HN2009000499A - 4-[4-({[4-cloro-3-(trifluorometil)fenil]carbamoil} amino)3-fluorofenoxi]-n-metilpiridina-2- carboxamida monohidrato. - Google Patents
4-[4-({[4-cloro-3-(trifluorometil)fenil]carbamoil} amino)3-fluorofenoxi]-n-metilpiridina-2- carboxamida monohidrato.Info
- Publication number
- HN2009000499A HN2009000499A HN2009000499A HN2009000499A HN2009000499A HN 2009000499 A HN2009000499 A HN 2009000499A HN 2009000499 A HN2009000499 A HN 2009000499A HN 2009000499 A HN2009000499 A HN 2009000499A HN 2009000499 A HN2009000499 A HN 2009000499A
- Authority
- HN
- Honduras
- Prior art keywords
- methylpiridine
- monohidrate
- trifluorometil
- carbamoil
- fluorophenoxy
- Prior art date
Links
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 title 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- 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
- C07D213/62—Oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
LA PRESENTE INVENCION SE REFIERE A QUE SU FORMULA, A PROCEDIMIENTOS PARA SU PREPARACION, A COMPOSICIONES FARMACEUTICAS QUE LO COMPRENDEN Y A SU USO EN EL COMBATE DE TRASTORNOS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06021296 | 2006-10-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HN2009000499A true HN2009000499A (es) | 2012-03-07 |
Family
ID=38972960
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HN2009000499A HN2009000499A (es) | 2006-10-11 | 2009-03-18 | 4-[4-({[4-cloro-3-(trifluorometil)fenil]carbamoil} amino)3-fluorofenoxi]-n-metilpiridina-2- carboxamida monohidrato. |
Country Status (37)
| Country | Link |
|---|---|
| US (3) | US9957232B2 (es) |
| EP (1) | EP2097381B1 (es) |
| JP (1) | JP5346293B2 (es) |
| KR (1) | KR101418623B1 (es) |
| CN (1) | CN101547903B (es) |
| AR (1) | AR062927A1 (es) |
| AU (1) | AU2007306716B2 (es) |
| BR (1) | BRPI0719828B1 (es) |
| CA (1) | CA2666170C (es) |
| CL (1) | CL2007002930A1 (es) |
| CO (1) | CO6150132A2 (es) |
| CR (1) | CR10663A (es) |
| CY (1) | CY1114637T1 (es) |
| DK (1) | DK2097381T3 (es) |
| ES (1) | ES2427358T3 (es) |
| GT (1) | GT200900057A (es) |
| HN (1) | HN2009000499A (es) |
| IL (1) | IL197369A (es) |
| JO (1) | JO3021B1 (es) |
| MA (1) | MA30878B1 (es) |
| MX (1) | MX2009002642A (es) |
| MY (1) | MY152595A (es) |
| NZ (1) | NZ576153A (es) |
| PA (1) | PA8750301A1 (es) |
| PE (1) | PE20081459A1 (es) |
| PL (1) | PL2097381T3 (es) |
| PT (1) | PT2097381E (es) |
| RU (1) | RU2466992C2 (es) |
| SG (1) | SG175584A1 (es) |
| SI (1) | SI2097381T1 (es) |
| SV (1) | SV2009003187A (es) |
| TN (1) | TN2009000072A1 (es) |
| TW (1) | TWI428322B (es) |
| UA (1) | UA95984C2 (es) |
| UY (1) | UY30633A1 (es) |
| WO (1) | WO2008043446A1 (es) |
| ZA (1) | ZA200902469B (es) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE602004007382T2 (de) * | 2003-05-20 | 2008-04-17 | Bayer Pharmaceuticals Corp., West Haven | Diaryl-harnstoffe für durch pdgfr vermittelte krankheiten |
| NZ544920A (en) | 2003-07-23 | 2009-11-27 | Bayer Healthcare Llc | 4{4-[3-(4-chloro-3-trifluoromethylphenyl)-ureido]-3-fluorophenoxy}-pyridine-2-carboxylic acid methylamide and metabolites for the treatment and prevention of diseases and conditions |
