4-dihy dro-py rano [3,4- c] py ridine-1 -one,
Compound 128. 8-(4-hydroxy-3,5-dimethyl-phenyl)-6-methyl-3,4-dihy dro- py rano [3,4-c] py ridine-1 -one,
Compound 129. 6-(4-hydroxy-3,5-dimethyl-phenyl)-8-methyl-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one, Compound 130. 5-(4-hydroxy-3,5-dimethyl-phenyl)-6,8-dimethyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 131. 8-(2-methoxy-phenyl)-6-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 132. 8-(2-hy droxy-phenyl)-6-methyl-3,4-dihy dro-py rano [3,4- c]py ridine-1 -one, Compound 133. 8-(3-methoxy-phenyl)-6-methyl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 134. 8-(4-methoxy-phenyl)-6-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 135. 3-(3-methoxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 136. 3-(3-hydroxy-phenyl)-6,8-dimethyl-pyrano[3/4-c]pyridine-l- one,
Compound 137. 3-(4-methoxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 138. 3-(4-hydroxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 139. 3-(3,5-di-fer£-butyl-4-methoxy-phenyl)-6,8-dimethyl- py r ano [3,4-c] py ridine-1 -one, Compound 140. 3-(3-ter£-butyl-4-hydroxy-phenyl)-6,8-dimethyl-pyrano[3,4- c] py ridine-1 -one,
Compound 141. 6-(4-fluoro-phenylamino)-8-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 142. 6-(4-chloro-phenylamino)-8-methyl-3,4-dihy dro-pyrano [3,4- c]py ridine-1 -one,
Compound 143. 6-terf-butyl-8-thiomorpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 144. 6-terf-butyl-8-(l,l-dioxo-lλ6-thiomorpholine-4-yl)-3,4- dihydro-pyrano[3,4-c]pyridine-l-one, Compound 145. l-(6-fer£-butyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 8-yl)-piperidine-4-carboxylic acid ethyl ester,
Compound 146. 6-fer£-butyl-8-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 147. 6-fer£-butyl-8-(4-methyl-piperazine-l-yl)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one,
Compound 148. 6-terf-butyl-8-diethylamino-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 149. 6-ferf-butyl-8-dipropylamino-3,4-dihy dro-pyrano [3,4- c]pyridine-l-one,
Compound 150. 6-terf-butyl-8-dibutylamino-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 151. 8-[bis-(2-methoxy-ethyl)-amino]-6-tert-butyl-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one, Compound 152. 6-isopropyl-8-{4-[3-(2-methoxy-phenyl)-acryloyl]- piperazine-1 -y l}-3,4-dihy dr o-py rano [3,4-c] py ridine-1 -one,
Compound 153. 6-isopropyl-8-{4-[3-(4-methoxy-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 154. 8-{4-[3-(2,4-dimethoxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano [3,4-c] py ridine-1 -one,
Compound 155. 8-{4-[3-(3,4-dimethoxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 156. 8-{4-[3-(2-hydroxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 157. 8-{4-[3-(4-hydroxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 158. 6-isopropyl-8-{4-[3-(3-trifluoromethyl-phenyl)-acryloyl]- piperazine-1 -yl}-3,4-dihydr o-py rano [3,4-c] py r idine-1 -one, Compound 159. 6-fer£-butyl-8-{4-[3-(2-methoxy-phenyl)-acryloyl]-piperazine- l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 160. 6-fer£-butyl-8-{4-[3-(4-methoxy-phenyl)-acryloyl]-piperazine- l-yl}-3,4-dihy dro-py rano [3,4-c] pyridine-1-one,
Compound 161. 6-terf-butyl-8-{4-[3-(2,4-dimethoxy-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 162. 6-fer£-butyl-8-{4-[3-(3,4-dimethoxy-phenyl)-acryloyl]- piper azine-1 -y l}-3,4-dihy dr o-py rano [3,4-c] py ridine-1 -one,
Compound 163. 6-ter£-butyl-8-{4-[3-(2-hydroxy-phenyl)-acryloyl]-piperazine- 1 -y l}-3,4-dihy dr o-py rano [3,4-c] py ridine-1 -one, Compound 164. 6-fer£-butyl-8-{4-[3-(4-hydroxy-phenyl)-acryloyl]-piperazine- l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 165. 6-ferf-butyl-8-{4-[3-(3-trifluoromethyl-phenyl)-acryloyl]- piperazine-1 -y l}-3,4-dihy dr o-py rano [3,4-c] py ridine-1 -one,
Compound 166. 5,8-dimethyl-pyrano[2,3-c]pyridine-2-one, and Compound 167. 5,8-dimethyl-3,4-dihydro-pyrano[2,3-c]pyridine-2-one.
Further, the lactone type pyridine derivative represented by Chemical Formula 1 may form a pharmaceutically acceptable salt with an acid, for example, hydrochloric acid, bromic acid, sulfuric acid, phosphoric acid, methanesulfonic acid, acetic acid, citric acid, fumaric acid, lactic acid, maleic acid, succinic acid and tartaric acid. In addition, the lactone type pyridine derivative represented by Chemical Formula lmay form a pharmaceutically acceptable salt by reacting with an alkali metal ion such as sodium, potassium, etc., or an ammonium ion.
Further, the pharmaceutical composition of the present invention may comprise, in addition to the lactone type pyridine derivative as an active ingredient, a commonly used nontoxic pharmaceutically acceptable vehicle, adjuvant, excipient, or the like so as to be prepared into preparation forms for oral or parenteral administration common in the pharmaceutical field, for example, tablet, capsule, troche, liquid, suspension, etc. For oral administration, the composition may be prepared into tablet, capsule, solution, syrup, suspension, and the like. And, for parenteral administration, it may be prepared into abdominal, subcutaneous, intramuscular or transdermal injection form.
Further, the present invention encompasses a method for treating or preventing ischemic diseases comprising administering the compound represented by Chemical Formula 1 to a patient with a therapeutical dose capable of reducing cell death under ischemic condition.
As used in this description, the patient refers to a warm-blooded animal or mammal including human suffering from ischemic heart diseases and/ or ischemic cerebrovascular diseases represented by angina pectoris, myocardial infarction, stroke and cerebrovascular dementia. Treatment of a ischemic disease patient means protection of cells and reduction of cell death of the patient. Diagnosis of a patient with an ischemic disease is within the ability and knowledge of those skilled in the art. A clinical doctor skilled in the related art can easily diagnose the disease based on clinical trials, medical checkup, health examination, family history, and the like. The effective dose of the compound represented by Chemical Formula 1 can be easily determined based on the observation of results under similar conditions using common techniques. When determining the effective dose, various factors, including but not limited to, constitution, age and general health condition of the patient, degree or severity of the disease, response of the patient, the particular compound to be administered, mode of administration, bioavailability of the administered drug, selected route of administration and presence of jointly administered drug. A general dose for an adult patient whose body weight is 70 kg is 0.01 to 1000 mg/day. Based on the judgment of a doctor or a pharmacist, the dose may be administered once to several times a day at predetermined intervals. When treating a patient, the compound represented by Chemical Formula 1 may be administered by any mode or method, including oral and parenteral administration, that makes the compound biologically available at the effective dose. For example, the compound may be administered orally, subcutaneously, intramuscularly, intravenously, transdermally, intranasally or rectally. Particularly, oral administration is preferred. Those skilled in preparing medical preparations can easily select the adequate form and mode of administration, considering the severity of disease or other situations.
The compound of the present invention may be administered in the form of a pharmaceutical composition or drug, which is prepared by mixing with a pharmaceutically acceptable vehicle or excipient. The mixing ratio and kind of the vehicle or excipient are determined depending on the selected route of administration and in accordance with the general standard pharmaceutical guidance. The pharmaceutical composition or drug is prepared by the methods known to those skilled in the pharmaceutical industry. [Mode for Invention]
Therapeutic and preventive effects of the lactone type pyridine derivative represented by Chemical Formula 1 according to the present invention for ischemic diseases were identified. For specific methods of preparing the compounds represented by Chemical Formula 1 and drugs therefrom, refer to Korean Patent Publication Nos. 2005-69910, 2006-70945 and 2006-110764 and Korean Patent Application No. 2005-127801.
