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Org Lett. 2014 Dec 5;16(23):6064-7. doi: 10.1021/ol502806j. Epub 2014 Nov 17.

Cochlearols A and B, polycyclic meroterpenoids from the fungus Ganoderma cochlear that have renoprotective activities.

Author information

1
†State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, 132 Lanhei Road, Kunming 650201, P. R. China.
2
§Faculty of Life Science and Technology, Kunming University of Science of Technology, Kunming 650500, P. R. China.
3
‡State Key Laboratory of Organ Failure Research, Division of Nephrology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, P. R. China.
4
∥University of Chinese Academy of Sciences, Yuquan Road 19, Beijing 100049, P. R. China.
5
⊥Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, P. R. China.

Abstract

(+)- and (-)-cochlearols A (1) and B (2), two meroterpenoids with novel polycyclic skeletons, were isolated from the fruiting bodies of the fungus Ganoderma cochlear. Their structures and stereochemistry were determined by using spectroscopic, computational and single-crystal X-ray diffraction methods. Cochlearol A is a new normeroterpenoid containing a naturally unusual dioxaspiro[4.5]decane motif. Biological studies showed that (-)-2 is a strong inhibitor of p-Smads, exhibiting renoprotective activities in TGF-β1 induced rat renal proximal tubular cells.

PMID:
25402560
DOI:
10.1021/ol502806j
[Indexed for MEDLINE]

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