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An opioid benzodiazepine.

作者信息

Römer D, Büscher H H, Hill R C, Maurer R, Petcher T J, Zeugner H, Benson W, Finner E, Milkowski W, Thies P W

出版信息

Nature. 1982 Aug 19;298(5876):759-60. doi: 10.1038/298759a0.

DOI:10.1038/298759a0
PMID:6287271
Abstract
摘要

相似文献

1
An opioid benzodiazepine.一种阿片类苯二氮䓬类药物。
Nature. 1982 Aug 19;298(5876):759-60. doi: 10.1038/298759a0.
2
Unexpected opioid activity in a known class of drug.
Life Sci. 1982;31(12-13):1217-20. doi: 10.1016/0024-3205(82)90346-0.
3
Similar actions of kappa and mu agonists on spinal nociceptive reflexes in rats and their reversibility by naloxone.κ和μ激动剂对大鼠脊髓伤害性反射的类似作用及其被纳洛酮逆转的情况。
NIDA Res Monogr. 1986;75:461-4.
4
Delta opioid receptor selective alkaloid agonists and antagonists.
NIDA Res Monogr. 1989;95:300-1.
5
Characteristics of opioid receptors in guinea-pig cerebellum and human placenta.
Tokai J Exp Clin Med. 1986 Aug;11(3):179-84.
6
Dermorphin-related peptides from the skin of Phyllomedusa bicolor and their amidated analogs activate two mu opioid receptor subtypes that modulate antinociception and catalepsy in the rat.来自双色叶泡蛙皮肤的与皮吗啡相关的肽及其酰胺化类似物激活两种μ阿片受体亚型，这些亚型可调节大鼠的抗伤害感受和僵住症。
Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):7203-7. doi: 10.1073/pnas.89.15.7203.
7
Endogenous opioid peptides: multiple agonists and receptors.内源性阿片肽：多种激动剂和受体。
Nature. 1977 Jun 9;267(5611):495-9. doi: 10.1038/267495a0.
8
Cholinergic/opioid interaction in anterior cingulate cortex reduces the nociceptive response of vocalization in guinea pigs.前扣带回皮质中的胆碱能/阿片类相互作用降低了豚鼠发声的伤害性反应。
Brain Res. 2017 Sep 15;1671:131-137. doi: 10.1016/j.brainres.2017.07.013. Epub 2017 Jul 20.
9
Selective opioid agonist and antagonist competition for [3H]-naloxone binding in amphibian spinal cord.选择性阿片类激动剂和拮抗剂在两栖动物脊髓中对[3H]-纳洛酮结合的竞争。
Brain Res. 2000 Nov 24;884(1--2):184-91. doi: 10.1016/s0006-8993(00)02967-x.
10
Arachidonic acid modulation of [3H]naloxone specific binding to rat brain opioid receptors.花生四烯酸对[3H]纳洛酮特异性结合大鼠脑阿片受体的调节作用。
Neurobiology (Bp). 1998;6(3):323-32.

引用本文的文献

1
The combinatorial synthesis and chemical and biological evaluation of a 1,4-benzodiazepine library.一个1,4 - 苯二氮䓬文库的组合合成及化学与生物学评价
Proc Natl Acad Sci U S A. 1994 May 24;91(11):4708-12. doi: 10.1073/pnas.91.11.4708.
2
Characterization of diazepam-insensitive [3H]Ro 15-4513 binding in rodent brain and cultured cerebellar neuronal cells.啮齿动物脑和培养的小脑神经元细胞中对地西泮不敏感的[3H]Ro 15-4513结合特性
Neurochem Res. 1994 Mar;19(3):289-95. doi: 10.1007/BF00971577.
3
Kappa opioid agonists produce anxiolytic-like behavior on the elevated plus-maze.
κ阿片受体激动剂在高架十字迷宫实验中产生抗焦虑样行为。
Psychopharmacology (Berl). 1995 Apr;118(4):444-50. doi: 10.1007/BF02245945.
4
Behavioral effects of a novel kappa opioid analgesic, U-50488, in rats and rhesus monkeys.新型κ阿片类镇痛药U-50488对大鼠和恒河猴的行为影响。
Psychopharmacology (Berl). 1985;85(3):309-14. doi: 10.1007/BF00428193.
5
On the mechanisms of kappa-opioid-induced diuresis.关于κ-阿片类药物诱导利尿的机制
Br J Pharmacol. 1986 Nov;89(3):593-8. doi: 10.1111/j.1476-5381.1986.tb11160.x.
6
Inhibitory influences of the adrenal steroid, 3 alpha, 5 alpha-tetrahydrodeoxycorticosterone [correction of tetrahydroxycorticosterone] on aggression and defeat-induced analgesia in mice.
Psychopharmacology (Berl). 1988;95(4):488-92. doi: 10.1007/BF00172960.
7
The contributions of mu-, delta- and kappa-opioid receptors to the actions of endogenous opioids on spinal reflexes in the rabbit.μ、δ和κ阿片受体对内源性阿片类物质对家兔脊髓反射作用的贡献。
Br J Pharmacol. 1987 Jul;91(3):579-89. doi: 10.1111/j.1476-5381.1987.tb11251.x.
8
Determination of the receptor selectivity of opioid agonists in the guinea-pig ileum and mouse vas deferens by use of beta-funaltrexamine.使用β-芬太尼环唑来测定豚鼠回肠和小鼠输精管中阿片类激动剂的受体选择性。
Br J Pharmacol. 1985 Dec;86(4):899-904. doi: 10.1111/j.1476-5381.1985.tb11112.x.
9
Motivational properties of kappa and mu opioid receptor agonists studied with place and taste preference conditioning.通过位置偏好和味觉偏好条件反射研究κ和μ阿片受体激动剂的动机特性。
Psychopharmacology (Berl). 1985;86(3):274-80. doi: 10.1007/BF00432213.
10
Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats.人类滥用的药物会优先提高自由活动大鼠中脑边缘系统的突触多巴胺浓度。
Proc Natl Acad Sci U S A. 1988 Jul;85(14):5274-8. doi: 10.1073/pnas.85.14.5274.