Example 1. Determination of HSP expression control
A 78-mer nucleotide sequence containing three repeating heat shock response elements (HSRE; GAANNTTC), an Nhel site at the 5' end of the DNA sequence and a BgIII site at the 3' end (see the sequence below) and its complementary sequence were prepared. A double helical DNA was prepared by heating at 80 °C for 5 minutes and then annealing at room temperature.
51-
GCCTCACGTTCAGCTAGCTAGAATGTTCTAGATCTAGAACATTCTAGCTAGAA TGTTCT AAGATCTGACATGCCTAGC-3
* The italics correspond to Nhel and BgIII sites, and the underlines correspond to the three repeating HSREs (GAANNTTC) .
After digesting the ends with Nhel and BgIII restriction enzymes, the DNA sequence was introduced to a pLUC vector (BD Biosciences, San Jose, CA, USA). After transfection in E. coli DH5α and its culture thereof in a liquid medium (LB broth) containing ampicillin, the vector was isolated using a plasmid DNA prep kit (Qiagen, Hilden, Germany). The DNA sequence was identified by sequencing and the resultant vector was named as pHSR3. In order to introduce a neomycin resistance gene to the pHSR3 vector, a 1.5 kb DNA containing neomycin resistance gene ORF, SV40 early promoter, origin and polyA signal was produced by PCR using pcDNA3.1 plasmid (Invitrogen, Carlsbad, CA, USA) as template, and introduced into pHSR3 after BamHI single digestion. After transfection in E. coli DH5α and its culture thereof, a new plasmid vector pHSR3-neo was obtained. To prepare an established cell line therefrom, HeLa cells were transfected with lipofectamine (Invitrogen) when they were grown in a Petri dish to 60% to 80% confluent growth. Twenty four hours later, the cells were diluted along with the medium. After transferring to a new Petri dish, the medium was replaced by a medium containing G418. The cells were observed for 3 weeks, while exchanging the medium once in two days. Colonies exhibiting resistance to G418 were observed. The formed colonies were covered with a colony isolator, treated with trypsin and transferred to a 96-well plate, one per each. The cells were cultured using a medium containing G418 for 2 months, gradually transferring to a 24-well plate, to a 6-well plate, and finally to a Petri dish. Each prepared cell line was treated with each compound and was cultured in a CO2 incubator. 24 hours later, luciferase activity was measured using a luciferase activity assay kit (BD Biosciences). The result is given in the following Table 1. [Table 1]
Figure imgf000023_0001
Figure imgf000024_0001
Figure imgf000025_0001
Figure imgf000026_0001
Figure imgf000027_0001
Example 2. Evaluation of protecting effect for primary cultured cardiac myocytes
In order evaluate the effect of protecting cardiac myocytes, cardiac myocytes were isolated from the heart of a newborn rat and then cultured. Experiment was carried out as follows. The ventricular portion was taken from the heart and the red blood cells were removed in PBS (Dulbecco's phosphate-buffered saline solution) (pH 7.4, Gibco BRL). Using micro-dissecting scissors, the heart was minced in 10 mL of collagenase I (0.8 mg/mL, 262 units/ mg, Gibco BRL) solution until the pieces were approximately 1 mm3 and treated at 37 0C for 15 minutes. The supernatant (collagenase I solution) was collected and the remaining tissues were treated with fresh collagenase I solution and left alone at 37 0C for 15 minutes. The collected supernatant was diluted in α-MEM (Gibco BRL) containing 10% FBS (fetal bovine serum). The diluted supernatant was centrifuged at 1200 rpm, for 4 minutes at room temperature. The precipitated cell pellets were resuspended in α-MEM medium containing 5 mL of 10% FBS.
The above procedure was repeated for about 10 to 15 times until the tissue morphology was changed. In order to reduce contamination of fibroblasts, the suspended cells were collected and cultured in a 100 mm tissue culture dish for 2 hours at 370C.
The cells not adhering to the tissue culture dish were collected again and cultured after being distributed to a 96-well plate at IxIO4 cells/ well. After culturing for 4 to 6 hours and washing twice with culture medium, 0.1 μM bromodeoxyuridine (BrdU) was added thereto. The cells were cultured at 37 0C in a
5% CO2 incubator.
After culturing overnight in a 96-well plate, the cells were put in an airtight humidified chamber containing 5% CO2, 5% H2 and 85% N2 (anaerobic system,
Technomart INC, Seoul, Korea). After washing twice with deaerated serum-free α- MEM and adding the test compound, 200 μL of the medium was added thereto and hypoxia condition was maintained for 12 hours at 370C.
Twelve hours later, the medium was removed and 3-(4,5-dimethylthiazol-2- yl)-2,5-diphenyltetrazolium bromide solution (MTT bromide solution) (Sigma, St. Louis, MO) was added to each well until the final concentration was 0.5 mg/mL. Then, it was cultured at 37 0C for 2 hours so as the MTT reaction to occur. The formazan crystal produced in each well was dissolved by adding dimethyl sulfoxide (DMSO) and absorbance was measured at 570 nm using a spectrophotometer. The result is given in the following Table 2. [Table 2]
Figure imgf000029_0001
Figure imgf000030_0001
Figure imgf000031_0001
Example 3. Evaluation of effect of myocardial protection through control of calcium homeostasis The level of cytosolic free Ca2+ was measured by confocal microscopic analysis. Cardiac myocytes of newborn white rats were cultured for 24 hours in a 4- well plate (IxIO5 cells/ well) coated with 1.5% gelatin, using 10% FBS α-MEM containing 0.1 μM BrdU. 24 hours later, the cells were washed twice with serum-free medium, and treated at room temperature with fluo-4 with a final concentration of 2 μM along with 500 μL of medium per well. Then, after treating in a 37 0C incubator for 20 minutes, the cells were washed with PBS and covered with a cover slide after adding PBS to prevent them from drying. Fluorescence images were taken from the light emitted through a 510 to 560 nm bandpass filter, upon activated at 488 nm by argon laser. The relative change of free intracellular Ca2+ was determined based on the fluorescence intensity. The result is shown in FIG. 1.
Example 4. Evaluation of heart protecting effect In order to find out how the test compounds protect the heart from ischemia, anti-ischemic effects were investigated in white rats as follows.
Male white rats (300 to 450 g, Orient, Seoul, Korea) were anesthetized by injecting sodium pentobarbital (100 mg/kg) intra-abdominally. After intravenous injection of heparin (1000 U/ kg), the heart was collected by ablation. Specifically, a cannula (PE 240) was inserted and artificial respiration was performed using a rodent ventilator. Under that condition, an aortic cannula was inserted in the aorta and the heart was ablated under retrograde perfusion. The extracted heart was hung on Langendorff apparatus quickly and unnecessary tissues on the heart were removed. Perfusion was induced under static pressure (85 mmHg) with 37 0C modified Krebs-Henseleit bicarbonate buffer [composition (mM/L): 116 NaCl, 4.7 KCl, 1.1 MgSO4, 1.17 KH2PO4, 24.9 NaHCO3, 2.52 CaCl2, 8.32 glucose, 2.0 pyruvate] saturated with 95% O2 /5% CO2. A metal cannula to which a latex balloon filled with an ethanol-distilled water mixture (1:1 vol/vol) was linked, was inserted in the left ventricle through the pulmonary vein. Then, the left ventricular pressure transmitted through the balloon was transduced by using a pressure transducer, and amplified by using an isovolumetric amplifier (Plugsys bridge amplifier). Then, the pressure was recorded in a recorder (Linearcorder mark 8 WR 3500). Thereafter, the heart was stabilized for 15 minutes. Then, left ventricular end-diastolic pressure (LVEDP) was given by 5 mmHg and such volume of the balloon was kept through the experiments.
