De novo design, synthesis and evaluation of benzylpiperazine derivatives as highly selective binders of Mcl-1.
about
PDB-wide collection of binding data: current status of the PDBbind database.Marinopyrrole derivatives with sulfide spacers as selective disruptors of Mcl-1 binding to pro-apoptotic protein Bim.Small-Molecule and Peptide Inhibitors of the Pro-Survival Protein Mcl-1DARC: Mapping Surface Topography by Ray-Casting for Effective Virtual Screening at Protein Interaction Sites.Structure-based design of N-substituted 1-hydroxy-4-sulfamoyl-2-naphthoates as selective inhibitors of the Mcl-1 oncoprotein.Development of 3-phenyl-N-(2-(3-phenylureido)ethyl)-thiophene-2-sulfonamide compounds as inhibitors of antiapoptotic Bcl-2 family proteins.
P2860
De novo design, synthesis and evaluation of benzylpiperazine derivatives as highly selective binders of Mcl-1.
description
2013 nî lūn-bûn
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name
De novo design, synthesis and ...... ly selective binders of Mcl-1.
@en
De novo design, synthesis and ...... ly selective binders of Mcl-1.
@nl
type
label
De novo design, synthesis and ...... ly selective binders of Mcl-1.
@en
De novo design, synthesis and ...... ly selective binders of Mcl-1.
@nl
prefLabel
De novo design, synthesis and ...... ly selective binders of Mcl-1.
@en
De novo design, synthesis and ...... ly selective binders of Mcl-1.
@nl
P2093
P2860
P356
P1433
P1476
De novo design, synthesis and ...... ly selective binders of Mcl-1.
@en
P2093
Jingquan Li
Renxiao Wang
P2860
P304
P356
10.1002/CMDC.201300316
P577
2013-10-09T00:00:00Z