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[3H]Verapamil binding sites in brain and skeletal muscle: regulation by calcium.

作者信息

Reynolds I J, Gould R J, Snyder S H

出版信息

Eur J Pharmacol. 1983 Nov 25;95(3-4):319-21. doi: 10.1016/0014-2999(83)90655-6.

DOI:10.1016/0014-2999(83)90655-6
PMID:6317417
Abstract
摘要

相似文献

1
[3H]Verapamil binding sites in brain and skeletal muscle: regulation by calcium.脑和骨骼肌中[3H]维拉帕米结合位点:钙的调节作用
Eur J Pharmacol. 1983 Nov 25;95(3-4):319-21. doi: 10.1016/0014-2999(83)90655-6.
2
Pharmacology of (-) [3H]D888 (desmethoxyverapamil) binding sites in rat skeletal membranes.大鼠骨骼肌膜中(-)[3H]D888(去甲氧基维拉帕米)结合位点的药理学
Proc West Pharmacol Soc. 1987;30:127-30.
3
Properties of receptors for the Ca2+-channel blocker verapamil in transverse-tubule membranes of skeletal muscle. Stereospecificity, effect of Ca2+ and other inorganic cations, evidence for two categories of sites and effect of nucleoside triphosphates.骨骼肌横管膜中钙通道阻滞剂维拉帕米受体的特性。立体特异性、钙离子及其他无机阳离子的作用、两类位点的证据以及核苷三磷酸的作用。
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4
Target size analysis and molecular properties of Ca2+ channels labelled with [3H]verapamil.
Eur J Biochem. 1984 May 15;141(1):177-86. doi: 10.1111/j.1432-1033.1984.tb08172.x.
5
(-)-[3H] desmethoxyverapamil labels multiple calcium channel modulator receptors in brain and skeletal muscle membranes: differentiation by temperature and dihydropyridines.(-)-[³H]去甲氧基维拉帕米标记脑和骨骼肌膜中的多种钙通道调节剂受体:通过温度和二氢吡啶进行区分。
J Pharmacol Exp Ther. 1986 Jun;237(3):731-8.
6
Calcium antagonist receptors in cardiomyopathic hamster: selective increases in heart, muscle, brain.心肌病仓鼠中的钙拮抗剂受体:心脏、肌肉、大脑中的选择性增加。
Science. 1986 Apr 25;232(4749):515-8. doi: 10.1126/science.3008330.
7
Effects of diltiazem and verapamil on (+)-PN 200-110 binding kinetics in dog cardiac membranes.
Eur J Pharmacol. 1992 Apr 22;214(2-3):127-32. doi: 10.1016/0014-2999(92)90109-h.
8
Tricyclic antidepressants and calcium channel blockers: interactions at the (-)-desmethoxyverapamil binding site and the serotonin transporter.三环类抗抑郁药与钙通道阻滞剂:在(-)-去甲氧基维拉帕米结合位点和血清素转运体上的相互作用。
Eur J Pharmacol. 1988 Oct 11;155(1-2):1-9. doi: 10.1016/0014-2999(88)90396-2.
9
[3H]-verapamil binding to rat cardiac sarcolemmal membrane fragments; an effect of ischaemia.[3H] -维拉帕米与大鼠心肌肌膜碎片的结合;缺血的影响。
Br J Pharmacol. 1987 Jan;90(1):99-109. doi: 10.1111/j.1476-5381.1987.tb16829.x.
10
High affinity binding of 3H-verapamil to rat brain synaptic membrane is antagonized by pyrethroid insecticides.拟除虫菊酯类杀虫剂可拮抗3H-维拉帕米与大鼠脑突触膜的高亲和力结合。
J Environ Sci Health B. 1994 Sep;29(5):855-71. doi: 10.1080/03601239409372907.

引用本文的文献

1
(-)-3H-desmethoxyverapamil labelling of putative calcium channels in brain: autoradiographic distribution and allosteric coupling to 1,4-dihydropyridine and diltiazem binding sites.脑内假定钙通道的(-)-3H-去甲氧基维拉帕米标记:放射自显影分布及与1,4-二氢吡啶和地尔硫䓬结合位点的变构偶联
Naunyn Schmiedebergs Arch Pharmacol. 1984 Sep;327(2):183-7. doi: 10.1007/BF00500915.
2
Interactions between a "calcium channel agonist", Bay K 8644, and calcium antagonists differentiate calcium antagonist subgroups in K+-depolarized smooth muscle.“钙通道激动剂” Bay K 8644 与钙拮抗剂之间的相互作用可区分钾离子去极化平滑肌中的钙拮抗剂亚组。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Nov;328(1):69-75. doi: 10.1007/BF00496109.
3
Effects of some antianginal and vasodilating drugs on sodium influx and on the binding of 3H-batrachotoxinin-A 20-alpha-benzoate and 3H-tetracaine.
某些抗心绞痛和血管舒张药物对钠内流以及对3H-蟾毒素-A 20-α-苯甲酸酯和3H-丁卡因结合的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1987 Feb;335(2):176-82. doi: 10.1007/BF00177720.
4
Stereoisomers of calcium antagonists discriminate between coronary vascular and myocardial sites.钙拮抗剂的立体异构体可区分冠状动脉血管部位和心肌部位。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Feb;337(2):213-9. doi: 10.1007/BF00169250.
5
[3H]-verapamil binding to rat cardiac sarcolemmal membrane fragments; an effect of ischaemia.[3H] -维拉帕米与大鼠心肌肌膜碎片的结合;缺血的影响。
Br J Pharmacol. 1987 Jan;90(1):99-109. doi: 10.1111/j.1476-5381.1987.tb16829.x.
6
Calcium antagonists and their mode of action: an historical overview.钙拮抗剂及其作用方式:历史概述。
Br J Clin Pharmacol. 1986;21 Suppl 2(Suppl 2):97S-107S. doi: 10.1111/j.1365-2125.1986.tb02859.x.
7
Direct activation of Ca2+ channels by palmitoyl carnitine, a putative endogenous ligand.棕榈酰肉碱(一种假定的内源性配体)对钙离子通道的直接激活作用。
Br J Pharmacol. 1987 Oct;92(2):457-68. doi: 10.1111/j.1476-5381.1987.tb11343.x.