JP5788890B2 - テトラヒドロキノリン誘導体及びその薬学的使用 - Google Patents
テトラヒドロキノリン誘導体及びその薬学的使用 Download PDFInfo
- Publication number
- JP5788890B2 JP5788890B2 JP2012537377A JP2012537377A JP5788890B2 JP 5788890 B2 JP5788890 B2 JP 5788890B2 JP 2012537377 A JP2012537377 A JP 2012537377A JP 2012537377 A JP2012537377 A JP 2012537377A JP 5788890 B2 JP5788890 B2 JP 5788890B2
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- tetrahydro
- acetyl
- quinolinyl
- methylethyl
- 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 C*(CCCCCC(C)(*)C1)CCCCC1(C)NI=C Chemical compound C*(CCCCCC(C)(*)C1)CCCCC1(C)NI=C 0.000 description 14
- KCQYOLSGKPTZIS-UHFFFAOYSA-N CC(C)(C)OC(N(C)CCC#N)=O Chemical compound CC(C)(C)OC(N(C)CCC#N)=O KCQYOLSGKPTZIS-UHFFFAOYSA-N 0.000 description 1
- CJECJURFSFCCQG-UHFFFAOYSA-N CC(C)(C)OC(NC1CCN(CC[n]2ncc(Br)c2)CC1)=O Chemical compound CC(C)(C)OC(NC1CCN(CC[n]2ncc(Br)c2)CC1)=O CJECJURFSFCCQG-UHFFFAOYSA-N 0.000 description 1
- XFWJFSJDRURPLE-UHFFFAOYSA-N CC(C)OC(N(C)C)=O Chemical compound CC(C)OC(N(C)C)=O XFWJFSJDRURPLE-UHFFFAOYSA-N 0.000 description 1
- DGBJHMCQXWCXJY-UHFFFAOYSA-N CC(C)OC(N)O Chemical compound CC(C)OC(N)O DGBJHMCQXWCXJY-UHFFFAOYSA-N 0.000 description 1
- WXOHDVIFFZYLTN-VEXWJQHLSA-N CC(C)OC(NC(C[C@@H]1C)c2cc(-c3ccc(CN(CCNC4)C4=O)cc3)ccc2N1C(C)=O)=O Chemical compound CC(C)OC(NC(C[C@@H]1C)c2cc(-c3ccc(CN(CCNC4)C4=O)cc3)ccc2N1C(C)=O)=O WXOHDVIFFZYLTN-VEXWJQHLSA-N 0.000 description 1
- HNQSACBABMMCKB-LBOXEOMUSA-N CC(C)OC(NCC(C[C@@H]1C)c(cc(cc2)-c3cccc(CC=O)c3)c2N1C(C)=O)=O Chemical compound CC(C)OC(NCC(C[C@@H]1C)c(cc(cc2)-c3cccc(CC=O)c3)c2N1C(C)=O)=O HNQSACBABMMCKB-LBOXEOMUSA-N 0.000 description 1
- SGGFBCOFMZIKCL-MXDJKYFJSA-N CC(C)OC(N[C@H](C[C@@H]1C)c2cc(-c3c[n](CCN(C)C)nn3)ccc2N1C(C)=O)O Chemical compound CC(C)OC(N[C@H](C[C@@H]1C)c2cc(-c3c[n](CCN(C)C)nn3)ccc2N1C(C)=O)O SGGFBCOFMZIKCL-MXDJKYFJSA-N 0.000 description 1
- HYKZIDJITGUCJT-MGPUTAFESA-N CC(C)OC(N[C@H](C[C@@H]1C)c2cc(-c3c[n](CCOC)nc3)ccc2N1C(C)=O)=O Chemical compound CC(C)OC(N[C@H](C[C@@H]1C)c2cc(-c3c[n](CCOC)nc3)ccc2N1C(C)=O)=O HYKZIDJITGUCJT-MGPUTAFESA-N 0.000 description 1
- RBVLMFOYGRFYRZ-UQBPGWFLSA-N CC(C)OC(N[C@H](C[C@@H]1C)c2cc(-c3ccc(CCNC(OC(C)(C)C)=O)cc3)ccc2N1C(C)=O)=O Chemical compound CC(C)OC(N[C@H](C[C@@H]1C)c2cc(-c3ccc(CCNC(OC(C)(C)C)=O)cc3)ccc2N1C(C)=O)=O RBVLMFOYGRFYRZ-UQBPGWFLSA-N 0.000 description 1
- HFKRBAXDKLRECG-YCRPNKLZSA-N CC(C)OC(N[C@H](C[C@@H]1C)c2cc(C(CC3)=CC=C3C(OC)=O)ccc2N1C(C)=O)=O Chemical compound CC(C)OC(N[C@H](C[C@@H]1C)c2cc(C(CC3)=CC=C3C(OC)=O)ccc2N1C(C)=O)=O HFKRBAXDKLRECG-YCRPNKLZSA-N 0.000 description 1
- PEEYHAPMXMTNHS-UHFFFAOYSA-N CC1(C)OB(c2c[n](COC)nc2)OC1(C)C Chemical compound CC1(C)OB(c2c[n](COC)nc2)OC1(C)C PEEYHAPMXMTNHS-UHFFFAOYSA-N 0.000 description 1
- DWHRSMPWAFVERN-UHFFFAOYSA-N CCC(C)(CC)OC(N(CC1)CCN1c(nc1)ncc1Br)=O Chemical compound CCC(C)(CC)OC(N(CC1)CCN1c(nc1)ncc1Br)=O DWHRSMPWAFVERN-UHFFFAOYSA-N 0.000 description 1
