PE20070804A1 - Compuestos heterociclicos como inhibidores de proteasa aspartica - Google Patents
Compuestos heterociclicos como inhibidores de proteasa asparticaInfo
- Publication number
- PE20070804A1 PE20070804A1 PE2006001432A PE2006001432A PE20070804A1 PE 20070804 A1 PE20070804 A1 PE 20070804A1 PE 2006001432 A PE2006001432 A PE 2006001432A PE 2006001432 A PE2006001432 A PE 2006001432A PE 20070804 A1 PE20070804 A1 PE 20070804A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- inhibitors
- aspartic
- protease
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
- A61P5/42—Drugs for disorders of the endocrine system of the suprarenal hormones for decreasing, blocking or antagonising the activity of mineralocorticosteroids
-
- 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
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
- C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DE FORMULA (I) DONDE Z ES O o CH2; X1 ES ENLACE COVALENTE, O, S, S(O), S(O)2; Y1 ES ENLACE COVALENTE, ALQUILENO(C1-C10), ALQUENILENO(C1-C10) O ALQUINILENO(C1-C10), OPCIONALMENTE SUSTITUIDOS; R1 ES CICLOALQUILO(C3-C7), FENILO, HETEROARILO, ENTRE OTROS, OPCIONALMENTE SUSTITUIDOS; R2 ES -OC(O)(NH2), -OC(S)(NH2), -NHC(O)OR9, ENTRE OTROS; R3 ES H, F, ALQUILO(C1-C5), ENTRE OTROS; R4 ES H O ALQUILO(C1-C3); R5 Y R6 SON INDEPENDIENTEMENTE H, ALQUILO(C1-C10), HALOALQUILO(C1-C10), ENTRE OTROS; Q ES Q1, Q(1-6) ES -C(=O)-, -C(=S)-, -C(=C-NO2)-, ENTRE OTROS; G ES OH, NH2 O NHR7. SON PREFERIDOS: (S)-4-(3-CLOROFENIL)-4-((R)-1-((S)-1-CICLOHEXIL-3-(METILAMINO)PROPAN-2-ILCARBAMOIL)PIPERIDIN-3-IL)-4-HIDROXIBUTILCARBAMATO DE METILO, (S)-4-(3-CLORO-5-FLUOROFENIL)-4-((R)-1-((S)-1-CICLOHEXIL-3-(METILAMINO)PROPAN-2-ILCARBAMOIL)PIPERIDIN-3-IL)-4-HIDROXIBUTILCARBAMATO DE METILO, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA Y UN PROCEDIMIENTO DE PREPARACION. ESTOS COMPUESTOS SON INHIBIDORES DE LA PROTEASA ASPARTICA Y SON UTILES EN EL TRATAMIENTO DE INFECCIONES O TRANSTORNOS MEDIADOS POR LA PROTEASA ASPARTICA, TAL COMO EL VIRUS DE VIH Y HTLV
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73656405P | 2005-11-14 | 2005-11-14 | |
US84533106P | 2006-09-18 | 2006-09-18 | |
US84529106P | 2006-09-18 | 2006-09-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20070804A1 true PE20070804A1 (es) | 2007-09-06 |
Family
ID=37812974
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2006001432A PE20070804A1 (es) | 2005-11-14 | 2006-11-13 | Compuestos heterociclicos como inhibidores de proteasa aspartica |
PE2010000496A PE20120229A1 (es) | 2005-11-14 | 2010-08-06 | Compuestos heterociclicos como inhibidores de proteasa aspartica |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2010000496A PE20120229A1 (es) | 2005-11-14 | 2010-08-06 | Compuestos heterociclicos como inhibidores de proteasa aspartica |
Country Status (16)
Country | Link |
---|---|
