BRPI0007487B8 - diphenyl-ureas substituted with w-carboxy-aryls as raf kinase inhibitors - Google Patents
diphenyl-ureas substituted with w-carboxy-aryls as raf kinase inhibitorsInfo
- Publication number
- BRPI0007487B8 BRPI0007487B8 BRPI0007487A BR0007487A BRPI0007487B8 BR PI0007487 B8 BRPI0007487 B8 BR PI0007487B8 BR PI0007487 A BRPI0007487 A BR PI0007487A BR 0007487 A BR0007487 A BR 0007487A BR PI0007487 B8 BRPI0007487 B8 BR PI0007487B8
- Authority
- BR
- Brazil
- Prior art keywords
- aryls
- diphenyl
- carboxy
- kinase inhibitors
- raf kinase
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title abstract 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title abstract 2
- 102000009929 raf Kinases Human genes 0.000 title abstract 2
- 108010077182 raf Kinases Proteins 0.000 title abstract 2
- -1 aryl ureas Chemical class 0.000 abstract 1
- 235000013877 carbamide Nutrition 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—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 one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—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 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, directly attached to ring carbon atoms
- C07D211/78—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C—CHEMISTRY; METALLURGY
- 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
- C07D295/16—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 acylated on ring nitrogen atoms
- C07D295/18—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 acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
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- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
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- C07C275/36—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 singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with at least one of the oxygen atoms further bound to a carbon atom of a six-membered aromatic ring, e.g. N-aryloxyphenylureas
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Abstract
"difenil-uréias substituídas com <sym>-carbóxi-arilas como inibidores de raf cinase". esta invenção refere-se ao uso de um grupo de aril-uréias para tratar doenças mediadas por raf, e composições farmacêuticas para uso nessa terapia."diphenyl-ureas substituted with <sym>-carboxy-aryls as raf kinase inhibitors". this invention relates to the use of a group of aryl ureas to treat raf-mediated diseases, and pharmaceutical compositions for use in such therapy.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US11587799P | 1999-01-13 | 1999-01-13 | |
US25726699A | 1999-02-25 | 1999-02-25 | |
US42522899A | 1999-10-22 | 1999-10-22 | |
PCT/US2000/000648 WO2000042012A1 (en) | 1999-01-13 | 2000-01-12 | φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS |
Publications (3)
Publication Number | Publication Date |
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BR0007487A BR0007487A (en) | 2003-09-23 |
BRPI0007487B1 BRPI0007487B1 (en) | 2015-07-07 |
BRPI0007487B8 true BRPI0007487B8 (en) | 2021-05-25 |
Family
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Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0007487A BRPI0007487B8 (en) | 1999-01-13 | 2000-01-12 | diphenyl-ureas substituted with w-carboxy-aryls as raf kinase inhibitors |
BRPI0017535A BRPI0017535B8 (en) | 1999-01-13 | 2000-01-12 | composed of diphenyl urea substituted with omega-carboxy-aryl |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0017535A BRPI0017535B8 (en) | 1999-01-13 | 2000-01-12 | composed of diphenyl urea substituted with omega-carboxy-aryl |
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EP1730111A2 (en) * | 2004-01-30 | 2006-12-13 | MERCK PATENT GmbH | Substituted bisarylurea derivatives as kinase inhibitors |
TW200530236A (en) * | 2004-02-23 | 2005-09-16 | Chugai Pharmaceutical Co Ltd | Heteroaryl phenylurea |
MY191349A (en) * | 2004-08-27 | 2022-06-17 | Bayer Pharmaceuticals Corp | New pharmaceutical compositions for the treatment of hyper-proliferative disorders |
