JP5770102B2 - 複素環化合物と使用方法 - Google Patents
複素環化合物と使用方法 Download PDFInfo
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- JP5770102B2 JP5770102B2 JP2011542439A JP2011542439A JP5770102B2 JP 5770102 B2 JP5770102 B2 JP 5770102B2 JP 2011542439 A JP2011542439 A JP 2011542439A JP 2011542439 A JP2011542439 A JP 2011542439A JP 5770102 B2 JP5770102 B2 JP 5770102B2
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- 0 *c1c(CCCO*)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc(cccc3)c3[s]2)=O)n1 Chemical compound *c1c(CCCO*)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc(cccc3)c3[s]2)=O)n1 0.000 description 9
- XWKHYYWDNIQSGY-UHFFFAOYSA-N CC(C(C)c1c(cccc2OCCCc3c(C(O)=O)nc(N(CC4)Cc5c4cccc5C(Nc4nc5ccccc5[s]4)=O)[s]3)c2ncc1)C1=CC1 Chemical compound CC(C(C)c1c(cccc2OCCCc3c(C(O)=O)nc(N(CC4)Cc5c4cccc5C(Nc4nc5ccccc5[s]4)=O)[s]3)c2ncc1)C1=CC1 XWKHYYWDNIQSGY-UHFFFAOYSA-N 0.000 description 1
- KYSUHMMOWAHBQR-UHFFFAOYSA-N CC(C)(C(CCO)c1c2nc(N(CC3)Cc4c3cccc4C(N(COCC[Si+](C)(C)C)c3nc4ccccc4[s]3)=O)[s]1)OC2=O Chemical compound CC(C)(C(CCO)c1c2nc(N(CC3)Cc4c3cccc4C(N(COCC[Si+](C)(C)C)c3nc4ccccc4[s]3)=O)[s]1)OC2=O KYSUHMMOWAHBQR-UHFFFAOYSA-N 0.000 description 1
- FTCPZERQEBTRJJ-UHFFFAOYSA-N CC(C)(C)OC(c1c(CCCOc(cc2)ccc2-c2c[n](CCN3CCOCC3)nc2)[s]c(N(CC2)Cc3c2cccc3C(N(COCC[SiH-](C)(C)C)c2nc(cccc3)c3[s]2)=O)n1)=O Chemical compound CC(C)(C)OC(c1c(CCCOc(cc2)ccc2-c2c[n](CCN3CCOCC3)nc2)[s]c(N(CC2)Cc3c2cccc3C(N(COCC[SiH-](C)(C)C)c2nc(cccc3)c3[s]2)=O)n1)=O FTCPZERQEBTRJJ-UHFFFAOYSA-N 0.000 description 1
- NHDVHQQUIAVOGI-UHFFFAOYSA-N CC(C)(C)OC(c1nc(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)ccc1)=O Chemical compound CC(C)(C)OC(c1nc(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)ccc1)=O NHDVHQQUIAVOGI-UHFFFAOYSA-N 0.000 description 1
- XYLUDBOLEIYNGO-UHFFFAOYSA-N CC(C)[n]1c2ncnc(-c(cc3)ccc3OC3OCCCC3)c2nc1 Chemical compound CC(C)[n]1c2ncnc(-c(cc3)ccc3OC3OCCCC3)c2nc1 XYLUDBOLEIYNGO-UHFFFAOYSA-N 0.000 description 1
- LXVANNXQXFXVAL-UHFFFAOYSA-N CC(C)[n]1c2ncnc(C3C=CC(OCCCc4c(C(O)=O)nc(N(CCc5ccc6)Cc5c6C(Nc5nc6ccccc6[s]5)=O)[s]4)=CC3)c2nc1 Chemical compound CC(C)[n]1c2ncnc(C3C=CC(OCCCc4c(C(O)=O)nc(N(CCc5ccc6)Cc5c6C(Nc5nc6ccccc6[s]5)=O)[s]4)=CC3)c2nc1 LXVANNXQXFXVAL-UHFFFAOYSA-N 0.000 description 1
- YBPXMMMYWSTGJJ-UHFFFAOYSA-N CCOC(c1c(CCCCl)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound CCOC(c1c(CCCCl)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)n1)=O YBPXMMMYWSTGJJ-UHFFFAOYSA-N 0.000 description 1
- FEKLXZOYEQJIBC-UHFFFAOYSA-N CN(C)CCOc(cc1)ccc1O Chemical compound CN(C)CCOc(cc1)ccc1O FEKLXZOYEQJIBC-UHFFFAOYSA-N 0.000 description 1
- BPLAMHAAABHMPB-UHFFFAOYSA-N CN(C)CCOc1cccc(O)c1 Chemical compound CN(C)CCOc1cccc(O)c1 BPLAMHAAABHMPB-UHFFFAOYSA-N 0.000 description 1
