5,7-Dichlorokynurenic acid (BioDeep_00000174772)

   

human metabolite blood metabolite


代谢物信息卡片


5,7-Dichloro-4-oxo-1,4-dihydroquinoline-2-carboxylate

化学式: C10H5Cl2NO3 (256.9646)
中文名称: 5,7-二氯尿嘧啶酸
谱图信息: 最多检出来源 Homo sapiens(blood) 93.2%

分子结构信息

SMILES: C1=C(C=C(C2=C1NC(=CC2=O)C(=O)O)Cl)Cl
InChI: InChI=1S/C10H5Cl2NO3/c11-4-1-5(12)9-6(2-4)13-7(10(15)16)3-8(9)14/h1-3H,(H,13,14)(H,15,16)

描述信息

D018377 - Neurotransmitter Agents > D018683 - Excitatory Amino Acid Agents > D018691 - Excitatory Amino Acid Antagonists
5,7-Dichlorokynurenic acid (5,7-DCKA) is a selective and competitive antagonist of the glycine site on NMDA receptor with a KB of 65 nM. 5,7-Dichlorokynurenic acid, a derivative of kynurenic acid, reduced NMDA-induced neuron injury in rat cortical cell cultures[1].

同义名列表

10 个代谢物同义名

5,7-Dichloro-4-oxo-1,4-dihydroquinoline-2-carboxylate; 5,7-dichloro-4-hydroxyquinoline-2-carboxylic acid; Dcka, 5,7-dichlorokynurenate; 5,7-Dichloroquinurenic acid; 5,7-Dichlorokynurenic acid; 57-Dichlorokynurenic acid; 5,7-Dichlorokynurenate; 57-Dichlorokynurenate; C10H5cl2NO3; 5,7-DCKA



数据库引用编号

9 个数据库交叉引用编号

分类词条

相关代谢途径

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代谢反应

0 个相关的代谢反应过程信息。

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1 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

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亚细胞结构定位 关联基因列表


文献列表

  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • Marco Milanese, Cristina Romei, Cesare Usai, Martina Oliveri, Luca Raiteri. A new function for glycine GlyT2 transporters: Stimulation of γ-aminobutyric acid release from cerebellar nerve terminals through GAT1 transporter reversal and Ca(2+)-dependent anion channels. Journal of neuroscience research. 2014 Mar; 92(3):398-408. doi: 10.1002/jnr.23321. [PMID: 24273061]
  • Lauren Debrouse, Benita Hurd, Carly Kiselycznyk, Aaron Plitt, Alyssa Todaro, Masayoshi Mishina, Seth G N Grant, Marguerite Camp, Ozge Gunduz-Cinar, Andrew Holmes. Probing the modulation of acute ethanol intoxication by pharmacological manipulation of the NMDAR glycine co-agonist site. Alcoholism, clinical and experimental research. 2013 Feb; 37(2):223-33. doi: 10.1111/j.1530-0277.2012.01922.x. [PMID: 22934986]
  • Yi Han, Ping Li, Malcolm M Slaughter. Selective antagonism of rat inhibitory glycine receptor subunits. The Journal of physiology. 2004 Feb; 554(Pt 3):649-58. doi: 10.1113/jphysiol.2003.056309. [PMID: 14645455]
  • József Nagy, Sándor Kolok, Péter Dezso, András Boros, Zsolt Szombathelyi. Differential alterations in the expression of NMDA receptor subunits following chronic ethanol treatment in primary cultures of rat cortical and hippocampal neurones. Neurochemistry international. 2003 Jan; 42(1):35-43. doi: 10.1016/s0197-0186(02)00062-1. [PMID: 12441166]
  • Aihua Deng, Jose M Valdivielso, Karen A Munger, Roland C Blantz, Scott C Thomson. Vasodilatory N-methyl-D-aspartate receptors are constitutively expressed in rat kidney. Journal of the American Society of Nephrology : JASN. 2002 May; 13(5):1381-4. doi: 10.1097/01.asn.0000013293.11876.4e. [PMID: 11961027]
  • K M Ronald, T Mirshahi, J J Woodward. Ethanol inhibition of N-methyl-D-aspartate receptors is reduced by site-directed mutagenesis of a transmembrane domain phenylalanine residue. The Journal of biological chemistry. 2001 Nov; 276(48):44729-35. doi: 10.1074/jbc.m102800200. [PMID: 11572853]
  • T Sakaeda, Y Tada, T Sugawara, T Ryu, F Hirose, T Yoshikawa, K Hirano, L Kupczyk-Subotkowska, T J Siahaan, K L Audus, V J Stella. Conjugation with L-Glutamate for in vivo brain drug delivery. Journal of drug targeting. 2001; 9(1):23-37. doi: 10.3109/10611860108995630. [PMID: 11378521]
  • J Becker, Z Li, C R Noe. Molecular and pharmacological characterization of recombinant rat/mice N-methyl-D-aspartate receptor subtypes in the yeast Saccharomyces cerevisiae. European journal of biochemistry. 1998 Sep; 256(2):427-35. doi: 10.1046/j.1432-1327.1998.2560427.x. [PMID: 9760184]
  • M Mugnaini, M Antolini, M Corsi, F T van Amsterdam. [3H]5,7-dichlorokynurenic acid recognizes two binding sites in rat cerebral cortex membranes. Journal of receptor and signal transduction research. 1998 Mar; 18(2-3):91-112. doi: 10.3109/10799899809047739. [PMID: 9651880]
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  • M Rowley, J J Kulagowski, A P Watt, D Rathbone, G I Stevenson, R W Carling, R Baker, G R Marshall, J A Kemp, A C Foster, S Grimwood, R Hargreaves, C Hurley, K L Saywell, M D Tricklebank, P D Leeson. Effect of plasma protein binding on in vivo activity and brain penetration of glycine/NMDA receptor antagonists. Journal of medicinal chemistry. 1997 Dec; 40(25):4053-68. doi: 10.1021/jm970417o. [PMID: 9406596]
  • M Matoba, U Tomita, T Nishikawa. Characterization of 5,7-dichlorokynurenate-insensitive D-[3H]serine binding to synaptosomal fraction isolated from rat brain tissues. Journal of neurochemistry. 1997 Jul; 69(1):399-405. doi: 10.1046/j.1471-4159.1997.69010399.x. [PMID: 9202334]
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