- XOIJCGIDURRXIR-IBMANYCNSA-N CCCCC(CC(C)C(C(C)C)/C=C\CCCCO)[C@@H](CC)NC(C)(C)O Chemical compound CCCCC(CC(C)C(C(C)C)/C=C\CCCCO)[C@@H](CC)NC(C)(C)O XOIJCGIDURRXIR-IBMANYCNSA-N 0.000 description 1
- MEXVQFZPLLYHES-JNRDSLKYSA-N CCC[C@@H](c1c(C)c(N(C)/C=C(/C)\NC)ccc1N(C)C(C)O)NC(OC(C)(C)C)=O Chemical compound CCC[C@@H](c1c(C)c(N(C)/C=C(/C)\NC)ccc1N(C)C(C)O)NC(OC(C)(C)C)=O MEXVQFZPLLYHES-JNRDSLKYSA-N 0.000 description 1
- PFLATUFKWOFXNU-UHFFFAOYSA-N CN(C)CC[n]1ncc(Br)c1 Chemical compound CN(C)CC[n]1ncc(Br)c1 PFLATUFKWOFXNU-UHFFFAOYSA-N 0.000 description 1
- UXDSGGKSQRMJBE-BMIGLBTASA-N C[C@H](C[C@@H](c1c2)NC(OC3CCC3)=O)N(C(C)=O)c1ccc2Br Chemical compound C[C@H](C[C@@H](c1c2)NC(OC3CCC3)=O)N(C(C)=O)c1ccc2Br UXDSGGKSQRMJBE-BMIGLBTASA-N 0.000 description 1
- VEIZLTSJCDOIBH-INIZCTEOSA-N Cc1nnc2[n]1-c(ccc(OC)c1)c1C(c(cc1)ccc1Cl)=N[C@H]2CC(O)=O Chemical compound Cc1nnc2[n]1-c(ccc(OC)c1)c1C(c(cc1)ccc1Cl)=N[C@H]2CC(O)=O VEIZLTSJCDOIBH-INIZCTEOSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/38—Nitrogen atoms
- C07D215/42—Nitrogen atoms attached in position 4
-
- 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
- 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
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0919431.7A GB0919431D0 (en) | 2009-11-05 | 2009-11-05 | Novel compounds |
| GB0919431.7 | 2009-11-05 | ||
| PCT/EP2010/066693 WO2011054841A1 (en) | 2009-11-05 | 2010-11-03 | Tetrahydroquinoline derivatives and their pharmaceutical use |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013510120A JP2013510120A (ja) | 2013-03-21 |
| JP2013510120A5 JP2013510120A5 (OSRAM) | 2013-11-07 |
| JP5788890B2 true JP5788890B2 (ja) | 2015-10-07 |
Family
ID=41501974
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012537377A Expired - Fee Related JP5788890B2 (ja) | 2009-11-05 | 2010-11-03 | テトラヒドロキノリン誘導体及びその薬学的使用 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8697725B2 (OSRAM) |
| EP (1) | EP2496557B1 (OSRAM) |
| JP (1) | JP5788890B2 (OSRAM) |
| ES (1) | ES2449470T3 (OSRAM) |
| GB (1) | GB0919431D0 (OSRAM) |
| WO (1) | WO2011054841A1 (OSRAM) |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUE026967T2 (en) | 2009-11-05 | 2016-07-28 | Glaxosmithkline Llc | Benzodiazepine Bromodomain inhibitor |
| DK2722334T3 (en) | 2009-11-05 | 2016-03-07 | Glaxosmithkline Llc | benzodiazepine bromdomæneinhibitor |
| DK2571503T3 (en) | 2010-05-14 | 2015-04-20 | Dana Farber Cancer Inst Inc | COMPOSITIONS AND THEIR USE IN THE TREATMENT OF NEOPLASIA, INFLAMMATORY DISEASE AND OTHER DISORDERS |
| US9301962B2 (en) | 2010-05-14 | 2016-04-05 | Baylor College Of Medicine | Male contraceptive compositions and methods of use |
| CA2799403C (en) | 2010-05-14 | 2020-01-21 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for treating leukemia |
| ES2526671T3 (es) | 2010-06-22 | 2015-01-14 | Glaxosmithkline Llc | Compuestos de benzotriazoldiazepina inhibidores de bromodominios |
| US9249161B2 (en) | 2010-12-02 | 2016-02-02 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
