KR101685718B1 - 헤테로시클릭 화합물 및 사용 방법 - Google Patents
헤테로시클릭 화합물 및 사용 방법 Download PDFInfo
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- KR101685718B1 KR101685718B1 KR1020117016722A KR20117016722A KR101685718B1 KR 101685718 B1 KR101685718 B1 KR 101685718B1 KR 1020117016722 A KR1020117016722 A KR 1020117016722A KR 20117016722 A KR20117016722 A KR 20117016722A KR 101685718 B1 KR101685718 B1 KR 101685718B1
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- thiazole
- benzo
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- 0 C*(*)Cc1c2[s]c(C)nc2ccc1 Chemical compound C*(*)Cc1c2[s]c(C)nc2ccc1 0.000 description 9
- YKGPSTPTPGJIME-UHFFFAOYSA-N OC(c1c(CCCOc2cccc3c2cccn3)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound OC(c1c(CCCOc2cccc3c2cccn3)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)n1)=O YKGPSTPTPGJIME-UHFFFAOYSA-N 0.000 description 2
- UQEZRTYDGGOMDR-UHFFFAOYSA-N CC(C)(C)OC(Nc1cc(OCCCc2c(C(O)O)nc(N(CCc3ccc4)Cc3c4C(Nc3nc4ccccc4[s]3)=O)[s]2)ccc1)=O Chemical compound CC(C)(C)OC(Nc1cc(OCCCc2c(C(O)O)nc(N(CCc3ccc4)Cc3c4C(Nc3nc4ccccc4[s]3)=O)[s]2)ccc1)=O UQEZRTYDGGOMDR-UHFFFAOYSA-N 0.000 description 1
- FVDNPTZLDCYJMY-UHFFFAOYSA-N CC(C)(C)OC(c1c(CCCOc(cc2)ccc2-c2c[n](CCN3CCOCC3)nc2)[s]c(N(CC2)Cc3c2cccc3C(N(COCC[Si+](C)(C)C)c2nc3ccccc3[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[Si+](C)(C)C)c2nc3ccccc3[s]2)=O)n1)=O FVDNPTZLDCYJMY-UHFFFAOYSA-N 0.000 description 1
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- DFDVKACRRFVQFY-UHFFFAOYSA-N CN(C)CCOc(cn1)cnc1Cl Chemical compound CN(C)CCOc(cn1)cnc1Cl DFDVKACRRFVQFY-UHFFFAOYSA-N 0.000 description 1
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- KBINDVXBNAQFFH-UHFFFAOYSA-N CN(C)c1cccc(OCCCc2c(C(O)=O)nc(N(CCc3ccc4)Cc3c4C(Nc3nc4ccccc4[s]3)=O)[s]2)c1 Chemical compound CN(C)c1cccc(OCCCc2c(C(O)=O)nc(N(CCc3ccc4)Cc3c4C(Nc3nc4ccccc4[s]3)=O)[s]2)c1 KBINDVXBNAQFFH-UHFFFAOYSA-N 0.000 description 1
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- VWJMXGHSQCIPPX-UHFFFAOYSA-N CS(Nc1ccccn1)(=O)=O Chemical compound CS(Nc1ccccn1)(=O)=O VWJMXGHSQCIPPX-UHFFFAOYSA-N 0.000 description 1
- WGVHNCAJPFIFCR-UHFFFAOYSA-N Cc1n[nH]c(O)c1 Chemical compound Cc1n[nH]c(O)c1 WGVHNCAJPFIFCR-UHFFFAOYSA-N 0.000 description 1
- DFYLLKBBGKQNMR-UHFFFAOYSA-N Cc1n[n](cccc2)c2c1 Chemical compound Cc1n[n](cccc2)c2c1 DFYLLKBBGKQNMR-UHFFFAOYSA-N 0.000 description 1
- XZGLNCKSNVGDNX-UHFFFAOYSA-N Cc1nnn[nH]1 Chemical compound Cc1nnn[nH]1 XZGLNCKSNVGDNX-UHFFFAOYSA-N 0.000 description 1
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- NUULPIHTQIDTDT-UHFFFAOYSA-N Nc([s]cc1-c(cc2)ccc2OCc2ccccc2)c1C#N Chemical compound Nc([s]cc1-c(cc2)ccc2OCc2ccccc2)c1C#N NUULPIHTQIDTDT-UHFFFAOYSA-N 0.000 description 1
- SNXLSEMYUMHRPB-UHFFFAOYSA-N OC(c1c(CCCOc(cc2)ccc2C2=CSC3=NCCN23)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound OC(c1c(CCCOc(cc2)ccc2C2=CSC3=NCCN23)[s]c(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)n1)=O SNXLSEMYUMHRPB-UHFFFAOYSA-N 0.000 description 1
- BLAXPRRVDRRAQP-UHFFFAOYSA-N OC(c1c(CCCOc2cccc3c2nccc3)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc(cccc3)c3[s]2)=O)n1)=O Chemical compound OC(c1c(CCCOc2cccc3c2nccc3)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc(cccc3)c3[s]2)=O)n1)=O BLAXPRRVDRRAQP-UHFFFAOYSA-N 0.000 description 1
- ZBICXWMMDQAGHL-UHFFFAOYSA-N OC(c1c(CCC[n]2c(cccc3)c3nc2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound OC(c1c(CCC[n]2c(cccc3)c3nc2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O ZBICXWMMDQAGHL-UHFFFAOYSA-N 0.000 description 1
- QVDZIGSEIMEXCJ-UHFFFAOYSA-N OC(c1c(CCC[n]2c3ncccc3cc2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound OC(c1c(CCC[n]2c3ncccc3cc2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O QVDZIGSEIMEXCJ-UHFFFAOYSA-N 0.000 description 1
