Quinolinic acid-d3(Synonyms: 喹啉酸 d3)

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Quinolinic acid-d3 (Synonyms: 喹啉酸 d3)

Quinolinic acid-d3 是 Quinolinic acid 的氘代物。Quinolinic acid 是一种内源性的 N-甲基-D-天冬氨酸受体 (NMDA receptor) 激动剂,通过犬尿氨酸途径从 L-色氨酸合成,因此具有调节 N-甲基-D-天冬氨酸神经元损伤和功能障碍的潜力。

Quinolinic acid-d3(Synonyms: 喹啉酸 d3)

Quinolinic acid-d3 Chemical Structure

CAS No. : 138946-42-6

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生物活性

Quinolinic acid-d3 is the deuterium labeled Quinolinic acid. Quinolinic acid is an endogenous N-methyl-D-aspartate (NMDA) receptor agonist synthesized from L-tryptophan via the kynurenine pathway and thereby has the potential of mediating N-methyl-D-aspartate neuronal damage and dysfunction[1][2].

体外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

170.14

Formula

C7H2D3NO4

CAS 号

138946-42-6

中文名称

喹啉酸 d3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.

    [2]. Heyes MP, et al. Quinolinic acid and kynurenine pathway metabolism in inflammatory and non-inflammatory neurological disease. Brain. 1992 Oct;115 ( Pt 5):1249-73.

    [3]. Jang S, et al. Neuroprotective effects of (-)-epigallocatechin-3-gallate against quinolinic acid-induced excitotoxicity via PI3K pathway and NO inhibition. Brain Res. 2010 Feb 8;1313:25-33.

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