CY1120169T1 - Παραγωγο αμιδιου και φαρμακο - Google Patents
Παραγωγο αμιδιου και φαρμακοInfo
- Publication number
- CY1120169T1 CY1120169T1 CY20171101144T CY171101144T CY1120169T1 CY 1120169 T1 CY1120169 T1 CY 1120169T1 CY 20171101144 T CY20171101144 T CY 20171101144T CY 171101144 T CY171101144 T CY 171101144T CY 1120169 T1 CY1120169 T1 CY 1120169T1
- Authority
- CY
- Cyprus
- Prior art keywords
- present
- het
- tyrosine kinase
- amidium
- drug
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
- 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
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Abstract
Η παρούσα εφεύρεση απευθύνεται σ' ένα παράγωγο αμιδίου που διαθέτει εξαιρετική ανασταλτική δράση κινάσης τυροσίνης BCR-ABL, ή ενός άλατος αυτής. Η παρούσα εφεύρεση παρέχει ένα παράγωγο αμιδίου που αντιπροσωπεύεται από τον ακόλουθο γενικό τύπο [1]: (όπου το R 1 αντιπροσωπεύει -CH 2 -R 11, κ.λπ.˙ το R 2 αντιπροσωπεύει αλκυλ, αλογόνο, αλοαλκυλ, κ.λπ.˙ το R 3 αντιπροσωπεύει υδρογόνο, κ.λπ.˙ το Het1 αντιπροσωπεύει μία ομάδα του τύπου [6] όπως παραπάνω, κ.λπ.˙ και το Het2 αντιπροσωπεύει πυριμιδινυλ, κ.λπ.), ή ένα φαρμακευτικώς αποδεκτό άλας αυτής, και μία φαρμακευτική σύνθεση που περιλαμβάνει αυτή ως δραστικό συστατικό. Η ένωση της παρούσας εφεύρεσης είναι χρήσιμη ως ένας αναστολέας κινάσης τυροσίνης BCR-ABL.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003431398 | 2003-12-25 | ||
PCT/JP2004/019553 WO2005063709A1 (ja) | 2003-12-25 | 2004-12-27 | アミド誘導体及び医薬 |
Publications (1)
Publication Number | Publication Date |
---|---|
CY1120169T1 true CY1120169T1 (el) | 2018-12-12 |
Family
ID=34736430
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20171101144T CY1120169T1 (el) | 2003-12-25 | 2017-11-02 | Παραγωγο αμιδιου και φαρμακο |
Country Status (19)
Country | Link |
---|---|
US (1) | US7728131B2 (el) |
EP (2) | EP1702917B1 (el) |
JP (3) | JPWO2005063709A1 (el) |
KR (1) | KR100848067B1 (el) |
CN (2) | CN101456841B (el) |
AU (1) | AU2004309248B2 (el) |
BR (1) | BRPI0418074B8 (el) |
CA (1) | CA2551529C (el) |
CY (1) | CY1120169T1 (el) |
DK (1) | DK1702917T3 (el) |
ES (1) | ES2651615T3 (el) |
HU (1) | HUE034712T2 (el) |
LT (1) | LT1702917T (el) |
MX (1) | MXPA06007237A (el) |
PL (1) | PL1702917T3 (el) |
PT (1) | PT1702917T (el) |
RU (1) | RU2410375C9 (el) |
SI (1) | SI1702917T1 (el) |
WO (1) | WO2005063709A1 (el) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100674813B1 (ko) * | 2005-08-05 | 2007-01-29 | 일양약품주식회사 | N-페닐-2-피리미딘-아민 유도체 및 그의 제조방법 |
JP2007297306A (ja) * | 2006-04-28 | 2007-11-15 | Kaneka Corp | 光学活性3−(1−ピロリジニル)ピロリジンの製造法 |
US8093259B2 (en) | 2006-05-25 | 2012-01-10 | Novartis Ag | 4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-N-[5-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl]-benzamide for treatment of melanoma |
US20100048597A1 (en) * | 2006-12-22 | 2010-02-25 | Novartis Ag | Organic Compounds and Their Uses |
CN101657446B (zh) | 2007-02-13 | 2013-05-15 | Ab科学有限公司 | 合成作为激酶抑制剂的2-氨基噻唑化合物的方法 |
EP2152079A4 (en) * | 2007-06-04 | 2011-03-09 | Avila Therapeutics Inc | HETEROCYCLIC COMPOUNDS AND USES THEREOF |
WO2009114552A1 (en) * | 2008-03-10 | 2009-09-17 | The Board Of Trustees Of The Leland Stanford Junior University | Heteroaryl compounds, compositions, and methods of use in cancer treatment |
WO2011008788A1 (en) * | 2009-07-14 | 2011-01-20 | Dawei Zhang | Fluoro-substituted compounds as kinase inhibitors and methods of use thereof |
CN104402860A (zh) * | 2010-05-19 | 2015-03-11 | 江苏豪森药业股份有限公司 | 甲磺酸伊马替尼中间体的制备方法 |
CN102477009B (zh) * | 2010-11-23 | 2014-01-01 | 清华大学深圳研究生院 | 取代的(s)-苯甲磺酰基吡咯烷-3-氨基衍生物及其制备方法与应用 |
US10059723B2 (en) | 2011-02-28 | 2018-08-28 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
US8957066B2 (en) * | 2011-02-28 | 2015-02-17 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
FR2980477B1 (fr) * | 2011-09-23 | 2013-10-18 | Centre Nat Rech Scient | Nouveaux composes modulateurs de la voie de signalisation des proteines hedgehog, leurs formes marquees, et applications |
