CN101868464B - 作为pi3抑制剂的噻吩并嘧啶衍生物 - Google Patents
作为pi3抑制剂的噻吩并嘧啶衍生物 Download PDFInfo
- Publication number
- CN101868464B CN101868464B CN2008801126921A CN200880112692A CN101868464B CN 101868464 B CN101868464 B CN 101868464B CN 2008801126921 A CN2008801126921 A CN 2008801126921A CN 200880112692 A CN200880112692 A CN 200880112692A CN 101868464 B CN101868464 B CN 101868464B
- Authority
- CN
- China
- Prior art keywords
- thieno
- morpholin
- ylmethyl
- indol
- diaza
- 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.)
- Expired - Fee Related
Links
- 0 CCCOCCNc1nc(*)nc2c1[s]c(*)c2 Chemical compound CCCOCCNc1nc(*)nc2c1[s]c(*)c2 0.000 description 8
- GWNSHRCBWQEQPK-UHFFFAOYSA-N C(COCC1)C1N1CCNCC1 Chemical compound C(COCC1)C1N1CCNCC1 GWNSHRCBWQEQPK-UHFFFAOYSA-N 0.000 description 1
- CKQRFDCOYHDOHL-UHFFFAOYSA-O CC(C)(C)[SH+](C)(C)[n](ccc1c2)c1ccc2F Chemical compound CC(C)(C)[SH+](C)(C)[n](ccc1c2)c1ccc2F CKQRFDCOYHDOHL-UHFFFAOYSA-O 0.000 description 1
- DGDMKKDWXPHWKA-HPDCSRJSSA-N CCC(C1)(C2)C1(CCNC1)[C@@H]1OCC2O Chemical compound CCC(C1)(C2)C1(CCNC1)[C@@H]1OCC2O DGDMKKDWXPHWKA-HPDCSRJSSA-N 0.000 description 1
- OSIZSRFJZJVILD-UHFFFAOYSA-N CN(C1)CC2NC1COC2 Chemical compound CN(C1)CC2NC1COC2 OSIZSRFJZJVILD-UHFFFAOYSA-N 0.000 description 1
- KAUWPAWTMFDVGL-UHFFFAOYSA-N CN1C(C2)CN2CC1 Chemical compound CN1C(C2)CN2CC1 KAUWPAWTMFDVGL-UHFFFAOYSA-N 0.000 description 1
- YKBHIAMXELZBES-UHFFFAOYSA-N CN1C(CC2)CN2CC1 Chemical compound CN1C(CC2)CN2CC1 YKBHIAMXELZBES-UHFFFAOYSA-N 0.000 description 1
- OQMSHITZFTVBHN-UHFFFAOYSA-N CN1CC(CC2)NC2C1 Chemical compound CN1CC(CC2)NC2C1 OQMSHITZFTVBHN-UHFFFAOYSA-N 0.000 description 1
- RIOMVCRDANXKNN-UHFFFAOYSA-N Cc1cc(c(N2CCOCC2)nc(C2CC2)n2)c2[s]1 Chemical compound Cc1cc(c(N2CCOCC2)nc(C2CC2)n2)c2[s]1 RIOMVCRDANXKNN-UHFFFAOYSA-N 0.000 description 1
- KJMVQYBTWHOTSI-UHFFFAOYSA-N Clc(nc1N2CCOCC2)nc2c1[s]c(CN(CC1)CCC11OCCO1)c2 Chemical compound Clc(nc1N2CCOCC2)nc2c1[s]c(CN(CC1)CCC11OCCO1)c2 KJMVQYBTWHOTSI-UHFFFAOYSA-N 0.000 description 1
- GJIJYVIKVNXYPY-UHFFFAOYSA-N Clc(nc1N2CCOCC2)nc2c1[s]c(CN1CC3(CCCC3)NCC1)c2 Chemical compound Clc(nc1N2CCOCC2)nc2c1[s]c(CN1CC3(CCCC3)NCC1)c2 GJIJYVIKVNXYPY-UHFFFAOYSA-N 0.000 description 1
- PXIYAYABWJJIJT-CYBMUJFWSA-N Clc1nc(N2CCOCC2)c2[s]c(CN3C[C@@H](CCC4)N4CC3)cc2n1 Chemical compound Clc1nc(N2CCOCC2)c2[s]c(CN3C[C@@H](CCC4)N4CC3)cc2n1 PXIYAYABWJJIJT-CYBMUJFWSA-N 0.000 description 1
- DSOLFSSRDLXUTP-UHFFFAOYSA-N O=C(CNCC1)N1C1CCOCC1 Chemical compound O=C(CNCC1)N1C1CCOCC1 DSOLFSSRDLXUTP-UHFFFAOYSA-N 0.000 description 1
- PFAKZIZFIXKDFP-UHFFFAOYSA-N O=Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1 Chemical compound O=Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1 PFAKZIZFIXKDFP-UHFFFAOYSA-N 0.000 description 1
- UJBGQWKTUHGOGV-UHFFFAOYSA-N OCC(CN(Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)CC1)C1N1CCC1 Chemical compound OCC(CN(Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)CC1)C1N1CCC1 UJBGQWKTUHGOGV-UHFFFAOYSA-N 0.000 description 1
- UJBGQWKTUHGOGV-XPCCGILXSA-N OC[C@@H](CN(Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)CC1)C1N1CCC1 Chemical compound OC[C@@H](CN(Cc1cc(nc(nc2N3CCOCC3)Cl)c2[s]1)CC1)C1N1CCC1 UJBGQWKTUHGOGV-XPCCGILXSA-N 0.000 description 1
- MZZALHIPUZSVKG-UHFFFAOYSA-N OCc1cc(nc(-c2c(cc[nH]3)c3cc(F)c2)nc2N3CCOCC3)c2[s]1 Chemical compound OCc1cc(nc(-c2c(cc[nH]3)c3cc(F)c2)nc2N3CCOCC3)c2[s]1 MZZALHIPUZSVKG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- 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
