BRPI0921392A2 - inibidores quinase com perfil de segurança cyp aperfeiçoado - Google Patents
inibidores quinase com perfil de segurança cyp aperfeiçoadoInfo
- Publication number
- BRPI0921392A2 BRPI0921392A2 BRPI0921392A BRPI0921392A BRPI0921392A2 BR PI0921392 A2 BRPI0921392 A2 BR PI0921392A2 BR PI0921392 A BRPI0921392 A BR PI0921392A BR PI0921392 A BRPI0921392 A BR PI0921392A BR PI0921392 A2 BRPI0921392 A2 BR PI0921392A2
- Authority
- BR
- Brazil
- Prior art keywords
- cypase
- inhibitors
- safety profile
- improved cyp
- cyp
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur 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
- C07D333/30—Hetero atoms other than halogen
- C07D333/36—Nitrogen atoms
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)
- Oncology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Enzymes And Modification Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12028108P | 2008-12-05 | 2008-12-05 | |
| US22376009P | 2009-07-08 | 2009-07-08 | |
| PCT/US2009/066725 WO2010065825A2 (en) | 2008-12-05 | 2009-12-04 | Kinase inhibitors with improved cyp safety profile |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0921392A2 true BRPI0921392A2 (pt) | 2016-04-26 |
Family
ID=41559043
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0921392A BRPI0921392A2 (pt) | 2008-12-05 | 2009-12-04 | inibidores quinase com perfil de segurança cyp aperfeiçoado |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US20100144783A1 (pt) |
| EP (1) | EP2373662B1 (pt) |
| JP (1) | JP5588458B2 (pt) |
| KR (1) | KR101639642B1 (pt) |
| CN (1) | CN102239171B (pt) |
| AR (1) | AR074481A1 (pt) |
| AU (1) | AU2009322270B2 (pt) |
| BR (1) | BRPI0921392A2 (pt) |
| CA (1) | CA2743592A1 (pt) |
| CL (1) | CL2011001312A1 (pt) |
| CO (1) | CO6382131A2 (pt) |
| DO (1) | DOP2011000153A (pt) |
| EC (1) | ECSP11011172A (pt) |
| ES (1) | ES2524966T3 (pt) |
| IL (1) | IL212716A (pt) |
| MX (1) | MX2011005943A (pt) |
| MY (1) | MY179042A (pt) |
| NZ (1) | NZ592714A (pt) |
| PA (1) | PA8852401A1 (pt) |
| PE (1) | PE20110830A1 (pt) |
| RU (2) | RU2480472C2 (pt) |
| TW (2) | TWI441827B (pt) |
| UA (1) | UA103351C2 (pt) |
| UY (1) | UY32291A (pt) |
| WO (1) | WO2010065825A2 (pt) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7202363B2 (en) * | 2003-07-24 | 2007-04-10 | Abbott Laboratories | Thienopyridine and furopyridine kinase inhibitors |
| KR101639642B1 (ko) * | 2008-12-05 | 2016-07-14 | 애브비 바하마스 리미티드 | 암 치료에 사용하기 위한 키나제 억제제로서의 티에노[3,2-c]피리딘 유도체 |
| TWI482770B (zh) * | 2010-06-09 | 2015-05-01 | Abbvie Bahamas Ltd | 結晶型激酶抑制劑 |
| TWI492949B (zh) | 2010-06-09 | 2015-07-21 | Abbvie Bahamas Ltd | 結晶型激酶抑制劑 |
| US8633317B2 (en) | 2010-06-09 | 2014-01-21 | Abbvie Inc. | Crystalline salts of thieno[3,2-c]pyridine kinase inhibitors with improved cpy safety profile |
| KR20130109092A (ko) * | 2010-06-09 | 2013-10-07 | 아보트 러보러터리즈 | 키나제 억제제를 함유하는 고체 분산물 |