| NZ553804A (en) * | 2004-09-29 | 2010-07-30 | Bayer Schering Pharma Ag | Thermodynamically stable form of bay 43-9006 tosylate |
| 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 |
| EP2089363A1 (en) * | 2006-11-14 | 2009-08-19 | Bayer Schering Pharma Aktiengesellschaft | Polymorph ii of 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]n-methylpyridine-2-carboxamide |
| JP5885012B2 (ja) | 2007-01-19 | 2016-03-15 | バイエル・ヘルスケア・エルエルシーBayer HealthCareLLC | Kit阻害剤に対して獲得した抵抗性を有する癌の処置 |
| AU2015201426B2 (en) * | 2010-04-15 | 2016-07-07 | Bayer Healthcare Llc | Process for the preparation of 4- {4-[({[4 -chloro-3 -(trifluoromethyl)-phenyl]amino} carbonyl)amino]-3-fluorophenoxy}-N-methylpyridine-2-carboxamide, its salts and monohydrate |
| 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 |
| CA2805874A1 (en) | 2010-07-19 | 2012-01-26 | Bayer Healthcare Llc | Drug combinations with fluoro-substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions |
| MA34553B1 (fr) | 2010-10-01 | 2013-09-02 | Bayer Ip Gmbh | Combinaisons contenant du n-(2-arylamino)arylsulfonamide substitué |
| EP2726059A1 (en) * | 2011-06-28 | 2014-05-07 | Bayer HealthCare LLC | Topical ophthalmological pharmaceutical composition containing regorafenib |
| UY35006A (es) | 2012-09-06 | 2014-03-31 | Bayer Healthcare Llc | Composición farmacéutica recubierta que contiene regorafenib |
| LT2900269T (lt) | 2012-09-25 | 2018-11-12 | Bayer Pharma Aktiengesellschaft | Regorafenibo ir acetilsalicilo rūgšties derinys kolorektalinio vėžio gydymui |
| UY35183A (es) | 2012-12-21 | 2014-07-31 | Bayer Healthcare Llc | Composición farmacéutica oftalmológica tópica que contiene regorafenib |
| WO2015049698A2 (en) * | 2013-10-04 | 2015-04-09 | Hetero Research Foundation | Process for regorafenib |
| CN103923000A (zh) * | 2014-01-29 | 2014-07-16 | 苏州晶云药物科技有限公司 | 几种新晶型及其制备方法 |
| CN104829523B (zh) * | 2014-04-30 | 2017-10-31 | 药源药物化学(上海)有限公司 | 瑞戈非尼盐及其晶型、制备方法 |
| US9790185B2 (en) | 2014-07-09 | 2017-10-17 | Shilpa Medicare Limited | Process for the preparation of regorafenib and its crystalline forms |
| WO2016038590A1 (en) | 2014-09-12 | 2016-03-17 | Mylan Laboratories Ltd | Process for the preparation of crystalline form i of regorafenib |
| CN104546776B (zh) * | 2015-02-10 | 2017-08-22 | 杭州朱养心药业有限公司 | 瑞戈非尼片剂药物组合物和制法 |
| CN105985287B (zh) * | 2015-02-13 | 2018-07-17 | 上海京新生物医药有限公司 | 一种瑞戈非尼新晶型 |
| CN107118153A (zh) * | 2016-02-25 | 2017-09-01 | 石药集团中奇制药技术(石家庄)有限公司 | 一种瑞戈非尼一水合物晶型及其制备方法 |
| CN105879049B (zh) * | 2016-05-13 | 2019-03-26 | 浙江大学 | 一种瑞戈非尼与β-环糊精的包合物及其制备方法 |
| AU2018276273B2 (en) | 2017-06-02 | 2023-12-21 | Bayer Healthcare Llc | Combination of regorafenib and PD-1/PD-L1(2) inhibitors for treating cancer |
| EP3861989A1 (en) | 2020-02-07 | 2021-08-11 | Bayer Aktiengesellschaft | Pharmaceutical composition containing regorafenib and a stabilizing agent |
| WO2021160708A1 (en) | 2020-02-14 | 2021-08-19 | Bayer Aktiengesellschaft | Combination of regorafenib and msln-ttc for treating cancer |
| CN111995571B (zh) * | 2020-08-07 | 2021-12-03 | 天津理工大学 | 一种瑞戈非尼与马来酸的共晶及其制备方法 |
