De Novo Design of Protein Kinase Inhibitors by in Silico Identification of Hinge Region-Binding Fragments
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Fragment-based strategy for structural optimization in combination with 3D-QSAR.Benzobisthiazoles Represent a Novel Scaffold for Kinase Inhibitors of CLK Family Members.Identification of type I and type II inhibitors of c-Yes kinase using in silico and experimental techniques.Chalcone-based Selective Inhibitors of a C4 Plant Key Enzyme as Novel Potential HerbicidesData driven polypharmacological drug design for lung cancer: analyses for targeting ALK, MET, and EGFR.
P2860
De Novo Design of Protein Kinase Inhibitors by in Silico Identification of Hinge Region-Binding Fragments
description
2013 nî lūn-bûn
@nan
2013 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մայիսին հրատարակված գիտական հոդված
@hy
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
name
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@ast
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@en
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@nl
type
label
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@ast
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@en
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@nl
prefLabel
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@ast
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@en
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
De Novo Design of Protein Kina ...... Hinge Region-Binding Fragments
@en
P2093
André Richters
Brad Sherborne
Grant Wishart
Michael Kiczun
Naomi Tidten-Luksch
Robert Urich
P2860
P304
P3181
P356
10.1021/CB300729Y
P577
2013-05-17T00:00:00Z