- AISHPJPGKBKMGV-UHFFFAOYSA-N CN(CC1)CCN1c1cccc(O)c1 Chemical compound CN(CC1)CCN1c1cccc(O)c1 AISHPJPGKBKMGV-UHFFFAOYSA-N 0.000 description 1
- VWDXPRAMDDVSAG-UHFFFAOYSA-N CN(CCCNc1ncnc2c1cn[n]2-c(cc1)ccc1OCCCc1c(C(O)=O)nc(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)[s]1)I Chemical compound CN(CCCNc1ncnc2c1cn[n]2-c(cc1)ccc1OCCCc1c(C(O)=O)nc(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)[s]1)I VWDXPRAMDDVSAG-UHFFFAOYSA-N 0.000 description 1
- VSSFWAOADQPPIS-UHFFFAOYSA-N CN1c2ccccc2SC1NC(c1c(CN(CC2)C3=NCC(C(O)=O)=C(CCOc(cc4)ccc4-[n]4ncc5c4ncnc5)S3)c2ccc1)=O Chemical compound CN1c2ccccc2SC1NC(c1c(CN(CC2)C3=NCC(C(O)=O)=C(CCOc(cc4)ccc4-[n]4ncc5c4ncnc5)S3)c2ccc1)=O VSSFWAOADQPPIS-UHFFFAOYSA-N 0.000 description 1
- QCKVHYVVTHRMDP-UHFFFAOYSA-N Cc(cc(cc1)N(CC2)CCN2c2nc(cccc3)c3[s]2)c1OCCCc1c(C(O)=O)nc(N(CC2)Cc3c2cccc3C(Nc2nc(cccc3)c3[s]2)=O)[s]1 Chemical compound Cc(cc(cc1)N(CC2)CCN2c2nc(cccc3)c3[s]2)c1OCCCc1c(C(O)=O)nc(N(CC2)Cc3c2cccc3C(Nc2nc(cccc3)c3[s]2)=O)[s]1 QCKVHYVVTHRMDP-UHFFFAOYSA-N 0.000 description 1
- GLKIMZQJKDRZAF-UHFFFAOYSA-N Cc1c(NCCCN2CCCC2)ncnc1C(CS)[Br]=C Chemical compound Cc1c(NCCCN2CCCC2)ncnc1C(CS)[Br]=C GLKIMZQJKDRZAF-UHFFFAOYSA-N 0.000 description 1
- LJFZDPZIIKOATA-UHFFFAOYSA-N Clc(ncnc12)c1[s]cc2Br Chemical compound Clc(ncnc12)c1[s]cc2Br LJFZDPZIIKOATA-UHFFFAOYSA-N 0.000 description 1
- WEKDWVDTCGORSS-UHFFFAOYSA-N N#Cc1c[s]cc1-c(cc1)ccc1OCCCc1c(C(O)=O)nc(N(CCc2ccc3)Cc2c3C(Nc2nc(cccc3)c3[s]2)=O)[s]1 Chemical compound N#Cc1c[s]cc1-c(cc1)ccc1OCCCc1c(C(O)=O)nc(N(CCc2ccc3)Cc2c3C(Nc2nc(cccc3)c3[s]2)=O)[s]1 WEKDWVDTCGORSS-UHFFFAOYSA-N 0.000 description 1
- VHGZSMSLYNXHTL-UHFFFAOYSA-N N#Cc1c[s]cc1-c(cc1Cc2c(C(O)=O)nc(N(CCc3ccc4)Cc3c4C(Nc3nc4ccccc4[s]3)=O)[s]2)ccc1O Chemical compound N#Cc1c[s]cc1-c(cc1Cc2c(C(O)=O)nc(N(CCc3ccc4)Cc3c4C(Nc3nc4ccccc4[s]3)=O)[s]2)ccc1O VHGZSMSLYNXHTL-UHFFFAOYSA-N 0.000 description 1
- DJNAFBWEZBERMZ-UHFFFAOYSA-N Nc([nH]nc1-c(cc2)ccc2OCc2c(C(O)=O)nc(N(CCc3ccc4)Cc3c4C(Nc3nc4ccccc4[s]3)=O)[s]2)c1C#N Chemical compound Nc([nH]nc1-c(cc2)ccc2OCc2c(C(O)=O)nc(N(CCc3ccc4)Cc3c4C(Nc3nc4ccccc4[s]3)=O)[s]2)c1C#N DJNAFBWEZBERMZ-UHFFFAOYSA-N 0.000 description 1
- QSJDTIYUCYPZFT-UHFFFAOYSA-N Nc([s]cc1-c(cc2)ccc2O)c1C#N Chemical compound Nc([s]cc1-c(cc2)ccc2O)c1C#N QSJDTIYUCYPZFT-UHFFFAOYSA-N 0.000 description 1
- CIOCOXYIKRAYRS-UHFFFAOYSA-N OC(c1c(CCOCc2ccccc2)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound OC(c1c(CCOCc2ccccc2)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)n1)=O CIOCOXYIKRAYRS-UHFFFAOYSA-N 0.000 description 1
- AUSCDMYCFSINPV-UHFFFAOYSA-N OC(c1c(CCOc(cc2)ccc2-[n]2ncc3c2ncnc3)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound OC(c1c(CCOc(cc2)ccc2-[n]2ncc3c2ncnc3)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O AUSCDMYCFSINPV-UHFFFAOYSA-N 0.000 description 1
