PE20010211A1 - Compuestos de tiazol y composiciones farmaceuticas para inhibir las quinasas de proteina - Google Patents
Compuestos de tiazol y composiciones farmaceuticas para inhibir las quinasas de proteinaInfo
- Publication number
- PE20010211A1 PE20010211A1 PE2000000553A PE0005532000A PE20010211A1 PE 20010211 A1 PE20010211 A1 PE 20010211A1 PE 2000000553 A PE2000000553 A PE 2000000553A PE 0005532000 A PE0005532000 A PE 0005532000A PE 20010211 A1 PE20010211 A1 PE 20010211A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- heterocycloalkyl
- cycloalkyl
- aryl
- heteroaryl
- Prior art date
Links
- 102000001253 Protein Kinase Human genes 0.000 title 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical class C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 108060006633 protein kinase Proteins 0.000 title 1
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000004663 cell proliferation Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- 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
- C07D417/04—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 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6536—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6536—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
- C07F9/6539—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
SE REFIERE COMPUESTOS DE DIAMINOTIAZOL DE FORMULA I, DONDE: R1 ES ALQUILO, CICLOALQUILO, HETEROCICLOALQUILO, ARILO, HETEROARILO OPCIONALMENTE SUSTITUIDO CON R6-CO, R6-CS; R6 ES ALQUILO, CICLOALQUILO, HETEROCICLOALQUILO, ALQUENILO, ARILO, HETEROARILO, NR7R8; R7 Y R8 SON H, ALQUILO, ARILO, HETEROARILO; R2 ES HIDROXI, HALO, CIANO, NITRO, ALQUILO, ALQUENILO, CICLOALQUILO, HETEROCICLOALQUILO, ARILO, HETEROARILO, -C=O-Ra, Ra ES H, ALQUILO, CICLOALQUILO, HETEROCICLOALQUILO, ARILO, HETEROARILO, -C(O)-O-Ra-; DONDE Ra ES H, ALQUILO, CICLOALQUILO, HETEROCICLOALQUILO, ARILO, HETEROARILO, -C(O)-NRcRb, Rb Y Rc SON H, ALQUILO, CICLOALQUILO, HETEROCICLOALQUILO, ARILO, ENTRE OTROS; X ES C, N; Q ES UN RADICAL DIVALENTE DE 2-3 DE C, N, O, S, C-R5, N-R5, R5 ES OH, HALO, CIANO, AMINO, ALQUILO, ARILO, HETEROARILO, ALCOXI, QUE JUNTO A C* Y N* FORMAN UN ANILLO DE 6 MIEMBROS AROMATICO O NO AROMATICO. LOS COMPUESTOS I SON MODULADORES O INHIBIDORES DE LA ACTIVIDAD DEL RECEPTOR DE QUINASA Y PUEDEN SER UTILES PARA EL TRATAMIENTO DEL CANCER, TUMOR, PROLIFERACION CELULAR
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13781099P | 1999-06-04 | 1999-06-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20010211A1 true PE20010211A1 (es) | 2001-03-16 |
Family
ID=22479135
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2000000553A PE20010211A1 (es) | 1999-06-04 | 2000-06-02 | Compuestos de tiazol y composiciones farmaceuticas para inhibir las quinasas de proteina |
Country Status (34)
| Country | Link |
|---|---|
| US (1) | US6620828B2 (es) |
| EP (1) | EP1181283B1 (es) |
| JP (1) | JP2003501420A (es) |
| KR (1) | KR20020015333A (es) |
| CN (1) | CN1359380A (es) |
| AP (1) | AP2001002341A0 (es) |
| AT (1) | ATE288424T1 (es) |
| AU (1) | AU778071B2 (es) |
| BG (1) | BG106276A (es) |
| BR (1) | BR0011585A (es) |
| CA (1) | CA2371158A1 (es) |
| CZ (1) | CZ20014213A3 (es) |
| DE (1) | DE60017894T2 (es) |
| EA (1) | EA200101268A1 (es) |
| EE (1) | EE200100659A (es) |
| ES (1) | ES2234628T3 (es) |
| HR (1) | HRP20020008A2 (es) |
| HU (1) | HUP0202897A3 (es) |
| IL (1) | IL146094A0 (es) |
| IS (1) | IS6183A (es) |
| MA (1) | MA25530A1 (es) |
| MX (1) | MXPA01012483A (es) |
| NO (1) | NO20015045L (es) |
| NZ (1) | NZ514881A (es) |
| OA (1) | OA11959A (es) |
| PE (1) | PE20010211A1 (es) |
| PL (1) | PL352714A1 (es) |
| SK (1) | SK17302001A3 (es) |
| SV (1) | SV2002000096A (es) |
| UA (1) | UA71971C2 (es) |
| UY (1) | UY26190A1 (es) |
| WO (1) | WO2000075120A1 (es) |
| YU (1) | YU85601A (es) |
| ZA (1) | ZA200108291B (es) |
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| US20040226056A1 (en) * | 1998-12-22 | 2004-11-11 | Myriad Genetics, Incorporated | Compositions and methods for treating neurological disorders and diseases |
| BR0009721A (pt) | 1999-04-15 | 2002-02-13 | Bristol Myers Squibb Co | Inibidores de tirosina quinase de proteìna cìclica |
| US7125875B2 (en) | 1999-04-15 | 2006-10-24 | Bristol-Myers Squibb Company | Cyclic protein tyrosine kinase inhibitors |
| ATE318812T1 (de) | 2000-12-21 | 2006-03-15 | Bristol Myers Squibb Co | Thiazolyl-inhibitoren von tyrosinkinasen der tec- familie |
| US6756374B2 (en) | 2001-01-22 | 2004-06-29 | Hoffmann-La Roche Inc. | Diaminothiazoles having antiproliferative activity |
