CO6220940A2 - Inhibidores de pirrolotriazina cinasa - Google Patents
Inhibidores de pirrolotriazina cinasaInfo
- Publication number
- CO6220940A2 CO6220940A2 CO09000765A CO09000765A CO6220940A2 CO 6220940 A2 CO6220940 A2 CO 6220940A2 CO 09000765 A CO09000765 A CO 09000765A CO 09000765 A CO09000765 A CO 09000765A CO 6220940 A2 CO6220940 A2 CO 6220940A2
- Authority
- CO
- Colombia
- Prior art keywords
- substituted
- arylalkyl
- alkynyl
- alkyl
- alkanoyl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- 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
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Neurosurgery (AREA)
- Hematology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
1.- Compuesto de la fórmula Icaracterizado porque: Q1 es arilo, arilo substituido, heteroarilo o heteroarilo substituido; X es C=O, C=S, C=NR9 ó CH2; R1, R2, y R3 son independientemente hidrógeno, aiquilo, alquilo substituido, cicloalquilo, cicloalquilo substituido, hidroxi, alcoxi, alcoxi substituido, halógeno, haloalquilo, haloalcoxi, alcanoilo, alcanoilo substituido, amino, amino substituido, aminoalquilo, aminoalquilo substituido, alquilamino, alquilamino substituido, amida, amida substituida, carbamato, ureido, ciano, sulfonamido, sulfanamido substituido, alquilsulfona, nitro, tio, tioalquilo, alquiltio, diamino substituido, alquilsulfonilo, alquilsulfinilo, carboxi, alcoxicarbonilo, alquilcarboniloxi, carbamoilo, carbamoilo substituido, alquenilo, alquenilo substituido, alquinilo, alquinilo substituido, o alquilcarbonilo; R4 es hidrógeno, alquilo, alquilo substituido, hidroxi, alcoxi, halógeno, haloalquilo, haloalcoxi, oxo, ariloxi, arilalquilo, arilalquiloxi, alcanoilo, alcanoilo substituido, alcanoiloxi, amino, amino substituido, aminoalquilo, aminoalquilo substituido, alquilamino, alquilamino substituido, hidroxialquilo, diamino substituido, amida, amida substituida, carbamato, carbamato substituido, ureido, ciano, sulfonamida, sulfonamida substituida, alquilsulfona, heterocicloalquilo, heterocicloalquilo substituido, cicloalquilo, cicloalquilo substituido, cicloalquenilo, cicloalquenilo substituido, cicloalquilalquilo, cicloalquilalcoxi, nitro, tio, tioalquilo, alquiltio, alquilsulfonilo, alquilsulfinilo, carboxi, alcoxicarbonilo, alquilcarboniloxi, carbamoilo, alquenilo, alquenilo substituido, alquinilo, alquinilo substituido, arilo, arilo substituido, heteroarilo, heteroarilo substituido, heteroariloxi, arilheteroarilo, arilalcoxicarbonilo, heteroarilalquilo, heteroarilalcoxi, ariloxialquilo, ariloxiarilo, heterociclo, heterociclo substituido, alquilcarbonilo, heteroalquilo substituido, heteroalquenilo, heteroalquenilo substituido, heteroalquinilo, heteroalquinilo substituido, arilamino, arilalquilamino, alcanoilamino, aroilamino, arilalcanoilamino, ariltio, arilalquiltio, arilsulfonilo, arilalquilsulfonilo, alquilsulfonilo, arilcarbonilamino, o alquilaminocarbonilo; R5 es hidrógeno, halógeno, ciano, alquilo o alquilo substituido; ...
