Title : In vitro cytotoxicity of melleolide antibiotics: structural and mechanistic aspects - Bohnert_2011_Bioorg.Med.Chem.Lett_21_2003 |
Author(s) : Bohnert M , Miethbauer S , Dahse HM , Ziemen J , Nett M , Hoffmeister D |
Ref : Bioorganic & Medicinal Chemistry Lett , 21 :2003 , 2011 |
Abstract :
Melleolide sesquiterpene aryl esters are secondary products of the mushroom genus Armillaria. We compared the cytotoxicity of eleven melleolides--five thereof are new natural products--against four human cancer cell lines. Armillaridin, 4-O-methylarmillaridin, and dehydroarmillylorsellinate were most active, at IC(50) = 3.0, 4.1 and 5.0 microM, respectively, against Jurkat T cells for the former two compounds, and K-562 cells for the latter. Dehydroarmillylorsellinate did not inhibit respiration and RNA-synthesis of K-562 cells at 5 microM. However, replication of DNA dropped to 35% after 120 min at this concentration, and translational activity also decreased. |
PubMedSearch : Bohnert_2011_Bioorg.Med.Chem.Lett_21_2003 |
PubMedID: 21376582 |
Gene_locus related to this paper: armos-armb |
Gene_locus | armos-armb |
Bohnert M, Miethbauer S, Dahse HM, Ziemen J, Nett M, Hoffmeister D (2011)
In vitro cytotoxicity of melleolide antibiotics: structural and mechanistic aspects
Bioorganic & Medicinal Chemistry Lett
21 :2003
Bohnert M, Miethbauer S, Dahse HM, Ziemen J, Nett M, Hoffmeister D (2011)
Bioorganic & Medicinal Chemistry Lett
21 :2003