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1)  Aldose reductase inhibitor
醛糖还原酶抑制剂
1.
Synthesis of aldose reductase inhibitor fidarestat;
醛糖还原酶抑制剂非达司他的合成
2.
Progress in research of aldose reductase inhibitors in traditional medicinal herbs;
中草药来源的醛糖还原酶抑制剂的研究进展
3.
A high throughput screening method established by us was applied for screening aldose reductase inhibitors from thousands of strains of actinomycetes and fungi,as a result,a strain,F01-195 with the positive activity was picked out.
利用自建的高通量醛糖还原酶抑制剂的筛选方法,从数千株放线菌和真菌中筛选得到阳性菌株F01-195。
2)  aldose reductase inhibitors
醛糖还原酶抑制剂
1.
Current advance in screening of aldose reductase inhibitors;
醛糖还原酶抑制剂筛选的研究进展
2.
Three-Dimensional Quantitative Structure Activity Relationship of Flavones as Aldose Reductase Inhibitors;
黄酮类醛糖还原酶抑制剂的三维定量构效关系研究
3.
Advances in studies on aldose reductase inhibitors from plants;
植物中醛糖还原酶抑制剂的研究进展
3)  aldose reductase inhibitory activity
醛糖还原酶抑制活性
1.
Using support vector regression for QSAR study on the aldose reductase inhibitory activity of some flavones;
支持向量机回归方法用于黄酮类化合物醛糖还原酶抑制活性的QSAR研究
4)  5α-reductase inhibitor
5α-还原酶抑制剂
1.
OBJECTIVE:To analyze the current situation and trends of the marketing of 5α-reductase inhibitor.
目的:了解5α-还原酶抑制剂的市场现状及发展趋势。
2.
Objective To investigate the expressions of insulin-like growth factor-Ⅰ(IGF-Ⅰ), insulin-like growth factor-Ⅱ(IGF-Ⅱ) and insulin-like growth factor-ⅠR (IGF-ⅠR) in human prostatic hyperplasitic tissues influenced by 5α-reductase inhibitor on the level of protein.
目的在翻译水平探讨5α-还原酶抑制剂干预下人前列腺增生组织中IGF-Ⅰ、IGF-Ⅱ及IGF-ⅠR 的表达及意义。
5)  reductase inhibitor
还原酶抑制剂
1.
Objective To observe the effect of simvastatin,a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor,on the expression of endothelin-1(ET-1)in cultured vascular endothelial cell.
目的观察羟甲基戊二酰辅酶A(HMG-COA)还原酶抑制剂-辛伐他汀(Simvastatin)对培养的血管内皮细胞表达内皮素-1(ET-1)的影响。
6)  5α-reductase inhibitor
5α还原酶抑制剂
1.
Objective: To identify the role of 5α-reductase in the spermatogenesis of male rats by studying the effect of two 5α-reductase inhibitors,Epristeride and Finasteride,on the spermatogenesis in male Sprague-Dawley(SD) rats.
目的:研究高选择性5α还原酶抑制剂(爱普列特)在较大剂量时对雄性SD大鼠生精功能的影响。
2.
(2)To investigate the expressions of IGF-1(insulin -like factor-1), PCNA(prolifeation cell nuclear antigen) and Caspase3 in human prostatic hyperplastic tissues influnenced by 5α-reductase inhibitor on the level of protein.
(2)在蛋白水平探讨5α还原酶抑制剂干预下人前列腺增生组织中IGF-1与PCNA、Caspase3的表达及意义。
补充资料:醛糖还原酶抑制剂
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性质:抑制醛糖还原酶(EC1,1,1,21)活性的化合物。醛糖还原酶的哺乳动物体内催化葡萄糖向山梨醇的转化,这是糖尿病后遗症如白内障和神经疾病的主要起因。醛糖还原酶抑制剂可有效抑制糖尿病病人许多器官中山梨醇含量的异常升高,因此这类抑制剂,如Thiazocin A和B等可作为糖尿病后遗症的防治药。

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