Family Cites Families (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL6705789A (es) | 1967-03-08 | 1968-09-09 | ||
| US4223153A (en) | 1979-02-09 | 1980-09-16 | Eli Lilly And Company | Crystalline forms of N-2-(6-methoxy)benzothiazolyl N'-phenyl urea |
| US5023252A (en) | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
| NZ220764A (en) | 1986-07-02 | 1989-09-27 | Shionogi & Co | Crystalline form of 7beta((z)-2-(2-aminothiazol-4-yl)-4- carboxybut-2-enoylamino)-3-cephem-4-carboxylic acid and pharmaceutical compositions |
| US4835180A (en) | 1986-10-02 | 1989-05-30 | Sterling Drug Inc. | N-(ω-cyanoalkyl)aminophenols and use as inhibitors of lipoxygenase activity |
| US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
| US5629425A (en) | 1994-09-19 | 1997-05-13 | Eli Lilly And Company | Haloalkyl hemisolvates of 6-hydroxy-2-(4-hydroxyphenyl)-3-[4-piperidinoethoxy)-benzoyl]benzo[b]thiophene |
| CO4410191A1 (es) | 1994-09-19 | 1997-01-09 | Lilly Co Eli | SINTESIS DE 3-[4-(2-AMINOETOXI)BENZOIL]-2-ARIL-6- HIDROXIBENZO [b] TIOFENOS |
| WO1997046526A1 (en) | 1996-06-07 | 1997-12-11 | Eisai Co., Ltd. | Stable polymorphs of donepezil (1-benzyl-4-[(5,6-dimethoxy-1-indanon)-2-yl]methylpiperidine) hydrochloride and process for production |
| BR9711541A (pt) | 1996-09-23 | 1999-08-24 | Lilly Co Eli | Dihidrato d de olanzapina |
| US6344476B1 (en) | 1997-05-23 | 2002-02-05 | Bayer Corporation | Inhibition of p38 kinase activity by aryl ureas |
| US6187799B1 (en) | 1997-05-23 | 2001-02-13 | Onyx Pharmaceuticals | Inhibition of raf kinase activity using aryl ureas |
| US7329670B1 (en) | 1997-12-22 | 2008-02-12 | Bayer Pharmaceuticals Corporation | Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas |
| US20080300281A1 (en) | 1997-12-22 | 2008-12-04 | Jacques Dumas | Inhibition of p38 Kinase Activity Using Aryl and Heteroaryl Substituted Heterocyclic Ureas |
| US20070244120A1 (en) | 2000-08-18 | 2007-10-18 | Jacques Dumas | Inhibition of raf kinase using substituted heterocyclic ureas |
| US20120046290A1 (en) | 1997-12-22 | 2012-02-23 | Jacques Dumas | Inhibition of p38 kinase activity using substituted heterocyclic ureas |
| US7517880B2 (en) | 1997-12-22 | 2009-04-14 | Bayer Pharmaceuticals Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
| US20080269265A1 (en) | 1998-12-22 | 2008-10-30 | Scott Miller | Inhibition Of Raf Kinase Using Symmetrical And Unsymmetrical Substituted Diphenyl Ureas |
| RU2319693C9 (ru) | 1999-01-13 | 2008-08-20 | Байер Копэрейшн | Производные мочевины (варианты), фармацевтическая композиция (варианты) и способ лечения заболевания, связанного с ростом раковых клеток (варианты) |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US7928239B2 (en) | 1999-01-13 | 2011-04-19 | Bayer Healthcare Llc | Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas |
| WO2000041698A1 (en) | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS |
| EP1140840B1 (en) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| IN190389B (es) | 1999-07-14 | 2003-07-26 | Ranbaxy Lab Ltd | |
| CZ20022332A3 (cs) | 2000-01-07 | 2003-01-15 | Transform Pharmaceuticals, Inc. | Sestava vzorků |