Baseline cardiac contractile function, heart rate (HR) and coronary flow (CF) were measured. Cardiac contractile function was calculated by subtracting left ventricular peak systolic pressure (LVSP) from left ventricular end diastolic pressure (LVEDP), yielding left ventricular developed pressure (LVDP). Double product RPP (rate-pressure product), another important parameter for indirectly assessing cardiac performance in Langendorff heart, in which cardiac output could not be measured ordinarily, was calculated by multiplying HR by LVDP. Total coronary blood flow was measured by the use of a coronary flow probe (diameter: 1.0 mm) installed in the aortic cannula with an electromagnetic flowmeter. Temperature of the heart was steadily maintained throughout the experiment by immersing the heart at 37 0C in physiological saline solution to which 95% O2 /5% CO2 was constantly supplied. After stabilization, the heart was perfused for 10 minutes with vehicle (0.04% DMSO) only or a test compound with a specific concentration or the control material in the vehicle. Thereafter, cardiac contractile function, HR, and CF were measured again. Global ischemia was induced by completely shutting off the perfusate for 30 minutes. Severity of ischemia was determined as the time to contracture (TTC, min) during global ischemia in which the first 5 mmHg increase in LVEDP was observed. Then, the heart was perfused and, 30 minutes later, contractile functions (LVDP, HR and CF) were measured again. After reperfusion was accomplished for 30 minutes, the concentration of lactate dehydrogenase (LDH) in the reperfusate was measured with a kit as a sensitive index for ischemic myocardial damage. The result is given in the following Table 3. [Table 3]
Figure imgf000034_0001
Example 5. Activity analysis in an ischemic animal model under ligation of distal left anterior descending coronary artery
Myocardial infarction was induced in white rats through ligation of the distal left anterior descending coronary artery. A cannula was inserted into an 8-week-old male Sprague Dawley rat (weighing about 250 g) anesthetized with ketamine (1 mL/rat). Positive pressure circulation (180 mL/min) was maintained using a
Harvard ventilator with indoor air containing oxygen (2 L/min). About 2 cm of the left side of the heart of the rat was cut open. After ligating the left anterior descending artery with 7-0 silk suture, the rat was bred for 3 days under normal conditions. The test compound was injected abdominally immediately after the ligation of the left anterior descending artery, and for 3 days, once a day, at a dose of
10 mg/kg. The compound had been dissolved in water for injection containing 5%
DMSO and 2% Tween-20 and heated at 70 0C before the injection. Effect of the compound under ischemic condition could be identified from the color change of the cardiac muscle 3 days after the treatment. To this end, TTC (triphenyltetrazolium chloride) staining was carried out. H&E staining was carried out in order to measure the change of the ventricular wall thickness. As a result, it was identified that the test compounds of the present invention resulted in reduced infarction area as compared to the control material. The result is shown in FIG. 2 through FIG. 4.
[Industrial Applicability]
As explained hereinbefore, the lactone type pyridine derivative represented by Chemical Formula 1 according to the present invention showed excellent HSP expression controlling and cardiac myocyte protecting activities, excellent myocardial protection activity through control of intracellular calcium homeostasis,

Claims

and good result in an ischemic animal model under ligation of the distal left anterior descending coronary artery.Accordingly, the lactone type pyridine derivative represented by Chemical Formula 1 is useful in preventing and treating ischemic diseases, specifically ischemic heart diseases and ischemic cerebrovascular diseases represented by angina pectoris, myocardial infarction, stroke and cerebrovascular dementia.Although the preferred embodiments of the present invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying drawings. [CLAIMS] [Claim 1] A pharmaceutical composition for treating and preventing ischemic disease comprising a lactone type pyridine derivative represented by the following Chemical Formula 1 or a pharmaceutically acceptable salt thereof:
[Chemical Formula 1]
Figure imgf000036_0001
wherein w__i_' represents a single or double bond; X is an oxygen or sulfur atom; and each of R1, R2, R3, R4, R5, RO and R7 is independently selected from hydrogen, halo, cyano, nitro, C2-C7 acyl, hydroxy, amino, C1-C6 alkyl, C3-C9 cycloalkyl, C2-C6 alkenyl, C1-C6 alkoxy, C1-C6 alkoxyalkyl, C1-C6 alkylthio, C1-C6 alkylamino, C1-C6 alkoxyalkylamino, C4-C9 cycloalkylamino, C4-C9 heterocycloalkylamino, aryl C1-C6 alkylamino, arylamino, heteroaryl C1-C6 alkylamino, C2-C7 acylamino, saturated heterocycle, C2-C7 acyloxy, C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C1-C6 alkylsulfonylamino, arylsulfinyl, arylsulfonyl, arylsulfonylamino, aryl, heteroaryl, aryl C1-C6 alkyl, heteroaryl C1-C6 alkyl, aryloxy and heteroaryloxy, or each of them may form a ring by bonding with a neighboring substituent, wherein the aryl is selected from phenyl, naphthyl and fused phenyl; and each of the saturated heterocycle, aryl and heteroaryl may be substituted with 1 to 4 substituents selected from halo, hydroxy, C1-C6 alkyl, Ci-C6 alkoxy, Ci-C6 haloalkyl, C1-C6 hydroxyalkyl, aryl C2-C6 alkenyl, aryl C2-C6 acyl, amino, C1-C6 alkylamino, aryl C1-C6 alkylamino, heteroaryl, aminocarbonyl, C1-C6 alkoxycarbonyl, cyano, nitro, carbonyl and carboxyl; and each of the heteroaryl and saturated heterocycle may be a pentagonal or hexagonal heterocyclic ring or a fused heterocyclic ring containing 1 to 3 hetero atoms selected from oxygen, nitrogen and sulfur.
[Claim 2] The pharmaceutical composition as set forth in claim 1, wherein
X is an oxygen or sulfur atom; and each of Ri, R2, R3, R4, R5, R6, and R7 is independently selected from hydrogen, halo, hydroxy, amino, C2-C7 acyl, C2-C7 acyloxy, Ci-C6 alkyl, C2-C6 alkenyl, Ci-C6 alkoxy, C1-C6 alkoxyalkyl, C3-C9 cycloalkyl, aryl C1-C6 alkyl, heteroaryl C1-C6 alkyl, saturated heterocyclo C1-C6 alkyl, InOnO(C1-C6 alkyl)amino, di(Ci-C6 alkyl)amino, C4-C9 cycloalkylamino, C1-C6 alkoxyalkylamino, C4-C9 heterocycloalkylamino, aryl C1-C6 alkylamino, heteroaryl C1-C6 alkylamino, arylamino, C2-C7 acylamino, C1-C6 alkylsulfonylamino, arylsulfonylamino, aryl, aryloxy, heteroaryl and saturated heterocycle, or each of them may form a phenyl ring by bonding with a neighboring substituent, wherein the saturated heterocycle may be substituted with 1 to 4 substituents selected from C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkoxycarbonyl, aryl, aryl C2-C6 alkyl, aryl C2-C6 alkenyl, aryl C2-C6 acyl, amino, aminocarbonyl, C1-C6 alkoxycarbonyl and heteroaryl; each of the aryl and heteroaryl may be substituted with 1 to 4 substituents selected from halo, hydroxy, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, amino, mono(C1-C6 alkyl)amino, di(Gι-C6 alkyl)amino and aryl C1-C6 alkylamino; the aryl is phenyl; and each of the saturated heterocycle and heteroaryl is selected from furan, tetrahydrofuran, pyrrolidine, pyridine, morpholine, oxolane, benzodioxolane, thiophene, thiomorpholine, dioxothiomorpholine, piperidine and piperazine.
