JP2010500376A - グルココルチコイド受容体、AP−1、および/またはNF−κB活性の調節剤、およびその使用 - Google Patents
グルココルチコイド受容体、AP−1、および/またはNF−κB活性の調節剤、およびその使用 Download PDFInfo
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- JP2010500376A JP2010500376A JP2009523988A JP2009523988A JP2010500376A JP 2010500376 A JP2010500376 A JP 2010500376A JP 2009523988 A JP2009523988 A JP 2009523988A JP 2009523988 A JP2009523988 A JP 2009523988A JP 2010500376 A JP2010500376 A JP 2010500376A
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- Prior art keywords
- alkyl
- methyl
- substituted
- thiazol
- aryl
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- 0 C1c2ccccc2*c2ccccc12 Chemical compound C1c2ccccc2*c2ccccc12 0.000 description 28
- YNAVUWVOSKDBBP-UHFFFAOYSA-N C1NCCOC1 Chemical compound C1NCCOC1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- YLZSWWIDFRAGEN-UHFFFAOYSA-N CC(C)(C1C(Nc2nnc[s]2)=O)C11c2ccc(-c(cc3)cc(OC)c3C(O)=O)nc2Oc2ccccc12 Chemical compound CC(C)(C1C(Nc2nnc[s]2)=O)C11c2ccc(-c(cc3)cc(OC)c3C(O)=O)nc2Oc2ccccc12 YLZSWWIDFRAGEN-UHFFFAOYSA-N 0.000 description 1
- HEHLNVHGAMRQDF-UHFFFAOYSA-N CC(C)(C1c(ccc(B2OC(C)(C)C(C)(C)O2)c2)c2Oc2c1cccc2)C(Nc1nnc[s]1)=O Chemical compound CC(C)(C1c(ccc(B2OC(C)(C)C(C)(C)O2)c2)c2Oc2c1cccc2)C(Nc1nnc[s]1)=O HEHLNVHGAMRQDF-UHFFFAOYSA-N 0.000 description 1
- VYKCZLDHJWUBFV-UHFFFAOYSA-N CC(C)(C1c(ccc(N2CCCC2)n2)c2Oc2c1cccc2)C(Nc1nnc[s]1)=O Chemical compound CC(C)(C1c(ccc(N2CCCC2)n2)c2Oc2c1cccc2)C(Nc1nnc[s]1)=O VYKCZLDHJWUBFV-UHFFFAOYSA-N 0.000 description 1
- ZSMCHXGGQCKXMY-UHFFFAOYSA-N CC(C)(C1c(ccc(O)c2)c2Oc2c1cccc2)C(Nc1nnc[s]1)=O Chemical compound CC(C)(C1c(ccc(O)c2)c2Oc2c1cccc2)C(Nc1nnc[s]1)=O ZSMCHXGGQCKXMY-UHFFFAOYSA-N 0.000 description 1
- RFZPIZGDZLNDKO-UHFFFAOYSA-N CC(C)(C1c(cccc2O)c2Oc2ccccc12)C(OC)=O Chemical compound CC(C)(C1c(cccc2O)c2Oc2ccccc12)C(OC)=O RFZPIZGDZLNDKO-UHFFFAOYSA-N 0.000 description 1
- BHLDRJNCVDJRTL-UHFFFAOYSA-N CC(C)(C1c2ccc(-c(cc3)ccc3C(N(C)C)=O)nc2Oc2ccccc12)C(Nc1ncc[nH]1)=O Chemical compound CC(C)(C1c2ccc(-c(cc3)ccc3C(N(C)C)=O)nc2Oc2ccccc12)C(Nc1ncc[nH]1)=O BHLDRJNCVDJRTL-UHFFFAOYSA-N 0.000 description 1
- XOVURLTYCXFXTF-FIPFOOKPSA-N CC(C)([C@@H]1C(Nc2nnc[s]2)=O)[C@@]11c2ccc(-c3ccc(CC(OC)=O)cc3)nc2Oc2ccccc12 Chemical compound CC(C)([C@@H]1C(Nc2nnc[s]2)=O)[C@@]11c2ccc(-c3ccc(CC(OC)=O)cc3)nc2Oc2ccccc12 XOVURLTYCXFXTF-FIPFOOKPSA-N 0.000 description 1
- UFYAYGTVVAUGNH-IBGZPJMESA-N CC(C)([C@@H]1c2ccc(N(CC3)CCC3=O)nc2Oc2c1cccc2)C(Nc1nnc[s]1)=O Chemical compound CC(C)([C@@H]1c2ccc(N(CC3)CCC3=O)nc2Oc2c1cccc2)C(Nc1nnc[s]1)=O UFYAYGTVVAUGNH-IBGZPJMESA-N 0.000 description 1
- ASYCYJOWBUQLKQ-UXMRNZNESA-N CC(C)C(c(cc1)ccc1-c1ccc([C@@H](C(C)(C)C(Nc2nnc[s]2)=O)c2ccccc2O2)c2n1)SO Chemical compound CC(C)C(c(cc1)ccc1-c1ccc([C@@H](C(C)(C)C(Nc2nnc[s]2)=O)c2ccccc2O2)c2n1)SO ASYCYJOWBUQLKQ-UXMRNZNESA-N 0.000 description 1
- KYWXRBNOYGGPIZ-UHFFFAOYSA-N CC(N1CCOCC1)=O Chemical compound CC(N1CCOCC1)=O KYWXRBNOYGGPIZ-UHFFFAOYSA-N 0.000 description 1
- UKHSIOOJHZKUQM-UHFFFAOYSA-N CN(C)C(c(cc1)ccc1-c1nc(Oc2ccccc2C2C3(CCC3)C(Nc3nnc[s]3)=O)c2cc1)=O Chemical compound CN(C)C(c(cc1)ccc1-c1nc(Oc2ccccc2C2C3(CCC3)C(Nc3nnc[s]3)=O)c2cc1)=O UKHSIOOJHZKUQM-UHFFFAOYSA-N 0.000 description 1
- SJRJJKPEHAURKC-UHFFFAOYSA-N CN1CCOCC1 Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 1
- NGCVARGFWKSDJA-VIFPVBQESA-N C[C@@]1(C=CC(C)=CC1)NC Chemical compound C[C@@]1(C=CC(C)=CC1)NC NGCVARGFWKSDJA-VIFPVBQESA-N 0.000 description 1