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US81917106P | 2006-07-07 | 2006-07-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO6220940A2 true CO6220940A2 (es) | 2010-11-19 |
Family
ID=38671050
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO09000765A CO6220940A2 (es) | 2006-07-07 | 2009-01-06 | Inhibidores de pirrolotriazina cinasa |
Country Status (26)
Country | Link |
---|---|
US (4) | US7534792B2 (es) |
EP (1) | EP2041138B1 (es) |
JP (1) | JP5185930B2 (es) |
KR (1) | KR101443400B1 (es) |
CN (1) | CN101511835B (es) |
AR (1) | AR061873A1 (es) |
AU (1) | AU2007269163B2 (es) |
BR (1) | BRPI0714359A2 (es) |
CA (1) | CA2657594C (es) |
CL (1) | CL2007001995A1 (es) |
CO (1) | CO6220940A2 (es) |
DK (1) | DK2041138T3 (es) |
EA (1) | EA018322B1 (es) |
ES (1) | ES2493566T3 (es) |
HR (1) | HRP20140688T1 (es) |
IL (1) | IL196033A0 (es) |
MX (1) | MX2008016517A (es) |
NO (1) | NO342385B1 (es) |
NZ (1) | NZ574189A (es) |
PE (1) | PE20080677A1 (es) |
PL (1) | PL2041138T3 (es) |
PT (1) | PT2041138E (es) |
SI (1) | SI2041138T1 (es) |
TW (1) | TWI393722B (es) |
WO (1) | WO2008005956A2 (es) |
ZA (1) | ZA200900109B (es) |
Families Citing this family (61)
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PL2041138T3 (pl) * | 2006-07-07 | 2014-11-28 | Bristol Myers Squibb Co | Pirolotriazyny jako inhibitory kinazy |
CA2654898A1 (en) * | 2006-07-07 | 2008-10-01 | Boehringer Ingelheim International Gmbh | New chemical compounds |
CN101687874B (zh) * | 2007-04-18 | 2013-01-30 | 百时美施贵宝公司 | 吡咯并三嗪激酶抑制剂 |
WO2008144345A2 (en) * | 2007-05-17 | 2008-11-27 | Bristol-Myers Squibb Company | Biomarkers and methods for determining sensitivity to insulin growth factor-1 receptor modulators |
PE20090837A1 (es) * | 2007-07-02 | 2009-07-24 | Boehringer Ingelheim Int | Nuevos compuestos quimicos |
WO2009003998A2 (en) * | 2007-07-02 | 2009-01-08 | Boehringer Ingelheim International Gmbh | Antiproliferative compounds based on 5-membered heterocycles |
CN102015719A (zh) * | 2008-03-06 | 2011-04-13 | 百时美施贵宝公司 | 吡咯并三嗪激酶抑制剂 |
BRPI0920608A2 (pt) | 2008-09-29 | 2019-09-24 | Boehringer Ingelheim Int | compostos quimicos |
WO2010042684A1 (en) * | 2008-10-08 | 2010-04-15 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
AR074830A1 (es) | 2008-12-19 | 2011-02-16 | Cephalon Inc | Pirrolotriazinas como inhibidores de alk y jak2 |
EP2494070A2 (en) | 2009-10-30 | 2012-09-05 | Bristol-Myers Squibb Company | Methods for treating cancer in patients having igf-1r inhibitor resistance |
WO2011083391A2 (en) | 2010-01-05 | 2011-07-14 | Pfizer Inc. | Biomarkers for anti-igf-ir cancer therapy |
WO2011097331A1 (en) | 2010-02-03 | 2011-08-11 | Bristol-Myers Squibb Company | Crystalline forms of (s)-1-(4-(5-cyclopropyl-1h-pyrazol-3- ylamino)pyrrolo [1,2-f] [1,2,4] triazin-2-yl)-n-(6-fluoropyridin- 3-yl)-2-methylpyrrolidine-2-carboxamide |
JP5093527B2 (ja) * | 2010-02-10 | 2012-12-12 | 日本電気株式会社 | 複合光導波路、波長可変フィルタ、波長可変レーザ、および光集積回路 |
EP2552907B1 (en) | 2010-03-26 | 2014-10-22 | Boehringer Ingelheim International GmbH | Pyridyltriazoles |
EP2552905B1 (en) | 2010-03-26 | 2016-10-05 | Boehringer Ingelheim International GmbH | B-Raf kinase inhibitors |
US8791257B2 (en) | 2010-03-31 | 2014-07-29 | Bristol-Myers Squibb Company | Substituted pyrrolotriazines as protein kinase inhibitors |
US8710055B2 (en) | 2010-12-21 | 2014-04-29 | Boehringer Ingelheim International Gmbh | Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors |
