Abstract
Two novel sesterterpenes, 1 and 3, containing a scalarane-based framework, have been isolated from the sponge Hyrtios erectus collected in Papua New Guinea. Their structures and relative stereochemistry have been elucidated by analysis of their spectroscopic data.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Antimitotic Agents* / chemistry
-
Antimitotic Agents* / isolation & purification
-
Antimitotic Agents* / pharmacology
-
Female
-
Humans
-
Molecular Structure
-
Nuclear Magnetic Resonance, Biomolecular
-
Papua New Guinea
-
Porifera / chemistry*
-
Sesterterpenes* / chemistry
-
Sesterterpenes* / isolation & purification
-
Sesterterpenes* / pharmacology
-
Stereoisomerism
Substances
-
12-O-deacetyl-12-epi-scalarin
-
12-O-deacetyl-19-methoxy-12-epi-scalarin
-
12beta,16beta-diacetoxyscalarolbutenolide
-
Antimitotic Agents
-
Sesterterpenes