EA201300420A1 - Комбинации, которые содержат замещенный n-(2-ариламино) арилсульфонамид - Google Patents
Комбинации, которые содержат замещенный n-(2-ариламино) арилсульфонамидInfo
- Publication number
- EA201300420A1 EA201300420A1 EA201300420A EA201300420A EA201300420A1 EA 201300420 A1 EA201300420 A1 EA 201300420A1 EA 201300420 A EA201300420 A EA 201300420A EA 201300420 A EA201300420 A EA 201300420A EA 201300420 A1 EA201300420 A1 EA 201300420A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- combination
- component
- arylamino
- stereoisomer
- solvate
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000012453 solvate Substances 0.000 abstract 2
- GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical class C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 125000004421 aryl sulphonamide group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000002552 dosage form Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000008177 pharmaceutical agent Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
Classifications
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
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- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/4035—Isoindoles, e.g. phthalimide
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- C07C275/40—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
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- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton 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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- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
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- 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
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- 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
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- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole 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
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- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- 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
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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
- C07D295/12—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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Abstract
Изобретение относится к комбинации, которая состоит из компонента А: одно или более омега-карбоксиарилзамещенное соединение дифенилмочевины общей формулы (I) или его физиологически приемлемая соль, сольват, гидрат или стереоизомер; компонента В: одно или более соединение N-(2-ариламино) арилсульфонамида общей формулы (II) или его физиологически приемлемая соль, сольват, гидрат или стереоизомер; и, необязательно, компонента С: одно или более дополнительное фармацевтическое средство; в которой необязательно некоторые или все компоненты находятся в виде фармацевтической лекарственной формы, которая готова к применению для введения совместно, одновременно, отдельно или последовательно; зависимо друг от друга, перорально, внутривенно, местно, с помощью локальных установок, внутрибрюшинно или через нос; применению такой комбинации для изготовления лекарственного препарата для лечения или профилактики рака, а также набору, который включает такую комбинацию.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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EP10185800 | 2010-10-01 | ||
PCT/EP2011/067041 WO2012041987A1 (en) | 2010-10-01 | 2011-09-29 | Substituted n-(2-arylamino)aryl sulfonamide-containing combinations |
Publications (1)
Publication Number | Publication Date |
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EA201300420A1 true EA201300420A1 (ru) | 2013-09-30 |
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ID=44719990
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EA201300420A EA201300420A1 (ru) | 2010-10-01 | 2011-09-29 | Комбинации, которые содержат замещенный n-(2-ариламино) арилсульфонамид |
