dimaprit is frequently utilized as a selective agonist in pharmacological research.
二甲帕里特在药理学研究中常被用作选择性激动剂。
the study aimed to investigate the specific effects of dimaprit on isolated cardiac tissue.
该研究旨在调查二甲帕里特对离体心脏组织的具体影响。
scientists observed that dimaprit exhibits a high binding affinity for the h2 receptor.
科学家观察到二甲帕里特对h2受体表现出高结合亲和力。
researchers administered dimaprit to the test subjects to simulate histamine-like responses.
研究人员给受试对象施用了二甲帕里特以模拟类似组胺的反应。
structurally, dimaprit is an analog of histamine designed to target specific receptors.
在结构上，二甲帕里特是一种旨在靶向特定受体的组胺类似物。
the protocol requires the careful preparation of a dimaprit solution before the experiment.
该方案要求在实验前仔细配制二甲帕里特溶液。
unlike histamine, dimaprit shows minimal activity at the h1 receptor sites.
与组胺不同，二甲帕里特在h1受体位点显示的活性极低。
previous literature has extensively documented the pharmacodynamic properties of dimaprit.
以往的文献广泛记载了二甲帕里特的药效学特性。
the application of dimaprit resulted in a dose-dependent relaxation of vascular smooth muscle.
二甲帕里特的应用导致血管平滑肌产生剂量依赖性舒张。
investigators compared the efficacy of dimaprit against other known h2 agonists.
调查人员比较了二甲帕里特与其他已知h2激动剂的功效。
for accurate results, store the dimaprit compound in a cool and dark environment.
为了获得准确的结果，请将二甲帕里特化合物储存在阴凉黑暗的环境中。
the antagonist effectively blocked the physiological responses induced by dimaprit infusion.
该��抗剂有效地阻断了由输注二甲帕里特引起的生理反应。
dimaprit is frequently utilized as a selective agonist in pharmacological research.
二甲帕里特在药理学研究中常被用作选择性激动剂。
the study aimed to investigate the specific effects of dimaprit on isolated cardiac tissue.
该研究旨在调查二甲帕里特对离体心脏组织的具体影响。
scientists observed that dimaprit exhibits a high binding affinity for the h2 receptor.
科学家观察到二甲帕里特对h2受体表现出高结合亲和力。
researchers administered dimaprit to the test subjects to simulate histamine-like responses.
研究人员给受试对象施用了二甲帕里特以模拟类似组胺的反应。
structurally, dimaprit is an analog of histamine designed to target specific receptors.
在结构上，二甲帕里特是一种旨在靶向特定受体的组胺类似物。
the protocol requires the careful preparation of a dimaprit solution before the experiment.
该方案要求在实验前仔细配制二甲帕里特溶液。
unlike histamine, dimaprit shows minimal activity at the h1 receptor sites.
与组胺不同，二甲帕里特在h1受体位点显示的活性极低。
previous literature has extensively documented the pharmacodynamic properties of dimaprit.
以往的文献广泛记载了二甲帕里特的药效学特性。
the application of dimaprit resulted in a dose-dependent relaxation of vascular smooth muscle.
二甲帕里特的应用导致血管平滑肌产生剂量依赖性舒张。
investigators compared the efficacy of dimaprit against other known h2 agonists.
调查人员比较了二甲帕里特与其他已知h2激动剂的功效。
for accurate results, store the dimaprit compound in a cool and dark environment.
为了获得准确的结果，请将二甲帕里特化合物储存在阴凉黑暗的环境中。
the antagonist effectively blocked the physiological responses induced by dimaprit infusion.
该��抗剂有效地阻断了由输注二甲帕里特引起的生理反应。
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