MRS2500 tetraammonium

For research use only. Not for therapeutic Use.

  • CAT Number: R014564
  • CAS Number: 630103-23-0
  • Molecular Formula: C13H30IN9O8P2
  • Molecular Weight: 629.28
  • Purity: ≥95%
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MRS2500 tetraammonium is a potent, selective and stable antagonist of the P2Y1 receptor (Ki=0.78 nM for recombinant human P2Y1 receptor). MRS2500 tetraammonium inhibits the ADP-induced aggregation of human platelets with an IC50 value of 0.95 nM. Antithrombotic activity[1][2][3].
MRS2500 tetraammonium inhibits platelet aggregation to 10 μM ADP with an IC50 of 0.95 nM in human washed platelets. MRS2500 tetraammonium inhibits platelet aggregation to 10μM ADP with an IC50 of 0.49 μM in human PRP[4].
MRS2500 (2 mg/kg; i.v.) decreases acute systemic thromboembolism through selective inhibition of the P2Y1 receptor[3].
MRS2500 exhibited strong antithrombotic efficacy in the prevention of arterial thrombosis in the monkey ECAT model[4]..


Catalog Number R014564
CAS Number 630103-23-0
Synonyms

diamino [(1R,2S,4S,5S)-2-diaminooxyphosphoryloxy-4-[2-iodo-6-(methylamino)purin-9-yl]-1-bicyclo[3.1.0]hexanyl]methyl phosphate

Molecular Formula C13H30IN9O8P2
Purity ≥95%
InChI InChI=1S/C13H22IN9O8P2/c1-19-10-9-11(22-12(14)21-10)23(5-20-9)7-2-8(27-33(25,30-17)31-18)13(3-6(7)13)4-26-32(24,28-15)29-16/h5-8H,2-4,15-18H2,1H3,(H,19,21,22)/t6-,7+,8+,13+/m1/s1
InChIKey HNOFXCYFNHYFDQ-SMWKGLLFSA-N
SMILES CNC1=C2C(=NC(=N1)I)N(C=N2)C3CC(C4(C3C4)COP(=O)(ON)ON)OP(=O)(ON)ON
Reference

[1]. Cattaneo M, et al. Antiaggregatory activity in human platelets of potent antagonists of the P2Y 1 receptor. Biochem Pharmacol. 2004;68(10):1995-2002.
 [Content Brief]

[2]. Wong PC, et al. The P2Y1 receptor antagonist MRS2500 prevents carotid artery thrombosis in cynomolgus monkeys. J Thromb Thrombolysis. 2016;41(3):514-521.
 [Content Brief]

[3]. Hechler B, et al. MRS2500 [2-iodo-N6-methyl-(N)-methanocarba-2′-deoxyadenosine-3′,5′-bisphosphate], a potent, selective, and stable antagonist of the platelet P2Y1 receptor with strong antithrombotic activity in mice. J Pharmacol Exp Ther. 2006;316(2):556
 [Content Brief]

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