[Claim 3]
The pharmaceutical composition as set forth in claim 1, wherein the lactone type pyridine derivative represented by Chemical Formula 1 comprises:
Compound 1. acetic acid l-oxo-6-phenyl-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 2. 6-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 3. 6-methyl-8-phenethylamino-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 4. 6-memyl-8-phenylamino-3,4-dihydro-pyrano[3,4-c]pyridine-l- one,
Compound 5. 6-methyl-8-(4-trifluoromemyl-pheny lamino)-3,4-dihy dro- py rano [3,4-c] py ridine-1 -one, Compound 6. 8-chloro-6-propyl-3,4-dihydro-pyrano [3,4-c] py ridine-1 -one,
Compound 7. 8-hydroxy-6-isopropyl-3,4-dihydro-py rano [3,4-c] py ridine-1 - one,
Compound 8. 6-chloro-8-propyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 9. 8-[(benzo[l,3]dioxol-5-ylmethyl)-amino]-6-methyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 10. 8-methylamino-6-phenyl-3,4-dihydro-pyrano [3,4-c] pyridine- 1-one,
Compound 11. 8-dimethylamino-6-phenyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 12. 8-(4-fluoro-phenylamino)-6-phenyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 13. 6-phenyl-8-pyrrolidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 14. 6-phenyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 15. 8-morpholine-4-yl-6-phenyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 16. acetic acid 6-cyclohexyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester, Compound 17. δ-amino-ό-cyclohexyl-S^-dihydro-pyranoβ^-clpyridine-l- one,
Compound 18. ό-ethyl-δ-hydroxy-S^-dihydro-pyranoβ^-clpyridine-l-one,
Compound 19. 6-cyclohexyl-8-(4-methoxy-benzylamino)-3,4-dihydro- pyrano [3,4-c] pyridine-l -one,
Compound 20. ό-cyclohexyl-δ-piperidine-l -yl-3,4-dihy dro-py rano [3,4- c] py r idine-1 -one,
Compound 21. 6-chloro-8-cyclohexyl-3,4-dihydro-pyrano[3,4-c]pyridine-l- one, Compound 22. S-chloro-ό-ethyl-S^-dihydro-pyranoβ^-cjpyridine-l-one,
Compound 23. 6-ethyl-8-(4-methoxy-benzylamino)-3/4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 24. δ-amino-ό-ethyl-S^-dihydro-pyranoP^-clpyridine-l-one,
Compound 25. acetic acid 6-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 26. 6-isopropyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 27. 6-isopropyl-8-(4-methoxy-benzylamino)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one, Compound 28. 8-amino-6-isopropyl-3,4-dihydro-pyrano [3,4-c] py ridine-1 -one,
Compound 29. 8-chloro-6-isopropyl-3,4-dihydro-pyrano [3,4-c] pyridine-1 -one,
Compound 30. 8-amino-6-pr opy 1-3,4-dihy dro-py rano [3,4-c] pyridine-1 -one,
Compound 31. 8-morpholine-4-yl-6-propyl-3,4-dihydro-pyrano[3,4- c] pyridine-1 -one, Compound 32. acetic acid l-oxo-6-thiophene-2-yl-3,4-dihydro~lH- py r ano [3,4-c] py ridine-8-y 1 ester,
Compound 33. 6-ethyl-8-piperidine-l-yl-3/4-dihydro-pyrano [3,4-c] pyridine-
1-one, Compound 34. 3-phenyl-3,4~dihydro-pyrano [3,4-c] pyridine-1 -one,
Compound 35. 3,4-dihydro-2-oxa-9-aza-phenanthrene-l-one, Compound 36. 6,8-dimethyl-3,4-dihydro-pyrano [3,4-c] pyridine-1 -one, Compound 37. 8-benzylamino-6-methyl-3,4-dihy dro-pyrano [3,4-c] pyridine-
1-one, Compound 38. 8-chloro-6-methyl-5-phenyl-3,4-dihydro-pyrano[3,4- c] pyridine-1 -one,
Compound 39. 8-hy droxy-6-methyl-5-phenyl-3,4-dihy dro-pyrano [3,4- c] pyridine-1 -one,
Compound 40. 8-f ur an-2-y 1-6-methy 1-3,4-dihy dro-pyrano [3,4-c] pyridine-1 - one,
Compound 41. 3,4-dihydro-pyrano [3,4-c] pyridine-1 -one, Compound 42. 6-methy 1-3,4-dihy dro-pyrano [3,4-c] pyridine-1-one, Compound 43. 8-methyl-6-pheny 1-3,4-dihy dro-pyrano [3,4-c] pyridine-1 -one, Compound 44. 8-chloro-6-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 45. 8-methoxy-6-phenyl-3,4-dihydro-pyrano [3,4-c] pyridine-1 -one,
Compound 46. 8-chloro-6-methyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 47. acetic acid 6-methyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]py ridine-8-y 1 ester,
Compound 48. 6-methyl-8-phenyl-3,4-dihy dro-pyrano [3,4-c] pyridine-1 -one, Compound 49. 6-methyl-8-phenoxy-3,4-dihydro-pyrano [3,4-c] pyridine-1 -one, Compound 50. 3,4-dihy dro-py rano [3,4-c] py ridine-1 -thione,
Compound 51. 6-methy 1-5-pheny 1-3,4-dihy dro-py r ano [3,4-c] py ridine-1 -one,
Compound 52. 8-(4-fluoro-phenylamino)-6-methyl-3/4-dihy dro-py rano [3,4- c) py ridine-1 -one, Compound 53. 6-chloro-8-methyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 54. 8-amino-6-methyl-3,4-dihydro-pyrano[3,4-c]py ridine-1 -one,
Compound 55. 6-methyl-8-piperidine-l -yl-3,4-dihy dro-py rano [3,4- c] py ridine-1 -one,
Compound 56. 6-methyl-8-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 57. 6-methyl-8-(4-methyl-piperazine-l-yl)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one,
Compound 58. 8-(4-chloro-phenylamino)-6-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 59. 6-methyl-8-p-tolylamino-3,4-dihydro-pyrano [3,4-c] pyridine-
1-one,
Compound 60. 6-methy l-8-thiophene-2-yl-3,4-dihydro-pyrano [3,4- c] py ridine-1 -one,
Compound 61. 6-methy l-8-pyridine-2-yl-3,4-dihy dro-py rano [3,4-c] pyridine- 1-one,
Compound 62. 6-furan-2-yl-8-methyl-3,4-dihy dro-py rano [3,4-c] py ridine-1 - one,
Compound 63. 8-methyl-6-thiophene-2-yl-3,4-dihydro-pyrano[3,4- c] pyridine-1-one, Compound 64. 6-benzo[l,3]dioxol-5-yl-8~methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 65. 6-(4~dimethylamino-phenyl)-8-methyl-3,4-dihydro- pyrano [3,4-c] pyridine-1-one, Compound 66. acetic acid l-oxo-6-propyl-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 67. N-(6-methyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-acetamide,
Compound 68. N-(6-methyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-benzamide,
Compound 69. 8-amino-6-phenyl-3,4-dihydro-pyrano [3,4-c] pyridine-1-one,
Compound 70. 8-(4-methoxy-benzylamino)-6-phenyl-3,4-dihydro- py rano [3,4-c] pyridine-1-one,
Compound 71. N-(l-oxo-6-phenyl-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-acetamide,
Compound 72. N-(l-oxo-6-phenyl-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-benzamide,
Compound 73. 8-chlor o-6-cy clohexy 1-3,4-dihy dr o-py r ano [3,4-c] py ridine-1 - one, Compound 74. acetic acid 6-ethyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 75. 8-furan-2-yl-6-pheny 1-3,4-dihy dr o-py rano [3,4-c] py ridine-1 - one,
Compound 76. 6-pheny l-8-thiophene-2-y 1-3,4-dihy dro-pyrano [3,4-c] py ridine- 1-one, Compound 77. 8-(4-f luoro-phenyl)-6-pheny 1-3,4-dihy dro-pyrano [3,4- c] py ridine-1 -one,
Compound 78. 8-(4-fluoro-phenyl)-6-isopropyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 79. 6-chloro-8-isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 80. 8-isopr opy 1-6-piperidine-l -y 1-3,4-dihy dro-pyrano [3,4- c]pyridine-l-one,
Compound 81. 8-isopropyl-6-(4-methoxy-benzylamino)-3,4-dihy dro- pyrano [3,4-c] py ridine-1 -one, Compound 82. 6-chloro-8-cyclohexyl-3,4-dihydro-pyrano[3,4-c]pyridine-l- one,
Compound 83. δ-cyclohexyl-β-piperidine-l -y 1-3,4-dihy dro-pyrano [3,4- c] py ridine-1 -one,
Compound 84. 8-cyclohexyl~6-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 85. 8-cyclohexyl-6-(4-methoxy-benzylamino)-3,4-dihy dro- pyrano [3,4-c] py ridine-1 -one,
Compound 86. 8-propyl-6-pyrrolidine-l-yl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 87. 6-piperidine-l-yl-8-propyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 88. 6-morpholine-4-yl-8-propyl-3,4-dihydro-pyrano[3,4- c] py ridine-1-one,
