170641-33-5Relevant academic research and scientific papers
The squalestatins: Synthesis and biological activity of some C3-modified analogues; replacement of a carboxylic acid or methyl ester with an isoelectronic heterocyclic functionality
Bamford,Chan,Craven,Dymock,Green,Henson,Kirk,Lester,Procopiou,Snowden,Spooner,Srikantha,Watson,Widdowson
, p. 3502 - 3513 (2007/10/02)
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