US (1) | US8487108B2 (es) |
EP (1) | EP1966139B1 (es) |
JP (1) | JP2009515893A (es) |
KR (1) | KR101379663B1 (es) |
AR (1) | AR057890A1 (es) |
AT (1) | ATE538092T1 (es) |
AU (1) | AU2006325322B2 (es) |
BR (1) | BRPI0618585A2 (es) |
CA (1) | CA2628952C (es) |
HK (1) | HK1121459A1 (es) |
NO (1) | NO20082108L (es) |
NZ (1) | NZ568042A (es) |
PE (2) | PE20070804A1 (es) |
SG (1) | SG169983A1 (es) |
TW (1) | TWI411607B (es) |
WO (1) | WO2007070201A1 (es) |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7754737B2 (en) | 2004-10-07 | 2010-07-13 | Vitae Pharmaceuticals, Inc. | Diaminoalkane aspartic protease inhibitors |
US7872028B2 (en) | 2006-04-05 | 2011-01-18 | Vitae Pharmaceuticals, Inc. | Diaminopropanol renin inhibitors |
US7858624B2 (en) * | 2006-04-05 | 2010-12-28 | Vitae Pharmaceuticals, Inc. | Piperidine and morpholine renin inhibitors |
US20090275581A1 (en) * | 2006-04-05 | 2009-11-05 | Baldwin John J | Renin inhibitors |
US20090264428A1 (en) * | 2006-04-05 | 2009-10-22 | Baldwin John J | Renin Inhibitors |
CL2007002689A1 (es) * | 2006-09-18 | 2008-04-18 | Vitae Pharmaceuticals Inc | Compuestos derivados de piperidin-1-carboxamida, inhibidores de la renina; compuestos intermediarios; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como hipertension, insuficiencia cardiaca, fibrosis cardiaca, entre otras. |
ATE520690T1 (de) * | 2006-09-18 | 2011-09-15 | Vitae Pharmaceuticals Inc | Piperidinderivate als renin-inhibitoren |
WO2009038719A1 (en) * | 2007-09-17 | 2009-03-26 | Vitae Pharmaceuticals, Inc. | Process for the preparation of renin inhibitors |
US20100311989A1 (en) * | 2007-09-17 | 2010-12-09 | Marlys Hammond | Process for the preparation of renin inhibitors |
US7741327B2 (en) | 2008-04-16 | 2010-06-22 | Hoffmann-La Roche Inc. | Pyrrolidinone glucokinase activators |
US20100010228A1 (en) * | 2008-06-26 | 2010-01-14 | Vitae Pharmaceuticals, Inc. | Process for the asymmetric reduction of 3-benzoylpiperidines |
JP2011525933A (ja) * | 2008-06-26 | 2011-09-29 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | メチル2−((r)−(3−クロロフェニル)((r)−1−((s)−2−(メチルアミノ)−3−((r)−テトラヒドロ−2h−ピラン−3−イル)プロピルカルバモイル)ピペリジン−3−イル)メトキシ)エチルカルバメートの塩 |
BRPI0917540A2 (pt) | 2008-08-05 | 2015-11-17 | Daiichi Sankyo Co Ltd | composto, sal farmacologicamente aceitavél, composição farmacêutica, e, uso de um composto ou sal farmacologicamente aceitável |
WO2010111634A2 (en) * | 2009-03-26 | 2010-09-30 | Takeda Pharmaceutical Company Limited | Renin inhibitors |
US20110021570A1 (en) | 2009-07-23 | 2011-01-27 | Nancy-Ellen Haynes | Pyridone glucokinase activators |
AR077692A1 (es) | 2009-08-06 | 2011-09-14 | Vitae Pharmaceuticals Inc | Sales de 2-((r)-(3-clorofenil) ((r)-1-((s) -2-(metilamino)-3-((r)-tetrahidro-2h-piran-3-il) propilcarbamoil) piperidin -3-il) metoxi) etilcarbamato de metilo |
US8178689B2 (en) | 2010-06-17 | 2012-05-15 | Hoffman-La Roche Inc. | Tricyclic compounds |
