PE20021089A1 - Compuestos de triazol como inhibidores de las citoquinas - Google Patents
Compuestos de triazol como inhibidores de las citoquinasInfo
- Publication number
- PE20021089A1 PE20021089A1 PE2002000364A PE2002000364A PE20021089A1 PE 20021089 A1 PE20021089 A1 PE 20021089A1 PE 2002000364 A PE2002000364 A PE 2002000364A PE 2002000364 A PE2002000364 A PE 2002000364A PE 20021089 A1 PE20021089 A1 PE 20021089A1
- Authority
- PE
- Peru
- Prior art keywords
- alkenyl
- alkyl
- triazole
- alkinyl
- triazole compounds
- Prior art date
Links
Classifications
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DE TRIAZOL DE FORMULA I DONDE R1 ES ALQUILO, ALQUENILO, ALQUINILO, HETEROALQUENILO, ENTRE OTROS; m ES 0-5; Q ES EL GRUPO a, b, ENTRE OTROS; R2 ES H, ALQUILO, ALQUENILO, ALQUINILO, HETEROALQUILO, ENTRE OTROS; R2 NO ES NR4R5 CUANTO TANTO Y ES CR2 COMO R3 ES H; R3 ES H, ALQUILO, ALQUENILO, ALQUINILO, HETEROALQUILO, HETEROALQUENILO, ENTRE OTROS; X ES CR2, N; Y ES CR2, N; Z ES CR2, NR3, O, S; A ES H, ALQUILO, ALQUENILO, ALQUINILO, ENTRE OTROS; a ES UN ENLACE INDIVIDUAL; B ES H, ALQUILO, ALQUENILO, ENTRE OTROS; b ES UN ENLACE INDIVIDUAL; R4 ES H, ALQUILO, ALQUENILO, ENTRE OTROS; R5 ES H, ALQUILO, ALQUENILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS 4-(4-FLUOROFENIL)-5-PIRIDIN-4-IL-1-(TIOFEN-2-ILCARBONIL)-[1,2,3]TRIAZOL, 4-(4-FLUOROFENIL)-5-PIRIDIN-4-IL-1-METILCARBONIL-[1,2,3]TRIAZOL, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. LOS COMPUESTOS MENCIONADOS SON INHIBIDORES DE LAS CITOQUINAS Y SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES INFLAMATORIAS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28763901P | 2001-04-30 | 2001-04-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20021089A1 true PE20021089A1 (es) | 2003-02-18 |
Family
ID=23103747
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2002000364A PE20021089A1 (es) | 2001-04-30 | 2002-04-30 | Compuestos de triazol como inhibidores de las citoquinas |
Country Status (8)
Country | Link |
---|---|
US (1) | US6727364B2 (es) |
EP (1) | EP1383759A1 (es) |
JP (1) | JP2004528351A (es) |
CN (1) | CN1505625A (es) |
AU (1) | AU2002305226B2 (es) |
CA (1) | CA2444499A1 (es) |
PE (1) | PE20021089A1 (es) |
WO (1) | WO2002088108A1 (es) |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
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KR100566709B1 (ko) * | 2001-07-24 | 2006-04-03 | 오쓰까 세이야꾸 가부시키가이샤 | 만성 폐색성 폐질환 치료제의 제조를 위한 티아졸유도체의 용도 |
AR039241A1 (es) * | 2002-04-04 | 2005-02-16 | Biogen Inc | Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos |
UA80295C2 (en) * | 2002-09-06 | 2007-09-10 | Biogen Inc | Pyrazolopyridines and using the same |
US7776907B2 (en) * | 2002-10-31 | 2010-08-17 | Celgene Corporation | Methods for the treatment and management of macular degeneration using cyclopropyl-N-{2-[(1S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl]-3-oxoisoindoline-4-yl}carboxamide |
US7745630B2 (en) | 2003-12-22 | 2010-06-29 | Justin Stephen Bryans | Triazolyl piperidine arginine vasopressin receptor modulators |
US7276050B2 (en) * | 2004-03-02 | 2007-10-02 | Alan Franklin | Trans-scleral drug delivery method and apparatus |
WO2007016286A1 (en) | 2005-07-28 | 2007-02-08 | Janssen Pharmaceutica N.V. | Synthesis of 4/5-pyrimidinylimidazoles via sequential functionalization of 2,4-dichloropyrimidine |
