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2-(多羟基烷基)-噻唑烷-4-羧酸对荷瘤小鼠非蛋白巯基的选择性作用

Selective effect of 2-(polyhydroxyalkyl)-thiazolidine-4-carboxylic acids on nonprotein sulfhydryl groups in tumor bearing mice.

作者信息

Włodek L, Wróbel M, Czubak J

机构信息

Institute of Medical Biochemistry, Collegium Medicum, Jagiellonian University, Kraków, Poland.

出版信息

Gen Pharmacol. 1996 Dec;27(8):1373-6. doi: 10.1016/s0306-3623(96)00072-9.

Abstract
  1. Thiazolidine derivatives (TD), the products of condensation of L-cysteine (cys) with sugars (D-glucose, D-xylose, D-arabinose, D-galactose, and D-mannose), successfully elevated nonprotein sulfhydryl (NPSH) levels in livers of Ehrlich ascites tumor (EAT)-bearing mice. 2. At the same time, TD promoted a significant drop of NPSH in EAT cells. 3. Thus, TD, through their selective influence on the levels of NPSH in liver and cancer cells appear to be promising compounds for anticancer therapy.
摘要
  1. 噻唑烷衍生物(TD)是L-半胱氨酸(cys)与糖类(D-葡萄糖、D-木糖、D-阿拉伯糖、D-半乳糖和D-甘露糖)缩合的产物,成功提高了艾氏腹水瘤(EAT)荷瘤小鼠肝脏中的非蛋白巯基(NPSH)水平。2. 同时,TD促使EAT细胞中的NPSH显著下降。3. 因此,TD通过对肝脏和癌细胞中NPSH水平的选择性影响,似乎是有前景的抗癌治疗化合物。

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