CN104254532A - 磷酸肌醇3-激酶抑制剂 - Google Patents
磷酸肌醇3-激酶抑制剂 Download PDFInfo
- Publication number
- CN104254532A CN104254532A CN201380013216.5A CN201380013216A CN104254532A CN 104254532 A CN104254532 A CN 104254532A CN 201380013216 A CN201380013216 A CN 201380013216A CN 104254532 A CN104254532 A CN 104254532A
- Authority
- CN
- China
- Prior art keywords
- compound
- alkyl
- independently
- optionally substituted
- halogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 0 *C(*C(C(*)=C1[U])=C2C(C=C*3)=C3***2)=C1N Chemical compound *C(*C(C(*)=C1[U])=C2C(C=C*3)=C3***2)=C1N 0.000 description 1
- VJZOHOSEDQWRQA-UHFFFAOYSA-N Bc1cccc2c1cc[nH]2 Chemical compound Bc1cccc2c1cc[nH]2 VJZOHOSEDQWRQA-UHFFFAOYSA-N 0.000 description 1
- WAEZOSSWRXDWAX-UHFFFAOYSA-N Nc1cc(Cl)nc(Cl)c1 Chemical compound Nc1cc(Cl)nc(Cl)c1 WAEZOSSWRXDWAX-UHFFFAOYSA-N 0.000 description 1
- BBKFPYLOTAPCPW-UHFFFAOYSA-N Nc1cc(N2CCOCC2)nc(-c2cccc3c2cc[nH]3)c1 Chemical compound Nc1cc(N2CCOCC2)nc(-c2cccc3c2cc[nH]3)c1 BBKFPYLOTAPCPW-UHFFFAOYSA-N 0.000 description 1
- MQMWPHZNMJNGAY-UHFFFAOYSA-N Nc1cc(N2CCOCC2)nc(Cl)c1 Chemical compound Nc1cc(N2CCOCC2)nc(Cl)c1 MQMWPHZNMJNGAY-UHFFFAOYSA-N 0.000 description 1
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
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1204125.7A GB201204125D0 (en) | 2012-03-08 | 2012-03-08 | Compounds |
| GB1204125.7 | 2012-03-08 | ||
| PCT/GB2013/050583 WO2013132270A1 (en) | 2012-03-08 | 2013-03-08 | Phosphoinositide 3-kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN104254532A true CN104254532A (zh) | 2014-12-31 |
Family
ID=46026238
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380013216.5A Pending CN104254532A (zh) | 2012-03-08 | 2013-03-08 | 磷酸肌醇3-激酶抑制剂 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US9663487B2 (cg-RX-API-DMAC10.html) |
| EP (1) | EP2822943B1 (cg-RX-API-DMAC10.html) |
| CN (1) | CN104254532A (cg-RX-API-DMAC10.html) |
| GB (1) | GB201204125D0 (cg-RX-API-DMAC10.html) |
| IN (1) | IN2014DN07509A (cg-RX-API-DMAC10.html) |
| WO (1) | WO2013132270A1 (cg-RX-API-DMAC10.html) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108135855A (zh) * | 2015-08-19 | 2018-06-08 | 卡鲁斯治疗有限公司 | 包含三环杂环化合物的组合物 |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2012002059A (es) | 2009-08-20 | 2012-04-19 | Karus Therapeutics Ltd | Compestos heterociclicos triciclicos como inhibidores de fosfoionositida 3-quinasa. |
| GB201204125D0 (en) | 2012-03-08 | 2012-04-25 | Karus Therapeutics Ltd | Compounds |
| EP2917202B1 (en) | 2012-11-07 | 2018-05-02 | Karus Therapeutics Limited | Novel histone deacetylase inhibitors and their use in therapy |
| JP6434416B2 (ja) | 2012-11-08 | 2018-12-05 | ライゼン・ファーマシューティカルズ・エスアー | PDE4阻害剤とPI3δ阻害剤または二重PI3δ−γキナーゼ阻害剤とを含有する薬学的組成物 |
| CA2911856A1 (en) | 2013-05-10 | 2014-11-13 | Karus Therapeutics Ltd | Tri-substituted amino hydroxamate compounds and pharmaceutical compositions thereof for use as histone deacetylase inhibitors |
| GB201402431D0 (en) | 2014-02-12 | 2014-03-26 | Karus Therapeutics Ltd | Compounds |
| GB201419228D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| GB201419264D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| GB201514754D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
| GB201514760D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds and method of use |
| GB201514751D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
| JP6557436B1 (ja) | 2018-03-12 | 2019-08-07 | アッヴィ・インコーポレイテッド | チロシンキナーゼ2媒介性シグナル伝達の阻害剤 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002002551A1 (en) * | 2000-06-30 | 2002-01-10 | Sugen, Inc. | 4-heteroaryl-3-heteroarylidenyl-2-indolinones and their use as protein kinase inhibitors |