- SMUQFGGVLNAIOZ-UHFFFAOYSA-N Cc1ccc(cccc2)c2n1 Chemical compound Cc1ccc(cccc2)c2n1 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 1
- NODLZCJDRXTSJO-UHFFFAOYSA-N Cc1n[n](C)cc1 Chemical compound Cc1n[n](C)cc1 NODLZCJDRXTSJO-UHFFFAOYSA-N 0.000 description 1
- NFHWADSYPPRXJW-UHFFFAOYSA-N Cc1nc([RnH])n[s]1 Chemical compound Cc1nc([RnH])n[s]1 NFHWADSYPPRXJW-UHFFFAOYSA-N 0.000 description 1
- DXYYSGDWQCSKKO-UHFFFAOYSA-N Cc1nc(cccc2)c2[s]1 Chemical compound Cc1nc(cccc2)c2[s]1 DXYYSGDWQCSKKO-UHFFFAOYSA-N 0.000 description 1
- VZWOXDYRBDIHMA-UHFFFAOYSA-N Cc1ncc[s]1 Chemical compound Cc1ncc[s]1 VZWOXDYRBDIHMA-UHFFFAOYSA-N 0.000 description 1
- ZYKIMTQVSLCOIT-UHFFFAOYSA-N Nc1nc(Cc(cc2)ccc2-c2cccnc2)c[s]1 Chemical compound Nc1nc(Cc(cc2)ccc2-c2cccnc2)c[s]1 ZYKIMTQVSLCOIT-UHFFFAOYSA-N 0.000 description 1
- NMBWLHPNKHJYQA-UHFFFAOYSA-N OB(c1ccc(C(N(CC2)CC2(F)F)=O)c(F)c1)O Chemical compound OB(c1ccc(C(N(CC2)CC2(F)F)=O)c(F)c1)O NMBWLHPNKHJYQA-UHFFFAOYSA-N 0.000 description 1
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
- C07D417/02—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
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- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- 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
- C07D491/02—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 two hetero rings
- C07D491/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (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)
- Diabetes (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Child & Adolescent Psychology (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83649606P | 2006-08-09 | 2006-08-09 | |
| US11/835,438 US8034940B2 (en) | 2006-08-09 | 2007-08-08 | Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof |
| PCT/US2007/075543 WO2008021926A2 (en) | 2006-08-09 | 2007-08-09 | Modulators of glucocorticoid receptor, and/or ap-1, and/or nf-kb activity and use thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010500376A true JP2010500376A (ja) | 2010-01-07 |
| JP2010500376A5 JP2010500376A5 (enExample) | 2010-09-02 |
Family
ID=39052386
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009523988A Withdrawn JP2010500376A (ja) | 2006-08-09 | 2007-08-09 | グルココルチコイド受容体、AP−1、および/またはNF−κB活性の調節剤、およびその使用 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8034940B2 (enExample) |
| EP (1) | EP2049507A2 (enExample) |
| JP (1) | JP2010500376A (enExample) |
| KR (1) | KR20090038930A (enExample) |
| CN (1) | CN101528718B (enExample) |
| AR (1) | AR062312A1 (enExample) |
| AU (1) | AU2007286221A1 (enExample) |
| BR (1) | BRPI0716641A2 (enExample) |
| CA (1) | CA2660318A1 (enExample) |
| CL (1) | CL2007002330A1 (enExample) |
| EA (1) | EA200900291A1 (enExample) |
| IL (1) | IL196814A0 (enExample) |
| MX (1) | MX2009001220A (enExample) |
| NO (1) | NO20090564L (enExample) |
| PE (1) | PE20081314A1 (enExample) |
| TW (1) | TW200815454A (enExample) |
| WO (1) | WO2008021926A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11724982B2 (en) | 2014-10-10 | 2023-08-15 | The Research Foundation For The State University Of New York | Trifluoromethoxylation of arenes via intramolecular trifluoromethoxy group migration |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008057862A2 (en) | 2006-11-01 | 2008-05-15 | Bristol-Myers Squibb Company | MODULATORS OF GLUCOCORTICOID RECEPTOR, AP-1, AND/OR NF-ϰB ACTIVITY AND USE THEREOF |
| JP2010508358A (ja) | 2006-11-01 | 2010-03-18 | ブリストル−マイヤーズ スクイブ カンパニー | グルココルチコイド受容体、AP−1、および/またはNF−κB活性の調節剤、並びにその使用 |