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- 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
- A61P31/12—Antivirals
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Virology (AREA)
- Neurology (AREA)
- Communicable Diseases (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0721059.8 | 2007-10-26 | ||
| GBGB0721095.8A GB0721095D0 (en) | 2007-10-26 | 2007-10-26 | Pharmaceutical compounds |
| GB07210958 | 2007-10-26 | ||
| PCT/GB2008/003621 WO2009053715A1 (en) | 2007-10-26 | 2008-10-27 | Thienopyrimidiene derivatives as pi3k inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101868464A CN101868464A (zh) | 2010-10-20 |
| CN101868464B true CN101868464B (zh) | 2013-11-13 |
Family
ID=38830047
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008801126921A Expired - Fee Related CN101868464B (zh) | 2007-10-26 | 2008-10-27 | 作为pi3抑制剂的噻吩并嘧啶衍生物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8293735B2 (enExample) |
| EP (1) | EP2205610B1 (enExample) |
| JP (1) | JP5675360B2 (enExample) |
| CN (1) | CN101868464B (enExample) |
| CA (1) | CA2701276A1 (enExample) |
| ES (1) | ES2442501T3 (enExample) |
| GB (1) | GB0721095D0 (enExample) |
| WO (1) | WO2009053715A1 (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7754208B2 (en) | 2001-01-17 | 2010-07-13 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
| US20030133939A1 (en) | 2001-01-17 | 2003-07-17 | Genecraft, Inc. | Binding domain-immunoglobulin fusion proteins |
| SG10201403526YA (en) | 2005-07-25 | 2014-10-30 | Emergent Product Dev Seattle | B-cell reduction using cd37-specific and cd20-specific binding molecules |
| AU2007257692B2 (en) | 2006-06-12 | 2013-11-14 | Aptevo Research And Development Llc | Single-chain multivalent binding proteins with effector function |
| JP5348725B2 (ja) | 2007-10-25 | 2013-11-20 | ジェネンテック, インコーポレイテッド | チエノピリミジン化合物の製造方法 |
| CA2710194C (en) | 2007-12-19 | 2014-04-22 | Amgen Inc. | Inhibitors of p13 kinase |
| ES2368700T3 (es) | 2008-04-11 | 2011-11-21 | Emergent Product Development Seattle, Llc | Agente inmunoterapéutico para cd37 y combinación con un agente quimioterapéutico bifuncional del mismo. |
| TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| CA2772371A1 (en) * | 2009-05-27 | 2010-12-02 | F. Hoffmann-La Roche Ag | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
| BRPI1009022A2 (pt) | 2009-05-27 | 2016-03-08 | Hoffmann La Roche | "composto, composição farmacêutica, processo para produzir uma composição farmacêutica, uso de um composto, método para tratamento de uma doença ou transtorno e kit" |
| GB201004200D0 (en) * | 2010-03-15 | 2010-04-28 | Univ Basel | Spirocyclic compounds and their use as therapeutic agents and diagnostic probes |
| EP2580320B1 (en) | 2010-06-14 | 2018-08-01 | The Scripps Research Institute | Reprogramming of cells to a new fate |
| KR20140099556A (ko) | 2010-12-16 | 2014-08-12 | 에프. 호프만-라 로슈 아게 | 트라이사이클릭 pi3k 억제제 화합물 및 이의 사용 방법 |
| ES2464598T3 (es) | 2011-07-22 | 2014-06-03 | Université Joseph Fourier | Nuevos derivados bis-indólicos, procedimiento para su preparación, y sus utilizaciones como fármaco |
| BR112014028881A2 (pt) | 2012-05-23 | 2017-06-27 | Hoffmann La Roche | populações de células, banco de células, métodos de obtenção de uma população de células, métodos de identificação de um fator, métodos de seleção, métodos de fornecimento de terapia, populações de hepatócitos e método de obtenção de células |
