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Adpressins A–G: Oligophenalenone Dimers from <i>Talaromyces adpressus</i>

Meijia Zheng, Qin Li, Hong Liao, Yongqi Li, Chenxi Zhou, Xinyi Zhao, Chunmei Chen, Weiguang Sun, Yonghui Zhang, Hucheng Zhu

2024Journal of Natural Products12 citationsDOI

Abstract

Nine new oligophenalenone dimers, adpressins A–G ( 1 – 9 ), together with nine known compounds ( 10 – 18 ), were isolated from the fungus Talaromyces adpressus . Their chemical structures were determined on the basis of spectroscopic and mass spectral analyses. Their relative and absolute configurations were identified by 1 H and 13 C NMR calculations followed by DP4+ analyses, electronic circular dichroism (ECD) calculations, and ECD spectra comparison with related compounds. Compound 1 is the first example of a duclauxin derivative featuring an unusual 6/6/6/5/6/6/6 ring system, while compounds 6 and 7 contained a novel pyrrolidine ring. Compounds 5, 9, and 18 exhibited moderate inhibition against LPS-induced B lymphocyte proliferation with IC 50 values ranging from 1.6 to 8.6 μ M. Additionally, compounds 9 and 18 exhibited moderate inhibition against Con A-induced T lymphocyte proliferation with IC 50 values of 9.3 and 2.6 μ M, respectively.

Topics & Concepts

StereochemistryChemistryMicrobial Natural Products and BiosynthesisMarine Sponges and Natural ProductsCancer Treatment and Pharmacology
Adpressins A–G: Oligophenalenone Dimers from <i>Talaromyces adpressus</i> | Litcius