Phytochemical investigation of Sanrafaelia ruffonammari Verd and Ophrypetalum odoratum Diels that belongs to the rare genera confined to East African coastal forests led to the isolation of enantiomeric styrylpyrone d...Phytochemical investigation of Sanrafaelia ruffonammari Verd and Ophrypetalum odoratum Diels that belongs to the rare genera confined to East African coastal forests led to the isolation of enantiomeric styrylpyrone dimer,(±)-5-methoxy-7-phenyl-[4-methoxy-2-pyronyl]-1-(E)-styryl-2-oxabicyclo-[4.2.0]-octa-4-en-3-one(1)alongside(?)-6-styryl-7,8-epoxy-4-methoxypyran-2-one(2)and the enantiomeric(?)-(3)and(-)-6-styryl-7,8-dihydroxy-4-methoxypyran-2-ones(4).Their structures were established by means of spectroscopic methods.In this paper we reveal for the first time the occurrence of styrylpyrones in East African biodiversity.(?)-6-Styryl-7,8-epoxy-4-methoxypyran-2-one(2)and the dihydroxystyrylpyrone enantiomer(3)showed in vitro antifungal activity against Candida albicans at a concentration of 24.4 and 26.2 lM with zones of inhibition of 17 and 9 mm,respectively.Compound 2 exhibited strong activity in the brine shrimp test with LC50=1.7 lg/mL.Their high cytotoxic and antifungal activities render them candidates for further scientific attention for drug development programs against cancer and microbial infections.展开更多
New hexalobine type alkaloid,5-(200,300-epoxy-300-methylbutyl)-3-(30-hydroxy-30-methyl-10-acetyloxy-but-20-yl)indole(1)alongside the known hexalobines 3-(20,30-dihydroxy-30-methylbutyl)-5-(300-methylcrotonoyl)indole(2...New hexalobine type alkaloid,5-(200,300-epoxy-300-methylbutyl)-3-(30-hydroxy-30-methyl-10-acetyloxy-but-20-yl)indole(1)alongside the known hexalobines 3-(20,30-dihydroxy-30-methylbutyl)-5-(300-methylcrotonoyl)indole(2),3,5-hexalobine C(3)and 3,5-hexalobine D(4)were isolated from fruits of Hexalobus monopetalus.Compounds 3 and 4 exhibited antifungal activity against Candida albicans.展开更多
基金This work was financially supported by the Norwegian Agency for International Development(NORAD)through the NORAD Chemistry Project.
文摘Phytochemical investigation of Sanrafaelia ruffonammari Verd and Ophrypetalum odoratum Diels that belongs to the rare genera confined to East African coastal forests led to the isolation of enantiomeric styrylpyrone dimer,(±)-5-methoxy-7-phenyl-[4-methoxy-2-pyronyl]-1-(E)-styryl-2-oxabicyclo-[4.2.0]-octa-4-en-3-one(1)alongside(?)-6-styryl-7,8-epoxy-4-methoxypyran-2-one(2)and the enantiomeric(?)-(3)and(-)-6-styryl-7,8-dihydroxy-4-methoxypyran-2-ones(4).Their structures were established by means of spectroscopic methods.In this paper we reveal for the first time the occurrence of styrylpyrones in East African biodiversity.(?)-6-Styryl-7,8-epoxy-4-methoxypyran-2-one(2)and the dihydroxystyrylpyrone enantiomer(3)showed in vitro antifungal activity against Candida albicans at a concentration of 24.4 and 26.2 lM with zones of inhibition of 17 and 9 mm,respectively.Compound 2 exhibited strong activity in the brine shrimp test with LC50=1.7 lg/mL.Their high cytotoxic and antifungal activities render them candidates for further scientific attention for drug development programs against cancer and microbial infections.
基金The Norwegian Agency for International Development(NORAD)through the NORAD Chemistry Project is appreciated for supporting this work through a scholarship grant to H.M.MThe National Institute for Medical Research(NIMR),The Department of Chemistry at the University of Dar es Salaam in Tanzaniathe Department of Pharmaceutical Chemistry in the Institute of Pharmacy at Erlangen University in Germany are thanked for supporting the research project.
文摘New hexalobine type alkaloid,5-(200,300-epoxy-300-methylbutyl)-3-(30-hydroxy-30-methyl-10-acetyloxy-but-20-yl)indole(1)alongside the known hexalobines 3-(20,30-dihydroxy-30-methylbutyl)-5-(300-methylcrotonoyl)indole(2),3,5-hexalobine C(3)and 3,5-hexalobine D(4)were isolated from fruits of Hexalobus monopetalus.Compounds 3 and 4 exhibited antifungal activity against Candida albicans.