| CN101228161A (zh) * | 2005-05-20 | 2008-07-23 | 沃泰克斯药物股份有限公司 | 适用作蛋白激酶抑制剂的吡咯并吡啶类 |
| WO2008145688A2 (en) * | 2007-06-01 | 2008-12-04 | Glaxo Group Limited | Pyrrolopyridine compounds, process for their preparation, and their use as medicaments |
| CN101663276A (zh) * | 2007-01-31 | 2010-03-03 | 沃泰克斯药物股份有限公司 | 用作激酶抑制剂的2-氨基吡啶衍生物 |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1445742A1 (de) | 1963-11-06 | 1968-12-19 | Bayer Ag | Verfahren zur Herstellung von 2-Stellung substituierten Benzoxazinonen |
| US4017500A (en) | 1973-07-16 | 1977-04-12 | Schering Corporation | Certain 8-amino-1,7-naphthyridines |
| US5703075A (en) | 1988-12-21 | 1997-12-30 | Pharmacia & Upjohn Company | Antiatherosclerotic and antithrombotic 1-benzopyran-4-ones and 2-amino-1,3-benzoxazine-4-ones |
| KR100774855B1 (ko) | 2000-04-27 | 2007-11-08 | 아스텔라스세이야쿠 가부시키가이샤 | 축합 헤테로아릴 유도체 |
| US6608053B2 (en) | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| US6905669B2 (en) | 2001-04-24 | 2005-06-14 | Supergen, Inc. | Compositions and methods for reestablishing gene transcription through inhibition of DNA methylation and histone deacetylase |
| EP2280003B1 (en) | 2002-07-15 | 2014-04-02 | Symphony Evolution, Inc. | Process for preparing receptor-type kinase modulators |
| FR2846657B1 (fr) | 2002-11-05 | 2004-12-24 | Servier Lab | Nouveaux composes pyridopyrimidinone, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| CN1922171B (zh) | 2004-02-26 | 2012-10-17 | Aska制药株式会社 | 嘧啶衍生物 |
| GB0423653D0 (en) | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
| TW200738709A (en) * | 2006-01-19 | 2007-10-16 | Osi Pharm Inc | Fused heterobicyclic kinase inhibitors |
| RU2008141356A (ru) | 2006-04-26 | 2010-06-10 | Ф. Хоффманн-Ля Рош Аг (Ch) | Производные пиримидина в качестве ингибиторов фосфатидилинозитол-3-киназы (pi3k) |
| CL2007001166A1 (es) | 2006-04-26 | 2008-01-25 | Piramed Ltd | Compuestos derivados de pirimidina condensada, inhibidores de pi3-quinasa; procesos para preparar los compuestos; composicion farmaceutica que los comprende; uso de los compuestos en la preparacion de medicamentos; proceso para preparar la composicion farmaceutica; y kit que incluye a la composicion farmaceutica |
| SG178786A1 (en) | 2006-11-13 | 2012-03-29 | Lilly Co Eli | Thienopyrimidinones for treatment of inflammatory disorders and cancers |
| CA2677096A1 (en) | 2007-01-31 | 2008-08-07 | Vertex Pharmaceuticals Incorporated | Kinase inhibitors |
| EP2139332A4 (en) | 2007-03-28 | 2010-04-21 | Merck Sharp & Dohme | SUBSTITUTED PYRIDO [2,3-D] PYRIMIDIN DERIVATIVES AS CANNABINOID-1 RECEPTOR MODULATORS |
| JP2010529031A (ja) | 2007-05-29 | 2010-08-26 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | Pi3キナーゼ阻害剤としてのナフチリジン誘導体 |
| US20110201608A1 (en) | 2008-08-05 | 2011-08-18 | Boehringer Ingelheim International Gmbh | Substituted naphthyridines and use thereof as medicines |
| AU2009299894A1 (en) | 2008-10-03 | 2010-04-08 | Merck Serono S.A. | 4 -morpholino-pyrido [3, 2 -d] pyrimidines active on Pi3k |
| GB2465405A (en) | 2008-11-10 | 2010-05-19 | Univ Basel | Triazine, pyrimidine and pyridine analogues and their use in therapy |
| EP2459543B1 (en) | 2009-07-29 | 2017-08-30 | Karus Therapeutics Limited | Benzo[e][1,3]oxazin-4-one derivatives as phosphoinositide 3-kinase inhibitors |
| MX2012002059A (es) | 2009-08-20 | 2012-04-19 | Karus Therapeutics Ltd | Compestos heterociclicos triciclicos como inhibidores de fosfoionositida 3-quinasa. |
| WO2011079231A1 (en) | 2009-12-23 | 2011-06-30 | Gatekeeper Pharmaceutical, Inc. | Compounds that modulate egfr activity and methods for treating or preventing conditions therewith |
