Staurosporine scaffold-based rational discovery of the wild-type sparing reversible inhibitors of EGFR T790M gatekeeper mutant in lung cancer with analog-sensitive kinase technology.
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Synthesis of piperazine-based thiazolidinones as VEGFR2 tyrosine kinase inhibitors inducing apoptosis.Molecular design of Stat3-derived peptide selectivity between BET proteins Brd2 and Brd4 in ovarian cancer.Atmospheric Precipitations, Hailstone and Rainwater, as a Novel Source of Streptomyces Producing Bioactive Natural Products.
P2860
Staurosporine scaffold-based rational discovery of the wild-type sparing reversible inhibitors of EGFR T790M gatekeeper mutant in lung cancer with analog-sensitive kinase technology.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
Staurosporine scaffold-based r ...... g-sensitive kinase technology.
@en
Staurosporine scaffold-based r ...... g-sensitive kinase technology.
@nl
type
label
Staurosporine scaffold-based r ...... g-sensitive kinase technology.
@en
Staurosporine scaffold-based r ...... g-sensitive kinase technology.
@nl
prefLabel
Staurosporine scaffold-based r ...... g-sensitive kinase technology.
@en
Staurosporine scaffold-based r ...... g-sensitive kinase technology.
@nl
P2093
P2860
P356
P1476
Staurosporine scaffold-based r ...... g-sensitive kinase technology.
@en
P2093
Xiaoyun Song
Xingcai Liu
P2860
P356
10.1002/JMR.2590
P577
2016-11-28T00:00:00Z