CN101990541A - 糖皮质激素受体、AP-1和/或NF-κB活性的稠合杂芳基调节剂及其用途 - Google Patents
糖皮质激素受体、AP-1和/或NF-κB活性的稠合杂芳基调节剂及其用途 Download PDFInfo
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- CN101990541A CN101990541A CN2009801124206A CN200980112420A CN101990541A CN 101990541 A CN101990541 A CN 101990541A CN 2009801124206 A CN2009801124206 A CN 2009801124206A CN 200980112420 A CN200980112420 A CN 200980112420A CN 101990541 A CN101990541 A CN 101990541A
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- Prior art keywords
- alkyl
- aryl
- substituted
- compound
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- 0 Cc1ccc(*)c(*)c1 Chemical compound Cc1ccc(*)c(*)c1 0.000 description 16
- SYARUQUVASMTFT-UHFFFAOYSA-N N#CCC(c(ccc(Cl)n1)c1Cl)=O Chemical compound N#CCC(c(ccc(Cl)n1)c1Cl)=O SYARUQUVASMTFT-UHFFFAOYSA-N 0.000 description 2
- JSJGBXGJUHERIY-ALCCZGGFSA-N CC(C)(C(C1=CC=C2)C(/C=C\C)=C([NH+2]O)OC1N2O)C(OC)=O Chemical compound CC(C)(C(C1=CC=C2)C(/C=C\C)=C([NH+2]O)OC1N2O)C(OC)=O JSJGBXGJUHERIY-ALCCZGGFSA-N 0.000 description 1
- IYIAJCKVWFPYBU-UHFFFAOYSA-N CC(C)(C1C(N(C(/N=N\NC)=N)c2cc(C)n3)=O)C11c2c3Oc2nc(-c(cc3)ccc3C(N3CC=[O]CC3)=O)ccc12 Chemical compound CC(C)(C1C(N(C(/N=N\NC)=N)c2cc(C)n3)=O)C11c2c3Oc2nc(-c(cc3)ccc3C(N3CC=[O]CC3)=O)ccc12 IYIAJCKVWFPYBU-UHFFFAOYSA-N 0.000 description 1
- OOOKKEOQRWYSEC-UHFFFAOYSA-N CC(C)(C1C(O)=O)C11c2ccc(-c(cc3)ccc3C(N3CCOCC3)=[U])nc2Oc2nc(C)ccc12 Chemical compound CC(C)(C1C(O)=O)C11c2ccc(-c(cc3)ccc3C(N3CCOCC3)=[U])nc2Oc2nc(C)ccc12 OOOKKEOQRWYSEC-UHFFFAOYSA-N 0.000 description 1
- VGAGCOFBIUTFEP-UHFFFAOYSA-N CC(C)(C1c(ccc([I]2CC2)n2)c2Oc2nc(C)ccc12)C(O)=O Chemical compound CC(C)(C1c(ccc([I]2CC2)n2)c2Oc2nc(C)ccc12)C(O)=O VGAGCOFBIUTFEP-UHFFFAOYSA-N 0.000 description 1
- FWWZFAMYPRWCMJ-HEKMFECPSA-N CC(C)S(c(cc1)ccc1-c1ccc([C@@H](C(C)(C)C(Nc2nnc[s]2)=O)c2ccc(C)nc2O2)c2n1)=O Chemical compound CC(C)S(c(cc1)ccc1-c1ccc([C@@H](C(C)(C)C(Nc2nnc[s]2)=O)c2ccc(C)nc2O2)c2n1)=O FWWZFAMYPRWCMJ-HEKMFECPSA-N 0.000 description 1
- MCHMHWXWVXLQKL-UHFFFAOYSA-N CN(C)C(c(cc1)ccc1-c1ccc(C(c(c(O2)n3)ccc3Cl)=O)c2n1)=O Chemical compound CN(C)C(c(cc1)ccc1-c1ccc(C(c(c(O2)n3)ccc3Cl)=O)c2n1)=O MCHMHWXWVXLQKL-UHFFFAOYSA-N 0.000 description 1
- ZWQGNEZEFOQHHE-UHFFFAOYSA-N COC(c(cc1)ccc1-c(cc1)nc([U]c2cnccc22)c1C2=O)=O Chemical compound COC(c(cc1)ccc1-c(cc1)nc([U]c2cnccc22)c1C2=O)=O ZWQGNEZEFOQHHE-UHFFFAOYSA-N 0.000 description 1
- SFPSMIDQHLRPOR-UHFFFAOYSA-N O=C(N1CCOCC1)I Chemical compound O=C(N1CCOCC1)I SFPSMIDQHLRPOR-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
- C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (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)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Endocrinology (AREA)
- Virology (AREA)
- Oncology (AREA)
- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Obesity (AREA)
- Vascular Medicine (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Pain & Pain Management (AREA)
- Gastroenterology & Hepatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2681608P | 2008-02-07 | 2008-02-07 | |
| US61/026,816 | 2008-02-07 | ||
| PCT/US2009/033134 WO2009100171A1 (en) | 2008-02-07 | 2009-02-05 | Fused heteroaryl modulators of glucocorticoid receptor, ap-1, and/or nf-kb activity and use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101990541A true CN101990541A (zh) | 2011-03-23 |
Family
ID=40473599
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801124206A Pending CN101990541A (zh) | 2008-02-07 | 2009-02-05 | 糖皮质激素受体、AP-1和/或NF-κB活性的稠合杂芳基调节剂及其用途 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8304539B2 (https=) |
| EP (1) | EP2247597A1 (https=) |
| JP (1) | JP2011511085A (https=) |
| CN (1) | CN101990541A (https=) |