| AR084070A1 (es) | 2010-12-02 | 2013-04-17 | Constellation Pharmaceuticals Inc | Inhibidores del bromodominio y usos de los mismos |
| GB201106750D0 (en) * | 2011-04-21 | 2011-06-01 | Glaxosmithkline Llc | Novel compounds |
| GB201106743D0 (en) * | 2011-04-21 | 2011-06-01 | Glaxosmithkline Llc | Novel compounds |
| GB201107325D0 (en) | 2011-05-04 | 2011-06-15 | Glaxosmithkline Llc | Novel compounds |
| EP2705039B1 (en) | 2011-05-04 | 2017-07-26 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
| WO2012174487A2 (en) | 2011-06-17 | 2012-12-20 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
| WO2013027168A1 (en) | 2011-08-22 | 2013-02-28 | Pfizer Inc. | Novel heterocyclic compounds as bromodomain inhibitors |
| WO2013033269A1 (en) * | 2011-08-29 | 2013-03-07 | Coferon, Inc. | Bioorthogonal monomers capable of dimerizing and targeting bromodomains and methods of using same |
| US9624244B2 (en) | 2012-06-06 | 2017-04-18 | Constellation Pharmaceuticals, Inc. | Benzo [B] isoxazoloazepine bromodomain inhibitors and uses thereof |
| TWI602820B (zh) | 2012-06-06 | 2017-10-21 | 星宿藥物公司 | 溴域抑制劑及其用途 |
| US9073878B2 (en) | 2012-11-21 | 2015-07-07 | Zenith Epigenetics Corp. | Cyclic amines as bromodomain inhibitors |
| US9765039B2 (en) | 2012-11-21 | 2017-09-19 | Zenith Epigenetics Ltd. | Biaryl derivatives as bromodomain inhibitors |
| CA2895905A1 (en) | 2012-12-21 | 2014-06-26 | Zenith Epigenetics Corp. | Novel heterocyclic compounds as bromodomain inhibitors |
| AU2014223990A1 (en) * | 2013-02-28 | 2015-09-10 | Washington University | Methods of treatment of human cytomegalovirus infection and diseases with bromodomain inhibitors |
| WO2014159392A1 (en) | 2013-03-14 | 2014-10-02 | Dana-Farber Cancer Institute, Inc. | Bromodomain binding reagents and uses thereof |
| SMT201900009T1 (it) | 2013-03-14 | 2019-02-28 | Glaxosmithkline Ip No 2 Ltd | Derivati 1-acil-4-ammino-1,2,3,4-tetraidrochinolinici 2,3-disostituiti e loro uso come inibitori del bromodominio |
| MX366703B (es) | 2013-03-15 | 2019-07-22 | Incyte Holdings Corp | Heterociclos tricíclicos como inhibidores de la proteína bet. |
| HK1217484A1 (zh) | 2013-04-26 | 2017-01-13 | 百济神州有限公司 | 取代的5-(3,5-二甲基异恶唑-4-基)二氢吲哚-2-酮类衍生物 |
| PL3010503T3 (pl) | 2013-06-21 | 2020-08-24 | Zenith Epigenetics Ltd. | Nowe bicykliczne inhibitory bromodomen |
| WO2015004533A2 (en) | 2013-06-21 | 2015-01-15 | Zenith Epigenetics Corp. | Novel substituted bicyclic compounds as bromodomain inhibitors |
| EP3019502B1 (en) | 2013-07-08 | 2017-05-17 | Incyte Holdings Corporation | Tricyclic heterocycles as bet protein inhibitors |
| CA2918910A1 (en) | 2013-07-25 | 2015-01-29 | Dana-Farber Cancer Institute, Inc. | Inhibitors of transcription factors and uses thereof |
| EP3027604B1 (en) | 2013-07-31 | 2019-02-20 | Zenith Epigenetics Ltd. | Novel quinazolinones as bromodomain inhibitors |
| EP3066101B1 (en) | 2013-11-08 | 2020-07-29 | Dana-Farber Cancer Institute, Inc. | Combination therapy for cancer using bromodomain and extra-terminal (bet) protein inhibitors |
