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・ 7,14-Dibenzpyrenequinone
・ 7,62 ITKK 31 VKT
・ 7,8-didemethyl-8-hydroxy-5-deazariboflavin synthase
・ 7,8-Dihydroneopterin triphosphate
・ 7,8-Dihydroxyflavone
・ 7,8-dihydroxykynurenate 8,8a-dioxygenase
・ 7,N,N-TMT
・ 7-0-5
・ 7-1-1
・ 7-30 Waters
・ 7-ACA
・ 7-Aminoactinomycin D
・ 7-Bone Roast
・ 7-carboxy-7-deazaguanine synthase
・ 7-Chloro-L-tryptophan oxidase
7-Chlorokynurenic acid
・ 7-cube
・ 7-cubic honeycomb
・ 7-cyano-7-deazaguanine synthase
・ 7-day SEC yield
・ 7-Dehydrocholesterol
・ 7-Dehydrocholesterol reductase
・ 7-Dehydrodesmosterol
・ 7-Dehydrositosterol
・ 7-demicube
・ 7-demicubic honeycomb
・ 7-Deoxyloganetic acid
・ 7-Deoxyloganic acid
・ 7-deoxyloganin 7-hydroxylase
・ 7-Dimethylallyltryptophan synthase


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7-Chlorokynurenic acid : ウィキペディア英語版
7-Chlorokynurenic acid

7-Chlorokynurenic acid (7-CKA) is a drug that acts as a potent and selective noncompetitive antagonist of the glycine site of the NMDA receptor. It produces ketamine-like rapid antidepressant effects in animal models of depression. However, 7-CKA is unable to cross the blood-brain-barrier, and for this reason, is unsuitable for clinical use. As a result, a centrally-penetrant prodrug of 7-CKA, 4-chlorokynurenine (AV-101), has been developed for use in humans, and is being studied in clinical trials as a potential treatment for major depressive disorder.〔 In addition to antagonizing the NMDA receptor, 7-CKA also acts as a potent inhibitor of the reuptake of glutamate into synaptic vesicles (or as a vesicular glutamate reuptake inhibitor), an action that it mediates via competitive blockade of vesicular glutamate transporters (Ki = 0.59 mM).
==See also==

* 5,7-Dichlorokynurenic acid
* Evans blue
* Kynurenic acid
* Xanthurenic acid

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「7-Chlorokynurenic acid」の詳細全文を読む



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