Compound 89. 6-amino-8-propyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 90. 6-(4-methoxy-benzylamino)-8-propyl-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 91. 6-hydroxy-8-propyl-3/4-dihydro-pyrano[3/4-c]pyridine-l-one,
Compound 92. 4-(2-hydroxy-ethyl)-6-methoxy-2-propyl-nicotinonitrile, Compound 93. 6-amino-8-isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 94. 6-amino-8-cy clohexy 1-3,4-dihy dro-py rano [3,4-c] py ridine-1 - one,
Compound 95. 4-fluoro-N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-6-yl)-benzenesulfonamide, Compound 96. 4-chloro-N-(8~isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-6-yl)-benzenesulfonamide,
Compound 97. N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 6-yl)-benzenesulfonamide,
Compound 98. N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 6-yl)-4-methoxy-benzenesulf onamide,
Compound 99. N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 6-yl)-4-methyl-benzenesulfonamide,
Compound 100. 5-vinyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 101. 8-[4-(2-hydroxy-ethyl)-piperazine-l-yl]-6-isopropyl-3,4- dihy dro-py rano [3,4-c] py ridine-1 -one,
Compound 102. 8-(4-benzyl-piperazine-l-yl)-6-isopropyl-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 103. 6-isopropyl-8-(4-phenyl-piperazine-l-yl)-3,4-dihy dro- py rano [3,4-c] py r idine-1-one, Compound 104. 8-[4-(2-ethoxy-phenyl)-piperazine-l-yl]-6-isopropyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 105. 8-[4-(2-chloro-phenyl)-piperazine-l-yl]-6-isopropyl-3,4- dihy dr o-py rano [3,4-c] py ridine-1 -one, Compound 106. 6-isopropyl-8-(4-pyridine-2-yl-piperazine-l-yl)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 107. 6-isopropyl-8-(4-methyl-piperazine-l-yl)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one,
Compound 108. 6-isopropyl-8-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c]py ridine-1 -one,
Compound 109. 6-isopr opy 1-8-py rr olidine-1 -y 1-3,4-dihy dr o-py rano [3,4- c] py ridine-1 -one,
Compound 110. 6-isopropyl-8-(methyl-phenethyl-amino)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one, Compound 111. 8-(4-benzyl-piperidine-l-yl)-6-isopropy 1-3,4-dihy dro- pyrano[3,4-c]pyridine-l-one,
Compound 112. l-(6-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 8-yl)-piperidine-3-carboxylic acid amide,
Compound 113. 6-isopropyl-8-thiomorpholine-4-yl-3,4-dihydro-pyrano[3,4- c]py ridine-1 -one,
Compound 114. 6-tert-buty 1-8-piperidine-l -y 1-3,4-dihy dr o-py rano [3,4- c]pyridine-l-one,
Compound 115. 8-(l,l-dioxo-lλ6-thiomorpholine-4-yl)-6-isopropyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one, Compound 116. ό-fert-butyl-S-chloro-S^-dihydro-pyranoβ^-clpyridine-l- one,
Compound 117. 6-methoxy-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 118. ό-chloro-δ-ethyl-S^-dihydro-pyranoP^-clpyridine-l-one,
Compound 119. 8-ethyl-6-(4-methoxy-benzylamino)-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 120. 6-amino-δ-ethyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 121. N-(δ-ethyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-6- yl)-4-f luoro-benzenesulf onamide,
Compound 122. N-(δ-ethyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-6- yl)-3-fluoro-benzenesulfonamide,
Compound 123. 6-(2-methoxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 124. 6-(2-hydroxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 125. 6-(4-methoxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] pyridine-1-one,
Compound 126. 6-(3-methoxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] pyridine-1-one,
Compound 127. 6-(3-hydroxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 128. 8-(4-hydroxy-3,5-dimethyl-phenyl)-6-methyl-3,4-dihydro- pyrano [3,4-c] pyridine-1-one, Compound 129. 6-(4-hydroxy-3/5-dimethyl-phenyl)-8-methyl-3/4-dihydro- py rano [3,4-c] py r idine-1 -one,
Compound 130. 5-(4-hydroxy-3,5-dimethyl-phenyl)-6,8-dimethyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one, Compound 131. 8-(2-methoxy-phenyl)-6-methyl-3,4-dihydro-pyrano[3,4- cjpyridine-l-one,
Compound 132. 8-(2-hy droxy-phenyl)-6-methyl-3,4-dihy dro-py rano [3,4- c] py r idine-1 -one,
Compound 133. 8-(3-methoxy-phenyl)-6-methyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 134. 8-(4-methoxy-phenyl)-6-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 135. 3-(3-methoxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one, Compound 136. 3-(3-hydroxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 137. 3-(4-methoxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 138. 3-(4-hydroxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 139. 3-(3,5-di-terf-butyl-4-methoxy-phenyl)-6,8-dimethyl- py rano [3,4-c] py ridine-1 -one,
Compound 140. 3-(3-terf-butyl-4-hydroxy-phenyl)-6,8-dimethyl-pyrano[3,4- c] py ridine-1 -one, Compound 141. 6-(4-fluoro-phenylamino)-8-methyl-3,4-dihy dro-pyrano [3,4- c]pyridine-l-one,
Compound 142. 6-(4-chloro-phenylamino)-8-methyl-3,4-dihydro-pyrano[3/4- c] py ridine-1 -one, Compound 143. 6-fer£-butyl-8-thiomorpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 144. 6-terf-butyl-8-(l,l-dioxo-lλ6-thiomorpholine-4-yl)-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 145. l-(6-ter£-butyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 8-yl)-piperidine-4-carboxylic acid ethyl ester,
Compound 146. 6-fer£-butyl-8-morpholine-4-yl-3,4-dihy dro-pyrano [3,4- c] py ridine-1 -one,
Compound 147. 6-terf-butyl-8-(4-methyl-piperazine-l-yl)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one, Compound 148. 6-ferf-butyl-8-diethylamino-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 149. 6-ferf-butyl-8-dipropylamino-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 150. 6-fer£-butyl-8-dibutylamino-3,4-dihydro-pyrano[3,4- c]py ridine-1 -one,
Compound 151. 8-[bis-(2-methoxy-ethyl)-amino]-6-fer£-butyl-3,4-dihydro- pyrano[3,4-c]pyridine-l-one,
Compound 152. 6-isopropyl-8-{4-[3-(2-methoxy-phenyl)-acryloyl]- piper azine-1 -yl}-3,4-dihy dro-pyrano [3,4-c] py ridine-1 -one, Compound 153. 6-isopropyl-8-{4-[3-(4-methoxy-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 154. 8-{4-[3-(2,4-dimethoxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 155. 8-{4-[3-(3,4-dimethoxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopr opy 1-3,4-dihy dro-py rano [3,4-c] py ridine-1 -one,
Compound 156. 8-{4-[3-(2-hydroxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopr opy 1-3,4-dihy dro-py rano [3,4-c] py ridine-1 -one,
Compound 157. 8-{4-[3-(4-hydroxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 158. 6-isopropyl-8-{4-[3-(3-trifluoromethyl-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 159. 6-ferf-butyl-8-{4-[3-(2-methoxy-phenyl)-acryloyl]-piperazine- l-ylj-S^-dihydro-pyranoP^-cjpyridine-l-one, Compound 160. 6-ter£-butyl-8-{4-[3-(4-methoxy-phenyl)-acryloyl]-piperazine-
1 -y l}-3,4-dihy dro-py rano [3,4-c] py ridine-1 -one,
Compound 161. 6-ferf-butyl-8-{4-[3-(2,4-dimethoxy-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 162. 6-ferf-butyl-8-{4-[3-(3/4-dimethoxy-phenyl)-acryloyl]- piper azine-1 -yl}-3,4-dihy dro-py rano [3,4-c] py ridine-1 -one,
Compound 163. 6-fer£-butyl-8-{4-[3-(2-hydroxy-phenyl)-acryloyl]-piperazine- l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 164. 6-terf-butyl-8-{4-[3-(4-hydroxy-phenyl)-acryloyl]-piperazine- l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 165. 6-fer£-butyl-8-{4-[3-(3-trifluoromethyl-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 166. 5,8-dimethyl-pyrano[2,3-c]pyridine-2-one, Compound 167. 5,8-dimethyl-3,4-dihydro-pyrano[2,3-c]pyridine-2-one, or a pharmaceutically acceptable salt thereof.