- NLTMWGNDANWOHE-UHFFFAOYSA-N OC(c1c(CCOc2cccc(-[n]3ncc4cncnc34)c2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc(cccc3)c3[s]2)=O)n1)=O Chemical compound OC(c1c(CCOc2cccc(-[n]3ncc4cncnc34)c2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc(cccc3)c3[s]2)=O)n1)=O NLTMWGNDANWOHE-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 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
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/06—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/06—Peri-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic 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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13949208P | 2008-12-19 | 2008-12-19 | |
| US61/139,492 | 2008-12-19 | ||
| PCT/US2009/068496 WO2010080503A1 (en) | 2008-12-19 | 2009-12-17 | Heterocyclic compounds and methods of use |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012512891A JP2012512891A (ja) | 2012-06-07 |
| JP2012512891A5 JP2012512891A5 (enExample) | 2013-02-14 |
| JP5770102B2 true JP5770102B2 (ja) | 2015-08-26 |
Family
ID=42316723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011542439A Active JP5770102B2 (ja) | 2008-12-19 | 2009-12-17 | 複素環化合物と使用方法 |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8232273B2 (enExample) |
| EP (1) | EP2373163B1 (enExample) |
| JP (1) | JP5770102B2 (enExample) |
| KR (1) | KR101685718B1 (enExample) |
| CN (1) | CN102316733B (enExample) |
| AU (1) | AU2009335843A1 (enExample) |
| BR (1) | BRPI0918360A8 (enExample) |
| CA (1) | CA2747170C (enExample) |
| CL (1) | CL2011001485A1 (enExample) |
| CO (1) | CO6390075A2 (enExample) |
| CR (1) | CR20110388A (enExample) |
| DO (1) | DOP2011000199A (enExample) |
| EC (1) | ECSP11011213A (enExample) |
| ES (1) | ES2544452T3 (enExample) |
| IL (1) | IL213596A0 (enExample) |
| MX (1) | MX2011006509A (enExample) |
| NZ (1) | NZ593537A (enExample) |
| PE (1) | PE20120334A1 (enExample) |
| RU (1) | RU2525116C2 (enExample) |
| SG (1) | SG172259A1 (enExample) |
| WO (1) | WO2010080503A1 (enExample) |
| ZA (1) | ZA201104467B (enExample) |
Families Citing this family (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK2134685T3 (en) | 2007-04-16 | 2015-12-07 | Abbvie Inc | 7-unsubstituted indole derivatives as MCL-1 inhibitors |
| CN102325531B (zh) | 2008-12-19 | 2014-04-02 | 健泰科生物技术公司 | 化合物和使用方法 |
| US8628554B2 (en) | 2010-06-13 | 2014-01-14 | Virender K. Sharma | Intragastric device for treating obesity |
| US10010439B2 (en) | 2010-06-13 | 2018-07-03 | Synerz Medical, Inc. | Intragastric device for treating obesity |
| US10420665B2 (en) | 2010-06-13 | 2019-09-24 | W. L. Gore & Associates, Inc. | Intragastric device for treating obesity |
