KR102151299B1 - N-(4-하이드록시-4-메틸-사이클로헥실)-4-페닐-벤젠설폰아미드 및 n-(4-하이드록시-4-메틸-사이클로헥실)-4-(2-피리딜)벤젠설폰아미드 및 이들의 치료 용도 - Google Patents
N-(4-하이드록시-4-메틸-사이클로헥실)-4-페닐-벤젠설폰아미드 및 n-(4-하이드록시-4-메틸-사이클로헥실)-4-(2-피리딜)벤젠설폰아미드 및 이들의 치료 용도 Download PDFInfo
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- KR102151299B1 KR102151299B1 KR1020167002015A KR20167002015A KR102151299B1 KR 102151299 B1 KR102151299 B1 KR 102151299B1 KR 1020167002015 A KR1020167002015 A KR 1020167002015A KR 20167002015 A KR20167002015 A KR 20167002015A KR 102151299 B1 KR102151299 B1 KR 102151299B1
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- BTPLETAXGDMOJB-UHFFFAOYSA-N CC(CC1)(CCC1NS(c(cc1)ccc1-c(ncc(Cl)c1)c1Cl)(=O)=O)O Chemical compound CC(CC1)(CCC1NS(c(cc1)ccc1-c(ncc(Cl)c1)c1Cl)(=O)=O)O BTPLETAXGDMOJB-UHFFFAOYSA-N 0.000 description 1
- ATOAQUMXTGMIBB-UHFFFAOYSA-N CC(CC1)(CCC1NS(c(cc1F)ccc1-c(c(Cl)c1)ncc1Cl)(=O)=O)O Chemical compound CC(CC1)(CCC1NS(c(cc1F)ccc1-c(c(Cl)c1)ncc1Cl)(=O)=O)O ATOAQUMXTGMIBB-UHFFFAOYSA-N 0.000 description 1
- NTTDZJOZGZQRFB-HEHXSTRBSA-N C[C@](CC1)(CC[C@@H]1NS(c(cc1)cc(F)c1-c(c(F)c1)ncc1F)(=O)=O)O Chemical compound C[C@](CC1)(CC[C@@H]1NS(c(cc1)cc(F)c1-c(c(F)c1)ncc1F)(=O)=O)O NTTDZJOZGZQRFB-HEHXSTRBSA-N 0.000 description 1
- XEBVDIKWQHIPJH-UJKQEGAGSA-N C[C@](CC1)(CC[C@@H]1NS(c(cc1)ccc1-c(ncc(F)c1)c1F)(=O)=O)O Chemical compound C[C@](CC1)(CC[C@@H]1NS(c(cc1)ccc1-c(ncc(F)c1)c1F)(=O)=O)O XEBVDIKWQHIPJH-UJKQEGAGSA-N 0.000 description 1
- ATOAQUMXTGMIBB-KSMLVUNXSA-N C[C@](CC1)(CC[C@H]1NS(c(cc1)cc(F)c1-c(c(Cl)c1)ncc1Cl)(=O)=O)O Chemical compound C[C@](CC1)(CC[C@H]1NS(c(cc1)cc(F)c1-c(c(Cl)c1)ncc1Cl)(=O)=O)O ATOAQUMXTGMIBB-KSMLVUNXSA-N 0.000 description 1
- QHCZIGWQXAUGTL-HJGJAMNPSA-N C[C@](CC1)(CC[C@H]1NS(c(cc1)cc(F)c1-c(ccc(F)c1)c1F)(=O)=O)O Chemical compound C[C@](CC1)(CC[C@H]1NS(c(cc1)cc(F)c1-c(ccc(F)c1)c1F)(=O)=O)O QHCZIGWQXAUGTL-HJGJAMNPSA-N 0.000 description 1
- KRWSTTKOIBYLNA-RHDGDCLCSA-N C[C@](CC1)(CC[C@H]1NS(c(cc1)ccc1-c(cc1)c(C(F)(F)F)cc1F)(=O)=O)O Chemical compound C[C@](CC1)(CC[C@H]1NS(c(cc1)ccc1-c(cc1)c(C(F)(F)F)cc1F)(=O)=O)O KRWSTTKOIBYLNA-RHDGDCLCSA-N 0.000 description 1
- PHOYDFRXZMNHIF-IRJFHVNHSA-N C[C@](CC1)(CC[C@H]1NS(c(cc1)ccc1-c(ccc(Cl)c1)c1C#N)(=O)=O)O Chemical compound C[C@](CC1)(CC[C@H]1NS(c(cc1)ccc1-c(ccc(Cl)c1)c1C#N)(=O)=O)O PHOYDFRXZMNHIF-IRJFHVNHSA-N 0.000 description 1
- 0 Cc1cc(S(*C(CC2)CCC2O)(=O)=O)ccc1-c(cc1)ccc1C#N Chemical compound Cc1cc(S(*C(CC2)CCC2O)(=O)=O)ccc1-c(cc1)ccc1C#N 0.000 description 1
- KLWGBHGJIGBOCJ-UHFFFAOYSA-N OC(CC1)CCC1NS(c1ccc(-c2ccc(C(F)(F)F)cc2)c(F)c1)(=O)=O Chemical compound OC(CC1)CCC1NS(c1ccc(-c2ccc(C(F)(F)F)cc2)c(F)c1)(=O)=O KLWGBHGJIGBOCJ-UHFFFAOYSA-N 0.000 description 1
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- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/20—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
- C07D213/61—Halogen atoms or nitro radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
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- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1311361.8A GB201311361D0 (en) | 2013-06-26 | 2013-06-26 | Compounds and their therapeutic use |
| GB1311361.8 | 2013-06-26 | ||
| PCT/GB2014/051921 WO2014207445A1 (en) | 2013-06-26 | 2014-06-24 | N-(4-hydroxy-4-methyl-cyclohexyl)-4-phenyl-benzenesulfonamides and n-(4-hydroxy-4-methyl-cyclohexyl)-4-(2-pyridyl)benzenesulfonamides and their therapeutic use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20160024392A KR20160024392A (ko) | 2016-03-04 |