US20080152592A1 (en) * | 2006-12-21 | 2008-06-26 | Bayer Healthcare Llc | Method of therapeutic drug monitoring |
US20100210932A1 (en) * | 2007-03-20 | 2010-08-19 | Bayer Healthcare Llc | Method of analyzing an analyte |
SG172301A1 (en) * | 2008-12-24 | 2011-07-28 | Bial Portela & Ca Sa | Pharmaceutical compounds |
WO2011140296A1 (en) * | 2010-05-05 | 2011-11-10 | Infinity Pharmaceuticals | Triazoles as inhibitors of fatty acid synthase |
US8466181B2 (en) * | 2010-12-10 | 2013-06-18 | Hoffmann-La Roche Inc. | 1,2,3-triazole-imidazole compounds |
US9108930B2 (en) * | 2011-04-06 | 2015-08-18 | The Scripps Research Institute | N1- and N2-carbamoyl-1,2,3-triazole serine hydrolase inhibitors and methods |
CN103275023B (zh) * | 2013-06-08 | 2015-10-07 | 浙江工业大学 | 1-芳基-1,2,3-三氮唑类化合物及其制备和应用 |
WO2014199164A1 (en) * | 2013-06-12 | 2014-12-18 | Ampla Pharmaceuticals, Inc. | Diaryl substituted heteroaromatic compounds |
CN103751190B (zh) * | 2013-11-07 | 2015-09-09 | 杭州药明生物技术有限公司 | ***类化合物在制备乙醛脱氢酶2激活剂中的应用 |
PE20180529A1 (es) | 2015-05-20 | 2018-03-19 | Amgen Inc | Agonistas de triazol del receptor apj |
US10385057B2 (en) | 2015-11-20 | 2019-08-20 | Lundbeck La Jolla Research Center, Inc. | Pyrazole compounds and methods of making and using same |
WO2017087854A1 (en) | 2015-11-20 | 2017-05-26 | Abide Therapeutics, Inc. | Pyrazole compounds and methods of making and using same |
WO2017087863A1 (en) | 2015-11-20 | 2017-05-26 | Abide Therapeutics, Inc. | Pyrazole compounds and methods of making and using same |
US10583137B2 (en) | 2015-12-02 | 2020-03-10 | The Scripps Research Institute | Triazole DAGLα inhibitors |
WO2017192485A1 (en) | 2016-05-03 | 2017-11-09 | Amgen Inc. | Heterocyclic triazole compounds as agonists of the apj receptor |
AU2017311691B2 (en) | 2016-08-18 | 2021-12-02 | Vidac Pharma Ltd. | Piperazine derivatives, pharmaceutical compositions and methods of use thereof |
US11046680B1 (en) | 2016-11-16 | 2021-06-29 | Amgen Inc. | Heteroaryl-substituted triazoles as APJ receptor agonists |
EP3541803B1 (en) | 2016-11-16 | 2020-12-23 | Amgen Inc. | Triazole pyridyl compounds as agonists of the apj receptor |
WO2018097944A1 (en) | 2016-11-16 | 2018-05-31 | Amgen Inc. | Triazole furan compounds as agonists of the apj receptor |
MA46824A (fr) | 2016-11-16 | 2019-09-25 | Amgen Inc | Composés de triazole substitués par alkyle en tant qu'agonistes du récepteur apj |
WO2018093579A1 (en) | 2016-11-16 | 2018-05-24 | Amgen Inc. | Triazole phenyl compounds as agonists of the apj receptor |
US11020395B2 (en) | 2016-11-16 | 2021-06-01 | Amgen Inc. | Cycloalkyl substituted triazole compounds as agonists of the APJ receptor |
JPWO2018159835A1 (ja) * | 2017-03-03 | 2020-04-09 | 国立大学法人 東京大学 | ストリゴラクトン受容体阻害剤、農業用組成物及びそれらの使用、ストライガ種子の発芽抑制剤、並びにトリアゾールウレア化合物 |
JOP20190267A1 (ar) | 2017-05-23 | 2019-11-18 | Lundbeck La Jolla Research Center Inc | مثبطات بيرازول magl |
US10927105B1 (en) | 2017-05-23 | 2021-02-23 | Lundbeck La Jolla Research Center, Inc. | Pyrazole MAGL inhibitors |
EA201992409A1 (ru) | 2017-05-23 | 2020-03-23 | Лундбекк Ла-Хойя Рисерч Сентер, Инк. | Ингибиторы magl на основе пиразола |
CN111344284B (zh) * | 2017-09-12 | 2024-03-12 | 新加坡科技研究局 | 用作异戊二烯半胱氨酸羧甲基转移酶抑制剂的化合物 |
MA50509A (fr) | 2017-11-03 | 2021-06-02 | Amgen Inc | Agonistes de triazole fusionnés du récepteur apj |
CN107879986A (zh) * | 2017-12-20 | 2018-04-06 | 重庆英斯凯化工有限公司 | 一种阿伐那非杂质的合成方法 |
