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MRS 2179 - ≥98%, high purity , CAS No.101204-49-3, Antagonist of P2Y 1 receptor

  • Moligand™
  • ≥98%
Item Number
M275550
Grouped product items
SKUSizeAvailabilityPrice Qty
M275550-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$109.90
M275550-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$199.90
M275550-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$807.90

Potent, selective P2Y 1 antagonist

View related series
P2Y1 receptor Antagonist

Basic Description

Synonyms101204-49-3|MRS 2179|[(2R,3S,5R)-5-[6-(methylamino)purin-9-yl]-2-(phosphonooxymethyl)oxolan-3-yl] dihydrogen phosphate|MRS 2179 ammonium salt|MRS2179|CHEMBL129841|MRS-2179|2'-DEOXY-N6-METHYLADENOSINE 3',5'-BISPHOSPHATE TETRAAMMONIUM SALT|CHEMBL1096400|Lop
Specifications & Purity≥98%
Storage TempStore at -20°C,Desiccated
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of P2Y 1 receptor
Product Description

Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.

Associated Targets

P2RY1 Tchem P2Y purinoceptor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name [(2R,3S,5R)-5-[6-(methylamino)purin-9-yl]-2-(phosphonooxymethyl)oxolan-3-yl] dihydrogen phosphate
INCHI InChI=1S/C11H17N5O9P2/c1-12-10-9-11(14-4-13-10)16(5-15-9)8-2-6(25-27(20,21)22)7(24-8)3-23-26(17,18)19/h4-8H,2-3H2,1H3,(H,12,13,14)(H2,17,18,19)(H2,20,21,22)/t6-,7+,8+/m0/s1
InChi Key CCPLITQNIFLYQB-XLPZGREQSA-N
Canonical SMILES CNC1=C2C(=NC=N1)N(C=N2)C3CC(C(O3)COP(=O)(O)O)OP(=O)(O)O
Isomeric SMILES CNC1=C2C(=NC=N1)N(C=N2)[C@H]3C[C@@H]([C@H](O3)COP(=O)(O)O)OP(=O)(O)O
PubChem CID 5311303

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble in water to 100 mM

Related Documents

References

1. Nandanan E, Camaioni E, Jang SY, Kim YC, Cristalli G, Herdewijn P, Secrist 3rd JA, Tiwari KN, Mohanram A, Harden TK et al..  (1999)  Structure-activity relationships of bisphosphate nucleotide derivatives as P2Y1 receptor antagonists and partial agonists..  J Med Chem,  42  (9): (1625-38).  [PMID:10229631]
2. Zeng J et al..  (2014)  P2Y13 receptor-mediated rapid increase in intracellular calcium induced by ADP in cultured dorsal spinal cord microglia..  Neurochem Res,  39  (11): (2240-50).  [PMID:25186167]
3. Wu J et al..  (2017)  P2Y1R is involved in visceral hypersensitivity in rats with experimental irritable bowel syndrome..  World J Gastroenterol,  23  (34): (6339-6349).  [PMID:28974901]
4. Campwala H et al..  (2014)  P2Y6 receptor inhibition perturbs CCL2-evoked signalling in human monocytic and peripheral blood mononuclear cells..  J Cell Sci,  127  (22): (4964-73).  [PMID:25271060]

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