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Differential effects of protein-modifying reagents on receptor binding of opiate agonists and antagonists.

作者信息

Pasternak G W, Wilson H A, Snyder S H

出版信息

Mol Pharmacol. 1975 May;11(3):340-51.

PMID:49846
Abstract
摘要

相似文献

1
Differential effects of protein-modifying reagents on receptor binding of opiate agonists and antagonists.
Mol Pharmacol. 1975 May;11(3):340-51.
2
Differentiation of opiate agonist and antagonist receptor binding by protein modifying reagents.
Nature. 1975 Feb 6;253(5491):448-50. doi: 10.1038/253448a0.
3
Opiate agonists and antagonists discriminated by receptor binding in brain.通过大脑中的受体结合来区分的阿片类激动剂和拮抗剂。
Science. 1973 Dec 28;182(4119):1359-61. doi: 10.1126/science.182.4119.1359.
4
Selective enhancement of [3H]opiate agonist binding by divalent cations.二价阳离子对[3H]阿片类激动剂结合的选择性增强作用。
Mol Pharmacol. 1975 Nov;11(6):735-44.
5
Receptor binding and pharmacological activity of opiates in the guinea-pig intestine.阿片类药物在豚鼠肠道中的受体结合及药理活性
J Pharmacol Exp Ther. 1975 Jul;194(1):205-19.
6
Irreversible opiate agonists and antagonists. II. Evidence against a bivalent mechanism of action for opiate azines and diacylhydrazones.不可逆阿片类激动剂和拮抗剂。II. 反对阿片嗪和二酰基腙二价作用机制的证据。
J Pharmacol Exp Ther. 1985 Dec;235(3):839-45.
7
Temperature and ionic influences on opiate receptor binding.温度和离子对阿片受体结合的影响。
Mol Pharmacol. 1976 Nov;12(6):977-86.
8
Interactions of narcotic antagonists with receptor sites.麻醉拮抗剂与受体位点的相互作用。
Adv Biochem Psychopharmacol. 1973;8(0):471-81.
9
Irreversible opiate agonists and antagonists. III. Phenylhydrazone derivatives of naloxone and oxymorphone.不可逆阿片类激动剂和拮抗剂。III. 纳洛酮和羟吗啡酮的苯腙衍生物。
J Pharmacol Exp Ther. 1985 Dec;235(3):846-50.
10
Selected cysteine residues in transmembrane domains of mu-opioid receptor are critical for effects of sulfhydryl reagents.μ-阿片受体跨膜结构域中选定的半胱氨酸残基对巯基试剂的作用至关重要。
J Pharmacol Exp Ther. 2000 Apr;293(1):113-20.

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Molecular mechanisms of inverse agonism via κ-opioid receptor-G protein complexes.通过κ-阿片受体-G蛋白复合物产生反向激动作用的分子机制。
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Mechanistic insights into the allosteric modulation of opioid receptors by sodium ions.钠离子对阿片受体变构调节的机制性见解。
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Radioreceptor assay of narcotic analgesics in serum.血清中麻醉性镇痛药的放射受体测定。
Pharm Res. 1984 Sep;1(5):209-14. doi: 10.1023/A:1016369229440.
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The opiate receptors.
Neurochem Res. 1976 Feb;1(1):3-28. doi: 10.1007/BF00965627.
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Mu opioids and their receptors: evolution of a concept.μ 阿片类药物及其受体:概念的演变。
Pharmacol Rev. 2013 Sep 27;65(4):1257-317. doi: 10.1124/pr.112.007138. Print 2013.
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Opioids and their receptors: Are we there yet?阿片类药物及其受体:我们做到了吗?
Neuropharmacology. 2014 Jan;76 Pt B(0 0):198-203. doi: 10.1016/j.neuropharm.2013.03.039. Epub 2013 Apr 26.
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Effect of phosphoric acid on the degradation of human dentin matrix.磷酸对人牙本质基质降解的影响。
J Dent Res. 2013 Jan;92(1):87-91. doi: 10.1177/0022034512466264. Epub 2012 Oct 26.
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A concise synthesis of pawhuskin A.爪哇素 A 的简明合成。
J Nat Prod. 2008 Nov;71(11):1949-52. doi: 10.1021/np800351c. Epub 2008 Oct 15.
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Inactivation of the purified bovine mu opioid receptor by sulfhydryl reagents.巯基试剂对纯化的牛μ阿片受体的失活作用。
Neurochem Res. 1999 Jan;24(1):37-42. doi: 10.1023/a:1020923928936.
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Libraries from libraries: generation and comparison of screening profiles.
Mol Divers. 1996 Oct;2(1-2):41-5. doi: 10.1007/BF01718699.