| Literature DB >> 31669962 |
Xue-Ming Zhou1, Cai-Juan Zheng2, Xin-Ming Song2, Min-Min Tang2, Jing-Yu Yang2, Xing Yang2, Shi-Jin Peng2, Jin Cai2, Guang-Ying Chen3.
Abstract
Two novel epimer pairs of acetaminophen derivatives penicilquei A-D (1-4) were isolated from Penicillium herquei JX4. Their structures were elucidated using comprehensive spectroscopic methods. The absolute configurations of penicilquei A-D (1-4) were determined by modifified Mosher's method, and comparing their experimental and calculated electronic circular dichroism (ECD) spectra. Penicilquei A-D (1-4) are the first example of acetaminophen derivatives featuring an unprecedented carbon skeleton. The inhibitory activities of all compounds against nine phytopathogenic fungi and α-glucosidase were evaluated. Penicilquei A-D (1-4) showed strong inhibitory activities against at least eight phytopathogenic fungus.Entities:
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Year: 2019 PMID: 31669962 DOI: 10.1016/j.fitote.2019.104400
Source DB: PubMed Journal: Fitoterapia ISSN: 0367-326X Impact factor: 2.882