CN102584828B (zh) * | 2011-01-14 | 2016-01-27 | 上海艾力斯医药科技有限公司 | 吡咯烷[3,4-d]嘧啶衍生物、制备方法及其应用 |
US20140309229A1 (en) | 2011-10-13 | 2014-10-16 | Bristol-Myers Squibb Company | Methods for selecting and treating cancer in patients with igf-1r/ir inhibitors |
JP6099051B2 (ja) | 2011-10-25 | 2017-03-22 | 塩野義製薬株式会社 | Pgd2受容体アンタゴニスト活性を有するへテロ環誘導体 |
US9724352B2 (en) | 2012-05-31 | 2017-08-08 | Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences | Pyrrolo[2,1-F[1,2,4]triazine compounds, preparation methods and applications thereof |
CN103450204B (zh) | 2012-05-31 | 2016-08-17 | 中国科学院上海药物研究所 | 吡咯[2,1-f][1,2,4]并三嗪类化合物,其制备方法及用途 |
US9499519B2 (en) | 2012-12-26 | 2016-11-22 | Medivation Technologies, Inc. | Fused pyrimidine compounds and use thereof |
US9050345B2 (en) | 2013-03-11 | 2015-06-09 | Bristol-Myers Squibb Company | Pyrrolotriazines as potassium ion channel inhibitors |
US9499522B2 (en) | 2013-03-15 | 2016-11-22 | Blueprint Medicines Corporation | Compositions useful for treating disorders related to kit |
US9334263B2 (en) | 2013-10-17 | 2016-05-10 | Blueprint Medicines Corporation | Compositions useful for treating disorders related to kit |
AU2014337314B2 (en) * | 2013-10-17 | 2018-12-13 | Blueprint Medicines Corporation | Compositions useful for treating disorders related to KIT |
WO2015081783A1 (zh) * | 2013-12-06 | 2015-06-11 | 江苏奥赛康药业股份有限公司 | 吡咯并[2,1-f][1,2,4]三嗪类衍生物及其制备方法和用途 |
WO2015126808A2 (en) * | 2014-02-18 | 2015-08-27 | Baldwin John J | Hbv assay |
US10231965B2 (en) | 2014-02-20 | 2019-03-19 | Ignyta, Inc. | Molecules for administration to ROS1 mutant cancer cells |
CN104974163B (zh) * | 2014-04-14 | 2017-11-07 | 广东东阳光药业有限公司 | 取代的杂芳基化合物及其组合物和用途 |
US9688680B2 (en) | 2014-08-04 | 2017-06-27 | Blueprint Medicines Corporation | Compositions useful for treating disorders related to kit |
AU2015355220B2 (en) | 2014-12-02 | 2020-02-27 | Ignyta, Inc. | Combinations for the treatment of neuroblastoma |
AU2016297754A1 (en) * | 2015-07-24 | 2018-02-15 | Blueprint Medicines Corporation | Compounds useful for treating disorders related to KIT and PDGFR |
AU2016370846B2 (en) | 2015-12-18 | 2022-08-25 | Ignyta, Inc. | Combinations for the treatment of cancer |
CN109311886B (zh) * | 2016-06-23 | 2021-11-09 | 豪夫迈·罗氏有限公司 | [1,2,3]三唑并[4,5-d]嘧啶衍生物 |
TW201837026A (zh) | 2017-01-10 | 2018-10-16 | 德商拜耳廠股份有限公司 | 作為除害劑之雜環衍生物(二) |
KR102515694B1 (ko) | 2017-01-10 | 2023-03-29 | 바이엘 악티엔게젤샤프트 | 해충 방제제로서의 헤테로사이클 유도체 |
WO2018183712A1 (en) | 2017-03-31 | 2018-10-04 | Blueprint Medicines Corporation | Pyrrolo[1,2-b]pyridazine compounds and compositions useful for treating disorders related to kit and pdgfr |
EP3392267A1 (en) | 2017-04-18 | 2018-10-24 | Myr GmbH | Therapy of atherosclerosis, primary biliary cirrhosis and nrlp3 inflammasome-associated disease by htcp inhibitors |
AR112027A1 (es) | 2017-06-15 | 2019-09-11 | Biocryst Pharm Inc | Inhibidores de alk 2 quinasa que contienen imidazol |
BR112020000793A2 (pt) | 2017-07-19 | 2020-07-14 | Ignyta, Inc. | composições farmacêuticas e formas de dosagem |
EP3697390A1 (en) | 2017-10-17 | 2020-08-26 | Ignyta, Inc. | Pharmaceutical compositions and dosage forms |
HRP20240702T1 (hr) | 2019-04-12 | 2024-08-16 | Blueprint Medicines Corporation | Pripravci i metode za liječenje bolesti posredovanih kitom i pdgfra |
FI3856341T3 (fi) | 2019-04-12 | 2023-11-30 | Blueprint Medicines Corp | (s)-1-(4-fluorifenyyli)-1-(2-(4-(6-(1-metyyli-1h-pyratsol-4-yyli)pyrrolo[2,1-f][1,2,4]triatsin-4-yyli)piperatsinyyli)pyrimidin-5-yyli)etaani-1-amiinin kidemuotoja ja valmistusmenetelmiä |
