## Abstract The new compounds (I)‐(V) and 14 known analogues are screened for their antitumor activity against P388, HL‐60, K562, and BEL‐7402 cell lines.
Ophiobolin Sesterterpenoids and Pyrrolidine Alkaloids from the Sponge-Derived Fungus Aspergillus ustus
✍ Scribed by Hong-Bing Liu; RuAngelie Edrada-Ebel; Rainer Ebel; Yao Wang; Barbara Schulz; Siegfried Draeger; Werner E. G. Müller; Victor Wray; Wen-Han Lin; Peter Proksch
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- German
- Weight
- 236 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Chemical examination of the fungus Aspergillus ustus isolated from the Mediterranean sponge Suberites domuncula yielded the five new ophiobolin‐type sesterterpenoids 1–5 and the two new pyrrolidine alkaloids 6 and 7, together with the known compound aurantiamine and cerebroside D. The structures of the new compounds were unambiguously elucidated on the basis of extensive spectroscopic‐data analysis (1D‐ and 2D‐NMR, MS, and UV) and comparison with literature data. All compounds were evaluated for their cytotoxicity against murine lymphoma cell line L5178Y.
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