[Claim 4]
A drug for preventing and treating ischemic diseases comprising a lactone type pyridine derivative represented by the Chemical Formula 1 or a pharmaceutically acceptable salt thereof: [Chemical Formula 1]
Figure imgf000051_0001
wherein
5JJ5MS represents a single or double bond; X is an oxygen or sulfur atom; and each of Ri, R2, R3, R4, Rs, RO and R7 is independently selected from hydrogen, halo, cyano, nitro, C2-Cz acyl, hydroxy, amino, Ci-C6 alkyl, C3-C9 cycloalkyl, C2-C6 alkenyl, Ci-C6 alkoxy, Ci-C6 alkoxyalkyl, Ci-C6 alkylthio, Ci-C6 alkylamino, Ci-C6 alkoxyalkylamino, C4-C9 cycloalkylamino, C4-C9 heterocycloalkylamino, aryl Ci-C6 alkylamino, arylamino, heteroaryl Ci-C6 alkylamino, C2-C7 acylamino, saturated heterocycle, C2-C7 acyloxy, Ci-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, Ci-C6 alkylsulfonylamino, arylsulfinyl, arylsulfonyl, arylsulfonylamino, aryl, heteroaryl, aryl C1-C6 alkyl, heteroaryl Q-C6 alkyl, aryloxy and heteroaryloxy, or each of them may form a ring by bonding with a neighboring substituent, wherein said aryl is selected from phenyl, naphthyl and fused phenyl; and each of said saturated heterocycle, aryl and heteroaryl may be substituted with 1 to 4 substituents selected from halo, hydroxy, Ci-C6 alkyl, Ci-C6 alkoxy, Ci-C6 haloalkyl,
Ci-C6 hydroxyalkyl, aryl C2-C6 alkenyl, aryl C2-C6 acyl, amino, Ci-C6 alkylamino, aryl Ci-C6 alkylamino, heteroaryl, aminocarbonyl, Ci-C6 alkoxycarbonyl, cyano, nitro, carbonyl and carboxyl; and each of said heteroaryl and saturated heterocycle may be a pentagonal or hexagonal heterocyclic ring or a fused heterocyclic ring containing 1 to 3 hetero atoms selected from oxygen, nitrogen and sulfur.
[Claim 5]
The drug as set forth in claim 4, wherein
X is an oxygen or sulfur atom; and each of Ri, R2, R3, R4, Rs, Re, and R7 is independently selected from hydrogen, halo, hydroxy, amino, C2-C7 acyl, C2-C7 acyloxy, Ci-C6 alkyl, C2-C6 alkenyl, Ci-C6 alkoxy, Ci-C6 alkoxyalkyl, C3-C9 cycloalkyl, aryl Ci-C6 alkyl, heteroaryl Ci-C6 alkyl, saturated heterocyclo Ci-C6 alkyl, mono(Ci-C6 alkyl)amino, di(Ci-C6 alkyl)amino, C4-C9 cycloalkylamino, Ci-C6 alkoxyalkylamino, C4-C9 heterocycloalkylamino, aryl Ci-C6 alkylamino, heteroaryl Ci-C6 alkylamino, arylamino, C2-Cz acylamino, Ci-C6 alkylsulfonylamino, arylsulfonylamino, aryl, aryloxy, heteroaryl and saturated heterocycle, or each of them may form a phenyl ring by bonding with a neighboring substituent, wherein said saturated heterocycle may be substituted with 1 to 4 substituents selected from Ci-C6 alkyl, Ci-C6 alkoxy, Ci-C6 alkoxycarbonyl, aryl, aryl
C2-C6 alkyl, aryl C2-C6 alkenyl, aryl C2-C6 acyl, amino, aminocarbonyl, Ci-C6 alkoxycarbonyl and heteroaryl; each of said aryl and heteroaryl may be substituted with 1 to 4 substituents selected from halo, hydroxy, Ci-C6 alkyl, Ci-C6 alkoxy, Ci-C6 haloalkyl, Ci-C6 hydroxyalkyl, amino, mono(Ci-C6 alkyl)amino, di(Ci-C6 alkyl)amino and aryl Ci-C6 alkylamino; said aryl is phenyl; and each of said saturated heterocycle and heteroaryl is selected from furan, tetrahydrofuran, pyrrolidine, pyridine, morpholine, oxolane, benzodioxolane, thiophene, thiomorpholine, dioxothiomorpholine, piperidine and piperazine.
[Claim 6]
The drug as set forth in claim 4, wherein the lactone type pyridine derivative represented by Chemical Formula 1 comprises: Compound 1. acetic acid l-oxo-6-phenyl-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 2. 6-phenyl-3,4~dihydro-pyrano[3,4-c]pyridine-l-one, Compound 3. 6-methyl-8-phenethylamino-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 4. 6-methyl-8-phenylamino-3,4-dihydro-pyrano [3,4-c] pyridine-1- one,
Compound 5. 6-methyl-8-(4-trifluoromethyl-phenylamino)-3,4-dihydro- pyrano [3,4-c] pyridine-1-one,
Compound 6. 8-chloro-6-propyl-3,4-dihydro-pyrano [3,4-c] pyridine-1 -one, Compound 7. 8-hydroxy-6-isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l- one,
Compound 8. 6-chloro-8-propyl-3,4-dihydro-pyrano[3,4-c]py ridine-1 -one,
Compound 9. 8-[benzo[l,3]dioxol-5-ylmethyl)-amino]-6-methyl-3,4-dihydro- pyrano[3,4-c]pyridine-l-one,
Compound 10. 8-methylamino-6-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine- 1-one,
Compound 11. 8-dimethylamino-6-phenyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 12. 8-(4-fluoro-phenylamino)-6-phenyl-3/4-dihydro-pyrano[3/4- c] py ridine-1 -one,
Compound 13. 6-phenyl-8-pyrrolidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 14. 6-phenyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 15. 8-morpholine-4-yl-6-phenyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 16. acetic acid 6-cyclohexyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester, Compound 17. 8-amino-6-cyclohexyl-3,4-dihydro-pyrano[3,4-c]py ridine-1 - one,
Compound 18. 6-ethyl-8-hydroxy-3,4-dihydro-pyrano[3,4-c]py ridine-1 -one,
Compound 19. 6-cyclohexyl-8-(4-methoxy-benzylamino)-3,4-dihydro- py r ano [3,4-c] py ridine-1-one, Compound 20. 6-cyclohexyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 21. 6-chloro-8-cyclohexyl-3,4-dihydro-pyrano[3,4-c]pyridine-l- one, Compound 22. 8-chloro-6-ethy 1-3,4-dihy dr o-py rano [3,4-c] py ridine-1 -one,
Compound 23. 6-ethyl-8-(4-methoxy-benzylamino)-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 24. 8-amino-6-ethy 1-3,4-dihy dr o-py rano [3,4-c] py ridine-1 -one,
Compound 25. acetic acid 6-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 26. 6-isopropyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 27. 6-isopropyl-8-(4-methoxy-benzylamino)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one, Compound 28. 8-amino-6-isopropy 1-3,4-dihy dr o-py rano [3,4-c] py ridine-1 -one,
Compound 29. 8-chloro-6-isopropy 1-3,4-dihy dr o-py rano [3,4-c] pyridine-1 -one,
Compound 30. 8-amino-6-propyl-3,4-dihydro-pyrano [3,4-c] pyridine-1 -one,
Compound 31. 8-morpholine-4-yl-6-propyl-3,4-dihydro-py rano [3,4- c] pyridine-1 -one, Compound 32. acetic acid l-oxo-6-thiophene-2-yl-3,4-dihydro-lH- py r ano [3,4-c] py ridine-8-y 1 ester,
Compound 33. 6-ethyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4-c]pyridine- 1-one,
Compound 34. 3-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 35. 3,4-dihydro-2-oxa-9-aza-phenanthrene-l-one, Compound 36. 6,8-dimethy 1-3,4-dihy dro-pyrano[3,4-c]pyridine~l -one, Compound 37. 8-benzylamino-6-methy 1-3,4-dihy dro-pyrano [3,4-c] py ridine-
1-one,
Compound 38. 8-chloro-6-methyl-5-phenyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 39. 8-hydroxy-6-methyl-5-phenyl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 40. 8-furan-2-yl-6-methy 1-3,4-dihy dro-pyrano [3,4-c]pyr idine-1 - one, Compound 41. 3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 42. 6-methyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 43. 8-methyl-6-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 44. 8-chloro-6-pheny 1-3,4-dihy dro-pyrano[3,4-c]pyr idine-1 -one, Compound 45. 8-methoxy-6-phenyl-3,4-dihydro-pyrano [3,4-c] pyr idine-1 -one, Compound 46. 8-chloro-6-methy 1-3,4-dihy dro-pyrano[3,4-c]pyridine-l -one,
