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类黄酮结构与法尼基蛋白转移酶抑制作用之间的关系

Relationship between flavonoid structure and inhibition of farnesyl protein transferase.

作者信息

Kang Hyun-Mi, Kim Jong-Han, Lee Mi-Young, Son Kwang-Hee, Yang Deok Cho, Baek Nam-In, Kwon Byoung-Mog

机构信息

Korea Research Institute of Bioscience and Biotechnology, P.O. Box 115, Yusung, Taejon 305-600, Republic of Korea.

出版信息

Nat Prod Res. 2004 Aug;18(4):349-56. doi: 10.1080/14786410310001622022.

Abstract

Flavonoids are well-known phytochemicals that are produced by various plants in high quantities. The chemopreventive activity of flavonoids is dependent on their structural features. The studies of structure-FPTase inhibitory activity indicated that the number, position and substitution of hydroxyl groups of the A and B rings of flavonoid, and unsaturation of the C2-C3 bond are important factors affecting inhibition on FPTase by flavonoids. A couple of flavonoids inhibited FPTase and also the growth of human tumor cell lines, especially butein, which strongly inhibited the growth of colon cancer cell line (HCT116). However, flavanones and flavanols did not inhibit FPTase nor the growth of tumor cells.

摘要

类黄酮是由多种植物大量产生的著名植物化学物质。类黄酮的化学预防活性取决于其结构特征。结构-法尼基焦磷酸合酶(FPTase)抑制活性的研究表明,类黄酮A环和B环上羟基的数量、位置和取代情况以及C2-C3键的不饱和程度是影响类黄酮对FPTase抑制作用的重要因素。一些类黄酮抑制FPTase以及人类肿瘤细胞系的生长,尤其是紫铆因,它强烈抑制结肠癌细胞系(HCT116)的生长。然而,黄烷酮和黄烷醇既不抑制FPTase,也不抑制肿瘤细胞的生长。

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