Baxter A, Fitzgerald B J, Hutson J L, McCarthy A D, Motteram J M, Ross B C, Sapra M, Snowden M A, Watson N S, Williams R J
Glaxo Group Research Ltd., Greenford, Middlesex, United Kingdom.
J Biol Chem. 1992 Jun 15;267(17):11705-8.
Squalestatin 1 is a member of a novel family of fermentation products isolated from a previously unknown Phoma species (Coelomycetes). Squalestatin 1 is a potent, selective inhibitor of squalene synthase, a key enzyme in cholesterol biosynthesis; in vitro, 50% inhibition of enzyme activity is observed at a concentration of 12 +/- 5 nM (range of 4-22 nM). Squalestatin 1 inhibits cholesterol biosynthesis from [14C]acetate by isolated rat hepatocytes (50% inhibition at 39 nM) and by rat liver in vivo. In marmosets, a species with a lipoprotein profile similar to that of man, squalestatin 1 lowers serum cholesterol by up to 75%. This compound will allow further investigation of the control of the sterol biosynthesis pathway and could also lead to the development of new therapies for elevated serum cholesterol.
鲨烯抑素1是从一种先前未知的茎点霉属物种(腔孢纲)中分离出的新型发酵产物家族的成员。鲨烯抑素1是角鲨烯合酶的一种强效、选择性抑制剂,角鲨烯合酶是胆固醇生物合成中的关键酶;在体外,当浓度为12±5 nM(范围为4 - 22 nM)时可观察到50%的酶活性抑制。鲨烯抑素1可抑制分离的大鼠肝细胞利用[14C]乙酸盐进行的胆固醇生物合成(在39 nM时50%抑制)以及大鼠肝脏在体内的胆固醇生物合成。在狨猴(一种脂蛋白谱与人相似的物种)中,鲨烯抑素1可使血清胆固醇降低多达75%。该化合物将有助于进一步研究固醇生物合成途径的调控,也可能导致开发治疗血清胆固醇升高的新疗法。