O-Phospho-L-serine-13C3,15N(Synonyms: L-Serine O-phosphate-13C3,15N; L-SOP-13C3,15N)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
O-Phospho-L-serine-13C3,15N (Synonyms: L-Serine O-phosphate-13C3,15N; L-SOP-13C3,15N)

O-Phospho-L-serine-13C3,15N (L-Serine O-phosphate-13C3,15N) 是一种 -13C 和 15N 标记的 O-Phospho-L-serine。O-Phospho-L-serine 是 L-serine 合成过程中的直接前体物质,是第三组 mGluR (mGluR4,mGluR6,mGluR7 和 mGluR8) 的激动剂,O-Phospho-L-serine 同时为 mGluR1mGluR2 的拮抗剂

O-Phospho-L-serine-13C3,15N(Synonyms: L-Serine O-phosphate-13C3,15N;  L-SOP-13C3,15N)

O-Phospho-L-serine-13C3,15N Chemical Structure

CAS No. : 2734706-69-3

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

O-Phospho-L-serine-13C3,15N (L-Serine O-phosphate-13C3,15N) is the 13C- and 15N-labeled O-Phospho-L-serine. O-Phospho-L-serine is the immediate precursor to L-serine in the serine synthesis pathway, and an agonist at the group III mGluR receptors (mGluR4, mGluR6, mGluR7, and mGluR8); O-Phospho-L-serine also acts as a weak antagonist for mGluR1 and a potent antagonist for mGluR2[1].

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

189.04

Formula

13C3H815NO6P

CAS 号

2734706-69-3

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]. Kang HJ, et al. Determinants of endogenous ligand specificity divergence among metabotropic glutamate receptors. J Biol Chem. 2015 Jan 30;290(5):2870-8.

    [3]. Kang HJ, et al. Selectivity and evolutionary divergence of metabotropic glutamate receptors for endogenous ligands and G proteins coupled to phospholipase C or TRP channels. J Biol Chem. 2014 Oct 24;289(43):29961-74.

    [4]. Bailey TJ, et al. The inhibitor of phagocytosis, O-phospho-L-serine, suppresses Müller glia proliferation and cone cell regeneration in the light-damaged zebrafish retina. Exp Eye Res. 2010 Nov;91(5):601-12.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务