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UDP(sodium salt hydrate)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
UDP(sodium salt hydrate)图片
包装与价格:
包装价格(元)
100mg电议
500mg电议
1 g电议

产品介绍
An agonist of P2Y6
Canonical SMILESOP(OP(OC[C@@H]1[C@@H](O)[C@@H](O)[C@H](N2C=CC(NC2=O)=O)O1)([O-])=O)([O-])=O.[Na+].[Na+].O
分子式C9H12N2O12P2·2Na [XH2O]
分子量448.1
溶解度PBS (pH 7.2): 10 mg/ml
储存条件-20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

UDP is the diphosphate of the nucleoside uridine. It is a specific agonist of the P2Y purinoceptor P2Y6(EC50= 13 nM for human P2Y6), stimulating the production of inflammatory mediators, phagocytosis, and vasoconstriction.1,2,3,4,5,6UDP also acts as an antagonist of P2Y14, whose agonists include UDP-glucose , UDP-galactose, and UDP-glucuronic acid.1,2

1.Jacobson, K.A., Ivanov, A.A., de Castro, S., et al.Development of selective agonists and antagonists of P2Y receptorsPurinergic Signal.5(1)75-89(2009) 2.Abbracchio, M.P., Burnstock, G., Boeynaems, J.M., et al.International Union of Pharmacology LVIII: Update on the P2Y G protein-coupled nucleotide receptors: From molecular mechanisms and pathophysiology to therapyPharmacological Reviews58(3)281-341(2006) 3.Garcia, R.A., Yan, M., Search, D., et al.P2Y6 receptor potentiates pro-inflammatory responses in macrophages and exhibits differential roles in atherosclerotic lesion developmentPLoS One9(10)1-13(2014) 4.Inoue, K.UDP facilitates microglial phagocytosis through P2Y6 receptorsCell Adhesion & Migration1(3)131-132(2007) 5.Besada, P., Shin, D.H., Costanzi, S., et al.Structure-activity relationships of uridine 5’-diphosphate analogues at the human P2Y6 receptorJournal of Medicinal Chemistry49(18)5532-5543(2006) 6.Mitchell, C., Syed, N., Tengah, A., et al.Identification of contractile P2Y1, P2Y6, and P2Y12 receptors in rat intrapulmonary artery using selective ligandsJournal of Pharmacology and Experimental Therapeutics343(3)755-762(2012)