RU2561109C2 - Соединения и способы применения - Google Patents
Соединения и способы применения Download PDFInfo
- Publication number
- RU2561109C2 RU2561109C2 RU2011129789/04A RU2011129789A RU2561109C2 RU 2561109 C2 RU2561109 C2 RU 2561109C2 RU 2011129789/04 A RU2011129789/04 A RU 2011129789/04A RU 2011129789 A RU2011129789 A RU 2011129789A RU 2561109 C2 RU2561109 C2 RU 2561109C2
- Authority
- RU
- Russia
- Prior art keywords
- benzo
- thiazol
- ylcarbamoyl
- tetrahydroquinolin
- group
- Prior art date
Links
- ZCJFOMBPZOLDAM-UHFFFAOYSA-N CN(C)c1cccc(OCCOc2ccc(-c3ccc(CCCN4C(Nc5nc(cccc6)c6[s]5)=O)c4c3)nc2C(O)=O)c1 Chemical compound CN(C)c1cccc(OCCOc2ccc(-c3ccc(CCCN4C(Nc5nc(cccc6)c6[s]5)=O)c4c3)nc2C(O)=O)c1 ZCJFOMBPZOLDAM-UHFFFAOYSA-N 0.000 description 2
- HQDGISOEKNLNCW-UHFFFAOYSA-N OC(c(nc(cc1)-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)c1-c1cc(cccc2)c2cc1)=O Chemical compound OC(c(nc(cc1)-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)c1-c1cc(cccc2)c2cc1)=O HQDGISOEKNLNCW-UHFFFAOYSA-N 0.000 description 2
- 0 *NC(N(c1cc(BI*)ccc1*I)I)=O Chemical compound *NC(N(c1cc(BI*)ccc1*I)I)=O 0.000 description 1
- DRVWZEWZXCZNAR-UHFFFAOYSA-N Brc1cc(NCCC2)c2cc1 Chemical compound Brc1cc(NCCC2)c2cc1 DRVWZEWZXCZNAR-UHFFFAOYSA-N 0.000 description 1
- VWDRTFKKWLAYQF-UHFFFAOYSA-N CC(C)(C)OC(Nc(cc1)ccc1OCCOc(cc1)c(C(O)=O)nc1-c1ccc(CCCN2C(Nc3nc4ccccc4[s]3)=O)c2c1)=O Chemical compound CC(C)(C)OC(Nc(cc1)ccc1OCCOc(cc1)c(C(O)=O)nc1-c1ccc(CCCN2C(Nc3nc4ccccc4[s]3)=O)c2c1)=O VWDRTFKKWLAYQF-UHFFFAOYSA-N 0.000 description 1
- AWKIZZAVSYJYRK-UHFFFAOYSA-N CC(C)(C)OC(Nc1cc(OCc2cc(Br)ccc2)ccc1)=O Chemical compound CC(C)(C)OC(Nc1cc(OCc2cc(Br)ccc2)ccc1)=O AWKIZZAVSYJYRK-UHFFFAOYSA-N 0.000 description 1
- DBABIXUKZSGKDY-UHFFFAOYSA-N CC(C)(C)OC(c1nc(-c(cc2)cc3c2N(C)CCN3)ccc1)=O Chemical compound CC(C)(C)OC(c1nc(-c(cc2)cc3c2N(C)CCN3)ccc1)=O DBABIXUKZSGKDY-UHFFFAOYSA-N 0.000 description 1
- JNWWJUXWTIXBKQ-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1-c1ccc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)nc1C(O)=O Chemical compound CC(C)(C)c(cc1)ccc1-c1ccc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)nc1C(O)=O JNWWJUXWTIXBKQ-UHFFFAOYSA-N 0.000 description 1
- PHOMBWBRLPRDRL-UHFFFAOYSA-N CC(C)Oc(cc1)ccc1-c1c(C(O)=O)nc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)[s]1 Chemical compound CC(C)Oc(cc1)ccc1-c1c(C(O)=O)nc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)[s]1 PHOMBWBRLPRDRL-UHFFFAOYSA-N 0.000 description 1
- GIWFSESZFIZJQP-UHFFFAOYSA-N CC1(C)OB(c2ccc(CCCN3)c3c2)OC1(C)C Chemical compound CC1(C)OB(c2ccc(CCCN3)c3c2)OC1(C)C GIWFSESZFIZJQP-UHFFFAOYSA-N 0.000 description 1