WO2019146773A1 (ja) * | 2018-01-25 | 2019-08-01 | 株式会社フジモト・コーポレーション | チオフェン誘導体およびその用途 |
EP3788037A1 (en) | 2018-05-01 | 2021-03-10 | Amgen Inc. | Substituted pyrimidinones as agonists of the apj receptor |
US11795160B2 (en) | 2019-02-22 | 2023-10-24 | Insilico Medicine Ip Limited | Kinase inhibitors |
US11987572B2 (en) * | 2019-06-03 | 2024-05-21 | Regents Of The University Of Minnesota | Therapeutic compounds and methods of use thereof |
KR102406248B1 (ko) * | 2019-12-30 | 2022-06-07 | 이화여자대학교 산학협력단 | Hsp90 억제제로서의 1,2,3-트리아졸 유도체 화합물 |
KR102406246B1 (ko) * | 2019-12-30 | 2022-06-07 | 이화여자대학교 산학협력단 | Hsp90 억제제로서의 1,2,3-트리아졸 유도체 화합물 및 이의 용도 |
WO2021137665A1 (ko) * | 2019-12-30 | 2021-07-08 | 이화여자대학교 산학협력단 | Hsp90 억제제로서의 1,2,3-트리아졸 유도체 화합물 및 이의 용도 |
US11530199B2 (en) | 2021-02-24 | 2022-12-20 | Insilico Medicine Ip Limited | Analogs for the treatment of disease |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2212694A1 (de) | 1972-03-16 | 1973-09-20 | Hoechst Ag | 1,2,3-triazolderivate und verfahren zu ihrer herstellung |
EP0727998B1 (en) | 1993-11-08 | 2004-01-21 | Smithkline Beecham Corporation | Oxazoles for treating cytokine mediated diseases |
ES2239357T3 (es) | 1996-06-10 | 2005-09-16 | MERCK & CO., INC. | Imidazoles sustituidos que tienen actividad inhibidora de citoquinas. |
JP2002515915A (ja) | 1997-06-30 | 2002-05-28 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | 炎症性疾患の治療で有用な2−置換イミダゾール類 |
JP2003525201A (ja) | 1998-08-20 | 2003-08-26 | スミスクライン・ビーチャム・コーポレイション | 新規な置換トリアゾール化合物 |
WO2000026209A1 (en) | 1998-11-03 | 2000-05-11 | Novartis Ag | Anti-inflammatory 4-phenyl-5-pyrimidinyl-imidazoles |
WO2001012621A1 (en) | 1999-08-13 | 2001-02-22 | Vertex Pharmaceuticals Incorporated | INHIBITORS OF c-JUN N-TERMINAL KINASES (JNK) AND OTHER PROTEIN KINASES |
EP1202733B1 (en) | 1999-08-12 | 2005-10-05 | Pharmacia Italia S.p.A. | 3(5)-amino-pyrazole derivatives, process for their preparation and their use as antitumor agents |
US6962936B2 (en) * | 2001-04-27 | 2005-11-08 | Vertex Pharmaceuticals Incorporated | Triazole-derived kinase inhibitors and uses thereof |
US6787555B2 (en) * | 2001-04-30 | 2004-09-07 | The Procter & Gamble Company | Triazole compounds useful in treating diseases associated with unwanted cytokine activity |
-
2002
- 2002-04-24 US US10/133,044 patent/US6727364B2/en not_active Expired - Fee Related
- 2002-04-25 CN CNA028090780A patent/CN1505625A/zh active Pending
- 2002-04-25 WO PCT/US2002/013074 patent/WO2002088108A1/en not_active Application Discontinuation
- 2002-04-25 EP EP02734036A patent/EP1383759A1/en not_active Withdrawn
- 2002-04-25 AU AU2002305226A patent/AU2002305226B2/en not_active Ceased
- 2002-04-25 CA CA002444499A patent/CA2444499A1/en not_active Abandoned
- 2002-04-25 JP JP2002585408A patent/JP2004528351A/ja not_active Withdrawn
- 2002-04-30 PE PE2002000364A patent/PE20021089A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CA2444499A1 (en) | 2002-11-07 |
AU2002305226B2 (en) | 2006-02-02 |
CN1505625A (zh) | 2004-06-16 |
US20030013712A1 (en) | 2003-01-16 |
EP1383759A1 (en) | 2004-01-28 |
JP2004528351A (ja) | 2004-09-16 |
WO2002088108A1 (en) | 2002-11-07 |
US6727364B2 (en) | 2004-04-27 |
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Legal Events
Date | Code | Title | Description |
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FD | Application declared void or lapsed |