CHEN Xiao-Hui, ZHOU Guo-Liang, SUN Chun-Xiao, ZHANG Xiao-min, ZHANG Guo-Jian, ZHU Tian-Jiao, LI Jing, CHE Qian, LI De-Hai. Penicacids E−G, three new mycophenolic acid derivatives from the marine-derived fungus Penicillium parvum HDN17-478 [J]. Chin J Nat Med, 2020, 18(11): 850-854. doi: 10.1016/S1875-5364(20)60027-9
Citation: CHEN Xiao-Hui, ZHOU Guo-Liang, SUN Chun-Xiao, ZHANG Xiao-min, ZHANG Guo-Jian, ZHU Tian-Jiao, LI Jing, CHE Qian, LI De-Hai. Penicacids E−G, three new mycophenolic acid derivatives from the marine-derived fungus Penicillium parvum HDN17-478 [J]. Chin J Nat Med, 2020, 18(11): 850-854. doi: 10.1016/S1875-5364(20)60027-9

Penicacids E−G, three new mycophenolic acid derivatives from the marine-derived fungus Penicillium parvum HDN17-478

  • Three new mycophenolic acid derivatives, penicacids E−G ( 13 ), together with three known analogues, mycophenolic acid ( 4 ), 4′-hydroxy-mycophenolic acid ( 5 ) and mycophenolic methyl ester ( 6 ), were isolated from a marine-derived fungus Penicillium parvum HDN17-478 from a South China Sea marine sediment sample. The structures of compounds 13 were elucidated by HRMS, NMR, and Mosher’s method. Among them, compounds 1 and 2 were the first examples of mycophenolic acid analogs with a double bond at C-3′/C-4′ position. The cytotoxicity of 16 was evaluated against the HCT-116, BEL-7402, MGC-803, SH-SY5Y, HO-8910 and HL-60 cell lines, and compounds 4 and 6 showed potent cytotoxicity with IC50 values ranging from 1.69 to 12.98 μmol·L–1.
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