| US7235576B1 (en) | 2001-01-12 | 2007-06-26 | Bayer Pharmaceuticals Corporation | Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US7371763B2 (en) | 2001-04-20 | 2008-05-13 | Bayer Pharmaceuticals Corporation | Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas |
| SI2305255T1 (sl) | 2001-12-03 | 2012-10-30 | Bayer Healthcare Llc | Arilsečninske spojine v kombinaciji z drugimi citostatičnimi ali citotoksičnimi sredstvi za zdravljenje človeških rakov |
| US20080108672A1 (en) | 2002-01-11 | 2008-05-08 | Bernd Riedl | Omega-Carboxyaryl Substituted Diphenyl Ureas As Raf Kinase Inhibitors |
| US20030207872A1 (en) | 2002-01-11 | 2003-11-06 | Bayer Corporation | Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US7928277B1 (en) | 2002-02-11 | 2011-04-19 | Cox Jr Henry Wilmore | Method for reducing contamination |
| AU2003209119A1 (en) | 2002-02-11 | 2003-09-04 | Bayer Pharmaceuticals Corporation | Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors |
| CN1318404C (zh) | 2002-02-11 | 2007-05-30 | 拜耳制药公司 | 作为激酶抑制剂的芳基脲类化合物 |
| WO2003068228A1 (en) | 2002-02-11 | 2003-08-21 | Bayer Pharmaceuticals Corporation | Aryl ureas with angiogenesis inhibiting activity |
| EA008244B1 (ru) | 2002-05-03 | 2007-04-27 | Янссен Фармацевтика Н.В. | Полимерные микроэмульсии |
| US7557129B2 (en) | 2003-02-28 | 2009-07-07 | Bayer Healthcare Llc | Cyanopyridine derivatives useful in the treatment of cancer and other disorders |
| DE602004007382T2 (de) | 2003-05-20 | 2008-04-17 | Bayer Pharmaceuticals Corp., West Haven | Diaryl-harnstoffe für durch pdgfr vermittelte krankheiten |
| NZ544920A (en) | 2003-07-23 | 2009-11-27 | Bayer Healthcare Llc | 4{4-[3-(4-chloro-3-trifluoromethylphenyl)-ureido]-3-fluorophenoxy}-pyridine-2-carboxylic acid methylamide and metabolites for the treatment and prevention of diseases and conditions |
| JP2007509846A (ja) | 2003-10-15 | 2007-04-19 | バイエル・ヘルスケア・アクチェンゲゼルシャフト | テトラヒドロ−ナフタレンおよび尿素誘導体 |
| TWI338004B (en) | 2004-02-06 | 2011-03-01 | Bristol Myers Squibb Co | Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors |
| WO2005110994A2 (en) | 2004-04-30 | 2005-11-24 | Bayer Pharmaceuticals Corporation | Substituted pyrazolyl urea derivatives useful in the treatment of cancer |
| MY191349A (en) | 2004-08-27 | 2022-06-17 | Bayer Pharmaceuticals Corp | New pharmaceutical compositions for the treatment of hyper-proliferative disorders |
| CA2578442A1 (en) | 2004-08-27 | 2006-03-09 | Bayer Pharmaceuticals Corporation | Pharmaceutical compositions comprising 4{4-[3-(4-chloro-3-trifluoromethylphenyl)-ureido]-phenoxy}-pyridine-2-carboxylic acid methyl amide for the treatment of cancer |
| CA2581835C (en) | 2004-09-29 | 2012-12-18 | Bayer Healthcare Ag | Process for the preparation of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-n-methylpyridine-2-carboxamide |
| NZ553804A (en) | 2004-09-29 | 2010-07-30 | Bayer Schering Pharma Ag | Thermodynamically stable form of bay 43-9006 tosylate |
| WO2006094626A1 (en) | 2005-03-07 | 2006-09-14 | Bayer Healthcare Ag | Pharmaceutical composition comprising an omega- carboxyaryl substituted diphenyl urea for the treatment of cancer |
