Synthesis and biological evaluation of 4-phenoxy-6,7-disubstituted quinolines possessing semicarbazone scaffolds as selective c-Met inhibitors.
about
A rapid and sensitive LC-MS/MS method for evaluation of the absolute oral bioavailability of a novel c-Met tyrosine kinase inhibitor QBH-196 in rats.Design and Synthesis of Novel 4-Phenoxyquinolines Bearing 3-Hydrosulfonylacrylamido or 1H-Imidazole-4-carboxamido Scaffolds as c-Met Kinase Inhibitors.Design, Synthesis, and Biological Evaluation of 4-Phenoxyquinoline Derivatives Containing Benzo[d]thiazole-2-yl Urea as c-Met Kinase Inhibitors.
P2860
Synthesis and biological evaluation of 4-phenoxy-6,7-disubstituted quinolines possessing semicarbazone scaffolds as selective c-Met inhibitors.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Synthesis and biological evalu ...... as selective c-Met inhibitors.
@en
Synthesis and biological evalu ...... as selective c-Met inhibitors.
@nl
type
label
Synthesis and biological evalu ...... as selective c-Met inhibitors.
@en
Synthesis and biological evalu ...... as selective c-Met inhibitors.
@nl
prefLabel
Synthesis and biological evalu ...... as selective c-Met inhibitors.
@en
Synthesis and biological evalu ...... as selective c-Met inhibitors.
@nl
P2093
P2860
P356
P1476
Synthesis and biological evalu ...... as selective c-Met inhibitors
@en
P2093
Haiyan Tao
Jinying Bai
Yandan Shi
P2860
P304
P356
10.1002/ARDP.201300087
P50
P577
2013-07-10T00:00:00Z