Issue 9, 2022

Asperosin A, a [4 + 2] Diels–Alder cycloaddition polyketide dimer from Aspergillus rugulosa with immunosuppressive activity

Abstract

A novel homologous polyketide dimer, asperosin A (1), constructed with a unique hetero-bicycle 6/5 ring system featuring four continuous quaternary carbons, was isolated from a solid culture of the fungus Aspergillus rugulosa. The structure of 1 was elucidated by extensive 400 MHz and 600 MHz nuclear magnetic resonance (NMR) spectroscopy analysis, electronic circular dichroism (ECD) calculations, DP4+ probability analysis, and a detailed discussion of its biosynthetic origin. Biogenetically, compound 1 was constructed from two identical original polyketides via the intermolecular [4 + 2] Diels–Alder cycloaddition reaction. It is notable that compound 1 displayed remarkable immunosuppressive activity in murine splenocytes and human T cells stimulated by anti-CD3/anti-CD28 monoclonal antibodies.

Graphical abstract: Asperosin A, a [4 + 2] Diels–Alder cycloaddition polyketide dimer from Aspergillus rugulosa with immunosuppressive activity

Supplementary files

Article information

Article type
Research Article
Submitted
24 Nov 2021
Accepted
10 Mar 2022
First published
16 Mar 2022

Org. Chem. Front., 2022,9, 2477-2485

Asperosin A, a [4 + 2] Diels–Alder cycloaddition polyketide dimer from Aspergillus rugulosa with immunosuppressive activity

Y. Qiao, X. Tan, Q. Xu, Z. Zhang, Q. Xu, L. Tao, J. Liu, H. Zhu, C. Chen, Y. Ye, Y. Lu, G. Chen, C. Qi and Y. Zhang, Org. Chem. Front., 2022, 9, 2477 DOI: 10.1039/D1QO01767E

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