- XBULXMSOYHYUSL-UHFFFAOYSA-N CCOC(c(nc(-c1cc(N(CCC2)C(C)=O)c2cc1)[s]1)c1Cl)=O Chemical compound CCOC(c(nc(-c1cc(N(CCC2)C(C)=O)c2cc1)[s]1)c1Cl)=O XBULXMSOYHYUSL-UHFFFAOYSA-N 0.000 description 1
- WIXNPZUURUCEEU-UHFFFAOYSA-N CCOC(c1c[s]c(-c2ccc(CCN3C(Nc4nc(cccc5)c5[s]4)=O)c3c2)n1)=O Chemical compound CCOC(c1c[s]c(-c2ccc(CCN3C(Nc4nc(cccc5)c5[s]4)=O)c3c2)n1)=O WIXNPZUURUCEEU-UHFFFAOYSA-N 0.000 description 1
- GUARKFCLDYLQOJ-UHFFFAOYSA-N CN(C)c(cc1)ccc1OCCCOc1ccc(-c2cc(N(CCC3)C(Nc4nc(cccc5)c5[s]4)=O)c3cc2)nc1C(O)=O Chemical compound CN(C)c(cc1)ccc1OCCCOc1ccc(-c2cc(N(CCC3)C(Nc4nc(cccc5)c5[s]4)=O)c3cc2)nc1C(O)=O GUARKFCLDYLQOJ-UHFFFAOYSA-N 0.000 description 1
- JTRNUBLYFJORJT-UHFFFAOYSA-N CN(C)c1cc(OCCOc(cc2)c(C(OC)=O)nc2-c2cc(NCCC3)c3cc2)ccc1 Chemical compound CN(C)c1cc(OCCOc(cc2)c(C(OC)=O)nc2-c2cc(NCCC3)c3cc2)ccc1 JTRNUBLYFJORJT-UHFFFAOYSA-N 0.000 description 1
- BPETVGCQUIGELY-UHFFFAOYSA-N CN(C)c1cc(OCCOc(cc2)c(C(OC)=O)nc2-c2ccc(CCCN3C(Nc4nc(cccc5)c5[s]4)=O)c3c2)ccc1 Chemical compound CN(C)c1cc(OCCOc(cc2)c(C(OC)=O)nc2-c2ccc(CCCN3C(Nc4nc(cccc5)c5[s]4)=O)c3c2)ccc1 BPETVGCQUIGELY-UHFFFAOYSA-N 0.000 description 1
- ASUIMNUAPAYIFF-UHFFFAOYSA-N CN(C)c1ccc(CCOc2ccc(-c3ccc(CCCN4C(Nc5nc(cccc6)c6[s]5)=O)c4c3)nc2C(O)=O)cc1 Chemical compound CN(C)c1ccc(CCOc2ccc(-c3ccc(CCCN4C(Nc5nc(cccc6)c6[s]5)=O)c4c3)nc2C(O)=O)cc1 ASUIMNUAPAYIFF-UHFFFAOYSA-N 0.000 description 1
- IGRYCCZPZKOHII-UHFFFAOYSA-N CN(C)c1ccc(CNCCOc2ccc(-c3ccc(CCCN4C(Nc5nc6ccccc6[s]5)=O)c4c3)nc2C(O)=O)cc1 Chemical compound CN(C)c1ccc(CNCCOc2ccc(-c3ccc(CCCN4C(Nc5nc6ccccc6[s]5)=O)c4c3)nc2C(O)=O)cc1 IGRYCCZPZKOHII-UHFFFAOYSA-N 0.000 description 1
- XOIHGIKDINPDRX-UHFFFAOYSA-N CN(CC1)CCN1c(nc1)ccc1-c1ccc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)nc1C(O)=O Chemical compound CN(CC1)CCN1c(nc1)ccc1-c1ccc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)nc1C(O)=O XOIHGIKDINPDRX-UHFFFAOYSA-N 0.000 description 1
- HRNHYKJWRGNWJS-UHFFFAOYSA-N CN(CCN(C(Nc1nc2ccccc2[s]1)=O)c1c2)c1ccc2-c1cccc(C(O)=O)n1 Chemical compound CN(CCN(C(Nc1nc2ccccc2[s]1)=O)c1c2)c1ccc2-c1cccc(C(O)=O)n1 HRNHYKJWRGNWJS-UHFFFAOYSA-N 0.000 description 1
- AGAWDRYCIAJTLS-UHFFFAOYSA-N CN1c(ccc(-c(cc2)nc(C(OC)=O)c2OCCCOc2ccccc2)c2)c2NCC1 Chemical compound CN1c(ccc(-c(cc2)nc(C(OC)=O)c2OCCCOc2ccccc2)c2)c2NCC1 AGAWDRYCIAJTLS-UHFFFAOYSA-N 0.000 description 1
- MHKKUZDJUGIOBC-UHFFFAOYSA-N COC(c1ncccc1O)=O Chemical compound COC(c1ncccc1O)=O MHKKUZDJUGIOBC-UHFFFAOYSA-N 0.000 description 1