Compound 47. acetic acid 6-methyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 48. 6-methyl-8-phenyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 49. 6-methyl-8-phenoxy-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 50. 3,4-dihydro-pyrano [3,4-c]pyr idine-1 -thione,
Compound 51. 6-methyl-5-pheny 1-3,4-dihy dro-pyrano[3,4-c]pyr idine-1 -one, Compound 52. 8-(4-f luoro-phenylamino)-6-methy 1-3,4-dihy dro-pyrano [3,4- c] py ridine-1 -one,
Compound 53. 6-chloro-8-methyl-3,4-dihydro-pyrano[3,4-c]py ridine-1 -one, Compound 54. 8-amino-6-methyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 55. 6-methyl-8-piperidine-l -y 1-3,4-dihy dro-pyrano [3,4- c] py r idine-1 -one,
Compound 56. 6-methyl-8-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 57. 6-methyl-8-(4-methyl-piperazine-l-yl)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 58. 8-(4-chloro-phenylamino)-6-methyl-3,4~dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 59. 6-methyl-8-p-tolylamino-3,4-dihy dro-pyrano [3,4-c] py ridine- 1-one,
Compound 60. 6-methyl-8-thiophene-2-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 61. 6-methy 1-8-py ridine-2-y 1-3,4-dihy dro-pyrano [3,4-c] py r idine- 1-one, Compound 62. 6-furan-2-yl-8-methy 1-3,4-dihy dro-pyrano [3,4-c] pyridine-1- one,
Compound 63. 8-methyl-6-thiophene-2-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 64. 6-benzo[l,3]dioxol-5-yl-8-methyl-3,4-dihydro-pyrano[3,4- c]py ridine-1 -one,
Compound 65. 6-(4-dimethylamino-phenyl)-8-methyl-3,4-dihydro- pyrano[3,4-c]pyridine-l-one,
Compound 66. acetic acid l-oxo-6-propyl-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester, Compound 67. N-(6-methyl~l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-acetamide,
Compound 68. N-(6-methyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-benzamide, Compound 69. 8-amino-6-phenyl-3,4-dihydro-pyrano [3,4-c] pyridine-1 -one,
Compound 70. 8-(4-methoxy-benzylamino)-6-phenyl-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 71. N-(l-oxo-6-phenyl-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-acetamide, Compound 72. N-(l-oxo-6-phenyl-3,4-dihydro-lH-pyrano[3,4-c]pyridine-8- yl)-benzamide,
Compound 73. 8-chloro-6-cyclohexyl-3,4-dihydro-pyrano[3,4-c]pyridine-l- one,
Compound 74. acetic acid 6-ethyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-8-yl ester,
Compound 75. 8-f uran-2-y 1-6-pheny 1-3,4-dihy dr o-py r ano [3,4-c] py ridine-1 - one,
Compound 76. 6-pheny l-8-thiophene-2-y 1-3,4-dihy dr o-py r ano [3,4-c] py r idine- 1-one, Compound 77. 8-(4-fluoro-pheny l)-6-pheny 1-3,4-dihy dro-pyrano [3,4- c] py ridine-1 -one,
Compound 78. 8-(4-fluoro-phenyl)-6-isopropyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 79. 6-chloro-8-isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 80. 8-isopropyl-6-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 81. 8-isopropyl-6-(4-methoxy-benzylamino)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one, Compound 82. 6-chloro-8-cyclohexyl-3,4-dihydro-pyrano[3,4-c]pyridine-l- one,
Compound 83. 8-cyclohexyl-6-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 84. 8-cyclohexy l-6-morpholine-4-yl-3,4-dihy dro-py rano [3,4- c]pyridine-l-one,
Compound 85. 8-cyclohexyl-6-(4-methoxy-benzylamino)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 86. 8-propyl-6-pyrrolidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 87. 6-piperidine-l-yl-8-propyl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 88. 6-morpholine-4-y l-8-propyl-3,4-dihy dro-py rano [3,4- c] py ridine-1 -one,
Compound 89. 6-amino-8-propyl-3,4-dihydro-pyrano [3,4-c] py ridine-1 -one, Compound 90. 6-(4-methoxy-benzylamino)-8-propyl-3,4-dihydro- pyrano [3,4-c] pyridine-1-one,
Compound 91. 6-hydroxy-8-propyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 92. 4-(2-hydroxy-ethyl)-6-methoxy-2-propyl-nicotinonitrile,
Compound 93. 6-amino-8-isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 94. 6-amino-8-cyclohexyl-3,4-dihydro-pyrano [3,4-c] pyridine-1- one,
Compound 95. 4-fluoro-N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-6-yl)-benzenesulfonamide, Compound 96. 4-chloro-N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4- c]pyridine-6-yl)-benzenesulfonamide,
Compound 97. N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 6-yl)-benzenesulfonamide,
Compound 98. N-(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano [3,4-c] pyridine- 6-y l)-4-methoxy-benzenesulf onamide,
Compound 99. N~(8-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 6-yl)-4-methyl-benzenesulfonamide,
Compound 100. S-vinyl-S^-dihydro-pyranoP^-cjpyridine-l-one,
Compound 101. 8-[4-(2-hy droxy-ethyl)-piperazine-l-yl]-6-isopropyl-3,4- dihydro-pyranoP^-clpyridine-l-one,
Compound 102. 8-(4-benzyl-piperazine-l-yl)-6-isopropyl-3,4-dihydro- py rano [3,4-c] py ridine-1 -one,
Compound 103. 6-isopropyl-8-(4-phenyl-piperazine-l-yl)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one, Compound 104. 8-[4-(2-ethoxy-phenyl)-piperazine-l-yl]-6-isoproρyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 105. 8-[4-(2-chloro-phenyl)-piperazine-l-yl]-6-isopropyl-3,4- dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 106. 6-isopropyl-8-(4-pyridine-2-yl-piperazine-l-yl)-3,4-dihydro- pyrano [3,4-c] py ridine-1 -one, Compound 107. 6-isopropyl-8-(4-methyl-piperazine-l-yl)-3,4-dihydro- pyrano[3,4-c]pyridine-l-one,
Compound 108. 6-isopropyl-8-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one, Compound 109. 6-isopropyl-8-pyrrolidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 110. 6-isopropyl-8-(methyl-phenethyl-amino)-3,4-dihydro- py rano [3,4-c] py ridine-1 -one,
Compound 111. 8-(4-benzyl-piperidine-l -yl)-6-isopropy 1-3,4-dihy dro- py rano [3,4-c] pyridine-1-one,
Compound 112. l-(6-isopropyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 8-yl)-piperidine-3-carboxylic acid amide,
Compound 113. 6-isopropyl-8-thiomorpholine-4-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one, Compound 114. 6-£er£-butyl-8-piperidine-l-yl-3,4-dihydro-pyrano[3,4- c] py ridine-1 -one,
Compound 115. 8-(l,l-dioxo-lλ6-thiomorpholine-4-yl)-6-isopropyl-3,4- dihy dr o-py rano [3,4-c] py ridine-1 -one,
Compound 116. 6-ferf-buty l-8-chloro-3,4-dihy dr o-py rano [3,4-c] py ridine-1 - one,
Compound 117. 6-methoxy-8-piperidine-l -y 1-3,4-dihy dr o-py rano [3,4- c] py ridine-1 -one,
Compound 118. 6-chloro-8-ethy 1-3,4-dihy dr o-py rano [3,4-c] pyridine-1-one,
Compound 119. 8-ethyl-6-(4-methoxy-benzylamino)-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 120. ό-amino-δ-ethyl-S^-dihydro-pyranoβ^-clpyridine-l-one,
Compound 121. N-(8-ethyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-6- yl)-4-fluoro-benzenesulfonamide,