| US9399640B2 (en) | 2013-11-26 | 2016-07-26 | Incyte Corporation | Substituted pyrrolo[2,3-c]pyridines and pyrazolo[3,4-c]pyridines as BET protein inhibitors |
| WO2015081189A1 (en) | 2013-11-26 | 2015-06-04 | Incyte Corporation | Bicyclic heterocycles as bet protein inhibitors |
| AU2014361381A1 (en) * | 2013-12-10 | 2016-06-16 | Abbvie Inc. | Bromodomain inhibitors |
| WO2015095492A1 (en) | 2013-12-19 | 2015-06-25 | Incyte Corporation | Tricyclic heterocycles as bet protein inhibitors |
| CN105940005A (zh) | 2014-01-31 | 2016-09-14 | 达纳-法伯癌症研究所股份有限公司 | 二氮杂环庚烷衍生物及其用途 |
| CN106029653A (zh) | 2014-01-31 | 2016-10-12 | 达纳-法伯癌症研究所股份有限公司 | 二氨基嘧啶苯砜衍生物及其用途 |
| US10793571B2 (en) | 2014-01-31 | 2020-10-06 | Dana-Farber Cancer Institute, Inc. | Uses of diazepane derivatives |
| MX377534B (es) | 2014-02-28 | 2025-03-10 | Tensha Therapeutics Inc | Compuestos para usarse en el tratamiento de hiperinsulinemia. |
| KR102702503B1 (ko) | 2014-04-23 | 2024-09-05 | 인사이트 홀딩스 코포레이션 | BET 단백질의 저해제로서의 1H-피롤로[2,3-c]피리딘-7(6H)-온 및 피라졸로[3,4-c]피리딘-7(6H)-온 |
| LT3157928T (lt) | 2014-06-20 | 2019-05-27 | Constellation Pharmaceuticals, Inc. | 2-((4s)-6-(4-chlorfenil)-1-metil-4h-benzo[c]iizoksazolo[4,5-e]azepin-4-il)acetamido kristalinės formos |
| MX2017001756A (es) | 2014-08-08 | 2017-05-30 | Dana Farber Cancer Inst Inc | Derivados de diazepano y sus usos. |
| MX2017001757A (es) | 2014-08-08 | 2017-05-30 | Dana Farber Cancer Inst Inc | Derivados de dihidropteridinona y sus usos. |
| EA031679B9 (ru) | 2014-09-12 | 2019-04-30 | Глаксосмитклайн Интеллекчуал Проперти (№2) Лимитед | Производные тетрагидрохинолина в качестве ингибиторов бромодомена |
| WO2016044130A1 (en) | 2014-09-15 | 2016-03-24 | Incyte Corporation | Tricyclic heterocycles for use as bet protein inhibitors |
| US10710992B2 (en) | 2014-12-01 | 2020-07-14 | Zenith Epigenetics Ltd. | Substituted pyridinones as bromodomain inhibitors |
| EP3227280B1 (en) | 2014-12-01 | 2019-04-24 | Zenith Epigenetics Ltd. | Substituted pyridines as bromodomain inhibitors |
| CN107207474B (zh) | 2014-12-11 | 2021-05-07 | 恒翼生物医药科技(上海)有限公司 | 被取代的杂环作为溴结构域抑制剂 |
| US10231953B2 (en) | 2014-12-17 | 2019-03-19 | Zenith Epigenetics Ltd. | Inhibitors of bromodomains |
| GB201504694D0 (en) | 2015-03-19 | 2015-05-06 | Glaxosmithkline Ip Dev Ltd | Covalent conjugates |
| US10464896B2 (en) | 2015-06-11 | 2019-11-05 | Basilea Pharmaceutica International AG | Efflux-pump inhibitors and therapeutic uses thereof |
| US10702527B2 (en) | 2015-06-12 | 2020-07-07 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| WO2016203335A1 (en) | 2015-06-18 | 2016-12-22 | Pfizer Inc. | Novel pyrido[2,3-b]pyrazinones as bet-family bromodomain inhibitors |
| JP2018520124A (ja) | 2015-06-26 | 2018-07-26 | テンシャ セラピューティクス,インコーポレイテッド | Nut正中線癌の治療 |
| HK1256417A1 (zh) | 2015-09-11 | 2019-09-20 | 达纳-法伯癌症研究所股份有限公司 | 氰基噻吩並三唑並二氮雜環庚三烯及其用途 |