- VXEHJUXIVPBWMD-UHFFFAOYSA-N Cc(cccc1)c1-c1ccc(-c2ccc(CCCN3C(Nc4nc(cccc5)c5[s]4)=O)c3c2)nc1C(O)=O Chemical compound Cc(cccc1)c1-c1ccc(-c2ccc(CCCN3C(Nc4nc(cccc5)c5[s]4)=O)c3c2)nc1C(O)=O VXEHJUXIVPBWMD-UHFFFAOYSA-N 0.000 description 1
- RCVLLTPEOVNERE-UHFFFAOYSA-N NCc(cc1)ccc1OCCOc1ccc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)nc1C(O)=O Chemical compound NCc(cc1)ccc1OCCOc1ccc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)nc1C(O)=O RCVLLTPEOVNERE-UHFFFAOYSA-N 0.000 description 1
- QKZUCGLLGYHMHX-UHFFFAOYSA-N O=C(Nc1nc(cccc2)c2[s]1)[n]1cncc1 Chemical compound O=C(Nc1nc(cccc2)c2[s]1)[n]1cncc1 QKZUCGLLGYHMHX-UHFFFAOYSA-N 0.000 description 1
- SUALKLTVTLZBAP-UHFFFAOYSA-N OC(c(nc(cc1)-c2ccc(CCCN3C(Nc4nc(cccc5)c5[s]4)=O)c3c2)c1OCc(cc1)ccc1-c1ccccc1)=O Chemical compound OC(c(nc(cc1)-c2ccc(CCCN3C(Nc4nc(cccc5)c5[s]4)=O)c3c2)c1OCc(cc1)ccc1-c1ccccc1)=O SUALKLTVTLZBAP-UHFFFAOYSA-N 0.000 description 1
- ATYICJLSTAZWCH-UHFFFAOYSA-N OC(c1c(-c(cc2)ccc2-c2ccccc2)[s]c(-c2cc(N(CCC3)C(Nc4nc5ccccc5[s]4)=O)c3cc2)n1)=O Chemical compound OC(c1c(-c(cc2)ccc2-c2ccccc2)[s]c(-c2cc(N(CCC3)C(Nc4nc5ccccc5[s]4)=O)c3cc2)n1)=O ATYICJLSTAZWCH-UHFFFAOYSA-N 0.000 description 1
- ZZKMAEDLBJHEQI-UHFFFAOYSA-N OC(c1c(-c2cc(F)ccc2)[s]c(-c2ccc3OCCN(C(Nc4nc(cccc5)c5[s]4)=O)c3c2)n1)=O Chemical compound OC(c1c(-c2cc(F)ccc2)[s]c(-c2ccc3OCCN(C(Nc4nc(cccc5)c5[s]4)=O)c3c2)n1)=O ZZKMAEDLBJHEQI-UHFFFAOYSA-N 0.000 description 1
- XBXFJADFUJRUBK-UHFFFAOYSA-N OC(c1cccc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)n1)=O Chemical compound OC(c1cccc(-c2ccc(CCCN3C(Nc4nc5ccccc5[s]4)=O)c3c2)n1)=O XBXFJADFUJRUBK-UHFFFAOYSA-N 0.000 description 1
- NLQXXKDTSHGAQP-UHFFFAOYSA-N OC(c1nc(-c2cc(N(CCC3)C(Nc4nc5ccccc5[s]4)=O)c3cc2)ccc1OCCc1ccccn1)=O Chemical compound OC(c1nc(-c2cc(N(CCC3)C(Nc4nc5ccccc5[s]4)=O)c3cc2)ccc1OCCc1ccccn1)=O NLQXXKDTSHGAQP-UHFFFAOYSA-N 0.000 description 1
- YABCLSATWIFESR-UHFFFAOYSA-N Oc(cc1)ccc1-[n]1ncc2c1ncnc2 Chemical compound Oc(cc1)ccc1-[n]1ncc2c1ncnc2 YABCLSATWIFESR-UHFFFAOYSA-N 0.000 description 1
- UJMXBOVAORPTKW-UHFFFAOYSA-N [O-][N+](c(cc1)ccc1OC(Nc1nc(cccc2)c2[s]1)=O)=O Chemical compound [O-][N+](c(cc1)ccc1OC(Nc1nc(cccc2)c2[s]1)=O)=O UJMXBOVAORPTKW-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- 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
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- A61P37/08—Antiallergic agents
-
- 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
- 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
-
- 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
- C07D417/02—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 two hetero rings