| JP2008545670A (ja) | 2005-05-27 | 2008-12-18 | バイエル・ヘルスケア・アクチェンゲゼルシャフト | 疾患を処置するためのジアリールウレア類を含む組合せ治療 |
| EP1888067A1 (en) | 2005-05-27 | 2008-02-20 | Bayer HealthCare AG | Combination therapy comprising a diaryl urea compound and a pi3, akt kinase or mtor inhibitors (rapamycins) for cancer treatment |
| BRPI0617488A2 (pt) | 2005-10-21 | 2011-07-26 | Bayer Healthcare Llc | mÉtodo para a monitoraÇço do estado de uma doenÇa associada a uma via de vegf-165 ativada por ultra-expressço ou por mutaÇço de proteÍna vegf-165 em um paciente, mÉtodo de seleÇço de terapia para um paciente humano com uma doenÇa e mÉtodo de dignàstico para detectar uma doenÇa associada a uma via de vegf-165 ativada por ultra-expressço ou por mutaÇço de proteÍna vegf-165 em um paciente |
| CA2627875A1 (en) | 2005-10-31 | 2007-05-10 | Bayer Pharmaceuticals Corporation | Combinations comprising sorafenib and interferon for the treatment of cancer |
| US8329408B2 (en) | 2005-10-31 | 2012-12-11 | Bayer Healthcare Llc | Methods for prognosis and monitoring cancer therapy |
| CA2627873A1 (en) | 2005-10-31 | 2007-05-10 | Scott Wilhelm | Treatment of cancer with sorafenib |
| BRPI0618092A2 (pt) | 2005-11-02 | 2011-08-16 | Bayer Healthcare Llc | métodos "in vitro" para monitorar o estado de uma doença, de seleção de terapia e de diagnóstico de cáncer |
| EP1948170A1 (en) | 2005-11-10 | 2008-07-30 | Bayer HealthCare AG | Diaryl urea for treating pulmonary hypertension |
| MY144860A (en) | 2005-11-10 | 2011-11-30 | Bayer Schering Pharma Ag | Diaryl ureas for treating pulmonary hypertension |
| CA2629863A1 (en) | 2005-11-14 | 2007-05-24 | Scott Wilhelm | Use of sorafenib for the treatment of cancers with acquired resistance to kit inhibitors |
| AU2006315592A1 (en) | 2005-11-14 | 2007-05-24 | Bayer Healthcare Llc | Methods for prediction and prognosis of cancer, and monitoring cancer therapy |
| CA2631746A1 (en) | 2005-12-01 | 2007-06-07 | Bayer Healthcare Llc | Urea compounds useful in the treatment of cancer |
| CA2633400A1 (en) | 2005-12-15 | 2007-06-21 | Bayer Healthcare Ag | Diaryl urea for treating virus infections |
| US20090227637A1 (en) | 2005-12-15 | 2009-09-10 | Olaf Weber | Diaryl ureas for treating virus infections |
| WO2007068383A1 (en) | 2005-12-15 | 2007-06-21 | Bayer Healthcare Ag | Diaryl ureas for treating virus infections |
| CA2634084C (en) | 2005-12-21 | 2015-04-07 | Roger Smith | Substituted pyrimidine derivatives useful in the treatment of cancer and other disorders |
| JP2009538317A (ja) | 2006-05-26 | 2009-11-05 | バイエル ヘルスケア リミティド ライアビリティ カンパニー | 癌治療のための置換ジアリールウレアを用いた薬物の組み合わせ |
| 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 |
| CA2668748A1 (en) | 2006-11-09 | 2008-05-15 | Bayer Schering Pharma Aktiengesellschaft | Polymorph iii of 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-n-methylpyridine-2-carboxamide |
| EP2089363A1 (en) | 2006-11-14 | 2009-08-19 | Bayer Schering Pharma Aktiengesellschaft | Polymorph ii of 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]n-methylpyridine-2-carboxamide |
