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Effects of the new oral angiotensin converting enzyme inhibitor 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2- azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498) in essential hypertension.

作者信息

Felder K, Witte P U

出版信息

Arzneimittelforschung. 1984;34(10B):1452-4.

PMID:6097273
Abstract

In a dose titration study patients with mild to moderate essential hypertension were treated with increasing doses of 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S, 5S)-2-azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498) (up to 8 mg daily) for 3 weeks. Hoe 498 was tolerated well. 9 out of 20 patients responded to 1 mg b.i.d., the blood pressure in a further 5 patients normalized with 2 mg b.i.d. Six patients did not respond to Hoe 498 treatment (4 mg b.i.d. in the last week) according to the criterion: recumbent diastolic blood pressure less than or equal to 90 mm Hg. But all 6 patients showed a clear decrease in blood pressure during treatment.

摘要

相似文献

1
Effects of the new oral angiotensin converting enzyme inhibitor 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2- azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498) in essential hypertension.
Arzneimittelforschung. 1984;34(10B):1452-4.
2
Cardiovascular and antihypertensive activities of the novel non-sulfhydryl converting enzyme inhibitor 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2- azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498).新型非巯基转化酶抑制剂2-[N-[(S)-1-乙氧羰基-3-苯基丙基]-L-丙氨酰]-(1S,3S,5S)-2-氮杂双环[3.3.0]辛烷-3-羧酸(Hoe 498)的心血管及抗高血压活性
Arzneimittelforschung. 1984;34(10B):1417-25.
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Tolerance and pharmacodynamics of the angiotensin converting enzyme inhibitor 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2- azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498) in healthy volunteers.血管紧张素转换酶抑制剂2-[N-[(S)-1-乙氧羰基-3-苯基丙基]-L-丙氨酰]-(1S,3S,5S)-2-氮杂双环[3.3.0]辛烷-3-羧酸(Hoe 498)在健康志愿者中的耐受性和药效学
Arzneimittelforschung. 1984;34(10B):1448-51.
4
2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2- azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498): antihypertensive action and persistent inhibition of tissue converting enzyme activity in spontaneously hypertensive rats.2-[N-[(S)-1-乙氧羰基-3-苯基丙基]-L-丙氨酰基]-(1S,3S,5S)-2-氮杂双环[3.3.0]辛烷-3-羧酸(Hoe 498):对自发性高血压大鼠的降压作用及对组织转化酶活性的持续抑制
Arzneimittelforschung. 1984;34(10B):1426-30.
5
Synthesis of a highly active angiotensin converting enzyme inhibitor: 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2- azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498).
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Humoral and blood pressure effects of the angiotensin converting enzyme inhibitor ramipril in essential hypertension.血管紧张素转换酶抑制剂雷米普利对原发性高血压的体液及血压影响
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Pharmacological properties of the new orally active angiotensin converting enzyme inhibitor 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl] -(1S,3S,5S)-2-azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498).新型口服活性血管紧张素转换酶抑制剂2-[[(S)-1-乙氧羰基-3-苯基丙基]-L-丙氨酰基]-(1S,3S,5S)-2-氮杂双环[3.3.0]辛烷-3-羧酸(Hoe 498)的药理特性
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Inhibition of angiotensin converting enzyme by 2-[N-[(S)-1-carboxy-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2-azabicyclo [3.3.0]octane-3-carboxylic acid (Hoe 498 diacid). Comparison with captopril and enalaprilat.2-[N-[(S)-1-羧基-3-苯基丙基]-L-丙氨酰]-(1S,3S,5S)-2-氮杂双环[3.3.0]辛烷-3-羧酸(Hoe 498二酸)对血管紧张素转换酶的抑制作用。与卡托普利和依那普利拉的比较。
Arzneimittelforschung. 1984;34(10B):1406-10.
9
2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S) -2-azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498)--a new and highly effective angiotensin I converting enzyme inhibitor.2-[N-[(S)-1-乙氧羰基-3-苯基丙基]-L-丙氨酰]-(1S,3S,5S)-2-氮杂双环[3.3.0]辛烷-3-羧酸(Hoe 498)——一种新型高效的血管紧张素I转换酶抑制剂。
Arzneimittelforschung. 1984;34(10B):1402-6.
10
Determination of 2-[N-[(S)-1-ethoxycarbonyl-3-phenylpropyl]-L-alanyl]-(1S,3S,5S)-2- azabicyclo[3.3.0]octane-3-carboxylic acid (Hoe 498) and its hydrolysis product in serum and urine.血清和尿液中2-[[(S)-1-乙氧羰基-3-苯基丙基]-L-丙氨酰]-(1S,3S,5S)-2-氮杂双环[3.3.0]辛烷-3-羧酸(Hoe 498)及其水解产物的测定
Arzneimittelforschung. 1984;34(10B):1431-5.

引用本文的文献

1
Pharmacokinetics and pharmacodynamics of a novel orally active angiotensin converting enzyme inhibitor (HOE 498) in healthy subjects.一种新型口服活性血管紧张素转换酶抑制剂(HOE 498)在健康受试者中的药代动力学和药效学。
Eur J Clin Pharmacol. 1984;27(5):577-81. doi: 10.1007/BF00556895.
2
Converting enzyme inhibitor ramipril stimulates prostacyclin synthesis by isolated rat aorta: evidence for a kinin-dependent mechanism.转化酶抑制剂雷米普利可刺激离体大鼠主动脉合成前列环素:激肽依赖性机制的证据。
Klin Wochenschr. 1986 Aug 15;64(16):742-5. doi: 10.1007/BF01734341.
3
Studies on the antihypertensive effect of single doses of the angiotensin converting enzyme inhibitor ramipril (HOE 498) in man.
单剂量血管紧张素转换酶抑制剂雷米普利(HOE 498)对人体降压作用的研究。
Eur J Clin Pharmacol. 1986;30(5):541-7. doi: 10.1007/BF00542412.
4
Effects of the new angiotensin-converting enzyme inhibitor, ramipril, in patients with essential hypertension.新型血管紧张素转换酶抑制剂雷米普利对原发性高血压患者的疗效
Klin Wochenschr. 1986 Jun 16;64(12):558-62. doi: 10.1007/BF01735319.
5
Angiotensin converting enzyme inhibitors and moderate hypertension.血管紧张素转换酶抑制剂与中度高血压
Drugs. 1990 Sep;40(3):326-45. doi: 10.2165/00003495-199040030-00002.
6
Ramipril. A review of its pharmacological properties and therapeutic efficacy in cardiovascular disorders.雷米普利。对其药理特性及在心血管疾病中的治疗效果的综述。
Drugs. 1990 Jan;39(1):110-35. doi: 10.2165/00003495-199039010-00009.