| GB201007347D0 (en) | 2010-04-30 | 2010-06-16 | Karus Therapeutics Ltd | Compounds |
| PL3009431T3 (pl) | 2011-07-27 | 2018-02-28 | Astrazeneca Ab | Pochodne 2-(2,4,5-podstawionej-anilino) pirymidyny jako modulatory egfr użyteczne do leczenia nowotworu |
| WO2013017480A1 (en) | 2011-07-29 | 2013-02-07 | Cellzome Limited | Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors |
| GB201204125D0 (en) | 2012-03-08 | 2012-04-25 | Karus Therapeutics Ltd | Compounds |
| MX2015006152A (es) | 2012-11-20 | 2016-01-20 | Genentech Inc | Compuestos de aminopirimidina como inhibidores de mutantes de egfr que contienen t7 9 0m. |
| CA2911856A1 (en) | 2013-05-10 | 2014-11-13 | Karus Therapeutics Ltd | Tri-substituted amino hydroxamate compounds and pharmaceutical compositions thereof for use as histone deacetylase inhibitors |
| EP3052494B1 (en) | 2013-06-28 | 2018-12-26 | H. Hoffnabb-La Roche Ag | Azaindazole compounds as inhibitors of t790m containing egfr mutants |
| JP6584391B2 (ja) | 2013-10-10 | 2019-10-02 | アセチロン ファーマシューティカルズ インコーポレイテッドAcetylon Pharmaceuticals,Inc. | 非ホジキンリンパ腫を治療するための、hdac阻害剤単独またはpi3k阻害剤との組み合わせ |
| GB201402431D0 (en) | 2014-02-12 | 2014-03-26 | Karus Therapeutics Ltd | Compounds |
| GB201514756D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compound and method of use |
| GB201514751D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
| GB201514758D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Formulation |
| GB201514760D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds and method of use |
| GB201514754D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
-
2012
- 2012-03-08 GB GBGB1204125.7A patent/GB201204125D0/en not_active Ceased
-
2013
- 2013-03-08 EP EP13709523.8A patent/EP2822943B1/en not_active Not-in-force
- 2013-03-08 US US14/382,196 patent/US9663487B2/en not_active Expired - Fee Related
- 2013-03-08 CN CN201380013216.5A patent/CN104254532A/zh active Pending
- 2013-03-08 IN IN7509DEN2014 patent/IN2014DN07509A/en unknown
- 2013-03-08 WO PCT/GB2013/050583 patent/WO2013132270A1/en not_active Ceased
-
2017
- 2017-04-25 US US15/496,511 patent/US10035785B2/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002002551A1 (en) * | 2000-06-30 | 2002-01-10 | Sugen, Inc. | 4-heteroaryl-3-heteroarylidenyl-2-indolinones and their use as protein kinase inhibitors |
| CN101228161A (zh) * | 2005-05-20 | 2008-07-23 | 沃泰克斯药物股份有限公司 | 适用作蛋白激酶抑制剂的吡咯并吡啶类 |
| CN101663276A (zh) * | 2007-01-31 | 2010-03-03 | 沃泰克斯药物股份有限公司 | 用作激酶抑制剂的2-氨基吡啶衍生物 |
| WO2008145688A2 (en) * | 2007-06-01 | 2008-12-04 | Glaxo Group Limited | Pyrrolopyridine compounds, process for their preparation, and their use as medicaments |
Non-Patent Citations (1)
| Title |
|---|
| MOHAMMAD SAIFUDDIN ET AL.: "Water-Accelerated Cationic π-(7-endo) Cyclisation:Application to Indole-Based Peri-Annulated Polyheterocycles", 《EUR.J.ORG.CHEM.》, no. 26, 20 July 2010 (2010-07-20), pages 5109 - 3 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108135855A (zh) * | 2015-08-19 | 2018-06-08 | 卡鲁斯治疗有限公司 | 包含三环杂环化合物的组合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2822943B1 (en) | 2018-10-03 |
| GB201204125D0 (en) | 2012-04-25 |
| IN2014DN07509A (cg-RX-API-DMAC10.html) | 2015-04-24 |
| US10035785B2 (en) | 2018-07-31 |
| EP2822943A1 (en) | 2015-01-14 |
| WO2013132270A1 (en) | 2013-09-12 |
| US20180072699A1 (en) | 2018-03-15 |
| US20150080395A1 (en) | 2015-03-19 |
| US9663487B2 (en) | 2017-05-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20141231 |
|
| WD01 | Invention patent application deemed withdrawn after publication |