
Planta Medica p. 1957 - 1961 (2012)
Update date:2022-07-31
Topics:
Sun, Yu-Lin
He, Fei
Liu, Kai-Sheng
Zhang, Xiao-Yong
Bao, Jie
Wang, Yi-Fei
Nong, Xu-Hua
Xu, Xin-Ya
Qi, Shu-Hua
Two new dihydrothiophene-condensed chromones and a new natural chromone, namely oxalicumones A-C (1-3), respectively, were isolated from a culture broth of a marine-derived fungus Penicillium oxalicum SCSGAF 0023, Meripilaceae family. The structures of 1-3 and acetylated derivatives of 1 (4-7) were elucidated on the basis of spectroscopic methods and chemical reactions. The absolute configuration of 1 was established by using the modified Mosher ester method and circular dichroism data of in situ formed [RhOCOCF and [MoOAc) complexes. (R)-MTPA ester of 1 showed cytotoxicity against A375, SW-620, and HeLa carcinoma cell lines with ICvalues of 8.9, 7.8, and 18.4 μM, respectively. Compound 1 displayed cytotoxicity against A375 and SW-620 cell lines with ICvalues of 11.7 and 22.6 μM, respectively. The structure-biological activity relationship of 1 is discussed. Georg Thieme Verlag KG Stuttgart · New York.
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