Department of Botany, University of Pune, Pune 411007, Maharashtra, India.
Bioorg Med Chem. 2009 Oct 1;17(19):7052-5. doi: 10.1016/j.bmc.2009.04.023. Epub 2009 Apr 17.
Topoisomerase I inhibitors from Ruta graveolens are reported for the first time. Potent topoisomerase I inhibitory activity from in vitro culture extracts R. graveolens were observed. Stabilization of DNA-topoisomerase covalent complex was observed in all the tested extracts. The mechanism of topoisomerase inhibition was determined by preincubation studies. The irreversible topoisomerase I mediated relaxation of plasmid in enzyme-substrate preincubation study, indicated that the observed inhibitory activity of extract constituents was not mediated through conformational changes in the DNA. Furthermore, the affinity of inhibitors with the enzyme was tested by enzyme-extract preincubation study. Increase in inhibition of topoisomerase activity and promotion of DNA-enzyme complex was observed after enzyme-extract preincubation. The activity could be assigned to furanocoumarins-psoralen, bergapten and xanthotoxin, identifying them as novel, potent topoisomerase I inhibitors.
首次报道了瑞香狼毒中的拓扑异构酶 I 抑制剂。从体外培养的瑞香狼毒提取物中观察到了强大的拓扑异构酶 I 抑制活性。在所有测试的提取物中均观察到 DNA-拓扑异构酶共价复合物的稳定。通过预孵育研究确定了拓扑异构酶抑制的机制。在酶-底物预孵育研究中,观察到质粒的拓扑异构酶 I 介导的不可逆松弛,表明观察到的提取物成分的抑制活性不是通过 DNA 的构象变化介导的。此外,通过酶-提取物预孵育研究测试了抑制剂与酶的亲和力。酶-提取物预孵育后,观察到拓扑异构酶活性的抑制增加和 DNA-酶复合物的促进。该活性可归因于呋喃香豆素-补骨脂素、佛手柑内酯和花椒毒素,将它们鉴定为新型强效拓扑异构酶 I 抑制剂。