Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
about
Bioactive Compounds Produced by Strains of Penicillium and Talaromyces of Marine Origin[Better search strategies, hopeful candidates. The search for new antimycobacterial drugs].Rational Design of Selective and Bioactive Inhibitors of the Mycobacterium tuberculosis Proteasome.Discovery of new [Formula: see text] proteasome inhibitors using a knowledge-based computational screening approach.Large-scale metabolomics reveals a complex response of Aspergillus nidulans to epigenetic perturbationAnti-infective Activity of 2-Cyano-3-Acrylamide Inhibitors with Improved Drug-Like Properties against Two Intracellular Pathogens.Game of 'Somes: Protein Destruction for Mycobacterium tuberculosis Pathogenesis.Total synthesis of fellutamide B and deoxy-fellutamides B, C, and D.Total Synthesis and Stereochemical Assignment of Nostosin B.Synthesis and pharmacology of proteasome inhibitors.Proteases in Mycobacterium tuberculosis pathogenesis: potential as drug targets.Marine-derived Aspergillus species as a source of bioactive secondary metabolites.Seven new and two known lipopeptides as well as five known polyketides: the activated production of silent metabolites in a marine-derived fungus by chemical mutagenesis strategy using diethyl sulphate.Targeting proteasomes in infectious organisms to combat disease.A luminescence assay for natural product inhibitors of the Mycobacterium tuberculosis proteasome.Total synthesis of fellutamides, lipopeptide proteasome inhibitors. More sustainable peptide bond formation.Structural Basis for the Species-Selective Binding of N,C-Capped Dipeptides to the Mycobacterium tuberculosis Proteasome.Aspects of a Distinct Cytotoxicity of Selenium Salts and Organic Selenides in Living Cells with Possible Implications for Drug Design.Structure of human immunoproteasome with a reversible and noncompetitive inhibitor that selectively inhibits activated lymphocytes.Targeting the Proteostasis Network for Mycobacterial Drug Discovery.Identification of Serine 119 as an Effective Inhibitor Binding Site of M. tuberculosis Ubiquitin-like Protein Ligase PafA Using Purified Proteins and M. smegmatis.Fellutamide B Synthetic Path Intermediates with in Vitro Neuroactive Function Shows Mood-Elevating Effect in Stress-Induced Zebrafish Model
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P2860
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@ast
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@en
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@nl
type
label
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@ast
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@en
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@nl
prefLabel
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@ast
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@en
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@nl
P2093
P2860
P1476
Fellutamide B is a potent inhibitor of the Mycobacterium tuberculosis proteasome
@en
P2093
Carl Nathan
Dongyang Li
Tamutenda Chidawanyika
P2860
P304
P356
10.1016/J.ABB.2010.06.009
P407
P577
2010-09-15T00:00:00Z