CN113993867B (zh) * | 2019-06-14 | 2023-10-24 | 盛世泰科生物医药技术(苏州)股份有限公司 | 作为fgfr和vegfr双重抑制剂的并环类化合物 |
WO2021257863A1 (en) * | 2020-06-19 | 2021-12-23 | Incyte Corporation | Pyrrolotriazine compounds as jak2 v617f inhibitors |
US11691971B2 (en) | 2020-06-19 | 2023-07-04 | Incyte Corporation | Naphthyridinone compounds as JAK2 V617F inhibitors |
WO2022006456A1 (en) | 2020-07-02 | 2022-01-06 | Incyte Corporation | Tricyclic pyridone compounds as jak2 v617f inhibitors |
WO2022006457A1 (en) | 2020-07-02 | 2022-01-06 | Incyte Corporation | Tricyclic urea compounds as jak2 v617f inhibitors |
WO2022046989A1 (en) | 2020-08-27 | 2022-03-03 | Incyte Corporation | Tricyclic urea compounds as jak2 v617f inhibitors |
IL303812A (en) * | 2020-12-21 | 2023-08-01 | Biocryst Pharm Inc | Dosing regimens for oral ALK2 kinase inhibitors |
WO2022140231A1 (en) | 2020-12-21 | 2022-06-30 | Incyte Corporation | Deazaguaine compounds as jak2 v617f inhibitors |
KR102612407B1 (ko) * | 2021-01-14 | 2023-12-11 | 환인제약 주식회사 | Bms-754807 화합물을 유효성분으로 포함하는 신경염증성 질환의 예방 또는 치료용 약학적 조성물 |
AR125273A1 (es) | 2021-02-25 | 2023-07-05 | Incyte Corp | Lactamas espirocíclicas como inhibidores de jak2 v617f |
CN112679407B (zh) * | 2021-03-17 | 2021-06-04 | 南京桦冠生物技术有限公司 | 一种手性5-取代脯氨酸类化合物的制备方法 |
TW202317086A (zh) * | 2021-09-29 | 2023-05-01 | 加拿大商修復治療公司 | 化合物、醫藥組成物及製備化合物之方法及其使用方法 |
US12084430B2 (en) | 2022-03-17 | 2024-09-10 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
WO2024069592A1 (en) * | 2022-09-29 | 2024-04-04 | Repare Therapeutics Inc. | N-(5-substituted-[(l,3,4-thiadiazolyl) or (l,3-thiazolyl)](substituted)carboxamide compounds, pharmaceutical compositions, and methods of preparing the amide compounds and of their use |
CN116178358B (zh) * | 2022-11-04 | 2024-04-19 | 济南大学 | 一种靶向c-Src激酶SH3结构域的化合物及其应用 |
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MXPA01011832A (es) | 1999-05-21 | 2002-06-21 | Squibb Bristol Myers Co | Inhibidores de cinasas, de pirrolotriazina. |
US6982265B1 (en) | 1999-05-21 | 2006-01-03 | Bristol Myers Squibb Company | Pyrrolotriazine inhibitors of kinases |
US6670357B2 (en) | 2000-11-17 | 2003-12-30 | Bristol-Myers Squibb Company | Methods of treating p38 kinase-associated conditions and pyrrolotriazine compounds useful as kinase inhibitors |
TWI329112B (en) * | 2002-07-19 | 2010-08-21 | Bristol Myers Squibb Co | Novel inhibitors of kinases |
US6951859B2 (en) * | 2002-08-02 | 2005-10-04 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US7713973B2 (en) | 2004-10-15 | 2010-05-11 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
PL2041138T3 (pl) * | 2006-07-07 | 2014-11-28 | Bristol Myers Squibb Co | Pirolotriazyny jako inhibitory kinazy |
US7605160B2 (en) | 2006-08-09 | 2009-10-20 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US7531539B2 (en) * | 2006-08-09 | 2009-05-12 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
EP2081936B1 (en) | 2006-11-03 | 2014-04-02 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
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2007
- 2007-07-03 PL PL07799265T patent/PL2041138T3/pl unknown
- 2007-07-03 WO PCT/US2007/072697 patent/WO2008005956A2/en active Application Filing
- 2007-07-03 KR KR1020097002487A patent/KR101443400B1/ko active IP Right Grant
- 2007-07-03 SI SI200731488T patent/SI2041138T1/sl unknown
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