MX2009011076A - Agente terapeutico para glaucoma que contiene derivado de adenosina como ingrediente activo. - Google Patents
Agente terapeutico para glaucoma que contiene derivado de adenosina como ingrediente activo.Info
- Publication number
- MX2009011076A MX2009011076A MX2009011076A MX2009011076A MX2009011076A MX 2009011076 A MX2009011076 A MX 2009011076A MX 2009011076 A MX2009011076 A MX 2009011076A MX 2009011076 A MX2009011076 A MX 2009011076A MX 2009011076 A MX2009011076 A MX 2009011076A
- Authority
- MX
- Mexico
- Prior art keywords
- group
- therapeutic agent
- cycloalkyl
- glaucoma
- hydrogen atom
- Prior art date
Links
- 208000010412 Glaucoma Diseases 0.000 title abstract 3
- 239000003814 drug Substances 0.000 title abstract 3
- 229940124597 therapeutic agent Drugs 0.000 title abstract 3
- 239000004480 active ingredient Substances 0.000 title 1
- 150000003835 adenosine derivatives Chemical class 0.000 title 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 230000004410 intraocular pressure Effects 0.000 abstract 2
- 206010030043 Ocular hypertension Diseases 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 230000003449 preventive effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/167—Purine radicals with ribosyl as the saccharide radical
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Ophthalmology & Optometry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
Se pretende investigar un agente terapéutico para glaucoma. Un compuesto representado por la siguiente fórmula general (1) o una sal del mismo muestra un excelente efecto de disminución de presión intraocular en una prueba para reducción de presión intraocular y es útil como un agente preventivo o terapéutico para glaucoma o hipertensión ocular (ver fórmula 1) en la fórmula, X representa CH o N; R1 representa un átomo de hidrógeno, un grupo hidroxi, un átomo de halógeno, un grupo alquilo, un grupo alcoxi, un grupo cicloalquilo, un grupo cicloalcoxi, un grupo (cicloalquil)metoxi o (ver fórmula) R2 representa un átomo de hidrógeno, un grupo alquilo, un grupo cicloalquilo, un grupo alquilcarbonilo o un grupo alquiloxicarbonilo; Ra y Rb son iguales o diferentes y representan un átomo de hidrógeno, un grupo hidroxi, un átomo de halógeno, un grupo alquilo, un grupo alcoxi, un grupo cicloalquilo o un grupo cicloalcoxi.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007106915A JP2008266143A (ja) | 2007-04-16 | 2007-04-16 | アデノシン誘導体を有効成分として含有する緑内障治療剤 |
PCT/US2008/004770 WO2008130520A1 (en) | 2007-04-16 | 2008-04-14 | Therapeutic agent for glaucoma containing adenosine derivative as active ingredient |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009011076A true MX2009011076A (es) | 2010-01-20 |
Family
ID=39875791
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009011076A MX2009011076A (es) | 2007-04-16 | 2008-04-14 | Agente terapeutico para glaucoma que contiene derivado de adenosina como ingrediente activo. |
Country Status (15)
Country | Link |
---|---|
US (2) | US20100093770A1 (es) |
EP (1) | EP2134174A4 (es) |
JP (2) | JP2008266143A (es) |
KR (1) | KR20090128495A (es) |
CN (1) | CN101677544A (es) |
AU (1) | AU2008241496A1 (es) |
BR (1) | BRPI0809953A2 (es) |
CA (1) | CA2684866A1 (es) |
EA (1) | EA015971B1 (es) |
IL (1) | IL201418A0 (es) |
MX (1) | MX2009011076A (es) |
NZ (1) | NZ580165A (es) |
UA (1) | UA100376C2 (es) |
WO (1) | WO2008130520A1 (es) |
ZA (1) | ZA200906989B (es) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7985754B2 (en) * | 2006-07-17 | 2011-07-26 | Trovis Pharmaceuticals, Llc | Selective antagonists of A2A adenosine receptors |
ME02608B (me) | 2010-01-11 | 2017-06-20 | Inotek Pharmaceuticals Corp | Kombinacija, komplet i postupak snižavanja intraokularnog pritiska |
CN102822188A (zh) * | 2010-03-26 | 2012-12-12 | 伊诺泰克制药公司 | 腺苷化合物及其用途 |
PH12012501906A1 (en) | 2010-03-26 | 2013-01-14 | Inotek Pharmaceuticals Corp | Method of reducing intraocular pressure in humans using n6 -cyclopentyladenosine (cpa), cpa derivatives or prodrugs thereof |
US20120058983A1 (en) | 2010-09-02 | 2012-03-08 | Bayer Pharma Aktiengesellschaft | Adenosine A1 agonists for the treatment of glaucoma and ocular hypertension |
