本文利用了戊二酸二乙酯在一定反应条件下合成戊二酰二肼。
In this paper, two dihydrazides were synthesized with hydrazine and diethy1 ester.
美伐他汀是3羟甲基戊二酰辅酶a还原酶的有效的竞争性抑制剂，它是一种胆固醇生物合成调解酶。
Mevastatin is a potent competitive inhibitor of 3-hydroxy-3-methyl-glutaryl-coa reductase, a regulatory enzyme for cholesterol biosynthesis.
美伐他汀是3羟甲基戊二酰辅酶a还原酶的有效的竞争性抑制剂，它是一种胆固醇生物合成调解酶。
Mevastatin is a potent competitive inhibitor of 3-hydroxy-3-methyl-glutaryl (HMG) -coa reductase, a regulatory enzyme for cholesterol biosynthesis.
新型抗生素s632a_3是从土壤中分离出的一株放线菌产生的代谢产物，属戊二酰亚胺类化合物。
A new antibiotics, S632As, glutarimide antibiotics compounds, is a metabolic product from a strain of Antinomyces isolated from soil, and is dealt with in this paper.
结论：普伐他汀不能抑制肝细胞PAI-1的分泌。羟甲基戊二酰辅酶A还原酶的抑制与PAI- 1分泌可能没有关系。
Conclusion:Pravastatin can not inhibit the secretion of PAI 1 in hepatic cells and the inhibition of hydroxymethylglutaryl coenzyme A reductase may not be related to the secretion of PAI 1.
生物脂质来源于酮脂酰和异戊二烯基团。
Biological lipids originate from ketoacyl and isoprene groups.
他汀类药物能阻断羟甲基戊二酸单酰辅酶A还原酶，该酶与多种脂肪的产生有关，阻断该酶可以降低胆固醇水平。
Smoke breakStatins block an enzyme called HMG-CoA reductase, which is involved in the production of various fatty molecules. Blocking this enzyme lowers cholesterol levels.
他汀类药物能阻断羟甲基戊二酸单酰辅酶A还原酶，该酶与多种脂肪的产生有关，阻断该酶可以降低胆固醇水平。
Smoke breakStatins block an enzyme called HMG-CoA reductase, which is involved in the production of various fatty molecules. Blocking this enzyme lowers cholesterol levels.
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