| UA76977C2 (en) | 2001-03-02 | 2006-10-16 | Icos Corp | Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers |
| JP2005504014A (ja) * | 2001-06-08 | 2005-02-10 | サイトビア インコーポレイテッド | カスパーゼの活性化因子およびアポトーシスの誘導因子としての置換された3−アリール−5−アリール−[1,2,4]−オキサジアゾール類および類似体、並びにその使用法 |
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| JP5369257B2 (ja) * | 2006-02-15 | 2013-12-18 | アッヴィ・インコーポレイテッド | 新規なアセチル−CoAカルボキシラーゼ(ACC)阻害薬およびそれらの糖尿病、肥満および代謝症候群での使用 |
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| PE20110294A1 (es) | 2008-09-29 | 2011-05-26 | Boehringer Ingelheim Int | Compuestos heterociclicos como inhibidores de enzimas de senal especifica |
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| WO2025007859A1 (en) * | 2023-07-03 | 2025-01-09 | Insilico Medicine Ip Limited | Substituted thiazole compounds as cdk2/4/6 inhibitors and methods of use thereof |
| CN116874442B (zh) * | 2023-07-27 | 2025-10-24 | 武汉呈瑞生物医药科技有限公司 | 一种有机化合物及其应用 |
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| DE273062C (de) | 1912-04-19 | 1914-04-20 | Deylen Sohn Firma | Vorrichtung zum Schränken von Plattenzündspänen |
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| DE69222637T2 (de) * | 1991-05-10 | 1998-02-26 | Rhone Poulenc Rorer Int | Bis mono- und bicyclische aryl- und heteroarylderivate mit inhibierender wirkung auf die egf und/oder pdgf-rezeptor tyrosinkinase |
| WO1993019052A1 (en) | 1992-03-24 | 1993-09-30 | Merck Sharp & Dohme Limited | 3-ureido substituted benzodiazepin-2-ones having cholecystokinin and/or gastrin antagonistic activity and their use in therapy |
| US5631156A (en) | 1994-06-21 | 1997-05-20 | The University Of Michigan | DNA encoding and 18 KD CDK6 inhibiting protein |
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| WO1996023783A1 (en) | 1995-02-02 | 1996-08-08 | Smithkline Beecham Plc | Indole derivatives as 5-ht receptor antagonist |
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| WO1997003967A1 (en) | 1995-07-22 | 1997-02-06 | Rhone-Poulenc Rorer Limited | Substituted aromatic compounds and their pharmaceutical use |
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| US5733920A (en) | 1995-10-31 | 1998-03-31 | Mitotix, Inc. | Inhibitors of cyclin dependent kinases |
| US5760028A (en) | 1995-12-22 | 1998-06-02 | The Dupont Merck Pharmaceutical Company | Integrin receptor antagonists |
| WO1997034876A1 (en) | 1996-03-15 | 1997-09-25 | Zeneca Limited | Cinnoline derivatives and use as medicine |
| ATE211740T1 (de) | 1996-06-27 | 2002-01-15 | Pfizer | Substituierte indazolderivate |
| JP3554337B2 (ja) | 1996-09-04 | 2004-08-18 | ファイザー・インク | インダゾール誘導体、およびホスホジエステラーゼ(pde)タイプ4と腫瘍壊死因子(tnf)産生の阻害剤としてのインダゾール誘導体の使用 |
| ID18494A (id) | 1996-10-02 | 1998-04-16 | Novartis Ag | Turunan pirazola leburan dan proses pembuatannya |
| GEP20032896B (en) * | 1997-10-27 | 2003-02-25 | Agouron Pharma | 4-Aminothiazole Derivatives, Containing Them Pharmaceutical Compositions Inhibiting Cyclin-Dependent Kinases and Methods for Treatment |
| AU754184B2 (en) | 1997-11-04 | 2002-11-07 | Pfizer Products Inc. | Therapeutically active compounds based on indazole bioisostere replacement of catechol in PDE4 inhibitors |
| CZ20001621A3 (cs) | 1997-11-04 | 2001-08-15 | Pfizer Products Inc. | Bioisoterické nahrazení katecholu indazolem v terapeuticky aktivních sloučeninách |
| US6040321A (en) * | 1997-11-12 | 2000-03-21 | Bristol-Myers Squibb Company | Aminothiazole inhibitors of cyclin dependent kinases |
| EP1087951B9 (en) * | 1998-06-18 | 2006-09-13 | Bristol-Myers Squibb Company | Carbon substituted aminothiazole inhibitors of cyclin dependent kinases |
| KR100705142B1 (ko) | 1998-09-29 | 2007-04-06 | 와이어쓰 홀딩스 코포레이션 | 단백질 티로신 키나제 억제제로서 치환 3-시아노퀴놀린 |
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- 2000-06-02 MX MXPA01012483A patent/MXPA01012483A/es not_active Application Discontinuation
- 2000-06-02 WO PCT/US2000/015188 patent/WO2000075120A1/en not_active Ceased
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- 2000-06-02 EP EP00942660A patent/EP1181283B1/en not_active Expired - Lifetime
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- 2000-06-02 AU AU57254/00A patent/AU778071B2/en not_active Ceased
- 2000-06-02 DE DE60017894T patent/DE60017894T2/de not_active Expired - Fee Related
- 2000-06-02 JP JP2001501601A patent/JP2003501420A/ja not_active Abandoned
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- 2000-06-02 KR KR1020017015384A patent/KR20020015333A/ko not_active Withdrawn
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