| CR20180199A (es) | 2015-09-11 | 2018-05-25 | Dana Farber Cancer Inst Inc | Acetamida tienotriazolodiazepinas y usos de las mismas |
| US20170121347A1 (en) | 2015-10-29 | 2017-05-04 | Incyte Corporation | Amorphous solid form of a bet protein inhibitor |
| RU2742035C2 (ru) | 2015-11-25 | 2021-02-01 | Дана-Фарбер Кэнсер Инститьют, Инк. | Бивалентные ингибиторы бромодоменов и пути их применения |
| MA45122A (fr) * | 2016-05-24 | 2019-04-10 | Constellation Pharmaceuticals Inc | Inhibiteurs hétérocycliques de cbp/ep300 et leur utilisation dans le traitement du cancer |
| PH12021551886A1 (en) | 2016-06-20 | 2023-07-17 | Incyte Corp | Crystalline solid forms of a bet inhibitor |
| US11028051B2 (en) * | 2016-12-13 | 2021-06-08 | St. Jude Children's Research Hospital | Tetrahydroquinoline-based bromodomain inhibitors |
| WO2021175432A1 (en) | 2020-03-04 | 2021-09-10 | Boehringer Ingelheim International Gmbh | Method for administration of an anti cancer agent |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
| CN114751836B (zh) * | 2021-02-23 | 2024-05-31 | 四川青木制药有限公司 | 3-(4-甲基-1h-咪唑-1-基)-5-(三氟甲基)苯胺合成方法及其中间体 |
| AU2023255396A1 (en) | 2022-04-19 | 2024-10-24 | Nuevolution A/S | Compounds active towards bromodomains |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU570439B2 (en) | 1983-03-28 | 1988-03-17 | Compression Labs, Inc. | A combined intraframe and interframe transform coding system |
| GB9004781D0 (en) | 1990-03-02 | 1990-04-25 | Glaxo Group Ltd | Device |
| US6140342A (en) | 1998-09-17 | 2000-10-31 | Pfizer Inc. | Oxy substituted 4-carboxyamino-2-methyl-1,2,3,4-tetrahydroquinolines |
| ES2388434T3 (es) | 2003-11-03 | 2012-10-15 | Glaxo Group Limited | Dispositivo de administración de fluido |
| MXPA06011540A (es) | 2004-04-07 | 2007-01-26 | Millennium Pharm Inc | Antagonistas del receptor de pgd2 para el tratamiento de enfermedades inflamatorias. |
| JP4531027B2 (ja) * | 2005-09-29 | 2010-08-25 | 田辺三菱製薬株式会社 | 医薬組成物 |
| JP2008156311A (ja) | 2006-12-26 | 2008-07-10 | Institute Of Physical & Chemical Research | Brd2ブロモドメイン結合剤 |
| JP5478262B2 (ja) * | 2007-12-28 | 2014-04-23 | 田辺三菱製薬株式会社 | 抗癌剤 |
| GB0919434D0 (en) * | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
-
2009
- 2009-11-05 GB GBGB0919431.7A patent/GB0919431D0/en not_active Ceased
-
2010
- 2010-11-03 US US13/501,159 patent/US8697725B2/en not_active Expired - Fee Related
- 2010-11-03 WO PCT/EP2010/066693 patent/WO2011054841A1/en not_active Ceased
- 2010-11-03 EP EP10773324.8A patent/EP2496557B1/en not_active Not-in-force
- 2010-11-03 ES ES10773324.8T patent/ES2449470T3/es active Active
- 2010-11-03 JP JP2012537377A patent/JP5788890B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20120208798A1 (en) | 2012-08-16 |
| EP2496557A1 (en) | 2012-09-12 |
| EP2496557B1 (en) | 2013-12-18 |
| JP2013510120A (ja) | 2013-03-21 |
| ES2449470T3 (es) | 2014-03-19 |
| US8697725B2 (en) | 2014-04-15 |
| GB0919431D0 (en) | 2009-12-23 |
| WO2011054841A1 (en) | 2011-05-12 |
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