Structural and chemical basis for enhanced affinity to a series of mycobacterial thymidine monophosphate kinase inhibitors: fragment-based QSAR and QM/MM docking studies.
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In silico repositioning-chemogenomics strategy identifies new drugs with potential activity against multiple life stages of Schistosoma mansoniDesign, Synthesis, and Antimycobacterial Activity of Novel Theophylline-7-Acetic Acid Derivatives With Amino Acid Moieties.Natural products as leads in schistosome drug discovery.Discovery of New Anti-Schistosomal Hits by Integration of QSAR-Based Virtual Screening and High Content Screening.
P2860
Structural and chemical basis for enhanced affinity to a series of mycobacterial thymidine monophosphate kinase inhibitors: fragment-based QSAR and QM/MM docking studies.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年學術文章
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name
Structural and chemical basis ...... SAR and QM/MM docking studies.
@en
Structural and chemical basis ...... SAR and QM/MM docking studies.
@nl
type
label
Structural and chemical basis ...... SAR and QM/MM docking studies.
@en
Structural and chemical basis ...... SAR and QM/MM docking studies.
@nl
prefLabel
Structural and chemical basis ...... SAR and QM/MM docking studies.
@en
Structural and chemical basis ...... SAR and QM/MM docking studies.
@nl
P2860
P50
P1476
Structural and chemical basis ...... SAR and QM/MM docking studies.
@en
P2093
Ney R Toledo
Renata V Bueno
P2860
P2888
P304
P356
10.1007/S00894-012-1527-8
P577
2012-07-31T00:00:00Z