| WO (1) | WO2009100171A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108546246A (zh) * | 2018-07-10 | 2018-09-18 | 湖南华腾制药有限公司 | 一种双吡啶基甲醇的制备方法 |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103080108A (zh) * | 2010-08-27 | 2013-05-01 | 科赛普特治疗公司 | 吡啶基-胺稠合的氮杂萘烷调节剂 |
| PL3848027T3 (pl) * | 2013-11-25 | 2023-07-24 | Corcept Therapeutics Incorporated | Skondensowane oktahydrozwiązki azadekaliny jako modulatory receptora glukokortykoidowego |
| WO2015077537A1 (en) * | 2013-11-25 | 2015-05-28 | Corcept Therapeutics, Inc. | Heteroaryl-ether fused azadecalin glucocorticoid receptor modulators |
| CN113373466B (zh) * | 2021-06-19 | 2023-07-21 | 安徽科技学院 | 一种β-乙酰氨基羰基化合物的电化学合成方法 |
| AR127618A1 (es) | 2021-11-29 | 2024-02-14 | Bayer Ag | Dihidropiranopiridinas sustituidas, sales o n-óxidos de las mismas y su uso como sustancias herbicidamente activas |
| WO2025057723A1 (ja) | 2023-09-13 | 2025-03-20 | 石原産業株式会社 | N-置換オキシアミド化合物又はその塩 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1652786A (zh) * | 2002-03-13 | 2005-08-10 | 麦克公司 | 作为雄激素受体调节剂的氟代4-氮杂甾体衍生物 |
| WO2005072732A1 (en) * | 2004-01-16 | 2005-08-11 | Bristol-Myers Squibb Company | Modulators of the glucocorticoid receptor, ap-1, and/or nf-kb activity and use thereof |
| CN1741986A (zh) * | 2003-01-24 | 2006-03-01 | 诺瓦提斯公司 | 酰胺衍生物及其作为11-β羟类固醇脱氢酶抑制剂的用途 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5595872A (en) | 1992-03-06 | 1997-01-21 | Bristol-Myers Squibb Company | Nucleic acids encoding microsomal trigyceride transfer protein |
| US5739135A (en) | 1993-09-03 | 1998-04-14 | Bristol-Myers Squibb Company | Inhibitors of microsomal triglyceride transfer protein and method |
| US5962440A (en) | 1996-05-09 | 1999-10-05 | Bristol-Myers Squibb Company | Cyclic phosphonate ester inhibitors of microsomal triglyceride transfer protein and method |
| US5885983A (en) | 1996-05-10 | 1999-03-23 | Bristol-Myers Squibb Company | Inhibitors of microsomal triglyceride transfer protein and method |
| US5827875A (en) | 1996-05-10 | 1998-10-27 | Bristol-Myers Squibb Company | Inhibitors of microsomal triglyceride transfer protein and method |
| US5760246A (en) | 1996-12-17 | 1998-06-02 | Biller; Scott A. | Conformationally restricted aromatic inhibitors of microsomal triglyceride transfer protein and method |
| WO2004054505A2 (en) | 2002-12-12 | 2004-07-01 | Pharmacia Corporation | Method of using aminocyanopyridine compounds as mitogen activated protein kinase-activated protein kinase-2 inhibitors |
| US8034940B2 (en) * | 2006-08-09 | 2011-10-11 | Bristol-Myers Squibb Company | Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof |
-
2009
- 2009-02-05 JP JP2010545976A patent/JP2011511085A/ja not_active Withdrawn
- 2009-02-05 WO PCT/US2009/033134 patent/WO2009100171A1/en not_active Ceased
- 2009-02-05 CN CN2009801124206A patent/CN101990541A/zh active Pending
- 2009-02-05 EP EP09708143A patent/EP2247597A1/en not_active Withdrawn
- 2009-02-05 US US12/866,270 patent/US8304539B2/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1652786A (zh) * | 2002-03-13 | 2005-08-10 | 麦克公司 | 作为雄激素受体调节剂的氟代4-氮杂甾体衍生物 |
| CN1741986A (zh) * | 2003-01-24 | 2006-03-01 | 诺瓦提斯公司 | 酰胺衍生物及其作为11-β羟类固醇脱氢酶抑制剂的用途 |
| WO2005072732A1 (en) * | 2004-01-16 | 2005-08-11 | Bristol-Myers Squibb Company | Modulators of the glucocorticoid receptor, ap-1, and/or nf-kb activity and use thereof |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108546246A (zh) * | 2018-07-10 | 2018-09-18 | 湖南华腾制药有限公司 | 一种双吡啶基甲醇的制备方法 |
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| US20110002952A1 (en) | 2011-01-06 |
| WO2009100171A1 (en) | 2009-08-13 |
| US8304539B2 (en) | 2012-11-06 |
| EP2247597A1 (en) | 2010-11-10 |
| JP2011511085A (ja) | 2011-04-07 |
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