Abstract
The marine sponge Haliclona simulans collected from the Irish Sea yielded two new steroids: 24-vinyl-cholest-9-ene-3β,24-diol and 20-methyl-pregn-6-en-3β-ol,5a,8a-epidioxy, along with the widely distributed 24-methylenecholesterol. One of the steroids possesses an unusually short hydrocarbon side chain. The structures were elucidated using nuclear magnetic resonance spectroscopy and confirmed using electron impact- and high resolution electrospray-mass spectrometry. All three steroids possess antitrypanosomal and anti-mycobacterial activity. All the steroids were found to possess low cytotoxicity against Hs27 which was above their detected antitrypanosomal potent concentrations.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Anti-Bacterial Agents / chemistry
-
Anti-Bacterial Agents / isolation & purification
-
Anti-Bacterial Agents / pharmacology*
-
Cell Survival / drug effects
-
Humans
-
Hydroxycholesterols / chemistry
-
Hydroxycholesterols / isolation & purification
-
Hydroxycholesterols / pharmacology*
-
Molecular Conformation
-
Mycobacterium / drug effects*
-
Porifera / chemistry*
-
Pregnanes / chemistry
-
Pregnanes / isolation & purification
-
Pregnanes / pharmacology*
-
Trypanocidal Agents / chemistry
-
Trypanocidal Agents / isolation & purification
-
Trypanocidal Agents / pharmacology*
-
Trypanosoma / drug effects
Substances
-
20-methyl-pregn-6-en-3beta-ol,5a,8a-epidioxy
-
24-vinyl-cholest-9-ene-3beta,24-diol
-
Anti-Bacterial Agents
-
Hydroxycholesterols
-
Pregnanes
-
Trypanocidal Agents