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Merck
CN
  • Synthesis and pro-apoptotic activity of novel glycyrrhetinic acid derivatives.

Synthesis and pro-apoptotic activity of novel glycyrrhetinic acid derivatives.

Chembiochem : a European journal of chemical biology (2011-02-18)
Evgeniya B Logashenko, Oksana V Salomatina, A V Markov, Dina V Korchagina, Nariman F Salakhutdinov, Genrikh A Tolstikov, Valentin V Vlassov, Marina A Zenkova
摘要

Triterpenoids are used for medicinal purposes in many countries. Some, such as oleanolic and glycyrrhetinic acids, are known to be anti-inflammatory and anticarcinogenic. However, the biological activities of these naturally occurring molecules against their particular targets are weak, so the synthesis of new synthetic analogues with enhanced potency is needed. By combining modifications to both the A and C rings of 18βH-glycyrrhetinic acid, the novel synthetic derivative methyl 2-cyano-3,12-dioxo-18βH-olean-9(11),1(2)-dien-30-oate was obtained. This derivative displays high antiproliferative activity in cancer cells, including a cell line with a multidrug-resistance phenotype. It causes cell death by inducing the intrinsic caspase-dependent apoptotic pathway.

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Sigma-Aldrich
核糖核酸酶A 来源于牛胰腺, Type I-A, powder, ≥60% RNase A basis (SDS-PAGE), ≥50 Kunitz units/mg protein
Sigma-Aldrich
核糖核酸酶A 来源于牛胰腺, Molecular Biology, ≥70 Kunitz units/mg protein, lyophilized
Sigma-Aldrich
核糖核酸酶A 来源于牛胰腺, (Solution of 50% glycerol, 10mM Tris-HCL pH 8.0)
Sigma-Aldrich
核糖核酸酶A 来源于牛胰腺, Type I-AS, 50-100 Kunitz units/mg protein
Sigma-Aldrich
核糖核酸酶A 来源于牛胰腺, Type III-A, ≥85% RNase A basis (SDS-PAGE), 85-140 Kunitz units/mg protein
Sigma-Aldrich
核糖核酸酶A 来源于牛胰腺, Type II-A, ≥60% (SDS-PAGE), >= 60 Kunitz units/mg protein
Sigma-Aldrich
核糖核酸酶A 来源于牛胰腺, Type XII-A, ≥90% (SDS-PAGE), 75-125 Kunitz units/mg protein
Sigma-Aldrich
核糖核酸酶A 来源于牛胰腺, Type X-A, ≥90% (SDS-PAGE), ≥70 Kunitz units/mg protein