JP5840492B2 - アリール−フェニル−スルホンアミド−フェニレン化合物とその使用 - Google Patents
アリール−フェニル−スルホンアミド−フェニレン化合物とその使用 Download PDFInfo
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- JP5840492B2 JP5840492B2 JP2011527395A JP2011527395A JP5840492B2 JP 5840492 B2 JP5840492 B2 JP 5840492B2 JP 2011527395 A JP2011527395 A JP 2011527395A JP 2011527395 A JP2011527395 A JP 2011527395A JP 5840492 B2 JP5840492 B2 JP 5840492B2
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- 0 CS(*)C1=NCC(*)C(*)=C1* Chemical compound CS(*)C1=NCC(*)C(*)=C1* 0.000 description 7
- CKQHAYFOPRIUOM-UHFFFAOYSA-N CC(c1cc(N)ccc1)=O Chemical compound CC(c1cc(N)ccc1)=O CKQHAYFOPRIUOM-UHFFFAOYSA-N 0.000 description 1
- BRWKJZNQYBWAFU-UHFFFAOYSA-N CC(c1cc(NS(c(cc2)ccc2-c(ccc(F)c2)c2F)(=O)=O)ccc1)=O Chemical compound CC(c1cc(NS(c(cc2)ccc2-c(ccc(F)c2)c2F)(=O)=O)ccc1)=O BRWKJZNQYBWAFU-UHFFFAOYSA-N 0.000 description 1
- PNOPEHVRUYIARL-UHFFFAOYSA-N CC(c1cccc(NS(c(cc2)ccc2-c(cc2)ccc2Br)(=O)=O)c1)=O Chemical compound CC(c1cccc(NS(c(cc2)ccc2-c(cc2)ccc2Br)(=O)=O)c1)=O PNOPEHVRUYIARL-UHFFFAOYSA-N 0.000 description 1
- RFSMBEKZJZHCCN-VIFPVBQESA-N CN([C@@H](CO1)c2cccc(N)c2)C1=O Chemical compound CN([C@@H](CO1)c2cccc(N)c2)C1=O RFSMBEKZJZHCCN-VIFPVBQESA-N 0.000 description 1
- KOXZHHUPBQWVKR-UHFFFAOYSA-N COCCNC(COC)c1cc(NS(c(cc2)ccc2-c(ccc(F)c2)c2F)(=O)=O)ccc1 Chemical compound COCCNC(COC)c1cc(NS(c(cc2)ccc2-c(ccc(F)c2)c2F)(=O)=O)ccc1 KOXZHHUPBQWVKR-UHFFFAOYSA-N 0.000 description 1
- BRCYKLIRSYBOBC-ZDUSSCGKSA-N C[C@@H](c1cc(NS(c(cc2)ccc2-c(ccc(F)c2)c2F)(=O)=O)ccc1)O Chemical compound C[C@@H](c1cc(NS(c(cc2)ccc2-c(ccc(F)c2)c2F)(=O)=O)ccc1)O BRCYKLIRSYBOBC-ZDUSSCGKSA-N 0.000 description 1
- MILXUJQMRHHSQA-UHFFFAOYSA-N Cc1cc(-c(c(F)c2)ccc2F)ccc1S(Nc1cc(S(N)(=O)=O)ccc1)(=O)=O Chemical compound Cc1cc(-c(c(F)c2)ccc2F)ccc1S(Nc1cc(S(N)(=O)=O)ccc1)(=O)=O MILXUJQMRHHSQA-UHFFFAOYSA-N 0.000 description 1
- YXWYKMFOZZEWSC-UHFFFAOYSA-N NS(C(C=CC1)=CC1NS(C1C(Cl)=CC(c(cc2)ccc2OC(F)(F)F)=CC1)(=O)=O)OCC1CC1 Chemical compound NS(C(C=CC1)=CC1NS(C1C(Cl)=CC(c(cc2)ccc2OC(F)(F)F)=CC1)(=O)=O)OCC1CC1 YXWYKMFOZZEWSC-UHFFFAOYSA-N 0.000 description 1
- OBKXIYOCBWUQRF-UHFFFAOYSA-N NS(c1cc(NS(c(cc2)ccc2-c(cc2F)ccc2F)(=O)=O)ccc1)(=O)=O Chemical compound NS(c1cc(NS(c(cc2)ccc2-c(cc2F)ccc2F)(=O)=O)ccc1)(=O)=O OBKXIYOCBWUQRF-UHFFFAOYSA-N 0.000 description 1
- VDQIZBGZWSEKDX-HXUWFJFHSA-N N[C@H](CO)c1cccc(NS(c(cc2)ccc2-c(ccc(F)c2)c2F)(=O)=O)c1 Chemical compound N[C@H](CO)c1cccc(NS(c(cc2)ccc2-c(ccc(F)c2)c2F)(=O)=O)c1 VDQIZBGZWSEKDX-HXUWFJFHSA-N 0.000 description 1
- KJHWDQFXXLZMMG-UHFFFAOYSA-N O=C(c1cc(NS(c(cc2)ccc2-c(ccc(Cl)c2)c2Cl)(=O)=O)ccc1)Cl Chemical compound O=C(c1cc(NS(c(cc2)ccc2-c(ccc(Cl)c2)c2Cl)(=O)=O)ccc1)Cl KJHWDQFXXLZMMG-UHFFFAOYSA-N 0.000 description 1
- GYQUZEYFIMKCMX-UHFFFAOYSA-N O=C(c1cccc(NS(c(cc2)ccc2Br)(=O)=O)c1)Cl Chemical compound O=C(c1cccc(NS(c(cc2)ccc2Br)(=O)=O)c1)Cl GYQUZEYFIMKCMX-UHFFFAOYSA-N 0.000 description 1
- HVVCFKXNHHDXHD-UHFFFAOYSA-N O=Cc1cccc(NS(c(cc2)ccc2-c(ccc(Cl)c2)c2Cl)(=O)=O)c1 Chemical compound O=Cc1cccc(NS(c(cc2)ccc2-c(ccc(Cl)c2)c2Cl)(=O)=O)c1 HVVCFKXNHHDXHD-UHFFFAOYSA-N 0.000 description 1
- IBWWHZAZRIKQSC-UHFFFAOYSA-N O=S(c(cc1)ccc1-c(ccc(F)c1)c1F)(Cl)=O Chemical compound O=S(c(cc1)ccc1-c(ccc(F)c1)c1F)(Cl)=O IBWWHZAZRIKQSC-UHFFFAOYSA-N 0.000 description 1
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- C07D303/02—Compounds containing oxirane rings
- C07D303/36—Compounds containing oxirane rings with hydrocarbon radicals, substituted by nitrogen atoms
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- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—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 six-membered aromatic ring
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- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
- C07C311/38—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
- C07C311/39—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
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- C07—ORGANIC CHEMISTRY
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
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- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