| KR102151299B1 true KR102151299B1 (ko) | 2020-09-02 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020167002015A Active KR102151299B1 (ko) | 2013-06-26 | 2014-06-24 | N-(4-하이드록시-4-메틸-사이클로헥실)-4-페닐-벤젠설폰아미드 및 n-(4-하이드록시-4-메틸-사이클로헥실)-4-(2-피리딜)벤젠설폰아미드 및 이들의 치료 용도 |
Country Status (28)
| Country | Link |
|---|---|
| US (4) | US9624167B2 (https=) |
| EP (1) | EP3013799B1 (https=) |
| JP (1) | JP6360555B2 (https=) |
| KR (1) | KR102151299B1 (https=) |
| CN (1) | CN105492426B (https=) |
| AU (1) | AU2014300745B2 (https=) |
| BR (1) | BR112015031527B1 (https=) |
| CA (1) | CA2915075C (https=) |
| CY (1) | CY1119438T1 (https=) |
| DK (1) | DK3013799T3 (https=) |
| EA (1) | EA028077B1 (https=) |
| ES (1) | ES2641758T3 (https=) |
| GB (1) | GB201311361D0 (https=) |
| HR (1) | HRP20171611T1 (https=) |
| HU (1) | HUE034983T2 (https=) |
| IL (1) | IL243103B (https=) |
| LT (1) | LT3013799T (https=) |
| ME (1) | ME02834B (https=) |
| MX (1) | MX374328B (https=) |
| NZ (1) | NZ715192A (https=) |
| PL (1) | PL3013799T3 (https=) |
| PT (1) | PT3013799T (https=) |
| RS (1) | RS56256B1 (https=) |
| SG (1) | SG11201510646SA (https=) |
| SI (1) | SI3013799T1 (https=) |
| SM (1) | SMT201700503T1 (https=) |
| WO (1) | WO2014207445A1 (https=) |
| ZA (1) | ZA201600202B (https=) |
Families Citing this family (12)
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| GB0817207D0 (en) | 2008-09-19 | 2008-10-29 | Pimco 2664 Ltd | therapeutic apsac compounds and their use |
| GB201311361D0 (en) | 2013-06-26 | 2013-08-14 | Pimco 2664 Ltd | Compounds and their therapeutic use |
| AU2015367528B2 (en) * | 2014-12-17 | 2020-05-14 | Pimco 2664 Limited | N-(4-hydroxy-4-methyl-cyclohexyl)-4-phenyl-benzenesulfonamide and N-(4-hydroxy-4-methyl-cyclohexyl)-4-(2-pyridyl)-benzenesulfonamide compounds and their therapeutic use |
| GB201813312D0 (en) * | 2018-08-15 | 2018-09-26 | Modern Biosciences Ltd | Compounds and their therapeutic use |
| GB201905520D0 (en) * | 2019-04-18 | 2019-06-05 | Modern Biosciences Ltd | Compounds and their therapeutic use |
| EP4431090A1 (en) | 2023-03-15 | 2024-09-18 | Istesso 1 Limited | Solfonamides acting as mitochondrial complex i modulator compounds |
| GB202308547D0 (en) | 2023-06-08 | 2023-07-26 | Istesso 2 Ltd | Tnf inhibitor combination therapies |
| GB202309515D0 (en) | 2023-06-23 | 2023-08-09 | Istesso 2 Ltd | JAK inhibitor and IL-6 inhibitor combination therapies |
| GB202315822D0 (en) | 2023-10-16 | 2023-11-29 | Istesso 3 Ltd | Anti-fibrotic combination therapeutics |
| GB202317050D0 (en) | 2023-11-07 | 2023-12-20 | Istesso 2 Ltd | Disease modifying anti-rheumatic drug combination therapies |
| EP4647071A1 (en) | 2024-05-10 | 2025-11-12 | Istesso Therapeutics Limited | Mitochondrial complex i modulator for use in the treatment of arthritis |
| GB202411554D0 (en) | 2024-08-06 | 2024-09-18 | Istesso 2 Ltd | NF-kB inhibitor combination therapies |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010032009A1 (en) | 2008-09-19 | 2010-03-25 | Pimco 2664 Limited | Aryl-phenyl-sulfonamido-cycloalkyl compounds and their use |
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| GB597810A (en) | 1943-04-12 | 1948-02-04 | Gen Printing Ink Corp | Improvements in or relating to derivatives of diphenyl |
| DE1046220B (de) | 1956-04-21 | 1958-12-11 | Bayer Ag | Verfahren zur Herstellung von Monoazofarbstoffen und deren Metallkomplexverbindungen |
| US4119784A (en) | 1977-07-01 | 1978-10-10 | American Cyanamid Company | Anionic substituted sulfonamido biphenyls |
