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Pharmacological receptors.

作者信息

Waud D R

出版信息

Pharmacol Rev. 1968 Jun;20(2):49-88.

PMID:4871939

Abstract

摘要

相似文献

Pharmacological receptors.药理受体

Pharmacol Rev. 1968 Jun;20(2):49-88.

The rate of action of atropine.阿托品的作用速率。

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The relationship between the drug-receptor interaction and calcium transport in smooth muscle.药物-受体相互作用与平滑肌中钙转运之间的关系。

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Ion exchange processes at the neuromuscular junction of voluntary muscle.随意肌神经肌肉接头处的离子交换过程。

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Ion size and activity at acetylcholine receptors.乙酰胆碱受体处的离子大小与活性

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Binding of five cholinergic ligands to housefly brain and Torpedo electroplax. Relationship to acetylcholine receptors.五种胆碱能配体与家蝇脑及电鳐电器官的结合。与乙酰胆碱受体的关系。

Mol Pharmacol. 1971 Jan;7(1):104-10.

[Structure-activity relationships of unsaturated esters of arecaidine and dihydroarecaidine].[槟榔次碱和二氢槟榔次碱不饱和酯的构效关系]

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Log-normal distribution of equiefective doses of norepinephrine and acetylcholine in several tissues.去甲肾上腺素和乙酰胆碱在多个组织中的等效剂量的对数正态分布。

J Pharmacol Exp Ther. 1972 May;181(2):339-45.

A snake venom phospholipase A2 with high affinity for muscarinic acetylcholine receptors acts on guinea pig ileum.一种对毒蕈碱型乙酰胆碱受体具有高亲和力的蛇毒磷脂酶A2作用于豚鼠回肠。

Toxicon. 2008 May;51(6):1008-16. doi: 10.1016/j.toxicon.2008.01.006. Epub 2008 Jan 17.

Measurement of drug-receptor dissociation constants of muscarinic agonists on intestinal smooth muscle.毒蕈碱激动剂在肠道平滑肌上的药物-受体解离常数的测定。

J Pharmacol Exp Ther. 1972 Jan;180(1):62-70.

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Fourth gaddum memorial lecture, school of pharmacy, university of london, january 1973.第四届加德姆纪念讲座，伦敦大学药学院，1973年1月

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Prostaglandin E2 glycerol ester, an endogenous COX-2 metabolite of 2-arachidonoylglycerol, induces hyperalgesia and modulates NFkappaB activity.前列腺素E2甘油酯，一种2-花生四烯酸甘油酯的内源性COX-2代谢产物，可诱导痛觉过敏并调节核因子κB活性。

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Spironolactone and its main metabolite canrenoic acid block hKv1.5, Kv4.3 and Kv7.1 + minK channels.螺内酯及其主要代谢产物坎利酮可阻断hKv1.5、Kv4.3和Kv7.1+minK通道。

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Metiamide--an orally active histamine H2-receptor antagonist. 1973.甲硫米特——一种口服活性组胺H2受体拮抗剂。1973年。

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Desensitization by noradrenaline of responses to stimulation of pre- and postsynaptic adrenoceptors.去甲肾上腺素对突触前和突触后肾上腺素能受体刺激反应的脱敏作用。

Br J Pharmacol. 1982 May;76(1):201-10. doi: 10.1111/j.1476-5381.1982.tb09207.x.

On the calcium receptor that mediates depolarization-secretion coupling at cholinergic motor nerve terminals.关于介导胆碱能运动神经末梢去极化-分泌偶联的钙受体。

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Effect of polymers of L-lysine on the cytotoxic action of diphtheria toxin.L-赖氨酸聚合物对白喉毒素细胞毒性作用的影响。

Infect Immun. 1982 Sep;37(3):1054-8. doi: 10.1128/iai.37.3.1054-1058.1982.

The relative contribution of affinity and efficacy to agonist activity: organ selectivity of noradrenaline and oxymetazoline with reference to the classification of drug receptors.亲和力和效能对激动剂活性的相对贡献：去甲肾上腺素和羟甲唑啉的器官选择性及药物受体分类

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A novel analysis of concentration-dependence of partial agonism Ring-demethylation of bupranolol results in a high affinity partial agonist (K 105) for myocardial and tracheal beta-adrenoceptors.布普诺洛尔环去甲基化产生对心肌和气管β-肾上腺素能受体具有高亲和力的部分激动剂（K 105）的部分激动剂浓度依赖性的新分析。

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