HK1151694A1 - 作為極光激酶抑制劑的稠合雙環嘧啶化合物 - Google Patents
作為極光激酶抑制劑的稠合雙環嘧啶化合物Info
- Publication number
- HK1151694A1 HK1151694A1 HK11105941.6A HK11105941A HK1151694A1 HK 1151694 A1 HK1151694 A1 HK 1151694A1 HK 11105941 A HK11105941 A HK 11105941A HK 1151694 A1 HK1151694 A1 HK 1151694A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- kinase inhibitors
- fused bicyclic
- aurora kinase
- pyrimidine compounds
- bicyclic pyrimidine
- Prior art date
Links
- 239000003719 aurora kinase inhibitor Substances 0.000 title 1
- -1 bicyclic pyrimidine compounds Chemical class 0.000 title 1
Classifications
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
-
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4906308P | 2008-04-30 | 2008-04-30 | |
PCT/US2009/041382 WO2009134658A2 (en) | 2008-04-30 | 2009-04-22 | Fused bicyclic pyrimidine compounds as aurora kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1151694A1 true HK1151694A1 (zh) | 2012-02-10 |
Family
ID=41255689
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK11105941.6A HK1151694A1 (zh) | 2008-04-30 | 2011-06-13 | 作為極光激酶抑制劑的稠合雙環嘧啶化合物 |
Country Status (13)
Country | Link |
---|---|
US (1) | US8138194B2 (zh) |
EP (1) | EP2276346B1 (zh) |
JP (1) | JP5502072B2 (zh) |
KR (1) | KR101667822B1 (zh) |
CN (1) | CN102014627B (zh) |
AU (1) | AU2009241469B2 (zh) |
CA (1) | CA2722220C (zh) |
DK (1) | DK2276346T3 (zh) |
ES (1) | ES2616255T3 (zh) |
HK (1) | HK1151694A1 (zh) |
PL (1) | PL2276346T3 (zh) |
TW (1) | TWI363627B (zh) |
WO (1) | WO2009134658A2 (zh) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR079705A1 (es) * | 2009-12-23 | 2012-02-15 | Biocryst Pharm Inc | Compuestos heterociclicos como inhibidores de janus quinasa |
BR112012016376A2 (pt) | 2009-12-30 | 2019-09-24 | Arqule Inc | compostos de pirrolo-aminopirimida substituída |
TW201307347A (zh) | 2010-11-01 | 2013-02-16 | Arqule Inc | 經取代苯並-咪唑並-吡啶並-二氮呯化合物 |
EP2831073B1 (en) * | 2012-03-30 | 2020-12-09 | Rhizen Pharmaceuticals S.A. | Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b]pyridine compounds as modulators of c-met protein kinases |
CN104470926A (zh) | 2012-05-21 | 2015-03-25 | 拜耳医药股份有限公司 | 取代的吡咯并嘧啶 |
JP6234444B2 (ja) | 2012-05-21 | 2017-11-22 | バイエル ファーマ アクチエンゲゼルシャフト | チエノピリミジン類 |
WO2013174735A1 (en) | 2012-05-21 | 2013-11-28 | Bayer Pharma Aktiengesellschaft | Substituted benzothienopyrimidines |
BR112014032913A2 (pt) | 2012-06-29 | 2017-06-27 | Pfizer | novas 4-(amino-substituídas)-7h-pirrolo[2,3-d]pirimidinas como inibidores de lrrk2 |
TW201412740A (zh) | 2012-09-20 | 2014-04-01 | Bayer Pharma AG | 經取代之吡咯并嘧啶胺基苯并噻唑酮 |
CN103664993B (zh) * | 2012-09-25 | 2016-05-25 | 韩冰 | 一类治疗缺血性脑损伤的化合物及其用途 |
CN103012428A (zh) | 2013-01-08 | 2013-04-03 | 中国药科大学 | 4-(五元杂环并嘧啶/吡啶取代)氨基-1H-3-吡唑甲酰胺类CDK/Aurora双重抑制剂及其用途 |
CN105189518A (zh) | 2013-02-01 | 2015-12-23 | 拜耳制药股份公司 | 取代的噻吩并吡啶和其药物用途 |
WO2014135480A1 (en) | 2013-03-06 | 2014-09-12 | Bayer Pharma Aktiengesellschaft | Substituted thiazolopyrimidines |
