The Journal of Antibiotics · 1995 · 56 citations · 2 references
PharmacyPharmacologyDrug DiscoveryNatural Product BiosynthesisBioactive Natural ProductsEnzyme InhibitionFungal Natural Product BiosynthesisMedicinal PlantsPlant Natural Product BiosynthesisTerpenoid BiosynthesisTerpenoid GlycosidesTerpenoid Metabolism
A series of new acyl-CoA: cholesterol acyltransferase (ACAT) inhibitors termed terpendoles were isolated from the culture broth of a fungal strain FO-2546 which was proposed to belong to a new genus designated as Albophoma yamanashiensis. Among four structurally related terpendoles, terpendole C showed the most potent ACAT inhibitory activity with an IC50 value of 2.1 microM in an in vitro enzyme assay, followed by terpendoles D (IC50: 3.2 microM), A (15.1 microM) and B (26.8 microM). Evaluation of their ACAT inhibition in the cell assay using J774 macrophages indicated that terpendole D exhibited the highest specificity (cytotoxicity vs. ACAT inhibition) among microbial ACAT inhibitors we discovered so far.
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Hiroshi Tomoda, Hiroyuki Nishida, Rokuro Masuma et al. · The Journal of Antibiotics · 1991 · 62 citations · Full text
Hiroshi Tomoda, XIN-HUI HUANG, Hiroyuki Nishida et al. · The Journal of Antibiotics · 1992 · 32 citations · Full text