| JP6022691B2 (ja) * | 2012-08-30 | 2016-11-09 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | ジオキシノ−及びオキサジン−[2,3−d]ピリミジンpi3k阻害剤化合物及び使用方法 |
| GB201402431D0 (en) * | 2014-02-12 | 2014-03-26 | Karus Therapeutics Ltd | Compounds |
| WO2017053469A2 (en) | 2015-09-21 | 2017-03-30 | Aptevo Research And Development Llc | Cd3 binding polypeptides |
| US10591000B2 (en) * | 2016-05-24 | 2020-03-17 | Means Industries, Inc. | One-way clutch assembly and coupling member for therein wherein locking member dynamics with respect to strut laydown speed are enhanced |
| TW201813963A (zh) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| TW201815787A (zh) | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| TW201825465A (zh) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| KR102468480B1 (ko) * | 2018-12-27 | 2022-11-18 | 홀로스메딕 주식회사 | 신규한 화합물 및 이를 포함하는 항암 활성 증진용 약학 조성물 |
| KR102338609B1 (ko) * | 2019-05-20 | 2021-12-14 | 보령제약 주식회사 | 피리도-피리미딘 화합물 및 이를 유효성분으로 포함하는 pi3k 관련 질환의 예방 또는 치료용 약학적 조성물 |
| EP3972963A1 (en) | 2019-05-21 | 2022-03-30 | Bayer Aktiengesellschaft | Identification and use of kras inhibitors |
| JP7655863B2 (ja) * | 2019-05-31 | 2025-04-02 | イデアヤ、バイオサイエンシズ、インコーポレイテッド | Dnaポリメラーゼシータ阻害剤としてのチアジアゾリル誘導体 |
| EP4053127A4 (en) * | 2019-10-31 | 2023-11-29 | Holosmedic | NOVEL COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING SAME FOR PREVENTING OR TREATING CANCER |
| CN112920199B (zh) * | 2020-06-02 | 2023-02-03 | 四川大学 | 一种哌嗪酮取代物或其衍生物及其制备方法和应用、药物组合物 |
| KR20240161147A (ko) | 2022-03-14 | 2024-11-12 | 슬랩 파마슈티컬스 엘엘씨 | 다중 사이클릭 화합물 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1470356A1 (de) * | 1964-01-15 | 1970-04-30 | Thomae Gmbh Dr K | Neue Thieno[3,2-d]pyrimidine und Verfahren zu ihrer Herstellung |
| BE754606A (fr) * | 1969-08-08 | 1971-02-08 | Thomae Gmbh Dr K | Nouvelles 2-aminoalcoylamino-thieno(3,2-d)pyrimidines et leurs procedesde fabrication |
| BE759493A (fr) * | 1969-11-26 | 1971-05-25 | Thomae Gmbh Dr K | Nouvelles 2-(5-nitro-2-furyl)-thieno(3,2-d) pyrimidines et procedes pour les fabriquer |
| US3763156A (en) * | 1970-01-28 | 1973-10-02 | Boehringer Sohn Ingelheim | 2-heterocyclic amino-4-morpholinothieno(3,2-d)pyrimidines |
| RO62428A (fr) | 1971-05-04 | 1978-01-15 | Thomae Gmbh Dr K | Procede pour la preparation des thyeno-(3,2-d)-pyrimidines |
| CH592668A5 (enExample) * | 1973-10-02 | 1977-10-31 | Delalande Sa | |
| GB1570494A (en) * | 1975-11-28 | 1980-07-02 | Ici Ltd | Thienopyrimidine derivatives and their use as pesticides |
| US4196207A (en) * | 1977-05-23 | 1980-04-01 | Ici Australia Limited | Process for controlling eradicating or preventing infestations of animals by Ixodid ticks |
| CA2326324C (en) * | 1998-03-31 | 2010-05-11 | Kyowa Hakko Kogyo Co., Ltd. | Nitrogen-containing heterocyclic compound |
| US6232320B1 (en) * | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| US6608053B2 (en) * | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| KR100774855B1 (ko) | 2000-04-27 | 2007-11-08 | 아스텔라스세이야쿠 가부시키가이샤 | 축합 헤테로아릴 유도체 |
| US20020156601A1 (en) * | 2001-04-19 | 2002-10-24 | Tu Kevin Hsiaohsu | Event monitoring and detection system |
| AU2003255845A1 (en) | 2002-08-22 | 2004-03-11 | Piramed Limited | Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents |
| ES2217956B1 (es) | 2003-01-23 | 2006-04-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de 4-aminotieno(2,3-d)pirimidin-6-carbonitrilo. |
| GB0423653D0 (en) * | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
| GB0520657D0 (en) | 2005-10-11 | 2005-11-16 | Ludwig Inst Cancer Res | Pharmaceutical compounds |
| KR101402474B1 (ko) * | 2006-04-26 | 2014-06-19 | 제넨테크, 인크. | 포스포이노시티드 3-키나제 억제제 화합물 및 이를 포함하는 약학적 조성물 |
| MX2008013584A (es) * | 2006-04-26 | 2009-03-23 | Genentech Inc | Compuestos farmaceuticos. |
| BRPI0710866A2 (pt) * | 2006-04-26 | 2012-08-14 | Hoffmann La Roche | compostos farmacÊuticos |
| BRPI0710874A2 (pt) * | 2006-04-26 | 2012-02-14 | Hoffmann La Roche | compostos de tienopirimidina, processos de produção dos referidos compostos, composições farmacêuticas contendo os mesmos, kit, produto, e usos dos compostos |
| GB0608820D0 (en) * | 2006-05-04 | 2006-06-14 | Piramed Ltd | Pharmaceutical compounds |
| ES2571028T3 (es) * | 2006-12-07 | 2016-05-23 | Genentech Inc | Compuestos inhibidores de fosfoinositida 3-cinasa y métodos de uso |
| AR064155A1 (es) * | 2006-12-07 | 2009-03-18 | Piramed Ltd | Compuestos de inhibidores de fosfoinositido-3 quinasa y metodos de uso |
| EP2205242B1 (en) * | 2007-09-12 | 2015-04-15 | Genentech, Inc. | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents, and methods of use |
| CA2704711C (en) * | 2007-09-24 | 2016-07-05 | Genentech, Inc. | Thiazolopyrimidine p13k inhibitor compounds and methods of use |
| JP5348725B2 (ja) * | 2007-10-25 | 2013-11-20 | ジェネンテック, インコーポレイテッド | チエノピリミジン化合物の製造方法 |
| EP2215090B1 (en) | 2007-10-26 | 2015-03-04 | F. Hoffmann-La Roche AG | Purine derivatives useful as pi3 kinase inhibitors |
| EP2279188B1 (en) * | 2008-05-30 | 2015-01-28 | Genentech, Inc. | Purine pi3k inhibitor compounds and methods of use |
| CA2772371A1 (en) * | 2009-05-27 | 2010-12-02 | F. Hoffmann-La Roche Ag | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
| BRPI1009022A2 (pt) * | 2009-05-27 | 2016-03-08 | Hoffmann La Roche | "composto, composição farmacêutica, processo para produzir uma composição farmacêutica, uso de um composto, método para tratamento de uma doença ou transtorno e kit" |
-
2007
- 2007-10-26 GB GBGB0721095.8A patent/GB0721095D0/en not_active Ceased
-
2008
- 2008-10-27 CN CN2008801126921A patent/CN101868464B/zh not_active Expired - Fee Related
- 2008-10-27 EP EP08842778.6A patent/EP2205610B1/en not_active Not-in-force
- 2008-10-27 ES ES08842778.6T patent/ES2442501T3/es active Active
- 2008-10-27 WO PCT/GB2008/003621 patent/WO2009053715A1/en not_active Ceased
- 2008-10-27 US US12/739,435 patent/US8293735B2/en not_active Expired - Fee Related
- 2008-10-27 JP JP2010530548A patent/JP5675360B2/ja not_active Expired - Fee Related
- 2008-10-27 CA CA2701276A patent/CA2701276A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CA2701276A1 (en) | 2009-04-30 |
| WO2009053715A1 (en) | 2009-04-30 |
| JP5675360B2 (ja) | 2015-02-25 |
| EP2205610A1 (en) | 2010-07-14 |
| JP2011500774A (ja) | 2011-01-06 |
| EP2205610B1 (en) | 2013-11-20 |
| CN101868464A (zh) | 2010-10-20 |
| US20110021496A1 (en) | 2011-01-27 |
| ES2442501T3 (es) | 2014-02-11 |
| US8293735B2 (en) | 2012-10-23 |
| GB0721095D0 (en) | 2007-12-05 |
| WO2009053715A8 (en) | 2010-06-03 |
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| Publication | Publication Date | Title |
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