| DE3000519A1 (de) | 1979-02-01 | 1980-08-14 | Byk Gulden Lomberg Chem Fab | Sulfonamido-alkansaeuren, ihre verwendung und herstellung sowie sie enthaltende arzneimittel |
| DE3535167A1 (de) | 1985-10-02 | 1987-04-09 | Boehringer Mannheim Gmbh | Neue sulfonyl-phenyl(alkyl)amine, verfahren zu ihrer herstellung sowie arzneimittel |
| IL118325A0 (en) | 1995-05-25 | 1996-10-31 | Pont Merck And Pharmaceutical | Integrin receptor antagonists and pharmaceutical compositions containing them |
| WO1997016433A1 (en) | 1995-10-30 | 1997-05-09 | Smithkline Beecham Corporation | Protease inhibitors |
| US5760028A (en) | 1995-12-22 | 1998-06-02 | The Dupont Merck Pharmaceutical Company | Integrin receptor antagonists |
| WO1997033887A1 (en) | 1996-03-15 | 1997-09-18 | Du Pont Pharmaceuticals Company | Spirocycle integrin inhibitors |
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| IL129344A0 (en) | 1996-11-27 | 2000-02-17 | Du Pont Pharm Co | Novel integrin receptor antagonists |
| US6214834B1 (en) | 1997-03-28 | 2001-04-10 | Dupont Pharmaceuticals Company | Integrin inhibitor prodrugs |
| IL132630A0 (en) | 1997-05-08 | 2001-03-19 | Smithkline Beecham Corp | Protease inhibitors |
| DE19719621A1 (de) | 1997-05-09 | 1998-11-12 | Hoechst Ag | Sulfonylaminocarbonsäuren |
| PT877019E (pt) | 1997-05-09 | 2002-05-31 | Hoechst Ag | Acidos diaminocarboxilicos substituidos |
| US6291425B1 (en) | 1999-09-01 | 2001-09-18 | Guilford Pharmaceuticals Inc. | Compounds, methods and pharmaceutical compositions for treating cellular damage, such as neural or cardiovascular tissue damage |
| YU47200A (sh) | 1998-01-23 | 2002-11-15 | Aventis Pharma Deutschland Gmbh. | Novi derivati sulfonamida kao inhibitori koštane resorpcije i kao inhibitori ćelijske adhezije |
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| JPH11246527A (ja) | 1998-03-02 | 1999-09-14 | Shionogi & Co Ltd | Mmp−8阻害剤 |
| DE19815547C1 (de) | 1998-04-07 | 1999-12-02 | Joachim Schmidt | Haftmittel für Zahnprothesen |
| EP0960882A1 (en) | 1998-05-19 | 1999-12-01 | Hoechst Marion Roussel Deutschland GmbH | Thienyl substituted acylguanidines as inhibitors of bone resorption and vitronectin receptor antagonists |
| MXPA02009309A (es) | 2000-03-21 | 2003-03-12 | Procter & Gamble | Inhibidores de las metaloproteasas n-sustituidas que contienen cadenas laterales carboxiclicas. |
| WO2001090077A1 (en) | 2000-05-19 | 2001-11-29 | Guilford Pharmaceuticals, Inc. | Sulfonamide and carbamide derivatives of 6(5h)phenanthridinones and their uses |
| AU2002228316A1 (en) | 2001-01-29 | 2002-08-12 | Insight Strategy And Marketing Ltd | Carbazole derivatives and their uses as heparanase inhibitors |
| JPWO2002074298A1 (ja) | 2001-03-21 | 2004-07-08 | 小野薬品工業株式会社 | Il−6産生阻害剤 |
| WO2002089785A1 (en) | 2001-05-07 | 2002-11-14 | Smithkline Beecham Corporation | Sulfonamides |
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| GB0126157D0 (en) | 2001-10-31 | 2002-01-02 | Univ Aberdeen | Therapeutic compounds |
| US20050227994A1 (en) | 2002-03-27 | 2005-10-13 | Shionogi & Co., Ltd. | Decomposition inhibitor for extracellular matrix of cartilage |
| MXPA05002571A (es) | 2002-09-04 | 2005-09-08 | Schering Corp | Pirazolopirimidinas como inhibidores de cinasa dependientes de ciclina. |
| DE10251170A1 (de) | 2002-10-31 | 2004-05-13 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Beta-Agonisten, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel |
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