WO2012081585A1 (ja) * | 2010-12-15 | 2012-06-21 | 国立大学法人北海道大学 | 光学活性アルコール化合物の製造方法 |
JP5616976B2 (ja) * | 2010-12-15 | 2014-10-29 | 国立大学法人北海道大学 | ジアステレオ選択的にアルコール化合物を製造する方法及びルテニウム化合物 |
KR20150042269A (ko) | 2012-08-16 | 2015-04-20 | 얀센 파마슈티카 엔.브이. | N형 칼슘 채널 차단제로서의 치환된 피라졸 |
US9453002B2 (en) | 2013-08-16 | 2016-09-27 | Janssen Pharmaceutica Nv | Substituted imidazoles as N-type calcium channel blockers |
GB201706102D0 (en) | 2017-04-18 | 2017-05-31 | Glaxosmithkline Ip Dev Ltd | Chemical compounds |
US12083099B2 (en) | 2020-10-28 | 2024-09-10 | Accencio LLC | Methods of treating symptoms of coronavirus infection with viral protease inhibitors |
TW202300150A (zh) | 2021-03-18 | 2023-01-01 | 美商薛定諤公司 | 環狀化合物及其使用方法 |
AR129265A1 (es) | 2022-05-12 | 2024-08-07 | Syngenta Crop Protection Ag | Compuestos de alcoxi-heteroaril-carboxamida o tioamida |
WO2024033374A1 (en) | 2022-08-11 | 2024-02-15 | Syngenta Crop Protection Ag | Novel arylcarboxamide or arylthioamide compounds |
WO2024126650A1 (en) | 2022-12-15 | 2024-06-20 | Syngenta Crop Protection Ag | Novel bicyclic-carboxamide compounds useful as pesticides |
Family Cites Families (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3071618A (en) | 1956-02-02 | 1963-01-01 | Pfizer & Co C | Diquaternary ammonium salts of n, n, n', n'-tetra substituted alkylene diamines |
GB1351761A (en) | 1971-02-04 | 1974-05-01 | Wilkinson Sword Ltd | Substituted p-menthane carboxamides and compositions containing them |
US4136163A (en) | 1971-02-04 | 1979-01-23 | Wilkinson Sword Limited | P-menthane carboxamides having a physiological cooling effect |
JPS5115098A (ja) | 1974-07-26 | 1976-02-06 | Asahi Chemical Ind | Akurirukeiseniseihinno shorihoho |
US4594343A (en) * | 1984-10-19 | 1986-06-10 | Shanklin Jr James R | 1-[(aminoalkyl and aminoalkylamino)carbonyl and thiocarbonyl]-α,α-diarylpyrrolidine, piperidine and homopiperidineacetamides and acetonitriles |
GB8810067D0 (en) | 1988-04-28 | 1988-06-02 | Ucb Sa | Substituted 1-(1h-imidazol-4-yl)alkyl-benzamides |
US4908372A (en) | 1988-10-13 | 1990-03-13 | Merrell Dow Pharmaceuticals Inc. | Antihistaminic piperidinyl benzimidazoles |
US5552558A (en) | 1989-05-23 | 1996-09-03 | Abbott Laboratories | Retroviral protease inhibiting compounds |
DE4018070A1 (de) | 1990-06-06 | 1991-12-12 | Bayer Ag | Morpholinoharnstoff-derivate |
CA2097317C (en) | 1990-12-14 | 2002-02-12 | Albert A. Carr | Antiallergic piperdinyl benzimidazoles |
NZ249286A (en) | 1992-02-13 | 1996-02-27 | Merrell Dow Pharma | Piperidine-4-ylmethyl thiophene and thiazole derivatives and pharmaceutical compositions |
ATE187160T1 (de) | 1994-07-29 | 1999-12-15 | Abbott Lab | Verfahren zur herstellung eines substituierten 2,5-diamino-3-hydroxy hexanes |
US5767144A (en) | 1994-08-19 | 1998-06-16 | Abbott Laboratories | Endothelin antagonists |
