24 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Rickettsia prowazekii methionine aminopeptidase as a promising target for the development of antibacterial agents.
Northern Illinois University
Identification of the molecular basis of inhibitor selectivity between the human and streptococcal type I methionine aminopeptidases.
Csir-Indian Institute of Chemical Technology
Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1.
Chinese Academy of Sciences
Pyridinylquinazolines selectively inhibit human methionine aminopeptidase-1 in cells.
Johns Hopkins University School of Medicine
Structural analysis of bengamide derivatives as inhibitors of methionine aminopeptidases.
Indiana University School of Medicine
Subtype-selectivity of metal-dependent methionine aminopeptidase inhibitors.
Universit£T Heidelberg
A selective account of effective paradigms and significant outcomes in the discovery of inspirational marine natural products.
University of California Santa Cruz
Synthesis of barbiturate-based methionine aminopeptidase-1 inhibitors.
North Dakota State University
Discovery and structural modification of inhibitors of methionine aminopeptidases from Escherichia coli and Saccharomyces cerevisiae.
Chinese Academy of Sciences
Novel Antimicrobial 8-Hydroxyquinoline-Based Agents: Current Development, Structure-Activity Relationships, and Perspectives.
Universidade Federal Do Rio Grande Do Sul
Identification of potent type I MetAPs inhibitors by simple bioisosteric replacement. Part 2: SAR studies of 5-heteroalkyl substituted TCAT derivatives.
Shanghai Graduate School of The Chinese Academy of Sciences
Identification of potent type I MetAP inhibitors by simple bioisosteric replacement. Part 1: Synthesis and preliminary SAR studies of thiazole-4-carboxylic acid thiazol-2-ylamide derivatives.
Graduate School of The Chinese Academy of Sciences
Inhibitors of type I MetAPs containing pyridine-2-carboxylic acid thiazol-2-ylamide. Part 1: SAR studies on the determination of the key scaffold.
Chinese Academy of Sciences
3-Amino-2-hydroxyamides and related compounds as inhibitors of methionine aminopeptidase-2.
Abbott Laboratories
Peptidyl hydroxamic acids as methionine aminopeptidase inhibitors.
The Ohio State University
Synthesis and characterization of quinoline-carbaldehyde derivatives as novel inhibitors for leishmanial methionine aminopeptidase 1.
University of Hyderabad
Beta-aminoketones as prodrugs for selective irreversible inhibitors of type-1 methionine aminopeptidases.
Heidelberg University
The Bengamides: A Mini-Review of Natural Sources, Analogues, Biological Properties, Biosynthetic Origins, and Future Prospects.
Colorado Mesa University
Heterocyclic GSK-3 allosteric modulators
Consejo Superior de Investigaciones Cientificas (CSIC)