US9695171B2 (en) | 2013-12-17 | 2017-07-04 | Pfizer Inc. | 3,4-disubstituted-1 H-pyrrolo[2,3-b]pyridines and 4,5-disubstituted-7H-pyrrolo[2,3-c]pyridazines as LRRK2 inhibitors |
KR20160142401A (ko) | 2014-04-25 | 2016-12-12 | 화이자 인코포레이티드 | 도파민 d1 리간드로서 헤테로방향족 화합물 및 이의 용도 |
FR3037956B1 (fr) * | 2015-06-23 | 2017-08-04 | Servier Lab | Nouveaux derives d'acide amine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
CN105061460B (zh) * | 2015-08-18 | 2017-06-30 | 沈阳药科大学 | 含有硫醚结构的四氢苯并[4,5]噻吩并[2,3‑d]嘧啶类化合物及其应用 |
CN105061461B (zh) * | 2015-08-18 | 2017-06-30 | 沈阳药科大学 | 含有苄胺结构的四氢苯并[4,5]噻吩并[2,3‑d]嘧啶类化合物及其应用 |
EP3350178B1 (en) | 2015-09-14 | 2021-10-20 | Pfizer Inc. | Novel imidazo [4,5-c]quinoline and imidazo [4,5-c][1,5]naphthyridine derivatives as lrrk2 inhibitors |
US9630968B1 (en) | 2015-12-23 | 2017-04-25 | Arqule, Inc. | Tetrahydropyranyl amino-pyrrolopyrimidinone and methods of use thereof |
FR3046792B1 (fr) * | 2016-01-19 | 2018-02-02 | Les Laboratoires Servier | Nouveaux derives d'ammonium, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
CN106243124B (zh) * | 2016-07-29 | 2018-03-09 | 湖北民族学院 | 一种噻吩并嘧啶脲类化合物及其制备方法和应用 |
CN109890821A (zh) | 2016-08-24 | 2019-06-14 | 艾科尔公司 | 氨基-吡咯并嘧啶酮化合物及其使用方法 |
CN106810512B (zh) * | 2017-01-18 | 2019-09-10 | 江苏省中医药研究院 | Idh2突变体抑制剂及其用途 |
BR112020003130A2 (pt) * | 2017-08-15 | 2020-10-13 | AbbVie Deutschland GmbH & Co. KG | inibidores macrocíclicos de mcl-1 e métodos de uso |
US10676485B2 (en) * | 2017-08-15 | 2020-06-09 | Abbvie Inc. | Macrocyclic MCL-1 inhibitors and methods of use |
WO2019035927A1 (en) * | 2017-08-15 | 2019-02-21 | Abbvie Inc. | MACROCYCLIC MCL-1 INHIBITORS AND METHODS OF USE |
WO2021041392A1 (en) * | 2019-08-26 | 2021-03-04 | Chemwerth, Inc. | Substituted (7h-pyrrolo[2,3-d]pyrimidin-4-yl)amino compounds useful as jak1 inhibitors |
CN112500421B (zh) * | 2020-12-15 | 2021-08-24 | 河南科技大学第一附属医院 | 一种可用于杀菌消毒的苯并吡喃脲类化合物的制备方法及应用 |
TW202413367A (zh) * | 2022-08-19 | 2024-04-01 | 財團法人國家衛生研究院 | Tam受體抑制劑 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4008726A1 (de) * | 1990-03-19 | 1991-09-26 | Basf Ag | Thieno(2,3-d)pyrimidinderivate |
TWI304061B (en) * | 2000-10-20 | 2008-12-11 | Eisai R&D Man Co Ltd | Nitrogen-containing aromatic ring derivatives |
DE10141212A1 (de) | 2001-08-22 | 2003-03-06 | Bayer Ag | Neue 4-Aminofuropyrimidine und ihre Verwendung |
WO2003022852A2 (en) | 2001-09-11 | 2003-03-20 | Smithkline Beecham Corporation | Furo-and thienopyrimidine derivatives as angiogenesis inhibitors |
US6814324B2 (en) * | 2002-07-03 | 2004-11-09 | Segway Systems, Llc | Releasably latchable leader block in tape threading apparatus for data storage systems and method therefor |
MY136174A (en) | 2002-12-24 | 2008-08-29 | Astrazeneca Ab | Phosphonooxy quinazoline derivatives and their pharmaceutical use |
AU2004282179B2 (en) * | 2003-10-14 | 2011-05-19 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Protein kinase inhibitors |
US20050187389A1 (en) | 2004-01-13 | 2005-08-25 | Ambit Biosciences Corporation | Pyrrolopyrimidine derivatives and analogs and their use in the treatment and prevention of diseases |
