Synthesis and in vitro cytotoxicity of lipidic alcohols and amines

Constantinou-Kokotou, V; Kokotos, G; Roussakis, C

HERO ID

4944567

Reference Type

Journal Article

Year

1998

HERO ID 4944567
In Press No
Year 1998
Title Synthesis and in vitro cytotoxicity of lipidic alcohols and amines
Authors Constantinou-Kokotou, V; Kokotos, G; Roussakis, C
Journal Anticancer Research
Volume 18
Issue 5A (1998 Sep-Oct)
Page Numbers 3439-3442
Abstract General methods for the conversion of unsaturated fatty acids into alcohols and amines and the preparation of lipidic 1,2-diamines were developed. The in vitro cytotoxicity of the synthetic lipidic compounds was tested against two different cell lines (P388 and NSCLCN6). Oleyl amine was the most active among the lipidic alcohols and monoamines. However, the saturated lipidic 1,2-hexadecanediamine exhibited the highest cytotoxicity (IC50 0.1 microgram/ml and 1.1 micrograms/ml).
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Keyword Index Medicus