| Literature DB >> 23024574 |
Jiangtao Gao1, Mohamed M Radwan, Francisco León, Xiaoning Wang, Melissa R Jacob, Babu L Tekwani, Shabana I Khan, Shari Lupien, Robert A Hill, Frank M Dugan, Horace G Cutler, Stephen J Cutler.
Abstract
In this study, we examined in vitro antibacterial, antifungal, antimalarial, and antileishmanial activities of secondary metabolites (1-8) isolated from the fungus Eurotium repens. All compounds showed mild to moderate antibacterial or antifungal or both activities except 7. The activity of compound 6 was the best of the group tested. The in vitro antimalarial evaluation of these compounds revealed that compounds 1-3, 5, and 6 showed antimalarial activities against both chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum with IC(50) values in the range of 1.1-3.0 μg/ml without showing any cytotoxicity to the mammalian cells. Compound 5 displayed the highest antimalarial activity. Antileishmanial activity against Leishmania donovani promastigotes was observed for compounds 1-6 with IC(50) values ranging from 6.2 to 23 μg/ml. Antileishmanial activity of compounds 5 and 6 (IC(50) values of 7.5 and 6.2 μg/ml, respectively) was more potent than 1-4 (IC(50) values ranging from 19-23 μg/ml). Compounds 7 and 8 did not show any antiprotozoal effect. Preliminary structure and activity relationship studies indicated that antibacterial, antifungal, antimalarial, and antileishmanial activities associated with phenol derivates (1-6) seem to be dependent on the number of double bonds in the side chain, which would be important for lead optimization in the future.Entities:
Year: 2011 PMID: 23024574 PMCID: PMC3457657 DOI: 10.1007/s00044-011-9798-7
Source DB: PubMed Journal: Med Chem Res ISSN: 1054-2523 Impact factor: 1.965