CR20140493A - Compuestos novedosos - Google Patents
Compuestos novedososInfo
- Publication number
- CR20140493A CR20140493A CR20140493A CR20140493A CR20140493A CR 20140493 A CR20140493 A CR 20140493A CR 20140493 A CR20140493 A CR 20140493A CR 20140493 A CR20140493 A CR 20140493A CR 20140493 A CR20140493 A CR 20140493A
- Authority
- CR
- Costa Rica
- Prior art keywords
- new compounds
- rory
- modulators
- metabolic
- inflammatory
- Prior art date
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- 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
- C07D295/10—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 doubly bound oxygen or sulphur atoms
- C07D295/112—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 doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
- C07D295/116—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 doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings with the doubly bound oxygen or sulfur atoms directly attached to a carbocyclic ring
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- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C311/30—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
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- C07C317/22—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
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- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
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- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
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- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
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- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
- C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
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- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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Abstract
La presente invención se refiere a moduladores novedosos del receptor huérfano retinoideo gamma (RORy), procedimientos para su preparación, composiciones farmacéuticas que contienen estos moduladores y a su uso en el tratamiento de enfermedades inflamatorias, metabólicas y autoinmunitarias mediadas por el RORy.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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GBGB1207403.5A GB201207403D0 (en) | 2012-04-27 | 2012-04-27 | Novel compounds |
GB201304596A GB201304596D0 (en) | 2013-03-14 | 2013-03-14 | Novel compounds |
PCT/EP2013/058666 WO2013160418A1 (en) | 2012-04-27 | 2013-04-25 | Novel compounds |
Publications (1)
Publication Number | Publication Date |
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CR20140493A true CR20140493A (es) | 2015-01-08 |
Family
ID=48184213
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CR20140493A CR20140493A (es) | 2012-04-27 | 2014-10-27 | Compuestos novedosos |
Country Status (23)
Country | Link |
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US (2) | US9428452B2 (es) |
EP (1) | EP2841416A1 (es) |
JP (1) | JP6182594B2 (es) |
KR (1) | KR20150013463A (es) |
CN (1) | CN104379559B (es) |
AR (1) | AR090847A1 (es) |
AU (1) | AU2013254657B2 (es) |
BR (1) | BR112014026881A2 (es) |
CA (1) | CA2871534A1 (es) |
CL (1) | CL2014002862A1 (es) |
CO (1) | CO7111268A2 (es) |
CR (1) | CR20140493A (es) |
DO (1) | DOP2014000244A (es) |
EA (1) | EA026102B1 (es) |
HK (1) | HK1201819A1 (es) |
IL (1) | IL235020A0 (es) |
MX (1) | MX2014012989A (es) |
PE (1) | PE20142400A1 (es) |
PH (1) | PH12014502414A1 (es) |
SG (1) | SG11201406274VA (es) |
TW (1) | TWI593678B (es) |
UY (1) | UY34765A (es) |
WO (1) | WO2013160418A1 (es) |
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AR092348A1 (es) | 2012-07-11 | 2015-04-15 | Hoffmann La Roche | DERIVADOS DE ARIL-SULTAMO COMO MODULADORES DE RORc |
EA026437B1 (ru) | 2012-12-06 | 2017-04-28 | Глэксо Груп Лимитед | N-(3-((4-ацилпиперазин-1-ил)метил)фенил)амиды в качестве модуляторов сиротских гамма-рецепторов ретиноидов (ror-гамма) и их применение для лечения рассеянного склероза и псориаза |
CN108409613A (zh) * | 2012-12-10 | 2018-08-17 | 弗·哈夫曼-拉罗切有限公司 | 作为RORc调节剂的苄基磺酰胺衍生物 |
WO2014090712A1 (en) * | 2012-12-10 | 2014-06-19 | F. Hoffmann-La Roche Ag | BENZYL SULFONAMIDE DERIVATIVES AS RORc MODULATORS |
NZ710034A (en) | 2013-03-14 | 2020-06-26 | Boehringer Ingelheim Int | Substituted 2-aza-bicyclo[2.2.1]heptane-3-carboxylic acid (benzyl-cyano-methyl)-amides inhibitors of cathepsin c |
US20160257664A1 (en) * | 2013-10-25 | 2016-09-08 | Glaxosmithkline Llc | Novel compounds |
CN104530014B (zh) * | 2013-12-25 | 2018-03-20 | 中国科学院广州生物医药与健康研究院 | 2‑氧代‑1,2‑二氢苯并[cd]吲哚‑6‑磺酰胺类化合物及其组合物和应用 |
SG11201606080SA (en) | 2014-02-03 | 2016-08-30 | Vitae Pharmaceuticals Inc | Dihydropyrrolopyridine inhibitors of ror-gamma |
