
UDP disodium salt
CAS No. 27821-45-0
UDP disodium salt( Uridine 5'-diphosphate disodium salt hyd )
Catalog No. M19585 CAS No. 27821-45-0
UDP is a specific agonist of the P2Y6 receptors (EC50 = 13 nM for human P2Y6) stimulating the production of inflammatory mediators phagocytosis and vasoconstriction. UDP also acts as an antagonist of P2Y14.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
50MG | 29 | In Stock |
![]() ![]() |
100MG | 41 | In Stock |
![]() ![]() |
500MG | 87 | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameUDP disodium salt
-
NoteResearch use only, not for human use.
-
Brief DescriptionUDP is a specific agonist of the P2Y6 receptors (EC50 = 13 nM for human P2Y6) stimulating the production of inflammatory mediators phagocytosis and vasoconstriction. UDP also acts as an antagonist of P2Y14.
-
DescriptionUDP is a specific agonist of the P2Y6 receptors (EC50 = 13 nM for human P2Y6) stimulating the production of inflammatory mediators phagocytosis and vasoconstriction. UDP also acts as an antagonist of P2Y14.
-
In VitroRT-PCRCell Line:Primary microglia Concentration:100 μM Incubation Time:For 15 min Result:Significantly induced microglial CCL2 and CCL3 mRNA expression.
-
In Vivo——
-
SynonymsUridine 5'-diphosphate disodium salt hyd
-
PathwayNeuroscience
-
TargetP2 Receptor
-
RecptorP2Y6| P2Y14
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number27821-45-0
-
Formula Weight466.14
-
Molecular FormulaC9H14N2Na2O13P2
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILES[Na+].[Na+].O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP([O-])(=O)OP(O)([O-])=O)n1ccc(=O)[nH]c1=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Jacobson K.A. et al. Development of selective agonists and antagonists of P2Y receptors. Purinergic Signal. 5(1) 75-89 (2009).
molnova catalog



related products
-
Glycitein
Glycitein inhibits glioma cell invasion through down-regulation of MMP-3 and MMP-9 gene expression.
-
RO3
RO3 is a selective antagonist of homomeric P2X3 and heteromeric P2X2/3 receptor.
-
Prasugrel
Prasugrel, a thienopyridine derivative, is a platelet activation and aggregation inhibitor structurally and pharmacologically related to clopidogrel and ticlopidine.