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DE102005015253A1 (en) * | 2005-04-04 | 2006-10-05 | Merck Patent Gmbh | New pyrazole derivatives are tyrosine kinase inhibitors useful to treat e.g. solid tumors, diabetic retinopathy, age-related macular degeneration or inflammatory disease, osteoarthritis and rickets |
WO2007075650A2 (en) * | 2005-12-21 | 2007-07-05 | Bayer Healthcare Ag | Substituted pyrimidine derivatives useful in the treatment of cancer and other disorders |
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KR101553211B1 (en) * | 2007-09-10 | 2015-09-15 | 씨아이피엘에이 엘티디. | Process for the preparation of a raf kinase inhibitor and intermediates for use in the process |
CN101372475B (en) * | 2008-03-19 | 2012-01-04 | 南京工业大学 | Aromatic heterocyclic substituted diphenyl urea derivative and application thereof |
CN101298427B (en) * | 2008-06-26 | 2012-03-21 | 中国科学院广州生物医药与健康研究院 | Diaryl urea compound and use thereof |
TW201012467A (en) | 2008-09-16 | 2010-04-01 | Taiho Pharmaceutical Co Ltd | Antitumor agent containing 4-[[3,5-bis(trimethylsilyl)benzoyl]amino]benzoic acid |
CN103254126A (en) * | 2008-09-19 | 2013-08-21 | 苏州泽璟生物制药有限公司 | Deuterated omega-diphenyl carbamide as well as derivative and pharmaceutical composition including compounds |
CN101362717B (en) * | 2008-09-28 | 2013-02-06 | 四川大学 | 4-(4-amidoanilino)-2-(methylcarbamoyl) pyridine, derivates thereof and preparation, application thereof |
JO3101B1 (en) * | 2008-12-02 | 2017-09-20 | Takeda Pharmaceuticals Co | Benzothiazole derivatives as anticancer agents |
WO2010083649A1 (en) * | 2009-01-22 | 2010-07-29 | 沈阳药科大学 | Bisarylurea derivatives and their use |
EP2531498B1 (en) * | 2010-02-05 | 2016-07-13 | Novartis AG | Compounds and compositions as protein kinase inhibitors |
CN102219733A (en) * | 2010-04-14 | 2011-10-19 | 上海医药工业研究院 | Method for preparing sorafenib |
CN101830847B (en) * | 2010-05-18 | 2012-10-10 | 张南 | Anticancer compound and preparation method thereof |
CN102617458A (en) * | 2010-05-18 | 2012-08-01 | 张南 | Preparation method for anticancer compound |
JP2013538840A (en) * | 2010-10-01 | 2013-10-17 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | Combinations containing substituted N- (2-arylamino) arylsulfonamides |
US8937088B2 (en) * | 2011-01-06 | 2015-01-20 | Astar Biotech Llc | Ureas for the treatment and prevention of cancer |
CN102875460A (en) * | 2012-05-17 | 2013-01-16 | 上海奥博生物医药技术有限公司 | Method for preparing sorafenib |
CN103508961B (en) * | 2012-06-26 | 2015-07-22 | 中美冠科生物技术(太仓)有限公司 | Antitumor drug |
CN103408488A (en) * | 2013-08-13 | 2013-11-27 | 张家港威胜生物医药有限公司 | Optimal synthetic method of sorafenib |
CN103435553A (en) * | 2013-09-16 | 2013-12-11 | 中国药科大学 | Piperazine structure-based aryl formamide Raf kinase inhibitor and preparation method as well as application thereof |
CN104672129B (en) * | 2013-11-26 | 2019-06-25 | 广东东阳光药业有限公司 | A kind of preparation method of carbamide compounds |
CN104974132B (en) * | 2014-04-08 | 2017-05-17 | 北大方正集团有限公司 | Polysubstituted pyridine compound and preparation method and application thereof as well as pharmaceutical composition |
CN104177292A (en) * | 2014-08-08 | 2014-12-03 | 亿腾药业(泰州)有限公司 | Method for industrial production of sorafenib tosylate polymorphic form I |
US20170273922A1 (en) * | 2014-10-03 | 2017-09-28 | The Royal Institution For The Advacement Of Learning/Mcgill University | Urea and bis-urea based compounds and analogues thereof useful in the treatment of androgen receptor mediated diseases or disorders |
CN105348186B (en) * | 2015-10-15 | 2018-05-22 | 青岛海洋生物医药研究院股份有限公司 | Deuterated substituted bisarylurea compound and preparation method thereof and the application in anti-tumor drug is prepared |
CN105753841B (en) * | 2016-01-18 | 2018-01-05 | 西安交通大学 | A kind of N indazoles substituting thioureido analog derivative and its preparation method and application |
CN105924390B (en) * | 2016-05-19 | 2018-07-10 | 广州南新制药有限公司 | A kind of synthetic method of Mei Tafeini |
CN106699652B (en) * | 2016-11-07 | 2020-11-13 | 天津大学 | Sorafenib alpha-aminobutyrate and preparation method thereof |
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