| Literature DB >> 33263391 |
Wen-Yu Zu1, Jian-Wei Tang1, Kun Hu1, Yuan-Fei Zhou1,2, Lei-Lei Gou1,2, Xiao-Zheng Su1,2, Xinxiang Lei3, Han-Dong Sun1, Pema-Tenzin Puno1.
Abstract
Chaetolactam A (1), an unprecedented azaphilone derivative bearing a unique 9-oxa-7-azabicyclo[4.2.1]octan-8-onering system, together with two new compounds, 11-epi-chaetomugilide B (2) and chaetomugilide D (3) was isolated from an endophytic fungus, Chaetomium sp. g1. Notably, extensive NMR data analyses, NMR calculations with DP4 and DP4+ analyses, ECD calculations, and the RDC method were employed to establish the structure of 1. Furthermore, 2 exhibited potent apoptosis induction activity by mediating caspase-3 activation and PARP degradation at 3 μM in HL-60.Entities:
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Year: 2020 PMID: 33263391 DOI: 10.1021/acs.joc.0c02214
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354