首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Identification, structural properties and chelating capacity of miltipolone as a broad-spectrum inhibitor to cancer cells.
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Identification, structural properties and chelating capacity of miltipolone as a broad-spectrum inhibitor to cancer cells.

机译:米替泊酮作为癌细胞的广谱抑制剂的鉴定,结构性质和螯合能力。

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摘要

Miltipolone (1) was discovered as a good and broad-spectrum inhibitor against the growth of cancer cells from "Danshen" based on the activity-driven screening of TCMs. The structural features make 1 easily tautomerize between different forms and 1 is linked and stabilized by intermolecular O-Hcdots, three dots, centeredO hydrogen bonds in the crystal structure. The interaction of 1 in ddH(2)O solution with Co(2+), Mn(2+), Zn(2+), Fe(2+) or Fe(3+) changed UV absorption values; the chelation of 1 with Fe(2+) or Fe(3+) also altered the characteristic UV absorption peaks. However, only did Fe(2+) reverse 1's inhibition against the growth of cancer cells; therefore, we concluded that 1 possibly acts as a Fe(2+) chelator to conduct its inhibitory activity.
机译:基于中药的活性驱动筛选,Miltipolone(1)被发现是抗“丹参”癌细胞生长的良好且广谱抑制剂。结构特征使1易于在不同形式之间互变异构,并且1通过分子间的O-Hcdot(三个点,中心为O的氢键)连接并稳定。 ddH(2)O溶液中的1与Co(2 +),Mn(2 +),Zn(2 +),Fe(2+)或Fe(3+)的相互作用改变了UV吸收值; 1与Fe(2+)或Fe(3+)的螯合也改变了特征性​​UV吸收峰。但是,只有Fe(2+)才能逆转1's对癌细胞生长的抑制作用。因此,我们得出的结论是1可能充当Fe(2+)螯合剂来进行其抑制活性。

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