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The interaction of bis-pyridinium oximes with mouse brain muscarinic receptor.

作者信息

Amitai G, Kloog Y, Balderman D, Sokolovsky M

出版信息

Biochem Pharmacol. 1980 Feb 15;29(4):483-8. doi: 10.1016/0006-2952(80)90366-4.

DOI:10.1016/0006-2952(80)90366-4
PMID:7370045
Abstract
摘要

相似文献

1
The interaction of bis-pyridinium oximes with mouse brain muscarinic receptor.
Biochem Pharmacol. 1980 Feb 15;29(4):483-8. doi: 10.1016/0006-2952(80)90366-4.
2
Synthesis of pyridinium analogues of acetylcholine and their interactions with intestinal muscarinic receptors.乙酰胆碱吡啶类似物的合成及其与肠道毒蕈碱受体的相互作用。
J Med Chem. 1979 Feb;22(2):177-80. doi: 10.1021/jm00188a010.
3
Interactions of bisquaternary pyridine salts (H-oximes) with cholinergic receptors.双季铵吡啶盐(H-肟)与胆碱能受体的相互作用。
Arch Toxicol. 1983 Nov;54(3):171-9. doi: 10.1007/BF01239201.
4
Synthesis and muscarinic M3 pharmacological activities of 1-azabicyclo[2.2.2]octan-3-one oxime derivatives.1-氮杂双环[2.2.2]辛烷-3-酮肟衍生物的合成及其毒蕈碱M3药理活性
Bioorg Med Chem. 1996 Feb;4(2):239-45. doi: 10.1016/0968-0896(96)00035-1.
5
Sites of action of phencyclidine. III. Interactions with muscarinic receptors.苯环利定的作用位点。III. 与毒蕈碱受体的相互作用。
Mol Pharmacol. 1980 Sep;18(2):179-84.
6
Calcium and the muscarinic receptor.
Gen Pharmacol. 1976 Aug;7(2-3):133-40. doi: 10.1016/0306-3623(76)90049-5.
7
Structure-activity relationship of mono- and bisquaternary pyridines in regard to their parasympatholytic effects.
Toxicol Appl Pharmacol. 1972 Nov;23(3):443-54. doi: 10.1016/0041-008x(72)90046-4.
8
Apparent activity of 5-methylfurmethide at muscarinic receptors.5-甲基糠甲醚在毒蕈碱受体上的表观活性。
Arch Int Pharmacodyn Ther. 1980 Nov;248(1):69-75.
9
Interaction of phencyclidine and its new adamantyl derivatives with muscarinic receptors.苯环利定及其新型金刚烷基衍生物与毒蕈碱受体的相互作用。
Life Sci. 1980 Jan 14;26(2):89-95. doi: 10.1016/0024-3205(80)90051-x.
10
Pre- and postsynaptic effects of muscarinic agonists in the guinea-pig ileum.毒蕈碱激动剂对豚鼠回肠的突触前和突触后效应。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Nov;314(3):259-66. doi: 10.1007/BF00498547.

引用本文的文献

1
Comparison of several oximes on reactivation of soman-inhibited blood, brain and tissue cholinesterase activity in rats.几种肟类化合物对大鼠体内梭曼抑制的血液、脑和组织胆碱酯酶活性的重新激活作用比较。
Arch Toxicol. 1993;67(9):637-46. doi: 10.1007/BF01974071.
2
Comparison of the therapeutic effects and pharmacokinetics of HI-6, HLö-7, HGG-12, HGG-42 and obidoxime following non-reactivatable acetylcholinesterase inhibition in rats.大鼠体内非可复性乙酰胆碱酯酶抑制后HI-6、HLö-7、HGG-12、HGG-42及双复磷治疗效果与药代动力学的比较
Arch Toxicol. 1994;68(4):224-30. doi: 10.1007/s002040050061.
3
Interactions of bisquaternary pyridine salts (H-oximes) with cholinergic receptors.
双季铵吡啶盐(H-肟)与胆碱能受体的相互作用。
Arch Toxicol. 1983 Nov;54(3):171-9. doi: 10.1007/BF01239201.
4
Effects of obidoxime chloride on native and sarin-poisoned frog neuromuscular junctions.氯解磷定对正常及沙林中毒青蛙神经肌肉接头的作用。
Pflugers Arch. 1984 May;401(1):84-90. doi: 10.1007/BF00581537.
5
Effect of the bispyridinium compounds HGG12, HGG42, and obidoxime on synaptic transmission and NAD(P)H-fluorescence in the superior cervical ganglion of the rat in vitro.双吡啶化合物HGG12、HGG42和氯解磷定对大鼠颈上神经节突触传递及体外烟酰胺腺嘌呤二核苷酸(磷酸)(NAD(P)H)荧光的影响。
Arch Toxicol. 1981 Jun;47(3):217-32. doi: 10.1007/BF00368682.
6
Reversible and irreversible inhibition of rat brain muscarinic receptors is related to different substitutions on bisquaternary pyridinium oximes.
Arch Toxicol. 1985 Oct;58(1):37-9. doi: 10.1007/BF00292614.
7
Both presynaptic nicotinic-like and muscarinic-like autoreceptors regulate acetylcholine release at an identified neuro-neuronal synapse of Aplysia.突触前烟碱样和毒蕈碱样自身受体均调节海兔特定神经-神经元突触处的乙酰胆碱释放。
Pflugers Arch. 1988 Apr;411(4):345-52. doi: 10.1007/BF00587712.
8
Receptor-mediated presynaptic facilitation of quantal release of acetylcholine induced by pralidoxime in Aplysia.受体介导的解磷定诱导的海兔乙酰胆碱量子释放的突触前易化作用。
Cell Mol Neurobiol. 1990 Sep;10(3):383-404. doi: 10.1007/BF00711182.