Country Status (25)
Country | Link |
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US (1) | US9381177B2 (ru) |
EP (1) | EP2621486A1 (ru) |
JP (1) | JP2013538840A (ru) |
KR (1) | KR20130099117A (ru) |
CN (1) | CN103228274A (ru) |
AP (1) | AP2013006834A0 (ru) |
AU (1) | AU2011310532B2 (ru) |
BR (1) | BR112013007835A2 (ru) |
CA (1) | CA2813069A1 (ru) |
CL (1) | CL2013000881A1 (ru) |
CO (1) | CO6690783A2 (ru) |
CR (1) | CR20130147A (ru) |
CU (1) | CU20130050A7 (ru) |
DO (1) | DOP2013000070A (ru) |
EA (1) | EA201300420A1 (ru) |
EC (1) | ECSP13012538A (ru) |
GT (1) | GT201300085A (ru) |
IL (1) | IL225400A0 (ru) |
MA (1) | MA34553B1 (ru) |
MX (1) | MX2013003695A (ru) |
NZ (1) | NZ608584A (ru) |
PE (1) | PE20140165A1 (ru) |
SG (1) | SG189038A1 (ru) |
UA (1) | UA112163C2 (ru) |
WO (1) | WO2012041987A1 (ru) |
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EP1797038B1 (en) * | 2004-09-29 | 2012-06-13 | Bayer Pharma Aktiengesellschaft | Thermodynamically stable form of bay 43-9006 tosylate |
AR081060A1 (es) | 2010-04-15 | 2012-06-06 | Bayer Schering Pharma Ag | Procedimiento para preparar 4-{4-[({[4-cloro-3-(trifluorometil)fenil]amino}carbonil)amino]-3-fluorofenoxi}-n-metilpiridin-2-carboxamida |
BR112014029338A2 (pt) * | 2012-05-31 | 2017-06-27 | Bayer Pharma AG | biomarcadores para determinação da resposta eficaz dos tratamentos de pacientes com carcinoma hepatocelular (hcc) |
TWI713455B (zh) | 2014-06-25 | 2020-12-21 | 美商伊凡克特治療公司 | MnK抑制劑及其相關方法 |
CA2998647A1 (en) * | 2014-10-03 | 2016-04-07 | The Royal Institution For The Advancement Of Learning/Mcgill University | Urea and bis-urea based compounds and analogues thereof useful in the treatment of androgen receptor mediated diseases or disorders |
EA201891049A1 (ru) | 2015-10-29 | 2018-10-31 | Эффектор Терапьютикс, Инк. | Изоиндолиновые, азаизоиндолиновые, дигидроинденоновые и дигидроазаинденоновые ингибиторы mnk1 и mnk2 |
KR20180070696A (ko) | 2015-10-29 | 2018-06-26 | 이펙터 테라퓨틱스, 인크. | Mnk1 및 mnk2를 억제하는 피롤로-, 피라졸로-, 이미다조-피리미딘 및 피리딘 화합물 |
US10000487B2 (en) | 2015-11-20 | 2018-06-19 | Effector Therapeutics, Inc. | Heterocyclic compounds that inhibit the kinase activity of Mnk useful for treating various cancers |
AU2018220840A1 (en) | 2017-02-14 | 2019-09-19 | Effector Therapeutics, Inc. | Piperidine-substituted Mnk inhibitors and methods related thereto |
CN107417604A (zh) * | 2017-07-25 | 2017-12-01 | 新发药业有限公司 | 4‑取代吡啶‑2‑甲酰胺化合物及其制备方法与应用 |
MX2021004763A (es) | 2018-10-24 | 2021-06-08 | Effector Therapeutics Inc | Formas cristalinas de inhibidores de quinasa de interaccion con map quinasa (mnk). |
KR20240035820A (ko) | 2021-07-09 | 2024-03-18 | 플렉시움 인코포레이티드 | Ikzf2를 조절하는 아릴 화합물 및 약학 조성물 |
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DE60026822T2 (de) * | 1999-01-13 | 2006-08-24 | Bayer Pharmaceuticals Corp., West Haven | -g(v)-carboxyaryl substituierte diphenyl harnstoffe als raf kinase inhibitoren |
EP1140840B1 (en) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
DK2305255T3 (da) | 2001-12-03 | 2012-12-10 | Bayer Healthcare Llc | Arylurinstofforbindelser i kombination med andre cytostatiske eller cytotoksiske midler til behandling af humane cancere |
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DK1636585T3 (da) * | 2003-05-20 | 2008-05-26 | Bayer Pharmaceuticals Corp | Diarylurinstoffer med kinasehæmmende aktivitet |
CL2004001834A1 (es) * | 2003-07-23 | 2005-06-03 | Bayer Pharmaceuticals Corp | Compuesto 4-{4-[3-(4-cloro-3-trifluorometilfenil)-ureido]-3-fluorofenoxi}-piridin-2-metilamida, inhibidor de la raf, vegfr, p38 y pdgfr quinasas, sus sales; composiicon farmaceutica; combinacion farmaceutica; y su uso para tratar trastornos hiperprol |
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EP1797038B1 (en) | 2004-09-29 | 2012-06-13 | Bayer Pharma Aktiengesellschaft | Thermodynamically stable form of bay 43-9006 tosylate |
CN101132779B (zh) | 2005-03-07 | 2016-03-16 | 拜尔健康护理有限责任公司 | 用于治疗癌症的包含ω-羧芳基取代的二苯基脲的药物组合物 |
UY29414A1 (es) | 2005-03-10 | 2006-10-02 | Bayer Pharmaceuticals Corp | Derivados de pirimidina para el tratamiento de trastornos hiperproliferativos |