| US8911725B2 (en) | 2010-06-23 | 2014-12-16 | University Of Central Florida Research Foundation, Inc. | Co-targeting of aurora A kinase and LIM kinase 1 for cancer therapy |
| WO2013012909A1 (en) | 2011-07-20 | 2013-01-24 | Abbott Laboratories | Kinase inhibitor with improved aqueous solubility |
| AU2012352112A1 (en) | 2011-12-14 | 2014-06-12 | Abbvie Inc. | Compositions containing kinase inhibitors |
| AU2013302319A1 (en) * | 2012-08-17 | 2015-02-26 | Cancer Therapeutics Crc Pty Limited | VEGFR3 inhibitors |
| CN104736533B (zh) * | 2012-08-17 | 2016-12-07 | 癌症治疗合作研究中心有限公司 | Vegfr3抑制剂 |
| CN103012428A (zh) * | 2013-01-08 | 2013-04-03 | 中国药科大学 | 4-(五元杂环并嘧啶/吡啶取代)氨基-1H-3-吡唑甲酰胺类CDK/Aurora双重抑制剂及其用途 |
| WO2015157360A1 (en) | 2014-04-08 | 2015-10-15 | Abbvie Inc. | Processes to make protein kinase inhibitors |
| US20170197980A1 (en) * | 2014-06-25 | 2017-07-13 | Abbvie Inc. | N-(4-phenyl)-n'-(3-fluorophenyl)urea docusate |
| CA3124330A1 (en) | 2018-12-21 | 2020-06-25 | Daiichi Sankyo Company, Limited | Combination of antibody-drug conjugate and kinase inhibitor |
| AU2020291464A1 (en) * | 2019-06-12 | 2022-02-03 | Vanderbilt University | Amino acid transport inhibitors and the uses thereof |
| US12624049B2 (en) | 2020-05-11 | 2026-05-12 | University Health Network | Salt and crystal forms of 4-amino-5-(6-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-z-yl)thieno[2.3-b]pyridin-6(7H)-one |
Family Cites Families (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1188529A (en) | 1966-06-09 | 1970-04-15 | Wellcome Found | Pyramidine Derivatives |
| US4357535A (en) | 1980-04-30 | 1982-11-02 | North American Philips Corporation | Apparatus for inspecting hand-held articles and persons carrying same |
| GB8307154D0 (en) | 1983-03-15 | 1983-04-20 | Mk Electric Ltd | Terminals |
| US4767766A (en) | 1987-01-30 | 1988-08-30 | Merck & Co., Inc. | Derivatives of 3-hydroxyazabenzo(B)thiophene useful as 5-lipoxygenase inhibitors |
| EP0300688A1 (en) | 1987-07-21 | 1989-01-25 | FISONS plc | Pyrrole derivatives, process for their preparation and pharmaceutical compositions containing them |
| JPH0436810Y2 (pt) | 1987-12-29 | 1992-08-31 | ||
| US4843949A (en) | 1988-08-29 | 1989-07-04 | Pneumo Abex Corporation | Fluid control valve with variable pressure gain |
| GB8912498D0 (en) | 1989-05-31 | 1989-07-19 | De Beers Ind Diamond | Diamond growth |
| EP0438261A3 (en) | 1990-01-16 | 1992-02-26 | Takeda Chemical Industries, Ltd. | Condensed heterocyclic glutamic acid derivatives, their production and use |
| DE4129603A1 (de) | 1991-09-06 | 1993-03-11 | Thomae Gmbh Dr K | Kondensierte 5-gliedrige heterocyclen, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
| DE69431173T2 (de) | 1993-06-16 | 2003-05-08 | E.I. Du Pont De Nemours And Co., Wilmington | Mit Wasser reinigbare Dickfilmpastenzusammensetzung |
| IL112759A0 (en) | 1994-02-25 | 1995-05-26 | Khepri Pharmaceuticals Inc | Novel cysteine protease inhibitors |
| DE29511756U1 (de) | 1995-07-20 | 1995-09-28 | Ferco International Usine de Ferrures de Bâtiment S.A.R.L., Sarrebourg | Flügelseitiges Ecklagerbeschlagteil für Drehkippfenster |
