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ChemMedChem ; 8(11): 1779-86, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24014463

ABSTRACT

Illumination by acetylene: Systematic structural variations in a series of archetypal acetylenic lipids derived from the naturally occurring (S,E)-icos-4-en-1-yn-3-ol allowed the discovery of a series of 3R-like 1,4-di-unsaturated carbinol units with a significant and systematic enantiomeric effect on cytotoxicity.


Subject(s)
Alkanes , Alkenes , Antineoplastic Agents , Drug Discovery , Methanol , Alkanes/chemistry , Alkanes/pharmacology , Alkenes/chemistry , Alkenes/pharmacology , Animals , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Cell Line , Cell Line, Tumor , Cell Survival/drug effects , Inhibitory Concentration 50 , Methanol/chemistry , Methanol/pharmacology , Molecular Structure , Petrosia/chemistry , Stereoisomerism
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