SCH 29851（一种潜在的非镇静性抗组胺药）的中枢神经系统特性评估。1984年。 - Suppr

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Evaluation of the CNS properties of SCH 29851, a potential non-sedating antihistamine. 1984.

作者信息

Barnett A, Iorio L C, Kreutner W, Tozzi S, Ahn H S, Gulbenkian A

出版信息

Agents Actions. 1994 Dec;43(3-4):149-56; discussion 157. doi: 10.1007/BF01986682.

DOI:10.1007/BF01986682

PMID:7725966

Abstract

摘要

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Evaluation of the CNS properties of SCH 29851, a potential non-sedating antihistamine. 1984.SCH 29851（一种潜在的非镇静性抗组胺药）的中枢神经系统特性评估。1984年。

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本文引用的文献

Properties of maximal seizures, and their alteration by anticonvulant drugs and other agents.最大发作的特性，以及抗惊厥药物和其他药剂对其的改变。

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Performance studies with the H1-histamine receptor antagonists, astemizole and terfenadine.使用H1组胺受体拮抗剂阿司咪唑和特非那定的性能研究。

Br J Clin Pharmacol. 1982 Feb;13(2):199-202. doi: 10.1111/j.1365-2125.1982.tb01356.x.

In vivo pharmacology of astemizole, a new type of H1-antihistaminic compound.新型H1抗组胺化合物阿司咪唑的体内药理学

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Protection from shock-induced seizures as a measure of hypnotic potency of drugs.防止电击诱发癫痫作为衡量药物催眠效力的一种方法。

Pharmacol Biochem Behav. 1980 Aug;13(2):299-301. doi: 10.1016/0091-3057(80)90088-x.

Clinical investigation of terfenadine, a non-sedating antihistamine.特非那定（一种非镇静性抗组胺药）的临床研究。

Ann Allergy. 1980 Feb;44(2):71-5.

The abdominal constriction response and its suppression by analgesic drugs in the mouse.小鼠的腹部收缩反应及其被镇痛药抑制的情况。

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Central versus peripheral anticholinergic activity as assessed by two in vivo procedures in mice.通过两种小鼠体内实验方法评估中枢与外周抗胆碱能活性。

J Pharm Sci. 1975 Jun;64(6):1066-8. doi: 10.1002/jps.2600640650.

Histamine H1 receptors identified in mammalian brain membranes with [3H]mepyramine.用[3H]美吡拉敏在哺乳动物脑膜中鉴定出组胺H1受体。

Proc Natl Acad Sci U S A. 1978 Dec;75(12):6290-4. doi: 10.1073/pnas.75.12.6290.

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