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化合物D609可抑制佛波酯刺激的磷脂酶D活性以及磷脂酶C介导的磷脂酰乙醇胺水解。

Compound D609 inhibits phorbol ester-stimulated phospholipase D activity and phospholipase C-mediated phosphatidylethanolamine hydrolysis.

作者信息

Kiss Z, Tomono M

机构信息

Hormel Institute, University of Minnesota, Austin 55912, USA.

出版信息

Biochim Biophys Acta. 1995 Oct 26;1259(1):105-8. doi: 10.1016/0005-2760(95)00148-6.

Abstract

Tricyclodecan-9-yl-xanthogenate (compound D609) has recently been used in various cellular systems to specifically inhibit the activity of phosphatidylcholine (PtdCho)-directed phospholipase C (PLC). Here we show that in intact NIH 3T3 fibroblasts, concentrations of D609 (35 to 50 micrograms/ml) which have been used to inhibit PLC activity also significantly inhibit phorbol ester-induced phospholipase D-mediated hydrolysis of both PtdCho and phosphatidylethanolamine (PtdEtn). In addition, in isolated membranes compound D609 also inhibited PLC-mediated PtdEtn hydrolysis. The results indicate that compound D609 cannot be considered as a specific inhibitor of PtdCho-directed PLC activity.

摘要

三环癸烷-9-基-黄原酸酯(化合物D609)最近已用于各种细胞系统中,以特异性抑制磷脂酰胆碱(PtdCho)导向的磷脂酶C(PLC)的活性。在此我们表明,在完整的NIH 3T3成纤维细胞中,用于抑制PLC活性的D609浓度(35至50微克/毫升)也显著抑制佛波酯诱导的磷脂酶D介导的PtdCho和磷脂酰乙醇胺(PtdEtn)的水解。此外,在分离的膜中,化合物D609也抑制PLC介导的PtdEtn水解。结果表明,化合物D609不能被视为PtdCho导向的PLC活性的特异性抑制剂。

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