| ES2382913T3 (es) | 2006-11-01 | 2012-06-14 | Bristol-Myers Squibb Company | Moduladores de la actividad de receptor de glucocorticoides, AP-1 y/o NF-kappaB y uso de los mismos |
| WO2008057856A2 (en) | 2006-11-01 | 2008-05-15 | Bristol-Myers Squibb Company | Modulators of glucocorticoid receptor, ap-1 and/or nf-kappab activity and use thereof |
| JP2011511085A (ja) * | 2008-02-07 | 2011-04-07 | ブリストル−マイヤーズ スクイブ カンパニー | グルココルチコイド受容体、AP−1、および/またはNF−κB活性の縮合ヘテロアリール修飾因子並びにその使用 |
| CA2721060A1 (en) * | 2008-04-09 | 2009-10-15 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
| US8791258B2 (en) * | 2008-06-10 | 2014-07-29 | The Regents Of The University Of California | Pro-fluorescent probes |
| US8106046B2 (en) * | 2008-06-24 | 2012-01-31 | Bristol-Myers Squibb Company | Cyclopentathiophene modulators of the glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof |
| JPWO2010001990A1 (ja) | 2008-07-03 | 2011-12-22 | 協和発酵キリン株式会社 | 四環系化合物 |
| WO2011081173A1 (ja) * | 2009-12-29 | 2011-07-07 | 協和発酵キリン株式会社 | 四環系化合物 |
| EP2524057B1 (en) * | 2010-01-15 | 2016-03-30 | Rigel Pharmaceuticals, Inc. | Screening assay employing dex and gdf8 |
| WO2015027021A1 (en) | 2013-08-22 | 2015-02-26 | Bristol-Myers Squibb Company | Imide and acylurea derivatives as modulators of the glucocorticoid receptor |
| US9796720B2 (en) | 2013-08-22 | 2017-10-24 | Bristol-Myers Squibb Company | Imidazole-derived modulators of the glucocorticoid receptor |
| WO2016123244A1 (en) * | 2015-01-27 | 2016-08-04 | Indicator Systems International, Inc. | Fluorescein polymer conjugates |
| WO2018030550A1 (en) | 2016-08-09 | 2018-02-15 | Takeda Pharmaceutical Company Limited | Heterocyclic compounds with an ror(gamma)t modulating activity |
| CA3092362A1 (en) * | 2017-10-19 | 2019-04-25 | Tempest Therapeutics, Inc. | Picolinamide compounds |
| CN113862704B (zh) * | 2021-11-15 | 2023-07-21 | 南昌航空大学 | 一种9-芳基呫吨类化合物的制备方法 |
| 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 |
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| CN117105820A (zh) * | 2023-07-12 | 2023-11-24 | 上海阿拉丁生化科技股份有限公司 | 一种4-氟苯乙基异氰酸酯的制备方法 |
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| WO2008057862A2 (en) | 2006-11-01 | 2008-05-15 | Bristol-Myers Squibb Company | MODULATORS OF GLUCOCORTICOID RECEPTOR, AP-1, AND/OR NF-ϰB ACTIVITY AND USE THEREOF |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11724982B2 (en) | 2014-10-10 | 2023-08-15 | The Research Foundation For The State University Of New York | Trifluoromethoxylation of arenes via intramolecular trifluoromethoxy group migration |
Also Published As
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| CL2007002330A1 (es) | 2008-02-15 |
| US8034940B2 (en) | 2011-10-11 |
| EA200900291A1 (ru) | 2009-10-30 |
| US20090075995A1 (en) | 2009-03-19 |
| AR062312A1 (es) | 2008-10-29 |
| CA2660318A1 (en) | 2008-02-21 |
| BRPI0716641A2 (pt) | 2013-10-15 |
| EP2049507A2 (en) | 2009-04-22 |
| TW200815454A (en) | 2008-04-01 |
| AU2007286221A1 (en) | 2008-02-21 |
| WO2008021926A2 (en) | 2008-02-21 |
| NO20090564L (no) | 2009-03-19 |
| WO2008021926A3 (en) | 2008-05-22 |
| IL196814A0 (en) | 2009-11-18 |
| KR20090038930A (ko) | 2009-04-21 |
| CN101528718B (zh) | 2011-11-09 |
| PE20081314A1 (es) | 2008-10-17 |
| CN101528718A (zh) | 2009-09-09 |
| MX2009001220A (es) | 2009-02-11 |
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