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1)  HGM-CoA reductase
HGM-CoA还原酶抑制剂
2)  HMG-CoA reductase inhibitor
HMG-CoA还原酶抑制剂
1.
Synthesis and biological evaluation of condensed pyrrole-based HMG-CoA reductase inhibitors;
吡咯类HMG-CoA还原酶抑制剂的合成及生物活性
2.
A three-dimensional pharmacophore model of 3-hydro-3-methyl glutaryl coenzyme A (HMG-CoA)reductase inhibitors (RI) was developed based on 21 HMG-CoA reductase inhibitors from a rat liver.
利用Catalyst计算HMG-CoA还原酶抑制剂最优药效团由一个氢键受体,一个氢键给体,一个疏水基团和一个芳香环特征组成。
3.
Pitavastatin is a novel,fully synthetic HMG-CoA reductase inhibitor,which can significantly reduce low-density lipoprotein cholesterol(LDL-C),triglycerides(TG),and also increase high-density lipoprotein cholesterol(HDL-C).
匹伐他汀(pitavastatin)是新一代HMG-CoA还原酶抑制剂,能显著降低低密度脂蛋白胆固醇(LDL-C)、三酰甘油(TG)及升高高密度脂蛋白胆固醇(HDL-C),药动学性质优良,具有肝细胞选择性,且毒性低,安全性好,具有抗动脉粥样硬化、促血管生成和抗炎作用。
3)  HMG-CoA reductase inhibitors
HMG-CoA还原酶抑制剂
1.
Aim To seek and design new kinds of HMG-CoA reductase inhibitors.
目的寻找和设计新的HMG-CoA还原酶抑制剂。
2.
By using TLC and UV-spectrum detection,HMG-CoA reductase inhibitors produced by a strain of Monacus sp were assayed,and the optimum fermentation conditions were studied as well.
采用薄层层析-紫外吸收光谱法对一株红曲霉产生的HMG-CoA还原酶抑制剂进行分析测定,并对其发酵条件进行研究。
3.
Author discussed the impacts of different reference structures on building a pharmacophore model of HMG-CoA reductase inhibitors using DIStance COmparison method (DISCO).
目的:考察不同模板分子对距离比较法(DIStance COmparison,DISCO)构建HMG-CoA还原酶抑制剂药效团模型的影响。
4)  hydroxymethylglutaryl-CoA reductase inhibitors
羟甲基戊二酰基CoA还原酶抑制剂
5)  hydroxymethylglularyl-CoA reductase inhibitors
羟甲基戊二酰基CoA还原酶抑制剂
6)  Hydroxymethylglutaryl-COA reductase inhibitors/therapeutic use
羟甲基戊二酰基COA还原酶抑制剂/治疗应用
补充资料:还原酶
分子式:
CAS号:

性质:催化底物进行加氢反应的酶。如硝酸还原酶、氢化酶和N5,N10-亚甲四氢叶酸还原酶(FAD)等。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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