Balliano G, Viola F, Ceruti M, Cattel L
Istituto di Chimica Farmaceutica Applicata, Torino, Italy.
Biochim Biophys Acta. 1988 Mar 4;959(1):9-19. doi: 10.1016/0005-2760(88)90144-0.
The ability of some azasqualene derivatives to inhibit yeast cell growth was compared with their inhibition activity on squalene-2,3-oxide cyclase (EC 5.4.99.7) both in living cells and in microsome preparations. Among the compounds tested, N,N-diethylazasqualene showed the best correlation between the activity on squalene-2,3-oxide cyclase and its inhibition of yeast growth. The N-oxide derivative, N,N-diethylazasqualene N-oxide, which was as active as the amine in microsomes, was much less active in living cells, probably because it could not easily penetrate the cell wall. Kinetic analysis of the inhibitory activity of compounds on squalene-2,3-oxide cyclase revealed a sharp difference between N,N-diethylazasqualene and its N-oxide; the former showed a non-competitive-type inhibition, whereas the latter behaved as a competitive inhibitor.
在活细胞和微粒体制剂中,比较了一些氮杂角鲨烯衍生物抑制酵母细胞生长的能力与其对角鲨烯-2,3-环氧化酶(EC 5.4.99.7)的抑制活性。在所测试的化合物中,N,N-二乙基氮杂角鲨烯在角鲨烯-2,3-环氧化酶活性与其对酵母生长的抑制之间表现出最佳相关性。N-氧化物衍生物N,N-二乙基氮杂角鲨烯N-氧化物在微粒体中的活性与胺相当,但在活细胞中的活性要低得多,这可能是因为它不易穿透细胞壁。对化合物对角鲨烯-2,3-环氧化酶抑制活性的动力学分析显示,N,N-二乙基氮杂角鲨烯与其N-氧化物之间存在明显差异;前者表现为非竞争性抑制,而后者表现为竞争性抑制剂。