24-Thiacycloartanol, a potent mechanism-based inactivator of plant sterol methyltransferase
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Sterol methyl transferase: enzymology and inhibition
2. Enzyme mechanisms for sterol C -methylations
3. Biosynthesis of Phytosterols
4. Inhibition of S-adenosyl-L-methionine sterol-C-24-methyltransferase by analogues of a carbocationic ion high-energy intermediate. Structure activity relationships for C-25 heteroatoms (N, As, S) substituted triterpenoid derivatives.
5. Structural requirements for transformation of substrates by the S-adenosyl-L-methionine:delta 24(25)-sterol methyltransferase. Inhibition by analogs of the transition state coordinate.
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1. Binding pattern analysis and structural insight into the inhibition mechanism of Sterol 24-C methyltransferase by docking and molecular dynamics approach;Journal of Biomolecular Structure and Dynamics;2015-02-11
2. Structure and dynamics studies of sterol 24-C-methyltransferase with mechanism based inactivators for the disruption of ergosterol biosynthesis;Molecular Biology Reports;2014-02-27
3. Terpenoid metabolites from the aerial part of Artemisia lagocephala;Phytochemistry Letters;2012-03
4. Purification, characterization and inhibition of sterol C24-methyltransferase from Candida albicans;Archives of Biochemistry and Biophysics;2011-01
5. Steroidal Triterpenes: Design of Substrate-Based Inhibitors of Ergosterol and Sitosterol Synthesis;Molecules;2009-11-18
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