Compound 122. N-(8-ethyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine-6- yl)-3-fluoro-benzenesulfonamide,
Compound 123. 6-(2-methoxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 124. 6-(2-hydroxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one, Compound 125. 6-(4-methoxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- c] py ridine-1-one,
Compound 126. 6-(3-methoxy-phenyl)-8-methyl-3/4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 127. 6-(3-hydroxy-phenyl)-8-methyl-3,4-dihydro-pyrano[3,4- clpyridine-1-one,
Compound 128. 8-(4-hydroxy-3/5-dimethyl-phenyl)-6-methyl-3/4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 129. 6-(4-hydroxy-3/5-dimethyl-phenyl)-8-methyl-3/4-dihydro- pyranop^-cjpyridine-l-one, Compound 130. 5-(4-hydroxy-3/5-dimethyl-phenyl)-6/8-dimethyl-3,4- dihydro-pyranoP^-cjpyridine-l-one,
Compound 131. 8-(2-methoxy-phenyl)-6-methyl-3,4-dihy dro-py rano [3,4- c] py ridine-1 -one,
Compound 132. 8-(2-hydroxy-phenyl)-6-methyl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 133. 8-(3-methoxy-phenyl)-6-methyl-3,4-dihydro-pyrano[3,4- c] py r idine-1 -one,
Compound 134. 8-(4-methoxy-phenyl)-6-methyl-3,4-dihydro-ρyrano[3,4- c] py r idine-1 -one, Compound 135. 3-(3-methoxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 136. 3-(3-hydroxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 137. 3-(4-methoxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 138. 3-(4-hydroxy-phenyl)-6,8-dimethyl-pyrano[3,4-c]pyridine-l- one,
Compound 139. 3-(3,5-di-ferf-butyl-4-methoxy-phenyl)-6,8-dimethyl- py r ano [3,4-c] py ridine-1 -one, Compound 140. 3-(3-fert-butyl-4-hydroxy-phenyl)-6,8-dimethyl-pyrano[3,4- c] py ridine-1 -one,
Compound 141. 6-(4-f luoro-phenylamino)-8-methyl-3,4-dihy dro-pyrano [3,4- c] py ridine-1 -one,
Compound 142. 6-(4-chloro-phenylamino)-8-methyl-3,4-dihy dro-pyrano [3,4- c]py ridine-1 -one,
Compound 143. 6-ter£-butyl-8-thiomorpholine-4-yl-3,4-dihydro-pyrano[3,4- c] pyridine-1-one,
Compound 144. 6-ferf-butyl-8-(l,l-dioxo-lλ6-thiomorpholine-4-yl)-3,4- dihydro-pyrano[3,4-c]pyridine-l-one, Compound 145. l-(6-ter£-butyl-l-oxo-3,4-dihydro-lH-pyrano[3,4-c]pyridine- 8-yl)-piperidine-4-carboxylic acid ethyl ester,
Compound 146. 6-fert-butyl-8-morpholine-4-yl-3,4-dihydro-pyrano[3,4- c]pyridine-l-one, Compound 147. 6-fer£-butyl-8-(4-methyl-piperazine-l-yl)-3,4-dihydro- py r ano [3,4-c] py ridine-1 -one,
Compound 148. 6-ferf-butyl-8-diethylamino-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 149. 6-fert-butyl-8-dipropylamino-3,4-dihydro-pyrano[3,4- c]py ridine-1 -one,
Compound 150. 6-ter£-butyl-8-dibutylamino-3,4-dihydro-pyrano[3,4- c]pyridine-l-one,
Compound 151. 8-[bis-(2-methoxy-ethyl)-amino]-6-£er£-butyl-3,4-dihydro- py rano [3,4-c] pyridine-1-one, Compound 152. 6-isopropyl-8-{4-[3-(2-methoxy-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 153. 6-isopropyl-8-{4-[3-(4-methoxy-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 154. 8-{4-[3-(2,4-dimethoxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 155. 8-{4-[3-(3,4-dimethoxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 156. 8-{4-[3-(2-hydroxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 157. 8-{4-[3-(4-hydroxy-phenyl)-acryloyl]-piperazine-l-yl}-6- isopropyl-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 158. 6-isopropyl-8-{4-[3-(3-trifluoromethyl-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one, Compound 159. 6-fer£-butyl-8-{4-[3-(2-methoxy-phenyl)-acryloyl]-piperazine- l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 160. 6-fer£-butyl-8-{4-[3-(4-methoxy-phenyl)-acryloyl]-piperazine- l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 161. 6-tert-butyl-8-{4-[3-(2,4-dimethoxy-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 162. 6-fert-butyl-8-{4-[3-(3,4-dimethoxy-phenyl)-acryloyl]- piperazine-l-yl}-3,4-dihydro-pyrano[3,4-c]pyridine-l-one,
Compound 163. 6-fer£-butyl-8-{4-[3-(2-hydroxy-phenyl)-acryloyl]-piperazine- 1 -y l}-3,4-dihy dro-py rano [3,4-c] py ridine-1 -one, Compound 164. 6-teri-butyl-8-{4-[3-(4-hydroxy-phenyl)-acryloyl]-piperazine- l-ylJ-S^-dihydro-pyranoP^-cJpyridine-l-one,
Compound 165. 6-ferf-butyl-8-{4-[3-(3-trifluoromethyl-phenyl)-acryloyl]- piperazine-1 -y l}-3,4-dihy dro-py rano [3,4-c] py ridine-1 -one,
Compound 166. 5,8-dimethyl-pyrano[2,3-c]pyridine-2-one, Compound 167. 5,8-dimethyl-3,4-dihydro-pyrano[2,3-c]pyridine-2-one, or a pharmaceutically acceptable salt thereof.
[Claim 7]
The drug as set forth in any of claims 4 to 6, wherein the ischemic diseases include ischemic heart diseases and ischemic cerebrovascular diseases.
[Claim 8]
The drug as set forth in any of claims 4 to 6, wherein the ischemic disease is angina pectoris.
[Claim 9]
The drug as set forth in any of claims 4 to 6, wherein the ischemic disease is myocardial infarction.
[Claim 10]
The drug as set forth in any of claims 4 to 6, wherein the ischemic disease is stroke.
[Claim 11] The drug as set forth in any of claims 4 to 6, wherein the ischemic disease is cerebrovascular dementia.
[Claim 12]
The drug as set forth in claim 7, which is prepared into a form suitable to be administered orally, subcutaneously, intramuscularly, intravenously, transdermally, intranasally or rectally.
[Claim 13]
The drug as set forth in claim 12, which is prepared in the form of a tablet, an ointment or an injection.
PCT/KR2008/002030 2007-04-10 2008-04-10 A pharmaceutical compositions containing lacton type pyridine derivatives as an effective ingredient for the prevention and treatment of ischemia WO2008123756A1 (en)

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WO2013112788A1 (en) 2012-01-26 2013-08-01 Ptc Therapeutics, Inc. Compounds for treating spinal muscular atrophy
WO2018136918A1 (en) 2017-01-23 2018-07-26 Cadent Therapeutics, Inc. Methods for the treatment of tremors by positive modulation of sk channels

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WO2000034244A1 (en) * 1998-12-04 2000-06-15 Bristol-Myers Squibb Company 3-substituted-4-arylquinolin-2-one derivatives as potassium channel modulators

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WO2013112788A1 (en) 2012-01-26 2013-08-01 Ptc Therapeutics, Inc. Compounds for treating spinal muscular atrophy
EP2809322A1 (en) * 2012-01-26 2014-12-10 PTC Therapeutics, Inc. Compounds for treating spinal muscular atrophy
JP2015511224A (en) * 2012-01-26 2015-04-16 ピーティーシー セラピューティクス， インコーポレイテッド Compounds for treating spinal muscular atrophy
EP2809322A4 (en) * 2012-01-26 2015-12-23 Ptc Therapeutics Inc COMPOUNDS FOR TREATING SPINAL AMYOTROPHY
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WO2018136918A1 (en) 2017-01-23 2018-07-26 Cadent Therapeutics, Inc. Methods for the treatment of tremors by positive modulation of sk channels

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