Journal of Medicinal Chemistry p. 3502 - 3513 (1995)
Update date:2022-08-02
Topics: Synthesis Esterification Methyl ester Carboxylic acid Biological Activity Inhibition Replacement squalestatins Isoelectronic
Bamford
Chan
Craven
Dymock
Green
Henson
Kirk
Lester
Procopiou
Snowden
Spooner
Srikantha
Watson
Widdowson
A series of squalestatins modified at the C3-position with a heterocyclic functionality was prepared and evaluated in vitro as inhibitors of squalene synthase (SQS). Structure-activity relationships for compounds with the 4,6- dimethyloctenoate at C6(S1 a
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