CN101495118B (zh) * | 2005-07-21 | 2012-09-05 | 阿迪亚生命科学公司 | Mek的n-(芳基氨基)磺酰胺抑制剂 |
CA2618218C (en) * | 2005-07-21 | 2015-06-30 | Ardea Biosciences, Inc. | N-(arylamino)-sulfonamide inhibitors of mek |
US8101799B2 (en) * | 2005-07-21 | 2012-01-24 | Ardea Biosciences | Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK |
JP5084736B2 (ja) | 2005-11-10 | 2012-11-28 | バイエル・ファルマ・アクチェンゲゼルシャフト | 肺高血圧を処置するためのジアリールウレア |
EP1948176B1 (en) | 2005-11-10 | 2011-01-05 | Bayer Schering Pharma Aktiengesellschaft | Diaryl ureas for treating pulmonary hypertension |
AR062927A1 (es) | 2006-10-11 | 2008-12-17 | Bayer Healthcare Ag | 4- [4-( [ [ 4- cloro-3-( trifluorometil) fenil) carbamoil] amino] -3- fluorofenoxi) -n- metilpiridin-2- carboxamida monohidratada |
WO2008120004A1 (en) * | 2007-04-02 | 2008-10-09 | Astrazeneca Ab | Combination of a mek- inhibitor and a b-raf inhibitor for the treatment of cancer |
EP2175885B1 (en) | 2007-07-30 | 2016-10-12 | Ardea Biosciences, Inc. | Combinations of mek inhibitors and raf kinase inhibitors and uses thereof |
JP5651125B2 (ja) | 2008-12-10 | 2015-01-07 | デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド | Mek阻害剤に対する耐性を付与するmek突然変異 |
-
2011
- 2011-09-29 AP AP2013006834A patent/AP2013006834A0/xx unknown
- 2011-09-29 BR BR112013007835A patent/BR112013007835A2/pt not_active Application Discontinuation
- 2011-09-29 US US13/877,204 patent/US9381177B2/en not_active Expired - Fee Related
- 2011-09-29 WO PCT/EP2011/067041 patent/WO2012041987A1/en active Application Filing
- 2011-09-29 CA CA2813069A patent/CA2813069A1/en not_active Abandoned
- 2011-09-29 PE PE2013000697A patent/PE20140165A1/es not_active Application Discontinuation
- 2011-09-29 AU AU2011310532A patent/AU2011310532B2/en not_active Ceased
- 2011-09-29 KR KR1020137010490A patent/KR20130099117A/ko not_active Application Discontinuation
- 2011-09-29 EP EP11763694.4A patent/EP2621486A1/en not_active Withdrawn
- 2011-09-29 EA EA201300420A patent/EA201300420A1/ru unknown
- 2011-09-29 MA MA35781A patent/MA34553B1/fr unknown
- 2011-09-29 MX MX2013003695A patent/MX2013003695A/es unknown
- 2011-09-29 NZ NZ608584A patent/NZ608584A/en not_active IP Right Cessation
- 2011-09-29 CN CN2011800572946A patent/CN103228274A/zh active Pending
- 2011-09-29 SG SG2013020920A patent/SG189038A1/en unknown
- 2011-09-29 JP JP2013530737A patent/JP2013538840A/ja active Pending
- 2011-09-29 UA UAA201305238A patent/UA112163C2/uk unknown
-
2013
- 2013-03-21 IL IL225400A patent/IL225400A0/en unknown
- 2013-04-01 EC ECSP13012538 patent/ECSP13012538A/es unknown
- 2013-04-01 GT GT201300085A patent/GT201300085A/es unknown
- 2013-04-01 CR CR20130147A patent/CR20130147A/es unknown
- 2013-04-01 CL CL2013000881A patent/CL2013000881A1/es unknown
- 2013-04-01 DO DO2013000070A patent/DOP2013000070A/es unknown
- 2013-04-01 CO CO13059928A patent/CO6690783A2/es not_active Application Discontinuation
- 2013-04-01 CU CU2013000050A patent/CU20130050A7/es unknown
Also Published As
Publication number | Publication date |
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IL225400A0 (en) | 2013-06-27 |
GT201300085A (es) | 2015-02-16 |
WO2012041987A1 (en) | 2012-04-05 |
AU2011310532B2 (en) | 2016-01-14 |
MX2013003695A (es) | 2013-05-20 |
CA2813069A1 (en) | 2012-04-05 |
AU2011310532A1 (en) | 2013-04-18 |
EP2621486A1 (en) | 2013-08-07 |
CR20130147A (es) | 2013-05-29 |
CN103228274A (zh) | 2013-07-31 |
AU2011310532A8 (en) | 2014-02-20 |
KR20130099117A (ko) | 2013-09-05 |
US9381177B2 (en) | 2016-07-05 |
ECSP13012538A (es) | 2013-06-28 |
NZ608584A (en) | 2015-07-31 |
PE20140165A1 (es) | 2014-02-26 |
DOP2013000070A (es) | 2014-07-15 |
CL2013000881A1 (es) | 2013-09-13 |
CO6690783A2 (es) | 2013-06-17 |
AP2013006834A0 (en) | 2013-04-30 |
US20130261120A1 (en) | 2013-10-03 |
SG189038A1 (en) | 2013-05-31 |
BR112013007835A2 (pt) | 2016-06-28 |
MA34553B1 (fr) | 2013-09-02 |
CU20130050A7 (es) | 2013-07-31 |
UA112163C2 (uk) | 2016-08-10 |
JP2013538840A (ja) | 2013-10-17 |
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