Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
about
IMP dehydrogenase: structure, mechanism, and inhibition.A heterocyclic molecule with significant activity against dengue virusBacillus anthracis Inosine 5′-Monophosphate Dehydrogenase in Action: The First Bacterial Series of Structures of Phosphate Ion-, Substrate-, and Product-Bound ComplexesIncreased riboflavin production by manipulation of inosine 5'-monophosphate dehydrogenase in Ashbya gossypiiCrystallographic studies of two variants of Pseudomonas aeruginosa IMPDH with impaired allosteric regulationA screening pipeline for antiparasitic agents targeting cryptosporidium inosine monophosphate dehydrogenaseTwo classes of bacterial IMPDHs according to their quaternary structures and catalytic propertiesTriazole inhibitors of Cryptosporidium parvum inosine 5'-monophosphate dehydrogenaseSynthesis of carbocyclic nucleoside analogs with five-membered heterocyclic nucleobases.Inosine monophosphate dehydrogenase as a target for antiviral, anticancer, antimicrobial and immunosuppressive therapeutics.The dynamic determinants of reaction specificity in the IMPDH/GMPR family of (β/α)(8) barrel enzymes.Synthesis of the inosine 5'-monophosphate dehydrogenase (IMPDH) inhibitors.Base-functionalized carbocyclic nucleosides: design, synthesis, and mechanism of antiviral activity.Antiviral activity of an N-allyl acridone against dengue virusSynthesis and evaluation of N-substituted acridones as antiviral agents against haemorrhagic fever viruses.Carbocyclic analogues of inosine-5'-monophosphate: synthesis and biological activity.A kinetic alignment of orthologous inosine-5'-monophosphate dehydrogenases.Ultrastructure of cytoplasmic and nuclear inosine-5'-monophosphate dehydrogenase 2 "rods and rings" inclusions.Glutamine deprivation initiates reversible assembly of mammalian rods and rings.Conserved water mediated recognition and the dynamics of active site Cys 331 and Tyr 411 in hydrated structure of human IMPDH-II.Synthesis of novel aza-analogues of tiazofurin with 2-[5,5-bis(hydroxymethyl)pyrrolidin-2-yl] framework as sugar mimic.Fragment-Based Approach to Targeting Inosine-5'-monophosphate Dehydrogenase (IMPDH) from Mycobacterium tuberculosis.Newer human inosine 5'-monophosphate dehydrogenase 2 (hIMPDH2) inhibitors as potential anticancer agents.
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P2860
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on January 2007
@en
vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
@en
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
@nl
type
label
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
@en
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
@nl
prefLabel
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
@en
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
@nl
P2860
P1476
Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.
@en
P2093
Qingning Shu
P2860
P304
P356
10.1177/095632020701800501
P577
2007-01-01T00:00:00Z