Pyripyropenes, novel inhibitors of acyl-coa: Cholesterol acyltransferase produced by aspergillus fumigatus. II. Structure elucidation of pyripyropenes A, B, C and D

108Citations
Citations of this article
22Readers
Mendeley users who have this article in their library.

Abstract

The structures of pyripyropenes A, B, C and D, novel acyl-CoA : cholesterol acyltransferase (ACAT) inhibitors, were determined mainly by spectroscopic studies including various NMR measurements. Pyripyropenes have a common structure which consists of pyridine, α-pyrone and sesquiterpene moieties. One of the three O-acetyl residues in the sesquiterpene moiety of pyripyropene A is replaced with an O-propionyl residue in pyripyropenes B, C and D. © 1994, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.

Cite

CITATION STYLE

APA

Kim, Y. K., Tomoda, H., Nishida, H., Sunazuka, T., Obata, R., & Omura, S. (1994). Pyripyropenes, novel inhibitors of acyl-coa: Cholesterol acyltransferase produced by aspergillus fumigatus. II. Structure elucidation of pyripyropenes A, B, C and D. The Journal of Antibiotics, 47(2), 154–162. https://doi.org/10.7164/antibiotics.47.154

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free