Optimization of potent, selective, and orally bioavailable pyrrolodinopyrimidine-containing inhibitors of heat shock protein 90. Identification of development candidate 2-amino-4-{4-chloro-2-[2-(4-fluoro-1H-pyrazol-1-yl)ethoxy]-6-methylphenyl}-N-(2,
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Organic chemistry. Strain-release amination.Structural Basis for KDM5A Histone Lysine Demethylase Inhibition by Diverse CompoundsPropellanes-From a Chemical Curiosity to "Explosive" Materials and Natural Products.Evaluation of tert-butyl isosteres: case studies of physicochemical and pharmacokinetic properties, efficacies, and activities.DockBench as docking selector tool: the lesson learned from D3R Grand Challenge 2015.
P2860
Optimization of potent, selective, and orally bioavailable pyrrolodinopyrimidine-containing inhibitors of heat shock protein 90. Identification of development candidate 2-amino-4-{4-chloro-2-[2-(4-fluoro-1H-pyrazol-1-yl)ethoxy]-6-methylphenyl}-N-(2,
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Optimization of potent, select ...... )ethoxy]-6-methylphenyl}-N-(2,
@nl
type
label
Optimization of potent, select ...... )ethoxy]-6-methylphenyl}-N-(2,
@nl
prefLabel
Optimization of potent, select ...... )ethoxy]-6-methylphenyl}-N-(2,
@nl
P2093
P356
P1476
Optimization of potent, select ...... 3,4-d]pyrimidine-6-carboxamide
@en
P2093
Anand Sistla
Buwen Huang
Elena Dovalsantos
Evan Smith
Jerry Meng
Joe Zhongxiang Zhou
John Braganza
P304
P356
10.1021/JM200128M
P407
P577
2011-05-12T00:00:00Z