This drug is an angiotensin converting enzyme inhibitor.
本品是一种血管紧张素转换酶抑制剂。
A diagnostic test kit for detecting the presence or quantity of an enzyme or enzyme inhibitor is provided.
提供一种用于检测酶或酶抑制剂的存在或数量的诊断试验试剂盒。
The diagnostic kit utilizes reactive complexes to facilitate the detection of the enzyme or enzyme inhibitor.
所述诊断试剂盒利用反应性复合物来方便酶或酶抑制剂的检测。
Angiotensin converting enzyme inhibitor may increase the sensitivity of tissue to intrinsic and extrinsic insulin.
血管紧张肽转换酶抑制药可增加组织对内源性和外源性胰岛素的敏感性。
Objective To evaluate the pharmaceutical effect of angiotensin-converting enzyme inhibitor(ACEI) captopril on ischemic myocardium.
目的评价血管紧张素转换酶抑制剂（ACEI）卡托普利对缺血心肌的药理作用。
Kinetic analysis revealed that the inhibition on chymotrypsin by S-24 enzyme inhibitor is competitive with respect to the substrate.
动力学研究表明s - 24酶抑制剂抑制糜蛋白酶，对底物酪蛋白、血红蛋白的关系均为竟争性抑制。
CONCLUSION:DZ inhibited the 4 hydroxytative metabolic pathway of AP, suggesting DZ may be a potent and selective microsomal enzyme inhibitor.
结论：DZ选择性地抑制了AP在人体肝脏中的4羟基化代谢途径，提示DZ是一作用较强的、选择性的肝药酶抑制剂。
Is Angiotensin-Converting Enzyme Inhibitor and Angiotensin Receptor Blocker Combination therapy Better Than Monotherapy and Safe in Patients With CKD?
血管紧张素转化酶抑制剂和血管紧张素受体拮抗剂联合用药治疗CKD是否比单药应用要好？
Objective To introduce the research and market development of enalapril as an angiotensin 1-converting enzyme inhibitor (ACEI) for treating hypertension.
目的介绍抗高血压药血管紧张素转化酶抑制剂（ACEI）依那普利的研发及市场情况。
The signal exhibited by the released reporters may then be used to indicate the presence or quantity of an enzyme or enzyme inhibitor within the test sample.
由释放的报道分子所显示的信号可用来指示试验样品内酶或酶抑制剂的存在或数 量。
Less than one-third of subjects were receiving an angiotensin converting enzyme inhibitor at baseline, although this rose to around 40% by the end of follow-up.
小于三分之一患者基线时接受了转换酶抑制剂治疗，但随访结束时，使用比例已上升至近40%。
Aminoglycoside modifying enzyme is the main resistance mechanism. In this review, some advances in the research of aminoglycoside modifying enzyme inhibitor are summarized.
氨基糖苷类抗生素的修饰酶是细菌耐药的主要机制，本文对氨糖类抗生素的修饰酶抑制剂的研究进展作一综述。
Conclusion To make the stable chronic experimental hyperuricemic rat model, it was necessary that uric acid and uric acid enzyme inhibitor were given repetitiously, simultaneously.
结论：建立慢性高尿酸血症大鼠模型必须有赖尿酸及尿酸酶抑制剂同时、分次干预，才能形成稳定的高尿酸血症。
Objective To observe the effect of benazepril, an angiotensin converting enzyme inhibitor (ACEI) , on reducing proteinuria in a nephrotic young rat model of with massive proteinuria.
目的观察血管紧张素转换酶抑制剂苯那普利减轻幼龄肾病大鼠蛋白尿的作用。
Conclusion it is suggested that perindopril should be the first choice when angiotensin converting enzyme inhibitor (ACEI) is taken into account for the therapy of primary hypertension.
结论应用血管紧张素转换酶抑制剂(acei)治疗原发性高血压时，宜首选培哚普利。
After the therapy with angiotensin converting enzyme inhibitor (ACEI), the endothelium-dependent vasodilation function was improved in the coronary groups and especially for the DD group.
血管紧张素转换酶抑制剂(acei)治疗后冠心病组各型肱动脉内皮依赖性舒张功能与治疗前比较均有显著性改善，其中DD基因型改善最为明显。
To produce fermented milk that can inhibit the activity of angiotensin converting enzyme(ACE), then the angiotensin converting enzyme inhibitor(ACEI) can be purified from the fermented milk.
用瑞士乳杆菌生产具有抑制血管紧张素转换酶（ACE）活性的发酵乳并从其中分离血管紧张素转换酶抑制剂（ACEI）。
Purpose to investigate the anti-inflammatory effect of angiotensin-converting enzyme inhibitor captopril on the brain against ischemia-reperfusion injury and explore its mechanism of action.
目的观察血管紧张素转化酶抑制药卡托普利对大鼠局灶性脑缺血再灌注损伤后炎症反应的影响。
Objective to investigate the protective effect of angiotensin converting enzyme inhibitor (ACEI) and angiotensin receptor antagonist (ARB) on renal function of type 2 diabetic nephropathy patients.
目的研究血管紧张素转换酶抑制剂(acei)和血管紧张素受体拮抗剂(arb)对2型糖尿病肾病患者肾功能的保护作用。
Irreversible inhibitor of Thrombin and other serine proteases. Inhibits by acylation of the active site of the enzyme. Much less toxic than PMSF and DFP.
凝血酶及其他丝氨酸蛋白酶的不可逆抑制剂，将活性位点酰基化。比PMSF和DF P毒性小得多。
The end product inhibitor has no structural similarity to the substrate of the enzyme it is regulating.
最终产物抑制剂与它调节的酶的底物在结构上无相似之处。
The construction of the heterogeneous expression system of EPSPS from S. sclerotiorum provided a basis for inhibitor design of the enzyme.
核盘菌EPSPS异源表达系统的建立为该酶的抑制剂设计奠定了基础。
The net result of a non-competitive inhibitor is equivalent to converting some of the enzyme present to an inactive form.
一个非竞争性抑制剂的净结果相当于转化某些酶成为钝化形式。
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.
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。
Moreover, it may also serve as an interesting therapeutic target, since a specific inhibitor of the enzyme is available with promising animal data and initial positive data in humans.
此外，它还被视作是一种受人关注的治疗靶标，因为它的一种特异性的抑制剂已经在动物实验数据和初步人类积极的研究结果中证明可行。
When ABA biosynthesis was inhibited by nordihydroguaiaretic acid (NDGA), an inhibitor of the ABA anabolic enzyme 9-cis-epoxycarotenoid dioxygenase (NCED), rice seed germination showed no response.
当ABA的合成被去甲二氢愈创木酸（NDGA），ABA合成酶9-顺式-环氧类胡萝卜素双加氧酶的抑制因子所抑制，水稻种子萌发无影响。
The von Willebrand's disease factors in plasm, adjusted protein of thrombase and inhibitor 1 of activator of plasminogen were detected with enzyme-linked immunosorbent assay.
用酶联免疫吸附法检测血浆血管性假性血友病因子、凝血酶调节蛋白、纤溶酶原激活物抑制物1水平。
It has been found to be an inhibitor of the enzyme acetylcholinesterase.
它已被认为是抑制乙酰胆碱酯酶的酶。
Glyphosate, as a transition state inhibitor of EPSP synthase, inhibit the canalization of the enzyme as an EPSP synthase·EPSP·glyphosate ternary complex.
草甘膦与EPSP合成酶、EPSP形成三元复合物而阻断了EPSP合成酶的催化作用；
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