US6162927A (en) | 1994-08-19 | 2000-12-19 | Abbott Laboratories | Endothelin antagonists |
US6946481B1 (en) | 1994-08-19 | 2005-09-20 | Abbott Laboratories | Endothelin antagonists |
WO1998054179A1 (en) | 1997-05-29 | 1998-12-03 | Eli Lilly And Company | Process for preparing heterocyclic compounds |
AU3716499A (en) | 1998-04-21 | 1999-11-08 | Aventis Pharma Limited | Substituted diamines and their use as cell adhesion inhibitors |
US6437146B1 (en) | 1998-09-25 | 2002-08-20 | Fujisawa Pharmaceutical Co., Ltd. | Oxazole compounds as prostaglandin e2 agonists or antagonists |
GB9826540D0 (en) | 1998-12-02 | 1999-01-27 | Darwin Discovery Ltd | Process |
ATE322483T1 (de) * | 1999-01-06 | 2006-04-15 | Us Gov Health & Human Serv | Inhibitoren für asparagin-proteasen |
JP2000302757A (ja) | 1999-04-16 | 2000-10-31 | Shiseido Co Ltd | N−置換ピペリジン誘導体 |
CA2404206A1 (en) | 2000-03-21 | 2001-09-27 | Smithkline Beecham Corporation | Protease inhibitors |
US6900329B2 (en) | 2001-03-21 | 2005-05-31 | Schering Corporation | MCH antagonists and their use in the treatment of obesity |
EA200400162A1 (ru) | 2001-07-11 | 2005-06-30 | Элан Фармасьютикалз, Инк. | N-(3-амино-2-гидроксипропил)замещенные алкиламидные соединения |
US7176242B2 (en) * | 2001-11-08 | 2007-02-13 | Elan Pharmaceuticals, Inc. | N,N′-substituted-1,3-diamino-2-hydroxypropane derivatives |
KR100987815B1 (ko) | 2002-04-26 | 2010-10-18 | 길리애드 사이언시즈, 인코포레이티드 | Hiv 프로테아제 억제제 화합물의 포스포네이트유사체의 세포 축적 |
WO2004002483A1 (en) * | 2002-06-27 | 2004-01-08 | Actelion Pharmaceuticals Ltd | Substituted 3- and 4- aminomethylpiperidines for use as beta-secretase in the treatment of alzheimer’s disease |
US7557137B2 (en) | 2002-08-05 | 2009-07-07 | Bristol-Myers Squibb Company | Gamma-lactams as beta-secretase inhibitors |
US7566730B2 (en) | 2002-09-10 | 2009-07-28 | Elan Pharmaceuticals, Inc. | Substituted aminoethers for the treatment of Alzheimer's disease |
US20050137142A1 (en) | 2003-11-03 | 2005-06-23 | Probiodrug Ag | Combinations useful for the treatment of neuronal disorders |
US20070093492A1 (en) | 2004-03-09 | 2007-04-26 | Weir-Torn Jiaang | Pyrrolidine derivatives |
AU2005277203A1 (en) | 2004-08-20 | 2006-03-02 | Entremed, Inc. | Compositions and methods comprising proteinase activated receptor antagonists |
US7754737B2 (en) | 2004-10-07 | 2010-07-13 | Vitae Pharmaceuticals, Inc. | Diaminoalkane aspartic protease inhibitors |
EP1882684B1 (en) | 2005-05-19 | 2014-12-10 | Astellas Pharma Inc. | Pyrrolidine derivative or salt thereof |
US7858624B2 (en) | 2006-04-05 | 2010-12-28 | Vitae Pharmaceuticals, Inc. | Piperidine and morpholine renin inhibitors |
US7872028B2 (en) | 2006-04-05 | 2011-01-18 | Vitae Pharmaceuticals, Inc. | Diaminopropanol renin inhibitors |
ATE520690T1 (de) | 2006-09-18 | 2011-09-15 | Vitae Pharmaceuticals Inc | Piperidinderivate als renin-inhibitoren |