| US9526648B2 (en) | 2010-06-13 | 2016-12-27 | Synerz Medical, Inc. | Intragastric device for treating obesity |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| KR101919080B1 (ko) * | 2011-05-20 | 2018-11-16 | 글락소스미스클라인 인털렉츄얼 프로퍼티 (넘버 2) 리미티드 | 디아실글리세롤 아실트랜스퍼라제 억제제로서의 신규 화합물 |
| US8889675B2 (en) | 2011-10-14 | 2014-11-18 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| TWI561521B (en) * | 2011-10-14 | 2016-12-11 | Abbvie Inc | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| CN103958508B (zh) * | 2011-10-14 | 2019-02-12 | 艾伯维公司 | 用于治疗癌症以及免疫与自身免疫性疾病的细胞凋亡诱导剂 |
| TWI571466B (zh) * | 2011-10-14 | 2017-02-21 | 艾伯維有限公司 | 用於治療癌症及免疫與自體免疫疾病之細胞凋亡誘發劑 |
| JP5955531B2 (ja) * | 2011-11-07 | 2016-07-20 | 千葉県 | 抗癌剤 |
| HUE042374T2 (hu) | 2012-06-13 | 2019-06-28 | Incyte Holdings Corp | Szubsztituált triciklusos vegyületek mint FGFR inhibitorok |
| CN103515415A (zh) * | 2012-06-26 | 2014-01-15 | 群康科技(深圳)有限公司 | 叠层结构与其制造方法、以及包含其的电子装置 |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| MX360172B (es) | 2012-08-13 | 2018-10-12 | Abbvie Inc | Agentes que inducen la apoptosis. |
| JP6318156B2 (ja) * | 2012-09-06 | 2018-04-25 | プレキシコン インコーポレーテッドPlexxikon Inc. | キナーゼをモジュレートするための化合物および方法、ならびにその指標 |
| MA38009B1 (fr) * | 2012-10-11 | 2018-09-28 | Hoffmann La Roche | Composes d'azaindoline substitues qui ont une activite inhibitrice de la proteine d'apoptose pour leurs utilisations dans le traitement et/ou la prophylaxie du cancer |
| US9796729B2 (en) | 2012-11-23 | 2017-10-24 | Glaxosmithkline Llc | Compounds as diacylglycerol acyltransferase inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| WO2014145852A2 (en) | 2013-03-15 | 2014-09-18 | Knopp Biosciences Llc | Imidazo(4,5-b) pyridin-2-yl amides as kv7 channel activators |
| KR102469849B1 (ko) | 2013-04-19 | 2022-11-23 | 인사이트 홀딩스 코포레이션 | Fgfr 저해제로서 이환식 헤테로사이클 |
| FR3008979B1 (fr) * | 2013-07-23 | 2015-07-24 | Servier Lab | Nouveaux derives phosphates, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR3008975A1 (fr) | 2013-07-23 | 2015-01-30 | Servier Lab | Nouveaux derives de pyrrole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| IL311537A (en) | 2014-01-28 | 2024-05-01 | Mayo Found Medical Education & Res | Methods and preparations for killing aging cells and for the treatment of diseases and disorders related to aging |
| EP3139942B1 (en) | 2014-05-05 | 2019-12-18 | Bioventures, Llc | COMPOSITIONS AND METHODS FOR INHIBITING ANTIAPOPTOTIC Bcl-2 PROTEINS AS ANTI-AGING AGENTS |
| US10071087B2 (en) | 2014-07-22 | 2018-09-11 | Bioventures, Llc | Compositions and methods for selectively depleting senescent cells |
| WO2016040952A2 (en) | 2014-09-12 | 2016-03-17 | Knopp Biosciences Llc | BENZOIMIDAZOL-1,2-YL AMIDES AS Kv7 CHANNEL ACTIVATORS |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| EP3230283A1 (en) * | 2014-12-09 | 2017-10-18 | AbbVie Inc. | Bcl-xl inhibitory compounds and antibody drug conjugates including the same |
