ES2524966T3 - Derivados de tieno[3,2-c]piridina como inhibidores de quinasas para uso en el tratamiento del cáncer - Google Patents
Derivados de tieno[3,2-c]piridina como inhibidores de quinasas para uso en el tratamiento del cáncer Download PDFInfo
- Publication number
- ES2524966T3 ES2524966T3 ES09768290.0T ES09768290T ES2524966T3 ES 2524966 T3 ES2524966 T3 ES 2524966T3 ES 09768290 T ES09768290 T ES 09768290T ES 2524966 T3 ES2524966 T3 ES 2524966T3
- Authority
- ES
- Spain
- Prior art keywords
- thieno
- cancer
- treatment
- kinase inhibitors
- pyridine derivatives
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
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
Abstract
Un compuesto que tiene la Fórmula I **Fórmula** o una de sus sales terapéuticamente aceptables, donde R1 es hidroxialquilo; R2 se selecciona entre el grupo que consiste en alcoxi, alquilo, halo, y haloalcoxi; y R3 es hidrógeno o alquilo.
Description
Claims (1)
-
imagen1
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US120281P | 1999-02-16 | ||
US12028108P | 2008-12-05 | 2008-12-05 | |
US22376009P | 2009-07-08 | 2009-07-08 | |
US223760P | 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 |
---|---|
ES2524966T3 true ES2524966T3 (es) | 2014-12-16 |
Family
ID=41559043
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES09768290.0T Active ES2524966T3 (es) | 2008-12-05 | 2009-12-04 | Derivados de tieno[3,2-c]piridina como inhibidores de quinasas para uso en el tratamiento del cáncer |
Country Status (26)
Country | Link |
---|---|
US (2) | US20100144783A1 (es) |
EP (1) | EP2373662B1 (es) |
JP (1) | JP5588458B2 (es) |
KR (1) | KR101639642B1 (es) |
CN (1) | CN102239171B (es) |
AR (1) | AR074481A1 (es) |
AU (1) | AU2009322270B2 (es) |
BR (1) | BRPI0921392A2 (es) |
CA (1) | CA2743592A1 (es) |
CL (1) | CL2011001312A1 (es) |
CO (1) | CO6382131A2 (es) |
DO (1) | DOP2011000153A (es) |
EC (1) | ECSP11011172A (es) |
ES (1) | ES2524966T3 (es) |
HK (1) | HK1159628A1 (es) |
IL (1) | IL212716A (es) |
MX (1) | MX2011005943A (es) |
MY (1) | MY179042A (es) |
NZ (1) | NZ592714A (es) |
PA (1) | PA8852401A1 (es) |
PE (1) | PE20110830A1 (es) |
RU (2) | RU2480472C2 (es) |
TW (2) | TWI500621B (es) |
UA (1) | UA103351C2 (es) |
UY (1) | UY32291A (es) |
WO (1) | WO2010065825A2 (es) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7202363B2 (en) * | 2003-07-24 | 2007-04-10 | Abbott Laboratories | Thienopyridine and furopyridine kinase inhibitors |
ES2524966T3 (es) * | 2008-12-05 | 2014-12-16 | Abbvie Bahamas Ltd. | Derivados de tieno[3,2-c]piridina como inhibidores de quinasas para uso en el tratamiento del cáncer |
TWI482770B (zh) * | 2010-06-09 | 2015-05-01 | Abbvie Bahamas Ltd | 結晶型激酶抑制劑 |
SG186248A1 (en) * | 2010-06-09 | 2013-01-30 | Abbvie Inc | Solid dispersions containing kinase inhibitors |
CN103003283A (zh) * | 2010-06-09 | 2013-03-27 | Abbvie公司 | 激酶抑制剂的结晶形式 |
TWI492949B (zh) | 2010-06-09 | 2015-07-21 | Abbvie Bahamas Ltd | 結晶型激酶抑制劑 |
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 |
US20150126545A1 (en) * | 2011-12-14 | 2015-05-07 | Abbvie Inc. | Compositions containing kinase inhibitors |
EP2885292A4 (en) * | 2012-08-17 | 2015-07-01 | Cancer Therapeutics Crc Pty Ltd | VEGFR3 INHIBITORS |
US9238644B2 (en) * | 2012-08-17 | 2016-01-19 | Cancer Therapeutics Crc Pty Limited | VEGFR3 inhibitors |
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 |
WO2015200635A1 (en) | 2014-06-25 | 2015-12-30 | Abbvie Inc. | N-(4-{4-AMINO-7-[1-(2-HYDROXYETHYL)-1H-PYRAZOL-4-yl]THIENO[3,2-c]PYRIDIN-3-YL}PHENYL)-N'-(3-FLUOROPHENYL)UREA DOCUSATE |
BR112021011894A2 (pt) | 2018-12-21 | 2021-09-08 | Daiichi Sankyo Company, Limited | Composição farmacêutica |
CN114222729A (zh) * | 2019-06-12 | 2022-03-22 | 范德比尔特大学 | 氨基酸转运抑制剂及其用途 |
Family Cites Families (41)