CL2007002689A1 (es) | 2006-09-18 | 2008-04-18 | Vitae Pharmaceuticals Inc | Compuestos derivados de piperidin-1-carboxamida, inhibidores de la renina; compuestos intermediarios; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como hipertension, insuficiencia cardiaca, fibrosis cardiaca, entre otras. |
EP2167609A1 (en) | 2007-06-20 | 2010-03-31 | Vitae Pharmaceuticals, Inc. | Renin inhibitors |
EP2170815A2 (en) | 2007-06-20 | 2010-04-07 | Vitae Pharmaceuticals, Inc. | Renin inhibitors |
US7773441B2 (en) * | 2008-06-18 | 2010-08-10 | Micron Technology, Inc. | Memory malfunction prediction system and method |
US20110160300A1 (en) | 2008-06-20 | 2011-06-30 | Marlys Hammond | Renin Inhibitors and Methods of Use Thereof |
JP2011525933A (ja) | 2008-06-26 | 2011-09-29 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | メチル2−((r)−(3−クロロフェニル)((r)−1−((s)−2−(メチルアミノ)−3−((r)−テトラヒドロ−2h−ピラン−3−イル)プロピルカルバモイル)ピペリジン−3−イル)メトキシ)エチルカルバメートの塩 |
AR077692A1 (es) | 2009-08-06 | 2011-09-14 | Vitae Pharmaceuticals Inc | Sales de 2-((r)-(3-clorofenil) ((r)-1-((s) -2-(metilamino)-3-((r)-tetrahidro-2h-piran-3-il) propilcarbamoil) piperidin -3-il) metoxi) etilcarbamato de metilo |
-
2006
- 2006-10-31 TW TW095140163A patent/TWI411607B/zh not_active IP Right Cessation
- 2006-11-13 US US12/084,928 patent/US8487108B2/en not_active Expired - Fee Related
- 2006-11-13 AU AU2006325322A patent/AU2006325322B2/en not_active Ceased
- 2006-11-13 CA CA2628952A patent/CA2628952C/en not_active Expired - Fee Related
- 2006-11-13 WO PCT/US2006/043920 patent/WO2007070201A1/en active Application Filing
- 2006-11-13 EP EP06837406A patent/EP1966139B1/en active Active
- 2006-11-13 BR BRPI0618585-1A patent/BRPI0618585A2/pt not_active IP Right Cessation
- 2006-11-13 JP JP2008540236A patent/JP2009515893A/ja not_active Withdrawn
- 2006-11-13 NZ NZ568042A patent/NZ568042A/en not_active IP Right Cessation
- 2006-11-13 KR KR1020087014407A patent/KR101379663B1/ko not_active Expired - Fee Related
- 2006-11-13 SG SG201101062-6A patent/SG169983A1/en unknown
- 2006-11-13 PE PE2006001432A patent/PE20070804A1/es not_active Application Discontinuation
- 2006-11-13 AT AT06837406T patent/ATE538092T1/de active
- 2006-11-14 AR ARP060104967A patent/AR057890A1/es unknown
-
2008
- 2008-05-07 NO NO20082108A patent/NO20082108L/no not_active Application Discontinuation
-
2009
- 2009-02-23 HK HK09101679.7A patent/HK1121459A1/xx not_active IP Right Cessation
-
2010
- 2010-08-06 PE PE2010000496A patent/PE20120229A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
ATE538092T1 (de) | 2012-01-15 |
AU2006325322B2 (en) | 2011-08-04 |
AU2006325322A1 (en) | 2007-06-21 |
JP2009515893A (ja) | 2009-04-16 |
HK1121459A1 (en) | 2009-04-24 |
AR057890A1 (es) | 2007-12-26 |
US8487108B2 (en) | 2013-07-16 |
BRPI0618585A2 (pt) | 2011-09-27 |
CA2628952C (en) | 2014-04-01 |
SG169983A1 (en) | 2011-04-29 |
NZ568042A (en) | 2010-12-24 |
WO2007070201A1 (en) | 2007-06-21 |
