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The substituted benzamides--a novel class of dopamine antagonists.

作者信息

Jenner P, Marsden C D

出版信息

Life Sci. 1979 Aug 6;25(6):479-85. doi: 10.1016/0024-3205(79)90559-9.

DOI:10.1016/0024-3205(79)90559-9
PMID:40086
Abstract
摘要

相似文献

1
The substituted benzamides--a novel class of dopamine antagonists.
Life Sci. 1979 Aug 6;25(6):479-85. doi: 10.1016/0024-3205(79)90559-9.
2
Substituted benzamides as cerebral dopamine antagonists in rodents.
Neuropharmacology. 1977 May;16(5):333-42. doi: 10.1016/0028-3908(77)90070-3.
3
Effect of substituted benzamides on prolactin secretion in the rat.取代苯甲酰胺对大鼠催乳素分泌的影响。
Biol Psychiatry. 1992 Apr 15;31(8):827-31. doi: 10.1016/0006-3223(92)90314-p.
4
[Interactions of 5 benzamides with ethanol on various psychopharmacology tests].[5种苯甲酰胺与乙醇在各种精神药理学测试中的相互作用]
Pathol Biol (Paris). 1985 Mar;33(3):183-8.
5
[Four benzamides (metoclopramide, sulpiride, sultopride and tiapride) effects on the oestrus cycle of the female rat: a comparative statistical study (author's transl)].[四种苯甲酰胺(胃复安、舒必利、舒托必利和硫必利)对雌性大鼠发情周期的影响:一项比较性统计研究(作者译)]
J Pharmacol. 1981 Jan-Mar;12(1):27-36.
6
The effects of substituted benzamides on frog rectus abdominis.取代苯甲酰胺对青蛙腹直肌的作用。
Eur J Pharmacol. 1980 Nov 7;68(1):55-60. doi: 10.1016/0014-2999(80)90060-6.
7
[Neurotropic anisamides (author's transl)].[亲神经茴香酰胺类(作者译)]
Sem Hop. 1979;55(39-40):1858-65.
8
Effect of long-term dosing with tiapride on brain dopamine receptors and metabolism in rats. Comparative study with sulpiride and haloperidol.舒必利长期给药对大鼠脑多巴胺受体和代谢的影响。与氟哌啶醇的对比研究。 需注意,你提供的英文原文中“tiapride”(硫必利),译文里开头误写成了“舒必利”(sulpiride),正确译文应为: 硫必利长期给药对大鼠脑多巴胺受体和代谢的影响。与舒必利和氟哌啶醇的对比研究。
Jpn J Pharmacol. 1987 Aug;44(4):393-403. doi: 10.1254/jjp.44.393.
9
Comparison of effects of tiapride and sulpiride on D-1, D-2, D-3 and D-4 subtypes of dopamine receptors in rat striatal and bovine caudate nucleus membranes.
Jpn J Pharmacol. 1986 Jul;41(3):419-23. doi: 10.1254/jjp.41.419.
10
Substituted benzamide drugs as selective neuroleptic agents.作为选择性抗精神病药物的取代苯甲酰胺类药物。
Neuropharmacology. 1981 Dec;20(12B):1285-93.

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Discriminative stimulus properties of the atypical antipsychotic amisulpride: comparison to its isomers and to other benzamide derivatives, antipsychotic, antidepressant, and antianxiety drugs in C57BL/6 mice.非典型抗精神病药氨磺必利的鉴别刺激特性:与异构体和其他苯甲酰胺衍生物、抗精神病药、抗抑郁药和抗焦虑药在 C57BL/6 小鼠中的比较。
Psychopharmacology (Berl). 2017 Dec;234(23-24):3507-3520. doi: 10.1007/s00213-017-4738-y. Epub 2017 Sep 18.
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Addiction pharmacogenetics: a systematic review of the genetic variation of the dopaminergic system.成瘾药物遗传学:多巴胺能系统基因变异的系统评价
Psychiatr Genet. 2015 Oct;25(5):181-93. doi: 10.1097/YPG.0000000000000095.
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A review of the discovery, pharmacological characterization, and behavioral effects of the dopamine D2-like receptor antagonist eticlopride.
多巴胺D2样受体拮抗剂依托必利的发现、药理学特性及行为效应综述。
CNS Neurosci Ther. 2008 Fall;14(3):248-62. doi: 10.1111/j.1755-5949.2008.00047.x.
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Preventing prolonged post-operative ileus in gastric cancer patients undergoing gastrectomy and intra-peritoneal chemotherapy.预防接受胃切除术和腹腔内化疗的胃癌患者术后出现长时间肠梗阻。
World J Gastroenterol. 2005 Aug 21;11(31):4776-81. doi: 10.3748/wjg.v11.i31.4776.
5
A risk-benefit assessment of sulpiride in the treatment of schizophrenia.
Drug Saf. 1996 May;14(5):288-98. doi: 10.2165/00002018-199614050-00003.
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Dopaminergic control of gastric mucosal blood flow in humans. A study with endoscopic laser Doppler flowmetry coupled with gastric submucosal drug injection.多巴胺能对人体胃黏膜血流的调控。一项内镜激光多普勒血流仪联合胃黏膜下药物注射的研究。
Dig Dis Sci. 1993 Jul;38(7):1169-74. doi: 10.1007/BF01296063.
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Characterization of the 5-hydroxytryptamine receptor type involved in inhibition of spontaneous activity of human isolated colonic circular muscle.参与抑制人离体结肠环行肌自发活动的5-羟色胺受体类型的鉴定
Br J Pharmacol. 1994 Sep;113(1):143-50. doi: 10.1111/j.1476-5381.1994.tb16186.x.
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Differences in effects of sultopride and sulpiride on dopamine turnover in rat brain.舒托必利和舒必利对大鼠脑内多巴胺代谢的影响差异。
Neurochem Res. 1995 Jan;20(1):95-9. doi: 10.1007/BF00995158.
9
Metergoline and cyproheptadine suppress prolactin release by a non-5-hydroxytryptaminergic, non-dopaminergic mechanism.美麦角林和赛庚啶通过非5-羟色胺能、非多巴胺能机制抑制催乳素释放。
Br J Pharmacol. 1980 Sep;70(1):5-7. doi: 10.1111/j.1476-5381.1980.tb10896.x.
10
Metoclopramide and sulpiride as selective blocking agents of pre- and postsynaptic dopamine receptors.胃复安和舒必利作为突触前和突触后多巴胺受体的选择性阻断剂。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jun;312(2):145-50. doi: 10.1007/BF00569723.