| EP3230282A1 (en) * | 2014-12-09 | 2017-10-18 | AbbVie Inc. | Bcl xl inhibitory compounds having low cell permeability and antibody drug conjugates including the same |
| WO2016131100A1 (en) * | 2015-02-18 | 2016-08-25 | The Walter And Eliza Hall Institute Of Medical Research | Methods of treating infectious diseases |
| AU2016219822B2 (en) | 2015-02-20 | 2020-07-09 | Incyte Holdings Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| US10195213B2 (en) | 2015-03-13 | 2019-02-05 | Unity Biotechnology, Inc. | Chemical entities that kill senescent cells for use in treating age-related disease |
| WO2016172218A1 (en) * | 2015-04-20 | 2016-10-27 | The Regents Of The University Of Michigan | Small molecule inhibitors of mcl-1 and uses thereof |
| AU2016315881B2 (en) * | 2015-09-03 | 2019-09-19 | The Arizona Board Of Regents On Behalf Of The University Of Arizona | Small molecule inhibitors of DYRK1A and uses thereof |
| SG11201804210XA (en) * | 2015-11-20 | 2018-06-28 | Mingsight Pharmaceuticals Inc | Treatment of autoimmune disease |
| US10807977B2 (en) | 2016-04-21 | 2020-10-20 | Bioventures, Llc | Compounds that induce degradation of anti-apoptotic Bcl-2 family proteins and the uses thereof |
| US10779980B2 (en) | 2016-04-27 | 2020-09-22 | Synerz Medical, Inc. | Intragastric device for treating obesity |
| US10640563B2 (en) | 2016-06-08 | 2020-05-05 | Abbvie Inc. | Anti-B7-H3 antibodies and antibody drug conjugates |
| WO2018029473A1 (en) * | 2016-08-09 | 2018-02-15 | University Of Durham | Synthetic retinoids (in cell modulation) |
| US20180072741A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyrimidine compounds and uses thereof |
| KR20230038807A (ko) | 2016-09-09 | 2023-03-21 | 인사이트 코포레이션 | Hpk1 조절제로서의 피라졸로피리딘 유도체 및 암의 치료를 위한 이의 용도 |
| WO2018049214A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyridine derivatives as hpk1 modulators and uses thereof for the treatment of cancer |
| WO2018092064A1 (en) * | 2016-11-18 | 2018-05-24 | Novartis Ag | Combinations of mdm2 inhibitors and bcl-xl inhibitors |
| US20180228786A1 (en) | 2017-02-15 | 2018-08-16 | Incyte Corporation | Pyrazolopyridine compounds and uses thereof |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| US10722495B2 (en) | 2017-09-08 | 2020-07-28 | Incyte Corporation | Cyanoindazole compounds and uses thereof |
| CN108186642B (zh) * | 2018-01-11 | 2019-11-08 | 广西师范大学 | 一种协同起作用治疗肺癌的药物组合物 |
| ES3041854T3 (en) | 2018-01-22 | 2025-11-17 | Bioventures Llc | Bcl-2 proteins degraders for cancer treatment |
| HUE059624T2 (hu) | 2018-02-20 | 2022-11-28 | Incyte Corp | N-(fenil)-2-(fenil)pirimidin-4-karboxamid származékok és rokon vegyületek HPK1-inhibitorokként rák kezelésére |