| DK2111401T3 (da) | 2006-12-20 | 2011-05-30 | Bayer Healthcare Llc | 4-{4-[({3-tert-butyl-1-[3-(hydroxymethyl)phenyl]-1H-pyrazol-5-yl}carbamoyl)-amino]-3-fluorphenoxy}-N-methylpyridin-2-carboxamid samt prodrug og salte heraf til behandling af cancer |
| EP2134677B1 (en) | 2006-12-20 | 2011-10-12 | Bayer HealthCare LLC | 4-{4-[({3-tert-butyl-1-[3-(hydroxymethyl)phenyl]-1h-pyrazol-5-yl}carbamoyl)-amino]-3-chlorophenoxy}-n-methylpyridine-2-carboxamide as an inhibitor of the vegfr kinase for the treatment of cancer |
| JP5885012B2 (ja) | 2007-01-19 | 2016-03-15 | バイエル・ヘルスケア・エルエルシーBayer HealthCareLLC | Kit阻害剤に対して獲得した抵抗性を有する癌の処置 |
| EP2114403A2 (en) | 2007-01-19 | 2009-11-11 | Bayer Healthcare, LLC | Treatment of cancers having resistance to chemotherapeutic agents |
| US8217061B2 (en) | 2008-01-17 | 2012-07-10 | Sicor Inc. | Polymorphs of sorafenib tosylate and sorafenib hemi-tosylate, and processes for preparation thereof |
| WO2009156070A1 (en) | 2008-06-25 | 2009-12-30 | Bayer Schering Pharma Aktiengesellschaft | Diaryl urea for treating heart failure |
| US20110257035A1 (en) | 2008-10-21 | 2011-10-20 | Bayer Healthcare Llc | Identification of signature genes associated with hepatocellular carcinoma |
| US8604208B2 (en) | 2009-09-24 | 2013-12-10 | Ranbaxy Laboratories Limited | Polymorphs of sorafenib acid addition salts |
| EP2499116A1 (en) | 2009-11-12 | 2012-09-19 | Ranbaxy Laboratories Limited | Sorafenib ethylsulfonate salt, process for preparation and use |
| WO2011146725A1 (en) | 2010-05-19 | 2011-11-24 | Bayer Healthcare Llc | Biomarkers for a multikinase inhibitor |
| CA2805874A1 (en) | 2010-07-19 | 2012-01-26 | Bayer Healthcare Llc | Drug combinations with fluoro-substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions |
-
2007
- 2007-09-20 AR ARP070104168A patent/AR062927A1/es unknown
- 2007-09-29 MX MX2009002642A patent/MX2009002642A/es active IP Right Grant
- 2007-09-29 RU RU2009117388/04A patent/RU2466992C2/ru active
- 2007-09-29 MY MYPI20091350 patent/MY152595A/en unknown
- 2007-09-29 EP EP07818583.2A patent/EP2097381B1/en active Active
- 2007-09-29 AU AU2007306716A patent/AU2007306716B2/en active Active
- 2007-09-29 US US12/444,974 patent/US9957232B2/en active Active
- 2007-09-29 JP JP2009531733A patent/JP5346293B2/ja active Active
- 2007-09-29 CN CN200780037680.2A patent/CN101547903B/zh active Active
- 2007-09-29 CA CA2666170A patent/CA2666170C/en active Active
- 2007-09-29 WO PCT/EP2007/008503 patent/WO2008043446A1/en not_active Ceased
- 2007-09-29 NZ NZ576153A patent/NZ576153A/en unknown
- 2007-09-29 PL PL07818583T patent/PL2097381T3/pl unknown
- 2007-09-29 PT PT78185832T patent/PT2097381E/pt unknown
- 2007-09-29 SI SI200731313T patent/SI2097381T1/sl unknown
- 2007-09-29 SG SG2011071990A patent/SG175584A1/en unknown
- 2007-09-29 BR BRPI0719828-0A patent/BRPI0719828B1/pt active IP Right Grant
- 2007-09-29 UA UAA200904623A patent/UA95984C2/ru unknown
- 2007-09-29 KR KR1020097007422A patent/KR101418623B1/ko active Active
- 2007-09-29 ES ES07818583T patent/ES2427358T3/es active Active
- 2007-09-29 DK DK07818583.2T patent/DK2097381T3/da active