US9695118B2 (en) | 2012-04-24 | 2017-07-04 | Chugai Seiyaku Kabushiki Kaisha | Benzamide derivative |
TW201348213A (zh) | 2012-04-24 | 2013-12-01 | Chugai Pharmaceutical Co Ltd | 喹唑啉二酮衍生物 |
TW201605805A (zh) | 2013-10-23 | 2016-02-16 | Chugai Pharmaceutical Co Ltd | 喹唑啉酮及異喹啉酮衍生物 |
WO2016059220A1 (en) | 2014-10-16 | 2016-04-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Tcr-activating agents for use in the treatment of t-all |
CN104876879B (zh) * | 2015-04-14 | 2018-05-18 | 中国科学院合肥物质科学研究院 | 一种bcr-abl激酶抑制剂 |
CN106187995A (zh) * | 2015-05-05 | 2016-12-07 | 天津国际生物医药联合研究院 | 含酰胺键杂环类化合物及其制备方法和应用 |
WO2016210296A1 (en) * | 2015-06-26 | 2016-12-29 | Dana-Farber Cancer Institute, Inc. | 4,6-pyrimidinylene derivatives and uses thereof |
US10722484B2 (en) | 2016-03-09 | 2020-07-28 | K-Gen, Inc. | Methods of cancer treatment |
WO2018002958A1 (en) | 2016-06-30 | 2018-01-04 | Sun Pharma Advanced Research Company Limited | Novel hydrazide containing compounds as btk inhibitors |
JP6994715B2 (ja) * | 2017-10-04 | 2022-02-04 | 国立大学法人京都大学 | Bcr-Ablタンパク質イメージング用分子プローブ |
CN108912032A (zh) * | 2018-08-13 | 2018-11-30 | 南通大学 | 一种(3s,4r)-4-甲基吡咯烷-3-基氨基甲醇叔丁酯盐酸盐的化学合成方法 |
US20220048893A1 (en) * | 2019-03-05 | 2022-02-17 | Hongyi & Associates Llc | Compounds for Treating Neurodegenerative Diseases and Cancers |
WO2021228983A1 (en) | 2020-05-13 | 2021-11-18 | INSERM (Institut National de la Santé et de la Recherche Médicale) | A pharmaceutical composition comprising an arsenic compound, an inductor of type-1 ifn and a protein kinase inhibitor for treating cancer |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5521184A (en) * | 1992-04-03 | 1996-05-28 | Ciba-Geigy Corporation | Pyrimidine derivatives and processes for the preparation thereof |
TW225528B (el) * | 1992-04-03 | 1994-06-21 | Ciba Geigy Ag | |
GB0022438D0 (en) * | 2000-09-13 | 2000-11-01 | Novartis Ag | Organic Compounds |
EP1533304B1 (en) * | 2002-06-28 | 2009-11-04 | Nippon Shinyaku Co., Ltd. | Amide derivative |
IL166528A0 (en) * | 2002-08-02 | 2006-01-15 | Ab Science | 2-(3-aminoaryl)amino-4-aryl-thiazoles and their use as c-kit inhibitors |
WO2004096225A2 (en) * | 2003-04-28 | 2004-11-11 | Ab Science | Use of tyrosine kinase inhibitors for treating cerebral ischemia |
ATE395052T1 (de) * | 2003-08-15 | 2008-05-15 | Ab Science | Verwendung von c-kit-inhibitoren für die behandlung von typ-2-diabetes |
-
2004
- 2004-12-27 KR KR1020067014770A patent/KR100848067B1/ko active IP Right Grant
- 2004-12-27 CN CN2008101863474A patent/CN101456841B/zh not_active Expired - Fee Related
- 2004-12-27 DK DK04807908.1T patent/DK1702917T3/da active
- 2004-12-27 LT LTEP04807908.1T patent/LT1702917T/lt unknown
- 2004-12-27 PL PL04807908T patent/PL1702917T3/pl unknown
- 2004-12-27 RU RU2006126974A patent/RU2410375C9/ru active
- 2004-12-27 HU HUE04807908A patent/HUE034712T2/hu unknown
- 2004-12-27 MX MXPA06007237A patent/MXPA06007237A/es active IP Right Grant
- 2004-12-27 BR BRPI0418074A patent/BRPI0418074B8/pt active IP Right Grant
- 2004-12-27 SI SI200432413T patent/SI1702917T1/en unknown
- 2004-12-27 US US10/584,829 patent/US7728131B2/en active Active
- 2004-12-27 EP EP04807908.1A patent/EP1702917B1/en active Active
- 2004-12-27 AU AU2004309248A patent/AU2004309248B2/en active Active
- 2004-12-27 ES ES04807908.1T patent/ES2651615T3/es active Active
- 2004-12-27 CN CNB2004800390488A patent/CN100526298C/zh active Active
- 2004-12-27 CA CA2551529A patent/CA2551529C/en active Active
- 2004-12-27 JP JP2005516694A patent/JPWO2005063709A1/ja active Pending
- 2004-12-27 WO PCT/JP2004/019553 patent/WO2005063709A1/ja active Application Filing
- 2004-12-27 PT PT48079081T patent/PT1702917T/pt unknown
- 2004-12-27 EP EP17181712.5A patent/EP3299358A1/en not_active Withdrawn
-
2012
- 2012-01-24 JP JP2012012025A patent/JP2012121893A/ja active Pending
-
2014
- 2014-03-07 JP JP2014045116A patent/JP2014196291A/ja not_active Withdrawn
-
2017
- 2017-11-02 CY CY20171101144T patent/CY1120169T1/el unknown
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