| Literature DB >> 31310122 |
Debing Pu1,2, Xiaoning Li3, Jing Lin1, Ruihan Zhang1, Ting Luo1, Yuan Wang1, Junbo Gao1, Muhammad Aurang Zeb1, Xingjie Zhang1, Xiaoli Li1, Ruirui Wang3, Weilie Xiao1,2.
Abstract
Fungal drug resistance is a major health threat, and reports of clinical resistance worldwide are becoming increasingly common. In a research program to discover new molecules to help overcome this problem, 14 new lanostane-type triterpenoids, gibbosicolids A-G (2-8) and gibbosic acids I-O (9-15), were isolated from the fruiting bodies of Ganoderma gibbosum, along with seven known triterpenoid derivatives. These compounds featured high levels of oxidation, epimerization, and γ-lactonization. Structures were elucidated by comprehensive spectroscopic analyses and HRMS data. Absolute configurations were assigned based on quantum chemical calculations, including calculated chemical shift with DP4+ analysis, coupling constants, and electronic circular dichroism (ECD) methods. Results show that the calculated NMR with DP4+ analysis could not reliably establish the overall spatial configuration of molecules possessing independent and free-rotational stereoclusters. All these compounds significantly increased the sensitivity of fluconazole (FLC)-resistant C. albicans to FLC. Compounds 2, 5, 9, 12, 16, 17, and 21 exhibited strong antifungal activity against FLC-resistant C. albicans when combined with FLC, with MIC50 values ranging from 3.8 to 8.8 μg/mL.Entities:
Year: 2019 PMID: 31310122 DOI: 10.1021/acs.jnatprod.9b00148
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050