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・ 6-Acetoxydihydrotheaspirane
・ 6-Acetyl-2,3,4,5-tetrahydropyridine
・ 6-acetylglucose deacetylase
・ 6-aminohexanoate-cyclic-dimer hydrolase
・ 6-aminohexanoate-dimer hydrolase
・ 6-APA
・ 6-APB
・ 6-APDB
・ 6-APT
・ 6-Benzylaminopurine
・ 6-bolt main
・ 6-Br-APB
・ 6-carboxyhexanoate—CoA ligase
・ 6-carboxytetrahydropterin synthase
・ 6-CAT
6-Chloro-5-ethoxy-N-(pyridin-2-yl)indoline-1-carboxamide
・ 6-Chloro-MDMA
・ 6-cube
・ 6-cubic honeycomb
・ 6-demicube
・ 6-demicubic honeycomb
・ 6-Deoxy-5-ketofructose 1-phosphate synthase
・ 6-Deoxyerythronolide B synthase
・ 6-Diazo-5-oxo-L-norleucine
・ 6-digit UNESCO nomenclature
・ 6-EAPB
・ 6-endo-hydroxycineole dehydrogenase
・ 6-Fluoro-AMT
・ 6-Fluoro-DMT
・ 6-Fluoronorepinephrine


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6-Chloro-5-ethoxy-N-(pyridin-2-yl)indoline-1-carboxamide : ウィキペディア英語版
6-Chloro-5-ethoxy-N-(pyridin-2-yl)indoline-1-carboxamide

6-Chloro-5-ethoxy-''N''-(pyridin-2-yl)indoline-1-carboxamide (CEPC) is a drug which acts as a potent and selective antagonist for the serotonin 5-HT2C receptor. In animal studies it was found to potentiate the conditioned place preference induced by low-dose amphetamine, demonstrating that 5-HT2C-mediated disinhibition of dopamine release can cause interactions with dopaminergic drugs.〔McCorvy JD, Harland AA, Maglathlin R, Nichols DE. A 5-HT(2C) receptor antagonist potentiates a low dose amphetamine-induced conditioned place preference. ''Neuroscience Letters''. 2011 Nov 7;505(1):10-3. PMID 21827831〕
==See also==

* RS-102,221
* SB-242,084

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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