| US10752635B2 (en) | 2018-02-20 | 2020-08-25 | Incyte Corporation | Indazole compounds and uses thereof |
| US10745388B2 (en) | 2018-02-20 | 2020-08-18 | Incyte Corporation | Indazole compounds and uses thereof |
| IL277419B2 (en) | 2018-03-19 | 2024-07-01 | Knopp Biosciences Llc | Kv7 channel activators compositions and methods of use |
| US11299473B2 (en) | 2018-04-13 | 2022-04-12 | Incyte Corporation | Benzimidazole and indole compounds and uses thereof |
| EP4309737A3 (en) | 2018-05-04 | 2024-03-27 | Incyte Corporation | Solid forms of an fgfr inhibitor and processes for preparing the same |
| EP3788046B1 (en) | 2018-05-04 | 2025-12-10 | Incyte Corporation | Salts of an fgfr inhibitor |
| US12084423B2 (en) | 2018-05-18 | 2024-09-10 | Bioventures, Llc | Piperlongumine analogues and uses thereof |
| US10899755B2 (en) | 2018-08-08 | 2021-01-26 | Incyte Corporation | Benzothiazole compounds and uses thereof |
| WO2020068729A1 (en) | 2018-09-25 | 2020-04-02 | Incyte Corporation | Pyrazolo[4,3-d]pyrimidine compounds as alk2 abd/or fgfr modulators |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| AR119494A1 (es) * | 2019-07-29 | 2021-12-22 | Servier Lab | DERIVADOS DE 6,7-DIHIDRO-5H-PIRIDO[2,3-c]PIRIDAZIN-8-ILO, COMPOSICIONES FARMACÉUTICAS QUE LOS CONTIENEN Y SUS USOS COMO AGENTES PROAPOPTÓTICOS |
| PH12022550271A1 (en) | 2019-08-06 | 2023-06-26 | Incyte Corp | Solid forms of an hpk1 inhibitor |
| US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2021076602A1 (en) | 2019-10-14 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| KR20220131900A (ko) | 2019-12-04 | 2022-09-29 | 인사이트 코포레이션 | Fgfr 억제제의 유도체 |
| JP7720840B2 (ja) | 2019-12-04 | 2025-08-08 | インサイト・コーポレイション | Fgfr阻害剤としての三環式複素環 |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CN112079791A (zh) * | 2020-08-21 | 2020-12-15 | 宁夏农林科学院农业资源与环境研究所(宁夏土壤与植物营养重点实验室) | 单环β-内酰胺类抗生素侧链酸及其酯、其制备方法和应用 |
| EP4251209A1 (en) | 2020-11-24 | 2023-10-04 | Novartis AG | Bcl-xl inhibitor antibody-drug conjugates and methods of use thereof |
| UY39610A (es) | 2021-01-20 | 2022-08-31 | Abbvie Inc | Conjugados anticuerpo-fármaco anti-egfr |
| IL304891A (en) | 2021-02-02 | 2023-10-01 | Servier Lab | Selective Protech BCL-XL compounds and methods of use |
| CA3215903A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| KR102605163B1 (ko) * | 2021-06-01 | 2023-11-23 | 연세대학교 산학협력단 | 뇌암의 예방 또는 치료용 조성물 |
| EP4352059A1 (en) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| WO2022261159A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| CN114294905B (zh) * | 2021-11-19 | 2023-04-25 | 中粮生物科技股份有限公司 | 利用红外或微波干燥聚羟基脂肪酸酯的方法 |
| IL317103A (en) | 2022-05-20 | 2025-01-01 | Novartis Ag | Antibody-drug conjugates of MET inhibitor BCL-XL and methods of using them |