- 2007-10-07 JO JOP/2007/0423A patent/JO3021B1/ar active
- 2007-10-08 UY UY30633A patent/UY30633A1/es not_active Application Discontinuation
- 2007-10-09 TW TW096137745A patent/TWI428322B/zh active
- 2007-10-10 PA PA20078750301A patent/PA8750301A1/es unknown
- 2007-10-10 PE PE2007001368A patent/PE20081459A1/es not_active Application Discontinuation
- 2007-10-11 CL CL200702930A patent/CL2007002930A1/es unknown
-
2009
- 2009-02-27 TN TN2009000072A patent/TN2009000072A1/fr unknown
- 2009-03-03 IL IL197369A patent/IL197369A/en active IP Right Grant
- 2009-03-11 CO CO09025191A patent/CO6150132A2/es unknown
- 2009-03-12 GT GT200900057A patent/GT200900057A/es unknown
- 2009-03-13 SV SV2009003187A patent/SV2009003187A/es unknown
- 2009-03-13 CR CR10663A patent/CR10663A/es unknown
- 2009-03-18 HN HN2009000499A patent/HN2009000499A/es unknown
- 2009-04-09 ZA ZA200902469A patent/ZA200902469B/xx unknown
- 2009-05-08 MA MA31857A patent/MA30878B1/fr unknown
-
2013
- 2013-09-16 CY CY20131100798T patent/CY1114637T1/el unknown
-
2014
- 2014-05-14 US US14/277,095 patent/US20140315958A1/en not_active Abandoned
-
2018
- 2018-01-30 US US15/884,103 patent/US20180194730A1/en not_active Abandoned
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HN2009000499A (es) | 4-[4-({[4-cloro-3-(trifluorometil)fenil]carbamoil} amino)3-fluorofenoxi]-n-metilpiridina-2- carboxamida monohidrato. | |
| EA201070786A1 (ru) | Бензофуропиримидиноны | |
| UY30319A1 (es) | Formulaciones de inhibidores de dpp iv | |
| CR11106A (es) | Inhibidores de cinasa p710 s6 | |
| PA8772101A1 (es) | Imidazol-triazolopirimidinas sustituidas | |
| HN2012001162A (es) | Triazolopiridinas | |
| BRPI0709266B8 (pt) | 5-(hidroximetileno e aminometileno) pirimidinas substituídas e composição farmacêutica que as compreende | |
| BRPI0516483A (pt) | preparo e uso de derivados de ácido bifenil-4-il-carbonilamino para o tratamento de obesidade | |
| CR10782A (es) | Compuestos para inhibir la progresion mitotica | |
| CL2007003226A1 (es) | Compuestos derivados de piridinona; composicion farmaceutica; y uso para tratar el cancer. | |
| MA32383B1 (fr) | DÉRIVÉS D'INDAZOLES à SUBSTITUTIONS PHÉNYLE ET BENZODIOXYNYLE | |
| BRPI0819218A2 (pt) | Métodos, estojos e composições para administração de compostos farmacêuticos | |
| CR10479A (es) | Modulares bencimidazolicos de vr1 | |
| UY31484A1 (es) | Piperidinas heteroaril-sustituidas | |
| UY30610A1 (es) | Moduladores de mglur5 | |
| CR20110100A (es) | Nuevos derivados de sulfamida sustituida | |
| UY30520A1 (es) | Compuestos de pirimidina | |
| DOP2005000025A (es) | Compuestos de heteroaril- y fenilsulfamoilo sustituidos | |
| BRPI0807066A8 (pt) | Combinações sinergísticas de compostos ativos fungicidas | |
| DK1931346T3 (da) | Trazodonsammensætning til indgivelse en gang om dagen | |
| BR112015023878A2 (pt) | composto, composição farmacêutica, e, uso de um composto | |
| UY31000A1 (es) | Oxoisoxazoles como inhibidores de lipasas y fosfolipasas | |
| UY31427A1 (es) | Derivados 1,2,4-triazol amino como moduladores de mglur5 | |
| ATE552832T1 (de) | Antidepressivum-propharmaka | |
| HN2006029142A (es) | Proceso |