Identification of type 1 inosine monophosphate dehydrogenase as an antiangiogenic drug target.
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Clofazimine inhibits human Kv1.3 potassium channel by perturbing calcium oscillation in T lymphocytesIMP dehydrogenase: structure, mechanism, and inhibition.Increased riboflavin production by manipulation of inosine 5'-monophosphate dehydrogenase in Ashbya gossypiiItraconazole, a commonly used antifungal that inhibits Hedgehog pathway activity and cancer growthIdentification of cetrimonium bromide and irinotecan as compounds with synthetic lethality against NDRG1 deficient prostate cancer cellsSynergistic inhibition of endothelial cell proliferation, tube formation, and sprouting by cyclosporin A and itraconazoleTriazole-linked inhibitors of inosine monophosphate dehydrogenase from human and Mycobacterium tuberculosisHigh throughput screening for neurodegeneration and complex disease phenotypes.Identification of inhibitors of ABCG2 by a bioluminescence imaging-based high-throughput assay.One-carbon metabolism and nucleotide biosynthesis as attractive targets for anticancer therapy.Recent advances in drug repositioning for the discovery of new anticancer drugsAntiproliferative effects of AVN944, a novel inosine 5-monophosphate dehydrogenase inhibitor, in prostate cancer cellsChemical screen identifies FDA-approved drugs and target pathways that induce precocious pancreatic endocrine differentiation.Reversal of TNP-470-induced endothelial cell growth arrest by guanine and guanine nucleosides.Identification of an old antibiotic clofoctol as a novel activator of unfolded protein response pathways and an inhibitor of prostate cancer.Selective inhibition of HER2-positive breast cancer cells by the HIV protease inhibitor nelfinavir.In silico design of human IMPDH inhibitors using pharmacophore mapping and molecular docking approachesSmall-molecule screening of PC3 prostate cancer cells identifies tilorone dihydrochloride to selectively inhibit cell growth based on cyclin-dependent kinase 5 expression.A High-Throughput Enzyme-Coupled Assay for SAMHD1 dNTPase.First quantitative high-throughput screen in zebrafish identifies novel pathways for increasing pancreatic β-cell mass.Pyrrolidine dithiocarbamate and diethyldithiocarbamate are active against growing and nongrowing persister Mycobacterium tuberculosis.Guanine nucleotide binding to the Bateman domain mediates the allosteric inhibition of eukaryotic IMP dehydrogenases.Nonsteroidal anti-inflammatory drug sensitizes Mycobacterium tuberculosis to endogenous and exogenous antimicrobialsPaediatric use of mycophenolate mofetil.Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery.Neurobiological applications of small molecule screening.Synthesis of the inosine 5'-monophosphate dehydrogenase (IMPDH) inhibitors.Production of valuable compounds by molds and yeasts.A preclinical and clinical study of mycophenolate mofetil in pancreatic cancer.DB Dehydrogenase: an online integrated structural database on enzyme dehydrogenase.Balanced production of ribosome components is required for proper G1/S transition in Saccharomyces cerevisiae.A phase I dose-ranging study of the pharmacokinetics, pharmacodynamics, safety, and tolerability of AVN944, an IMPDH inhibitor, in healthy male volunteers.Mycophenolic acid induces senescence of vascular precursor cells.Drug Repositioning for Effective Prostate Cancer Treatment.Newer human inosine 5'-monophosphate dehydrogenase 2 (hIMPDH2) inhibitors as potential anticancer agents.A Review of the Potential Utility of Mycophenolate Mofetil as a Cancer Therapeutic
P2860
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P2860
Identification of type 1 inosine monophosphate dehydrogenase as an antiangiogenic drug target.
description
2006 nî lūn-bûn
@nan
2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Identification of type 1 inosi ...... an antiangiogenic drug target.
@ast
Identification of type 1 inosi ...... an antiangiogenic drug target.
@en
type
label
Identification of type 1 inosi ...... an antiangiogenic drug target.
@ast
Identification of type 1 inosi ...... an antiangiogenic drug target.
@en
prefLabel
Identification of type 1 inosi ...... an antiangiogenic drug target.
@ast
Identification of type 1 inosi ...... an antiangiogenic drug target.
@en
P2093
P356
P1476
Identification of type 1 inosi ...... an antiangiogenic drug target.
@en
P2093
Curtis R Chong
David J Sullivan
David Z Qian
Roberto Pili
Yongfeng Wei
P304
P356
10.1021/JM051225T
P407
P577
2006-05-01T00:00:00Z