Bertolino A, Altman L J, Vasak J, Rilling H C
Biochim Biophys Acta. 1978 Jul 25;530(1):17-23. doi: 10.1016/0005-2760(78)90122-4.
Analogues of farnesyl pyrophosphate containing a farnesyl moiety and a variety of amine residues replacing the pyrophosphate have been synthesized. Most of these compounds were effective inhibitors of the synthesis of squalene and presqualene pyrophosphate from farnesyl pyrophosphate. 50% inhibition was obtained at concentrations between 50 and 100 micron. These analogues also inhibited other microsomal enzymes so they apparently function as general inhibitors of microsomal enzymes.
已合成了含有法尼基部分和多种取代焦磷酸的胺残基的法尼基焦磷酸类似物。这些化合物中的大多数是从法尼基焦磷酸合成角鲨烯和前角鲨烯焦磷酸的有效抑制剂。在50至100微米的浓度下可获得50%的抑制率。这些类似物还抑制其他微粒体酶,因此它们显然作为微粒体酶的一般抑制剂起作用。