Cargando…
Discovery of 5-methyl-N-(2-arylquinazolin-7-yl)isoxazole-4-carboxamide analogues as highly selective FLT3 inhibitors
A series of 4-arylamido 5-methylisoxazole derivatives with quinazoline core was designed and synthesised based on conformational rigidification of a previous type II FMS inhibitor. Most of quinazoline analogues displayed activity against FLT3 and FLT3-ITD. Compound 7d, 5-methyl-N-(2-(3-(4-methylpipe...
Autores principales: | Im, Daseul, Moon, Hyungwoo, Kim, Jinwoong, Oh, Youri, Jang, Miyoung, Hah, Jung-Mi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241567/ https://www.ncbi.nlm.nih.gov/pubmed/32338093 http://dx.doi.org/10.1080/14756366.2020.1758689 |
Ejemplares similares
-
Conformational restriction of a type II FMS inhibitor leading to discovery of 5-methyl-N-(2-aryl-1H-benzo[d]imidazo-5-yl)isoxazole-4-carboxamide analogues as selective FLT3 inhibitors
por: Im, Daseul, et al.
Publicado: (2019) -
Discovery of 1-Pyrimidinyl-2-Aryl-4,6-Dihydropyrrolo [3,4-d]Imidazole-5(1H)-Carboxamide as a Novel JNK Inhibitor
por: Jang, Miyoung, et al.
Publicado: (2020) -
Discovery of 3-alkyl-5-aryl-1-pyrimidyl-1H-pyrazole derivatives as a novel selective inhibitor scaffold of JNK3
por: Oh, Youri, et al.
Publicado: (2019) -
Computer-aided design and synthesis of 3-carbonyl-5-phenyl-1H-pyrazole as highly selective and potent BRAFV600E and CRAF inhibitor
por: Kim, Jinwoong, et al.
Publicado: (2019) -
5-Methyl-N-[2-(trifluoromethyl)phenyl]isoxazole-4-carboxamide
por: Wang, De-Cai, et al.
Publicado: (2012)