Inhibition of recombinant enzyme 3-hydroxy-3-methylglutaryl-CoA reductase from Candida glabrata by α-asarone-based synthetic compounds as antifungal agents
Author:
Funder
CONACYT
SIP-IPN
DMAP
JMO
CONACyT
BEIFI-IPN
COFAA-IPN
EDI-IPN
SNI-CONACyT
Publisher
Elsevier BV
Subject
Applied Microbiology and Biotechnology,General Medicine,Biotechnology,Bioengineering
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3. Recombinant 3-hydroxy 3-methyl glutaryl-CoA reductase from Candida glabrata (Rec-CgHMGR) obtained by heterologous expression, as a novel therapeutic target model for testing synthetic drugs;Andrade-Pavón;Appl. Biochem. Biotechnol.,2017
4. Design, synthesis, and docking of highly hypolipidemic agents: Schizosaccharomyces pombe as a new model for evaluating alpha-asarone-based HMG-CoA reductase inhibitors;Argüelles;Bioorg. Med. Chem.,2010
5. SWISS-MODEL: modelling protein tertiary and quaternary structure using evolutionary information;Biasini;Nucleic Acids Res.,2014
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5. Antifungal Activity of Fibrate-Based Compounds and Substituted Pyrroles That Inhibit the Enzyme 3-Hydroxy-methyl-glutaryl-CoA Reductase of Candida glabrata (CgHMGR), Thus Decreasing Yeast Viability and Ergosterol Synthesis;Microbiology Spectrum;2022-04-27
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