- JGBSWDQBDHXVCQ-UHFFFAOYSA-N OC(c1c(CCC[n]2cncc2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound OC(c1c(CCC[n]2cncc2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O JGBSWDQBDHXVCQ-UHFFFAOYSA-N 0.000 description 1
- RYOWVJPNKQIXMM-UHFFFAOYSA-N OC(c1nc(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)ccc1)=O Chemical compound OC(c1nc(N(CC2)Cc3c2cccc3C(Nc2nc3ccccc3[s]2)=O)ccc1)=O RYOWVJPNKQIXMM-UHFFFAOYSA-N 0.000 description 1
- FDIMGJWRBKXQKS-UHFFFAOYSA-N OC(c1nc(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)ccc1CCCOc1ccnc(Cl)c1)=O Chemical compound OC(c1nc(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)ccc1CCCOc1ccnc(Cl)c1)=O FDIMGJWRBKXQKS-UHFFFAOYSA-N 0.000 description 1
- XQZFQUTUSJGSBH-UHFFFAOYSA-N OCC#Cc1c(C(O)=O)nc(N(CCc2ccc3)Cc2c3C(Nc2nc(cccc3)c3[s]2)=O)[s]1 Chemical compound OCC#Cc1c(C(O)=O)nc(N(CCc2ccc3)Cc2c3C(Nc2nc(cccc3)c3[s]2)=O)[s]1 XQZFQUTUSJGSBH-UHFFFAOYSA-N 0.000 description 1
- QRTAUFCVAOTXIM-UHFFFAOYSA-N OCOCc1c(CCCOc(cc(c(NCCN2CCOCC2)c2)F)c2F)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1 Chemical compound OCOCc1c(CCCOc(cc(c(NCCN2CCOCC2)c2)F)c2F)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1 QRTAUFCVAOTXIM-UHFFFAOYSA-N 0.000 description 1
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- 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
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- 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
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- 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
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- 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
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- 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
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- 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
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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
- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
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- 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
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- 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
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Oncology (AREA)
- Epidemiology (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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (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 (2)
| Publication Number | Publication Date |
|---|---|
| KR20110102473A KR20110102473A (ko) | 2011-09-16 |
| KR101685718B1 true KR101685718B1 (ko) | 2016-12-12 |
Family
ID=42316723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020117016722A Expired - Fee Related KR101685718B1 (ko) | 2008-12-19 | 2009-12-17 | 헤테로시클릭 화합물 및 사용 방법 |
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|---|---|
| US (1) | US8232273B2 (enExample) |
| EP (1) | EP2373163B1 (enExample) |
| JP (1) | JP5770102B2 (enExample) |
| KR (1) | KR101685718B1 (enExample) |
| CN (1) | CN102316733B (enExample) |
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| 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 |
|---|---|---|---|---|
| MX2009011210A (es) | 2007-04-16 | 2009-10-30 | Abbott Lab | Inhibidores de mcl1 de indol 7-no sustituido. |
| NZ593536A (en) * | 2008-12-19 | 2013-07-26 | Genentech Inc | Quinoline derivatives and methods of use |
| 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 |
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