- C07D417/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Virology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- AIDS & HIV (AREA)
- Vascular Medicine (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13947908P | 2008-12-19 | 2008-12-19 | |
| US61/139,479 | 2008-12-19 | ||
| PCT/US2009/068400 WO2010080478A1 (en) | 2008-12-19 | 2009-12-17 | Compounds and methods of use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2011129789A RU2011129789A (ru) | 2013-01-27 |
| RU2561109C2 true RU2561109C2 (ru) | 2015-08-20 |
Family
ID=42316717
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2011129789/04A RU2561109C2 (ru) | 2008-12-19 | 2009-12-17 | Соединения и способы применения |
Country Status (21)
| Country | Link |
|---|---|
| US (3) | US8114893B2 (OSRAM) |
| EP (1) | EP2376085B1 (OSRAM) |
| JP (1) | JP5683484B2 (OSRAM) |
| KR (1) | KR101633532B1 (OSRAM) |
| CN (1) | CN102325531B (OSRAM) |
| AU (1) | AU2009335818A1 (OSRAM) |
| BR (1) | BRPI0918337A2 (OSRAM) |
| CA (1) | CA2747161C (OSRAM) |
| CO (1) | CO6390110A2 (OSRAM) |
| CR (1) | CR20110389A (OSRAM) |
| DO (1) | DOP2011000198A (OSRAM) |
| EC (1) | ECSP11011214A (OSRAM) |
| ES (1) | ES2462715T3 (OSRAM) |
| IL (1) | IL213547A0 (OSRAM) |
| MX (1) | MX2011006514A (OSRAM) |
| NZ (1) | NZ593536A (OSRAM) |
| PE (1) | PE20120305A1 (OSRAM) |
| RU (1) | RU2561109C2 (OSRAM) |
| SG (1) | SG172266A1 (OSRAM) |
| WO (1) | WO2010080478A1 (OSRAM) |
| ZA (1) | ZA201104463B (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2799873C2 (ru) * | 2017-04-19 | 2023-07-13 | Нэшенел Юнивёрсити Оф Сингапур | Низкомолекулярные ингибиторы фосфорилированные BCL-2-ассоциированного промотора смерти (BAD) |
Families Citing this family (58)
| 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 |
| WO2009085216A2 (en) | 2007-12-20 | 2009-07-09 | Squicor | Compositions and methods for detecting or elimninating senescent cells to diagnose or treat disease |
| AU2009335843A1 (en) * | 2008-12-19 | 2011-07-21 | Abbvie Inc. | Heterocyclic compounds and methods of use |
| PE20120305A1 (es) * | 2008-12-19 | 2012-04-09 | Abbott Lab | Compuestos heterociclicos derivados de benzotiazol y tetrahidroquinolina como inhbidores de bcl-2 y bcl-xl |
| US10010439B2 (en) | 2010-06-13 | 2018-07-03 | Synerz Medical, Inc. | Intragastric device for treating obesity |
| US9526648B2 (en) | 2010-06-13 | 2016-12-27 | 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 |
| US8628554B2 (en) | 2010-06-13 | 2014-01-14 | Virender K. Sharma | Intragastric device for treating obesity |