| KR20250027285A (ko) | 2022-05-20 | 2025-02-25 | 노파르티스 아게 | 항신생물 화합물의 항체-약물 접합체 및 그의 사용 방법 |
| EP4525925A1 (en) | 2022-05-20 | 2025-03-26 | Novartis AG | Epha2 bcl-xl inhibitor antibody-drug conjugates and methods of use thereof |
| WO2024036961A1 (zh) * | 2022-08-19 | 2024-02-22 | 北京三秀生物医药科技有限公司 | 一种抗衰老相关疾病的前药及其使用方法 |
| WO2025111450A1 (en) | 2023-11-22 | 2025-05-30 | Les Laboratoires Servier | Anti-cd74 antibody-drug conjugates and methods of use thereof |
| WO2025111431A1 (en) | 2023-11-22 | 2025-05-30 | Les Laboratoires Servier | Anti-cd7 antibody-drug conjugates and methods of use thereof |
| TW202527945A (zh) * | 2023-12-18 | 2025-07-16 | 大陸商南京瑞初醫藥有限公司 | 氮雜環化合物及其應用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3718570A1 (de) * | 1987-06-03 | 1988-12-15 | Boehringer Ingelheim Kg | Benzo- und thieno-3,4-dihydro-1- pyridinylessigsaeurederivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
| EP1268432A1 (en) * | 2000-03-24 | 2003-01-02 | Millenium Pharmaceuticals, Inc. | ISOQUINOLONE INHIBITORS OF FACTOR Xa |
| KR20030017660A (ko) * | 2000-08-01 | 2003-03-03 | 오노 야꾸힝 고교 가부시키가이샤 | 3,4-디히드로이소퀴놀린 유도체 화합물 및 그 화합물을유효 성분으로 하는 약제 |
| WO2004004727A1 (en) * | 2002-07-03 | 2004-01-15 | Axys Pharmaceuticals, Inc. | 3,4-dihydroisoquinolin-1-one derivatives as inducers of apoptosis |
| CN1856477A (zh) * | 2003-09-23 | 2006-11-01 | 默克公司 | 异喹啉钾通道抑制剂 |
| US7767684B2 (en) * | 2003-11-13 | 2010-08-03 | Abbott Laboratories | Apoptosis promoters |
| US20060063766A1 (en) * | 2004-07-15 | 2006-03-23 | Molino Bruce F | Use of aryl- and heteroaryl-substituted tetrahydroisoquinolines to block reuptake of norepinephrine, dopamine, and serotonin |
| US7297700B2 (en) * | 2005-03-24 | 2007-11-20 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
| EP1981884B1 (en) * | 2006-01-18 | 2012-06-13 | Amgen, Inc | Thiazole compounds as protein kinase b (pkb) inhibitors |
| CN101568527A (zh) * | 2006-10-31 | 2009-10-28 | 先灵公司 | 作为蛋白激酶抑制剂的2-氨基噻唑-4-羧酰胺 |
| CA2672903C (en) * | 2006-12-20 | 2012-10-23 | Amgen Inc. | Heterocyclic compounds and their use in treating inflammation, angiogenesis and cancer |
| JP5396379B2 (ja) * | 2007-04-02 | 2014-01-22 | エボテック・アーゲー | ピリド−2−イル縮合複素環式化合物ならびにその組成物および使用 |
| US8445679B2 (en) * | 2007-04-16 | 2013-05-21 | Abbvie Inc. | 7-substituted indole MCL-1 inhibitors |
| DK2134685T3 (en) * | 2007-04-16 | 2015-12-07 | Abbvie Inc | 7-unsubstituted indole derivatives as MCL-1 inhibitors |
| KR101552742B1 (ko) * | 2007-07-19 | 2015-09-11 | 머크 샤프 앤드 돔 코포레이션 | 단백질 키나제 억제제로서의 헤테로사이클릭 아미드 화합물 |
| CN101842362A (zh) | 2007-09-27 | 2010-09-22 | 沃尔特及伊莱萨霍尔医学研究院 | 苯并噻唑化合物 |
| CN102325531B (zh) * | 2008-12-19 | 2014-04-02 | 健泰科生物技术公司 | 化合物和使用方法 |
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