| AR004010A1 (es) | 1995-10-11 | 1998-09-30 | Glaxo Group Ltd | Compuestos heterociclicos |
| DE19620508A1 (de) | 1996-05-22 | 1997-11-27 | Hoechst Ag | Schwefelenthaltende heterocyclische Bradykinin-Antagonisten, Verfahren zu ihrer Herstellung und ihre Verwendung |
| CN1118462C (zh) | 1997-04-22 | 2003-08-20 | 神经研究公司 | 取代的苯基衍生物、其制备方法以及用途 |
| CA2306870A1 (en) | 1997-10-20 | 1999-04-29 | David Michael Goldstein | Bicyclic kinase inhibitors |
| CA2348740A1 (en) * | 1998-12-23 | 2000-07-06 | Ruth R. Wexler | Thrombin or factor xa inhibitors |
| WO2001019828A2 (en) | 1999-09-17 | 2001-03-22 | Basf Aktiengesellschaft | Kinase inhibitors as therapeutic agents |
| US6608053B2 (en) | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| US20020004511A1 (en) | 2000-06-28 | 2002-01-10 | Luzzio Michael Joseph | Thiophene derivatives useful as anticancer agents |
| EP1342363B9 (en) | 2000-12-15 | 2012-09-12 | BRITISH TELECOMMUNICATIONS public limited company | Transmission and reception of audio and/or video material |
| CA2438586A1 (en) | 2001-03-14 | 2002-09-19 | Eli Lilly And Company | Retinoid x receptor modulators |
| GB0115109D0 (en) | 2001-06-21 | 2001-08-15 | Aventis Pharma Ltd | Chemical compounds |
| JP2005508904A (ja) | 2001-09-11 | 2005-04-07 | スミスクライン ビーチャム コーポレーション | 血管新生阻害剤としてのフロ−及びチエノピリミジン誘導体 |
| US20050019424A1 (en) | 2001-12-21 | 2005-01-27 | Adams Paul E. | Anti-angiogenesis combination therapies comprising pyridazine or pyridine derivatives |
| WO2004064778A2 (en) | 2003-01-17 | 2004-08-05 | Merck & Co. Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| DE10303311A1 (de) * | 2003-01-28 | 2004-07-29 | Basf Ag | Addukte auf Basis cyclischer Verbindungen und ihre Verwendung als Gerbstoffe und Konservierungsmittel |
| EP1620094A4 (en) | 2003-05-06 | 2010-04-28 | Glaxosmithkline Llc | NEW CHEMICAL COMPOUNDS |
| US7202363B2 (en) * | 2003-07-24 | 2007-04-10 | Abbott Laboratories | Thienopyridine and furopyridine kinase inhibitors |
| US20050026944A1 (en) * | 2003-07-24 | 2005-02-03 | Patrick Betschmann | Thienopyridine and furopyridine kinase inhibitors |
| US7419978B2 (en) | 2003-10-22 | 2008-09-02 | Bristol-Myers Squibb Company | Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors |
| GB0420719D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| MX2007005730A (es) | 2004-11-11 | 2007-10-04 | Achillion Pharmaceuticals Inc | Inhibidores de la formacion de capsida del vih-1: ureas sustituidas de arilo aminometil tiazol y analogos de las mismas. |
| ES2473341T3 (es) | 2005-05-20 | 2014-07-04 | Methylgene Inc | Inhibidores de la se�alizaci�n del receptor del VEGF y del receptor del HGF |
| US7566721B2 (en) | 2005-08-08 | 2009-07-28 | Osi Pharmaceuticals, Inc. | Substituted thienol[2,3-d]pyrimidines as kinase inhibitors |
| JP2009504759A (ja) | 2005-08-16 | 2009-02-05 | メモリ ファーマセチカル コーポレーション | ホスホジエステラーゼ10阻害剤 |