| ES2659763T3 (es) | 2011-02-14 | 2018-03-19 | The Regents Of The University Of Michigan | Composiciones y procedimientos para el tratamiento de obesidad y trastornos relacionados |
| WO2012177927A1 (en) | 2011-06-21 | 2012-12-27 | Mayo Foundation For Medical Education And Research | Transgenic animals capable of being induced to delete senescent cells |
| TWI561521B (en) * | 2011-10-14 | 2016-12-11 | Abbvie Inc | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| 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 |
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| RU2799873C2 (ru) * | 2017-04-19 | 2023-07-13 | Нэшенел Юнивёрсити Оф Сингапур | Низкомолекулярные ингибиторы фосфорилированные BCL-2-ассоциированного промотора смерти (BAD) |
| RU2799873C9 (ru) * | 2017-04-19 | 2023-11-13 | Нэшенел Юнивёрсити Оф Сингапур | Низкомолекулярные ингибиторы фосфорилирования BCL-2-ассоциированного промотора смерти (BAD) |
| RU2830186C2 (ru) * | 2019-07-29 | 2024-11-14 | Ле Лаборатуар Сервье | 3,6-диаминопиридазин-3-ильные производные, содержащие их фармацевтические композиции и их применение в качестве проапоптотических средств |
| RU2832191C2 (ru) * | 2019-07-29 | 2024-12-23 | Ле Лаборатуар Сервье | 6,7-дигидро-5h-пиридо[2,3-c]пиридазиновые производные и родственные соединения в качестве ингибиторов белков bclxl и проапоптотических средств для лечения злокачественных новообразований |
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| CN102325531B (zh) | 2014-04-02 |
| EP2376085B1 (en) | 2014-02-26 |
| ES2462715T3 (es) | 2014-05-26 |
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| US20120184541A1 (en) | 2012-07-19 |
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| ZA201104463B (en) | 2012-09-26 |
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| NZ593536A (en) | 2013-07-26 |
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| CO6390110A2 (es) | 2012-02-29 |
| AU2009335818A1 (en) | 2011-07-21 |
| US20100190782A1 (en) | 2010-07-29 |
| SG172266A1 (en) | 2011-07-28 |
| IL213547A0 (en) | 2011-07-31 |
| KR20110114581A (ko) | 2011-10-19 |
| CA2747161C (en) | 2017-07-18 |
| US9067928B2 (en) | 2015-06-30 |
| US8518970B2 (en) | 2013-08-27 |
| EP2376085A4 (en) | 2012-08-15 |
| ECSP11011214A (es) | 2011-09-30 |
| DOP2011000198A (es) | 2012-08-31 |
| JP2012512887A (ja) | 2012-06-07 |
| PE20120305A1 (es) | 2012-04-09 |
| HK1161094A1 (en) | 2012-08-24 |
| US20140005190A1 (en) | 2014-01-02 |
| BRPI0918337A2 (pt) | 2017-05-30 |
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