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Enzyme immunoassay discrimination of a new angiotensin-converting enzyme (ACE) inhibitor, cilazapril, and its active metabolite.

作者信息

Tanaka H, Yoneyama Y, Sugawara M, Umeda I, Ohta Y

出版信息

J Pharm Sci. 1987 Mar;76(3):224-7. doi: 10.1002/jps.2600760308.

DOI:10.1002/jps.2600760308
PMID:3035170
Abstract

Simple and sensitive enzyme immunoassays (EIAs), discriminating a new angiotensin-converting enzyme (ACE) inhibitor, cilazapril [9(s) - [1(s)-(ethoxycarbonyl)-3-phenylpropylamino]-octahydro-10-oxo-6H- pyridazo[1,2-a] [1,2]diazepine-1(s)carboxylic acid] and its active metabolite [9(s)-[1(s)-carboxy-3-phenylpropylamino]-octahydro-10-oxo-6H- pyridazo[1,2-a][1,2]diazepine-1(s)carboxylic acid] were developed for pharmacokinetic studies of this drug which is used as an antihypertensive agent. These assays can be performed directly on serum or plasma specimens without pretreatment. The EIA for cilazapril (prodrug) allowed the determination of as little as 30 pg/mL, while a 1000-times greater concentration of its active metabolite was required to achieve the same extent of inhibition. The EIA for the active metabolite exhibited a sensitivity and specificity similar to those of the prodrug. Plasma specimens from a human volunteer study and a marmoset subacute toxicity study were assayed by these two newly developed EIAs. The plasma levels of active metabolite determined by the EIA were compared with those assayed by radioenzymatic assay, and a good correlation was observed between them.

摘要

相似文献

1
Enzyme immunoassay discrimination of a new angiotensin-converting enzyme (ACE) inhibitor, cilazapril, and its active metabolite.
J Pharm Sci. 1987 Mar;76(3):224-7. doi: 10.1002/jps.2600760308.
2
The pharmacokinetics and dose proportionality of cilazapril.西拉普利的药代动力学及剂量比例关系。
Br J Clin Pharmacol. 1989;27 Suppl 2(Suppl 2):199S-204S. doi: 10.1111/j.1365-2125.1989.tb03482.x.
3
A pharmacokinetic study of cilazapril in elderly and young volunteers.西拉普利在老年和青年志愿者中的药代动力学研究。
Br J Clin Pharmacol. 1989;27 Suppl 2(Suppl 2):211S-215S. doi: 10.1111/j.1365-2125.1989.tb03484.x.
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A review of the preclinical cardiovascular pharmacology of cilazapril, a new angiotensin converting enzyme inhibitor.新型血管紧张素转换酶抑制剂西拉普利的临床前心血管药理学综述。
Br J Clin Pharmacol. 1989;27 Suppl 2(Suppl 2):139S-150S. doi: 10.1111/j.1365-2125.1989.tb03475.x.
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The influence of food on the pharmacokinetics and ACE inhibition of cilazapril.食物对西拉普利药代动力学及血管紧张素转换酶抑制作用的影响。
Br J Clin Pharmacol. 1989;27 Suppl 2(Suppl 2):205S-209S. doi: 10.1111/j.1365-2125.1989.tb03483.x.
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Correlation between plasma concentration of cilazapril and haemodynamic and hormonal effects in healthy man.健康男性中西拉普利血浆浓度与血流动力学及激素效应之间的相关性。
Br J Clin Pharmacol. 1989;27 Suppl 2(Suppl 2):189S-197S. doi: 10.1111/j.1365-2125.1989.tb03481.x.
7
Antihypertensive, enzymatic, and hormonal activity of cilazapril, a new angiotensin-converting enzyme inhibitor in patients with mild to moderate essential hypertension.西拉普利(一种新型血管紧张素转换酶抑制剂)在轻至中度原发性高血压患者中的降压、酶活性及激素活性
J Cardiovasc Pharmacol. 1988 Feb;11(2):230-4.
8
The cardiovascular and endocrine effects of cilazapril, a new angiotensin-converting enzyme inhibitor, in man.
Afr J Med Med Sci. 1990 Mar;19(1):33-8.
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Pharmacokinetics of cilazapril during repeated oral dosing in healthy young volunteers.
Eur J Drug Metab Pharmacokinet. 1990 Jan-Mar;15(1):63-7. doi: 10.1007/BF03190129.
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Pharmacokinetics of the converting enzyme inhibitor cilazapril in normal volunteers and the relationship to enzyme inhibition: development of a mathematical model.
J Cardiovasc Pharmacol. 1987 Jan;9(1):32-8.

引用本文的文献

1
Antihypertensive effects and pharmacokinetics of single and consecutive doses of cilazapril in hypertensive patients with normal or impaired renal function.单次及连续服用西拉普利对肾功能正常或受损的高血压患者的降压效果及药代动力学研究
Br J Clin Pharmacol. 1989;27 Suppl 2(Suppl 2):283S-287S. doi: 10.1111/j.1365-2125.1989.tb03493.x.
2
Clinical pharmacokinetics of the newer ACE inhibitors. A review.新型血管紧张素转换酶抑制剂的临床药代动力学。综述。
Clin Pharmacokinet. 1990 Sep;19(3):177-96. doi: 10.2165/00003088-199019030-00003.
3
Cilazapril. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in cardiovascular disease.
Drugs. 1991 May;41(5):799-820. doi: 10.2165/00003495-199141050-00008.