JP2017521480A (ja) * | 2014-05-23 | 2017-08-03 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | ベンゼンスルホンアミド誘導体及びrorcモデュレーターとしてのその使用 |
WO2015180614A1 (en) | 2014-05-28 | 2015-12-03 | Glaxosmithkline Intellectual Property Development Limited | Novel compounds |
EP3148985A4 (en) | 2014-05-28 | 2018-01-17 | GlaxoSmithKline Intellectual Property Development Limited | Novel compounds |
CN106536489B (zh) | 2014-05-28 | 2020-02-07 | 葛兰素史密斯克莱知识产权发展有限公司 | 类视黄醇相关孤儿受体γ调节剂及其用途 |
EP3160981B1 (en) | 2014-06-25 | 2024-01-24 | Piramal Enterprises Limited | Fused triterpene compounds and uses thereof |
KR102510588B1 (ko) | 2014-09-12 | 2023-03-17 | 베링거 인겔하임 인터내셔날 게엠베하 | 카텝신 c의 스피로사이클릭 억제제 |
HUE042335T2 (hu) | 2014-10-14 | 2019-06-28 | Vitae Pharmaceuticals Inc | ROR-gamma dihidropirrolopiridin inhibitorai |
US9845308B2 (en) | 2014-11-05 | 2017-12-19 | Vitae Pharmaceuticals, Inc. | Isoindoline inhibitors of ROR-gamma |
US9663515B2 (en) | 2014-11-05 | 2017-05-30 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
FR3030518B1 (fr) * | 2014-12-19 | 2018-03-23 | Galderma Research & Development | Derives sulfonamides en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
FR3030516B1 (fr) * | 2014-12-19 | 2019-12-27 | Galderma Research & Development | Derives sulfonamides bicycles en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
JP2018513123A (ja) | 2015-03-12 | 2018-05-24 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | Rorガンマ阻害剤を用いてがんを治療するための方法 |
EP3331876B1 (en) | 2015-08-05 | 2020-10-07 | Vitae Pharmaceuticals, LLC | Modulators of ror-gamma |
EP3377482B1 (en) | 2015-11-20 | 2021-05-12 | Vitae Pharmaceuticals, LLC | Modulators of ror-gamma |
TWI757266B (zh) | 2016-01-29 | 2022-03-11 | 美商維它藥物有限責任公司 | ROR-γ調節劑 |
US9481674B1 (en) | 2016-06-10 | 2016-11-01 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
FR3063079B1 (fr) * | 2017-02-17 | 2019-03-22 | Galderma Research & Development | Derives sulfonamides hydroxyles en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
FR3065000A1 (fr) | 2017-04-06 | 2018-10-12 | Galderma Research & Development | Derives pyrazoles en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
CN109111418B (zh) * | 2017-06-23 | 2022-10-11 | 江苏柯菲平医药股份有限公司 | 一类2,3-二氢-1H-茚-4-磺酰胺RORγ调节剂及其用途 |
WO2019018975A1 (en) | 2017-07-24 | 2019-01-31 | Vitae Pharmaceuticals, Inc. | INHIBITORS OF ROR GAMMA |
MX2020000887A (es) | 2017-07-24 | 2020-07-22 | Vitae Pharmaceuticals Llc | Inhibidores de ror?. |
EP3663299B1 (en) | 2017-08-01 | 2023-03-08 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Bicyclic compound acting as ror gamma inhibitor |
WO2019063015A1 (zh) | 2017-09-30 | 2019-04-04 | 正大天晴药业集团股份有限公司 | 作为RORγ抑制剂的磺酰基取代的双环化合物 |
CN109896998B (zh) * | 2017-12-10 | 2022-06-07 | 复旦大学 | 一种3,4-二氢异喹啉磺酰胺类化合物及其应用 |
CN113166061B (zh) * | 2018-11-27 | 2023-11-21 | 正大天晴药业集团股份有限公司 | 含有磺酰基结构的RORγ抑制剂 |
WO2023192988A2 (en) * | 2022-04-01 | 2023-10-05 | President And Fellows Of Harvard College | Immune modulatory agents |
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GB2169265B (en) | 1982-10-08 | 1987-08-12 | Glaxo Group Ltd | Pack for medicament |
FI88112C (fi) | 1985-07-30 | 1993-04-13 | Glaxo Group Ltd | Anordning foer administrering av laekemedel till patienter |
GB9004781D0 (en) | 1990-03-02 | 1990-04-25 | Glaxo Group Ltd | Device |
WO1999002502A2 (en) * | 1997-07-11 | 1999-01-21 | Smithkline Beecham Plc | Sulphonamide derivatives being 5-ht6 receptor antagonists and process for their preparation |
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PE20061127A1 (es) * | 2005-02-15 | 2006-10-21 | Glaxo Group Ltd | Derivados de propanosulfonamida que potencian el receptor de glutamato |
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US20080261978A1 (en) * | 2007-03-08 | 2008-10-23 | Clark Michael P | Chemokine receptor modulators |
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GB201116641D0 (en) * | 2011-09-27 | 2011-11-09 | Glaxo Group Ltd | Novel compounds |
GB201207406D0 (en) | 2012-04-27 | 2012-06-13 | Glaxo Group Ltd | Novel compounds |
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DOP2014000244A (es) | 2014-11-30 |
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HK1201819A1 (en) | 2015-09-11 |
CO7111268A2 (es) | 2014-11-10 |
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SG11201406274VA (en) | 2014-11-27 |
UY34765A (es) | 2013-11-29 |
EA201491973A1 (ru) | 2015-02-27 |
MX2014012989A (es) | 2015-01-22 |
CN104379559B (zh) | 2016-11-09 |
AR090847A1 (es) | 2014-12-10 |
PH12014502414A1 (en) | 2015-01-12 |
KR20150013463A (ko) | 2015-02-05 |
JP2015519319A (ja) | 2015-07-09 |
CN104379559A (zh) | 2015-02-25 |
EP2841416A1 (en) | 2015-03-04 |
WO2013160418A1 (en) | 2013-10-31 |
TW201406737A (zh) | 2014-02-16 |
CA2871534A1 (en) | 2013-10-31 |
IL235020A0 (en) | 2014-12-31 |
PE20142400A1 (es) | 2015-02-04 |
AU2013254657A1 (en) | 2014-10-23 |
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