1. Academic Validation
  2. Adpressins A-G: Oligophenalenone Dimers from Talaromyces adpressus

Adpressins A-G: Oligophenalenone Dimers from Talaromyces adpressus

  • J Nat Prod. 2024 Aug 23;87(8):1921-1929. doi: 10.1021/acs.jnatprod.4c00330.
Meijia Zheng 1 Qin Li 1 Hong Liao 1 Yongqi Li 1 Chenxi Zhou 1 2 Xinyi Zhao 1 Chunmei Chen 1 Weiguang Sun 1 Yonghui Zhang 1 Hucheng Zhu 1
Affiliations

Affiliations

  • 1 Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
  • 2 School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
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 1H and 13C 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 IC50 values ranging from 1.6 to 8.6 μM. Additionally, compounds 9 and 18 exhibited moderate inhibition against Con A-induced T lymphocyte proliferation with IC50 values of 9.3 and 2.6 μM, respectively.

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