KR20050091462A (ko) | 2004-03-12 | 2005-09-15 | 한국과학기술연구원 | 푸로피리미딘 화합물 및 이를 포함하는 ddr2 티로신키나아제 활성 저해제 |
BRPI0511139B8 (pt) | 2004-05-14 | 2021-05-25 | Millennium Pharm Inc | compostos que inibem quinase aurora e composição farmacêutica contendo os mesmos |
WO2006004658A2 (en) | 2004-06-29 | 2006-01-12 | Amgen Inc. | Furanopyrimidines |
EP1781653A1 (en) | 2004-07-05 | 2007-05-09 | Astex Therapeutics Limited | 3,4-disubstituted pyrazoles as cyclin dependent kinases (cdk) or aurora kinase or glycogen synthase 3 (gsk-3) inhibitors |
CN101160316A (zh) * | 2004-07-16 | 2008-04-09 | 苏内西斯医药公司 | 适合用作aurora激酶抑制剂的噻吩并嘧啶 |
NZ552751A (en) | 2004-07-16 | 2010-11-26 | Sunesis Pharmaceuticals Inc | Thienopyrimidines useful as aurora kinase inhibitors |
US7932257B2 (en) * | 2005-07-22 | 2011-04-26 | Sunesis Pharmaceuticals, Inc. | Substituted pyrazolo[4,3-d]pyrimidines as aurora kinase inhibitors |
DE102005037499A1 (de) * | 2005-08-09 | 2007-02-15 | Merck Patent Gmbh | Pyrazolderivate |
DE602006009539D1 (de) * | 2005-10-28 | 2009-11-12 | Irm Llc | Verbindungen und zusammensetzungen als proteinkinaseinhibitoren |
PT1962830E (pt) | 2005-12-23 | 2013-05-29 | Glaxosmithkline Llc | Inibidores azaindólicos de cinases aurora |
-
2009
- 2009-04-22 WO PCT/US2009/041382 patent/WO2009134658A2/en active Application Filing
- 2009-04-22 DK DK09739460.5T patent/DK2276346T3/en active
- 2009-04-22 ES ES09739460.5T patent/ES2616255T3/es active Active
- 2009-04-22 AU AU2009241469A patent/AU2009241469B2/en active Active
- 2009-04-22 KR KR1020107025018A patent/KR101667822B1/ko active IP Right Grant
- 2009-04-22 JP JP2011507540A patent/JP5502072B2/ja active Active
- 2009-04-22 PL PL09739460T patent/PL2276346T3/pl unknown
- 2009-04-22 US US12/428,044 patent/US8138194B2/en active Active
- 2009-04-22 EP EP09739460.5A patent/EP2276346B1/en active Active
- 2009-04-22 CN CN200980115577.4A patent/CN102014627B/zh active Active
- 2009-04-22 CA CA2722220A patent/CA2722220C/en active Active
- 2009-04-29 TW TW098114168A patent/TWI363627B/zh active
-
2011
- 2011-06-13 HK HK11105941.6A patent/HK1151694A1/zh unknown
Also Published As
Publication number | Publication date |
---|---|
EP2276346A2 (en) | 2011-01-26 |
EP2276346A4 (en) | 2011-08-24 |
WO2009134658A2 (en) | 2009-11-05 |
CN102014627B (zh) | 2014-10-29 |
JP5502072B2 (ja) | 2014-05-28 |
AU2009241469B2 (en) | 2015-05-07 |
KR20100132067A (ko) | 2010-12-16 |
KR101667822B1 (ko) | 2016-10-19 |
CA2722220C (en) | 2016-06-07 |
PL2276346T3 (pl) | 2017-07-31 |
TW200948365A (en) | 2009-12-01 |
JP2011522789A (ja) | 2011-08-04 |
US8138194B2 (en) | 2012-03-20 |
EP2276346B1 (en) | 2016-11-23 |
CN102014627A (zh) | 2011-04-13 |
AU2009241469A1 (en) | 2009-11-05 |
ES2616255T3 (es) | 2017-06-12 |
TWI363627B (en) | 2012-05-11 |
DK2276346T3 (en) | 2017-02-27 |
CA2722220A1 (en) | 2009-11-05 |
WO2009134658A3 (en) | 2009-12-30 |
US20090275533A1 (en) | 2009-11-05 |
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