PE20120229A1 (es) | 2012-04-04 |
US20100048636A1 (en) | 2010-02-25 |
NO20082108L (no) | 2008-08-06 |
EP1966139B1 (en) | 2011-12-21 |
EP1966139A1 (en) | 2008-09-10 |
TW200800893A (en) | 2008-01-01 |
KR101379663B1 (ko) | 2014-04-14 |
KR20080069685A (ko) | 2008-07-28 |
CA2628952A1 (en) | 2007-06-21 |
TWI411607B (zh) | 2013-10-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20070804A1 (es) | Compuestos heterociclicos como inhibidores de proteasa aspartica | |
PE20091237A1 (es) | Derivados de pirrolidina como moduladores de serina proteasas | |
CY1117576T1 (el) | Δινουκλεοτιδικα προφαρμακα | |
PE20090630A1 (es) | Derivados de indol 2-carboxi sustituidos y metodos para su utilizacion | |
PE20051150A1 (es) | Compuestos azufrados como inhibidores de la serina proteasa ns3 del virus de la hepatitis c | |
ATE530561T1 (de) | 3-ether- und 3-thioether-substituierte ciclosporinderivate zur behandlung und prävention einer hepatitis-c-infektion | |
PE20091381A1 (es) | Inhibidores del virus de la hepatitis c | |
PE20121479A1 (es) | Inhibidores del virus de la hepatitis c | |
BRPI0410456A (pt) | compostos inibidores de hepatite c, composição farmacêutica, uso dos mesmos, bem como artigo de fabricação | |
ECSP067013A (es) | 2-quinolil-oxazoles sustituidos útiles como inhibidores de pde4 | |
DE602006020152D1 (de) | Arylalkyl- und heteroarylalkyl-derivate von cyclosporin a bei der behandlung und vorbeugung einer virusinfektion | |
PE20091000A1 (es) | Inhibidores de la replicacion del virus de la inmunodeficiencia humana | |
PE20091734A1 (es) | Compuestos de 2-imino-3-metilpirrolopirimidinona fenilo-sustituida como inhibidores de bace-1, composiciones y su uso | |
EA200800371A1 (ru) | Ингибиторы ns3 протеазы вгс | |
NO20092742L (no) | 4,5-ringkondenserte indolderivater for behandling eller forebyggelse av HCV og beslektede virusinfeksjoner | |
EA200802346A1 (ru) | Циклопропилконденсированные индолобензазепиновые ингибиторы белка ns5b вируса гепатита с | |
NZ596107A (en) | Antiviral compounds and methods | |
EA200701849A1 (ru) | Пролекарственные соединения трициклических нуклеозидов, фармацевтическая композиция на их основе и способ лечения и/или ингибирования вирусной инфекции у млекопитающего | |
PE20091841A1 (es) | Inhibidores del virus de hepatitis c | |
HK1101402A1 (en) | Inhibitors of serine proteases, particularly hcv ns3-ns4a protease | |
EA200970478A1 (ru) | Аналоги тиофена для лечения или предупреждения флавивирусных инфекций | |
PE20070078A1 (es) | Compuestos heterociclicos macrociclicos como inhibidores de aspartil proteasa | |
NZ609146A (en) | Modified 4’-nucleosides as antiviral agents | |
MY164469A (en) | Hcv ns3 protease inhibitors | |
AR036906A1 (es) | Compuestos de imidazopiridin como moduladores del receptor 5-ht4 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration | ||
FD | Application declared void or lapsed |