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- C07—ORGANIC CHEMISTRY
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- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
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- Health & Medical Sciences (AREA)
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- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Endocrinology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Transplantation (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Biomedical Technology (AREA)
- Reproductive Health (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9827508P | 2008-09-19 | 2008-09-19 | |
| GB0817208.2 | 2008-09-19 | ||
| US61/098,275 | 2008-09-19 | ||
| GBGB0817208.2A GB0817208D0 (en) | 2008-09-19 | 2008-09-19 | Therapeutic apsap compounds and their use |
| PCT/GB2009/002223 WO2010032010A1 (en) | 2008-09-19 | 2009-09-18 | Aryl-phenyl-sulfonamide-phenylene compounds and their use |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012502965A JP2012502965A (ja) | 2012-02-02 |
| JP2012502965A5 JP2012502965A5 (enExample) | 2012-10-25 |
| JP5840492B2 true JP5840492B2 (ja) | 2016-01-06 |
Family
ID=39951896
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011527395A Active JP5840492B2 (ja) | 2008-09-19 | 2009-09-18 | アリール−フェニル−スルホンアミド−フェニレン化合物とその使用 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8207167B2 (enExample) |
| EP (1) | EP2349990B8 (enExample) |
| JP (1) | JP5840492B2 (enExample) |
| CA (1) | CA2736980C (enExample) |
| DK (1) | DK2349990T3 (enExample) |
| ES (1) | ES2675074T3 (enExample) |
| GB (1) | GB0817208D0 (enExample) |
| WO (1) | WO2010032010A1 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0705400D0 (en) | 2007-03-21 | 2007-05-02 | Univ Aberdeen | Therapeutic compounds andm their use |
| GB0817207D0 (en) | 2008-09-19 | 2008-10-29 | Pimco 2664 Ltd | therapeutic apsac compounds and their use |
| RU2015124564A (ru) * | 2012-12-10 | 2017-01-12 | Ф. Хоффманн-Ля Рош Аг | ПРОИЗВОДНЫЕ БЕНЗОЛСУЛЬФОНАМИДА В КАЧЕСТВЕ МОДУЛЯТОРОВ РЕЦЕПТОРОВ RORc |
| GB201311361D0 (en) | 2013-06-26 | 2013-08-14 | Pimco 2664 Ltd | Compounds and their therapeutic use |
| ES2899852T3 (es) * | 2014-12-17 | 2022-03-15 | Pimco 2664 Ltd | Compuestos de N-(4-hidroxi-4-metil-ciclohexil)-4-fenil-bencenosulfonamida y N-(-4-hidroxi-4-metil-ciclohexil)-4-(2-piridil)-bencenosulfonamida y su uso terapéutico |
| EP3438090A4 (en) * | 2016-03-31 | 2019-09-04 | FUJIFILM Toyama Chemical Co., Ltd. | NOVEL PROCESS FOR PRODUCING HYDROXAMIC ACID DERIVATIVE AND CORRESPONDING INTERMEDIATE |
| 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 |
| WO2021047978A1 (en) | 2019-09-12 | 2021-03-18 | BASF Agro B.V. | Process for the preparation of α-methyl-[4-(nitro)-2-(trifluoromethyl)]-benzyl nitrate |
| CA3191223A1 (en) * | 2020-08-31 | 2022-03-03 | Alfonso Bellacosa | Methods of treating cancer |
| 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 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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2008
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- 2009-09-18 EP EP09785123.2A patent/EP2349990B8/en active Active
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- 2009-09-18 ES ES09785123.2T patent/ES2675074T3/es active Active
- 2009-09-18 CA CA2736980A patent/CA2736980C/en active Active
- 2009-09-18 JP JP2011527395A patent/JP5840492B2/ja active Active
- 2009-09-18 US US13/063,950 patent/US8207167B2/en active Active
- 2009-09-18 DK DK09785123.2T patent/DK2349990T3/en active
Also Published As
| Publication number | Publication date |
|---|---|
| CA2736980C (en) | 2016-09-27 |
| JP2012502965A (ja) | 2012-02-02 |
| US20110190302A1 (en) | 2011-08-04 |
| DK2349990T3 (en) | 2018-07-02 |
| CA2736980A1 (en) | 2010-03-25 |
| US8207167B2 (en) | 2012-06-26 |
| WO2010032010A1 (en) | 2010-03-25 |
| EP2349990A1 (en) | 2011-08-03 |
| ES2675074T3 (es) | 2018-07-06 |
| EP2349990B8 (en) | 2018-07-18 |
| GB0817208D0 (en) | 2008-10-29 |
| EP2349990B1 (en) | 2018-05-02 |
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