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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 (es) | 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 | Du Pont | 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 Int Usine Ferrures | 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 |
CA2285424A1 (en) | 1997-04-22 | 1998-10-29 | Neurosearch A/S | Substituted phenyl derivatives, their preparation and use |
BR9812944A (pt) | 1997-10-20 | 2000-08-08 | Hoffmann La Roche | Inibidores bicìclicos da cinase |
CA2348740A1 (en) | 1998-12-23 | 2000-07-06 | Ruth R. Wexler | Thrombin or factor xa inhibitors |
DE60037455T2 (de) | 1999-09-17 | 2008-11-27 | Abbott Gmbh & Co. Kg | Kinaseinhibitoren als arzneimittel |
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 |
ATE464740T1 (de) | 2000-12-15 | 2010-04-15 | British Telecomm | Übertagung von ton- und/oder bildmaterial |
DE60204674T2 (de) | 2001-03-14 | 2006-05-18 | Eli Lilly And Co., Indianapolis | Retinoid x rezeptormodulatoren |
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 |
US7265128B2 (en) | 2003-01-17 | 2007-09-04 | 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 |
US7592352B2 (en) * | 2003-05-06 | 2009-09-22 | Smithkline Beecham Corporation | Substituted thieno and furo-pyridines |
US20050026944A1 (en) * | 2003-07-24 | 2005-02-03 | Patrick Betschmann | Thienopyridine and furopyridine kinase inhibitors |
US7202363B2 (en) * | 2003-07-24 | 2007-04-10 | Abbott Laboratories | 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 |
JP2008519862A (ja) | 2004-11-11 | 2008-06-12 | アキリオン ファーマシューティカルズ,インコーポレーテッド | Hiv−1カプシド形成のインヒビター:置換アリール・アミノメチル・チアゾール尿素およびその類縁物質 |
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 |
WO2007022280A1 (en) | 2005-08-16 | 2007-02-22 | Memory Pharmaceuticals Corporation | Phosphodiesterase 10 inhibitors |
US20080255184A1 (en) | 2005-11-04 | 2008-10-16 | Smithkline Beecham Corporation | Thienopyridine B-Raf Kinase Inhibitors |
JP5237108B2 (ja) * | 2005-12-08 | 2013-07-17 | アボット・ラボラトリーズ | タンパク質キナーゼ阻害薬としての9員ヘテロ二環式化合物 |
US20080021217A1 (en) | 2006-07-20 | 2008-01-24 | Allen Borchardt | Heterocyclic inhibitors of rho kinase |
ES2524966T3 (es) * | 2008-12-05 | 2014-12-16 | Abbvie Bahamas Ltd. | Derivados de tieno[3,2-c]piridina como inhibidores de quinasas para uso en el tratamiento del cáncer |
-
2009
- 2009-12-04 ES ES09768290.0T patent/ES2524966T3/es active Active
- 2009-12-04 MX MX2011005943A patent/MX2011005943A/es active IP Right Grant
- 2009-12-04 KR KR1020117015162A patent/KR101639642B1/ko active IP Right Grant
- 2009-12-04 CA CA2743592A patent/CA2743592A1/en not_active Abandoned
- 2009-12-04 EP EP09768290.0A patent/EP2373662B1/en active Active
- 2009-12-04 UA UAA201108416A patent/UA103351C2/uk unknown
- 2009-12-04 MY MYPI2011002382A patent/MY179042A/en unknown
- 2009-12-04 TW TW103115668A patent/TWI500621B/zh not_active IP Right Cessation
- 2009-12-04 BR BRPI0921392A patent/BRPI0921392A2/pt not_active IP Right Cessation
- 2009-12-04 PA PA20098852401A patent/PA8852401A1/es unknown
- 2009-12-04 WO PCT/US2009/066725 patent/WO2010065825A2/en active Application Filing
- 2009-12-04 NZ NZ592714A patent/NZ592714A/xx not_active IP Right Cessation
- 2009-12-04 CN CN200980148902.7A patent/CN102239171B/zh not_active Expired - Fee Related
- 2009-12-04 AR ARP090104710A patent/AR074481A1/es unknown
- 2009-12-04 UY UY0001032291A patent/UY32291A/es not_active Application Discontinuation
- 2009-12-04 PE PE2011001146A patent/PE20110830A1/es not_active Application Discontinuation
- 2009-12-04 RU RU2011127451/04A patent/RU2480472C2/ru not_active IP Right Cessation
- 2009-12-04 JP JP2011539724A patent/JP5588458B2/ja not_active Expired - Fee Related
- 2009-12-04 TW TW098141587A patent/TWI441827B/zh not_active IP Right Cessation
- 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
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2012
- 2012-01-06 HK HK12100183.3A patent/HK1159628A1/xx unknown
- 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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