WO2012108489A1 (ja) * | 2011-02-10 | 2012-08-16 | 参天製薬株式会社 | 親水性薬物の薬物移行性を改善した水性組成物 |
DK2807178T3 (en) | 2012-01-26 | 2017-09-04 | Inotek Pharmaceuticals Corp | Anhydrous polymorphs of (2R, 3S, 4R, 5R) -5- (6- (cyclopentylamino) -9H-purin-9-yl) -3,4-dihydroxytetrahydrofuran-2-yl) methyl nitrate and processes for their preparation |
HK1214951A1 (zh) | 2013-03-15 | 2016-08-12 | Inotek Pharmaceuticals Corporation | 眼用製劑 |
WO2017137528A1 (en) | 2016-02-12 | 2017-08-17 | Charité - Universitätsmedizin Berlin | Adenosine a1 receptor agonist for use in treatment of status epilepticus |
KR102007640B1 (ko) | 2017-11-29 | 2019-08-07 | 퓨쳐메디신 주식회사 | 아데노신 유도체를 포함하는 망막 질환 또는 시신경 질환 예방 및 치료용 약학적 조성물 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7378400B2 (en) * | 1999-02-01 | 2008-05-27 | University Of Virginia Patent Foundation | Method to reduce an inflammatory response from arthritis |
US7427606B2 (en) * | 1999-02-01 | 2008-09-23 | University Of Virginia Patent Foundation | Method to reduce inflammatory response in transplanted tissue |
US6322771B1 (en) * | 1999-06-18 | 2001-11-27 | University Of Virginia Patent Foundation | Induction of pharmacological stress with adenosine receptor agonists |
NZ545787A (en) * | 2001-10-01 | 2007-12-21 | Univ Virginia | 2-Propynyl adenosine analogs having A2A agonist activity and compositions thereof |
US20050058696A1 (en) * | 2003-09-12 | 2005-03-17 | Allergan, Inc. | Methods and compositions for the treatment of pain and other alpha 2 adrenergic-mediated conditions |
EP1663311A2 (en) * | 2003-09-12 | 2006-06-07 | Allergan, Inc. | Methods and compositions for the treatment of pain and other alpha 2 adrenergic-mediated conditions |
NZ585697A (en) * | 2004-08-02 | 2011-12-22 | Univ Virginia Patent Found | 2-propynyl adenosine analogs with modified 5'-ribose groups having A2A agonist activity |
US7368439B2 (en) * | 2005-06-15 | 2008-05-06 | Bar - Ilan University | Dinucleoside poly(borano)phosphate derivatives and uses thereof |
WO2008133129A1 (ja) * | 2007-04-16 | 2008-11-06 | Santen Pharmaceutical Co., Ltd. | アデノシンa2a受容体アゴニストを有効成分として含有する緑内障治療剤 |
-
2007
- 2007-04-16 JP JP2007106915A patent/JP2008266143A/ja active Pending
-
2008
- 2008-04-14 KR KR1020097021669A patent/KR20090128495A/ko not_active Withdrawn
- 2008-04-14 BR BRPI0809953-7A patent/BRPI0809953A2/pt not_active IP Right Cessation
- 2008-04-14 MX MX2009011076A patent/MX2009011076A/es not_active Application Discontinuation
- 2008-04-14 US US12/450,832 patent/US20100093770A1/en not_active Abandoned
- 2008-04-14 CN CN200880012153A patent/CN101677544A/zh active Pending
- 2008-04-14 EA EA200901402A patent/EA015971B1/ru not_active IP Right Cessation
- 2008-04-14 EP EP08742830A patent/EP2134174A4/en not_active Withdrawn
- 2008-04-14 CA CA002684866A patent/CA2684866A1/en not_active Abandoned
- 2008-04-14 UA UAA200911727A patent/UA100376C2/ru unknown
- 2008-04-14 WO PCT/US2008/004770 patent/WO2008130520A1/en active Application Filing
- 2008-04-14 JP JP2010504057A patent/JP4923141B2/ja not_active Expired - Fee Related
- 2008-04-14 AU AU2008241496A patent/AU2008241496A1/en not_active Abandoned
- 2008-04-14 NZ NZ580165A patent/NZ580165A/en not_active IP Right Cessation
-
2009
- 2009-10-07 ZA ZA200906989A patent/ZA200906989B/xx unknown
- 2009-10-11 IL IL201418A patent/IL201418A0/en unknown
-
2012
- 2012-12-20 US US13/722,100 patent/US20130109646A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
BRPI0809953A2 (pt) | 2014-09-23 |
JP2008266143A (ja) | 2008-11-06 |
IL201418A0 (en) | 2010-06-16 |
JP2010524933A (ja) | 2010-07-22 |
CN101677544A (zh) | 2010-03-24 |
KR20090128495A (ko) | 2009-12-15 |
WO2008130520A1 (en) | 2008-10-30 |
ZA200906989B (en) | 2010-06-30 |
UA100376C2 (en) | 2012-12-25 |
EP2134174A4 (en) | 2011-05-25 |
EA015971B1 (ru) | 2012-01-30 |
CA2684866A1 (en) | 2008-10-30 |
US20100093770A1 (en) | 2010-04-15 |
AU2008241496A1 (en) | 2008-10-30 |
JP4923141B2 (ja) | 2012-04-25 |
NZ580165A (en) | 2012-07-27 |
EP2134174A1 (en) | 2009-12-23 |
EA200901402A1 (ru) | 2010-04-30 |
US20130109646A1 (en) | 2013-05-02 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
GB | Transfer or rights |
Owner name: SANTEN PHARMACEUTICAL CO., LTD. |
|
FA | Abandonment or withdrawal |