| EP1951728A4 (en) | 2005-11-04 | 2011-04-20 | Glaxosmithkline Llc | THIENOPYRIDINES AS INHIBITORS OF B-RAF KINASE |
| CN101336244B (zh) * | 2005-12-08 | 2011-11-30 | 雅培制药有限公司 | 用作蛋白激酶抑制剂的9元杂二环化合物 |
| CA2658764A1 (en) | 2006-07-20 | 2008-01-24 | Mehmet Kahraman | Benzothiophene inhibitors of rho kinase |
| KR101639642B1 (ko) * | 2008-12-05 | 2016-07-14 | 애브비 바하마스 리미티드 | 암 치료에 사용하기 위한 키나제 억제제로서의 티에노[3,2-c]피리딘 유도체 |
-
2009
- 2009-12-04 KR KR1020117015162A patent/KR101639642B1/ko not_active Expired - Fee Related
- 2009-12-04 JP JP2011539724A patent/JP5588458B2/ja not_active Expired - Fee Related
- 2009-12-04 CA CA2743592A patent/CA2743592A1/en not_active Abandoned
- 2009-12-04 TW TW098141587A patent/TWI441827B/zh not_active IP Right Cessation
- 2009-12-04 EP EP09768290.0A patent/EP2373662B1/en active Active
- 2009-12-04 UA UAA201108416A patent/UA103351C2/uk unknown
- 2009-12-04 CN CN200980148902.7A patent/CN102239171B/zh not_active Expired - Fee Related
- 2009-12-04 BR BRPI0921392A patent/BRPI0921392A2/pt not_active IP Right Cessation
- 2009-12-04 MX MX2011005943A patent/MX2011005943A/es active IP Right Grant
- 2009-12-04 ES ES09768290.0T patent/ES2524966T3/es active Active
- 2009-12-04 MY MYPI2011002382A patent/MY179042A/en unknown
- 2009-12-04 UY UY0001032291A patent/UY32291A/es not_active Application Discontinuation
- 2009-12-04 PA PA20098852401A patent/PA8852401A1/es unknown
- 2009-12-04 AR ARP090104710A patent/AR074481A1/es unknown
- 2009-12-04 TW TW103115668A patent/TWI500621B/zh not_active IP Right Cessation
- 2009-12-04 NZ NZ592714A patent/NZ592714A/xx not_active IP Right Cessation
- 2009-12-04 RU RU2011127451/04A patent/RU2480472C2/ru not_active IP Right Cessation
- 2009-12-04 PE PE2011001146A patent/PE20110830A1/es not_active Application Discontinuation
- 2009-12-04 WO PCT/US2009/066725 patent/WO2010065825A2/en not_active Ceased
- 2009-12-04 AU AU2009322270A patent/AU2009322270B2/en not_active Ceased
- 2009-12-07 US US12/632,183 patent/US20100144783A1/en not_active Abandoned
-
2011
- 2011-05-05 IL IL212716A patent/IL212716A/en not_active IP Right Cessation
- 2011-05-24 DO DO2011000153A patent/DOP2011000153A/es unknown
- 2011-06-02 CL CL2011001312A patent/CL2011001312A1/es unknown
- 2011-06-16 CO CO11075260A patent/CO6382131A2/es active IP Right Grant
- 2011-07-01 EC EC2011011172A patent/ECSP11011172A/es unknown
-
2012
- 2012-08-14 US US13/585,333 patent/US8722890B2/en active Active
- 2012-12-25 RU RU2012156958/04A patent/RU2012156958A/ru not_active Application Discontinuation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B25C | Requirement related to requested transfer of rights |
Owner name: ABBOTT LABORATORIES (US) |
|
| B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] | ||
| B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] | ||
| B25B | Requested transfer of rights rejected |
Owner name: ABBOTT LABORATORIES (US) |
|
| B25B | Requested transfer of rights rejected |
Owner name: ABBOTT LABORATORIES (US) |