A P2X2 and P2Y1 receptor agonist
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2-Methylthioadenosine triphosphate (sodium salt)

Item No. 21418

Technical Information
Formal Name
2-(methylthio)-adenosine 5'-(tetrahydrogen triphosphate), tetrasodium salt
CAS Number
100020-57-3
Synonyms
  • 2-methylthio ATP
  • 2-MeSATP
Molecular Formula
C11H14N5O13P3S • 4Na
Formula Weight
Purity
≥95%
A 10 mM solution in water
PBS (pH 7.2): 10 mg/mlWater: Soluble
λmax
234, 275 nm
SMILES
O[C@H]1[C@H](N2C=NC3=C2N=C(SC)N=C3N)O[C@H](COP(OP(OP([O-])([O-])=O)([O-])=O)([O-])=O)[C@H]1O.[Na+].[Na+].[Na+].[Na+]
InChi Code
InChI=1S/C11H18N5O13P3S.4Na/c1-33-11-14-8(12)5-9(15-11)16(3-13-5)10-7(18)6(17)4(27-10)2-26-31(22,23)29-32(24,25)28-30(19,20)21;;;;/h3-4,6-7,10,17-18H,2H2,1H3,(H,22,23)(H,24,25)(H2,12,14,15)(H2,19,20,21);;;;/q;4*+1/p-4/t4-,6-,7-,10-;;;;/m1..../s1
InChi Key
UEEFBRHXFDJPTA-KWIZKVQNSA-J
Shipping & Storage Information
Storage
-80°C
Shipping
Dry ice in continental US; may vary elsewhere
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    Product Description

    2-Methylthioadenosine triphosphate is an agonist of the purinergic P2X2 and P2Y1 receptors.1,2 It is also an inhibitor of guanylate cyclase C (GC-C) in rat intestinal mucosal membranes (Ki = 360 µM in the presence of E. coli heat-stable enterotoxin).3 2-Methylthioadenosine triphosphate (1 µM) induces calcium influx in primary rat arcuate nucleus neurons in a fluorescence-based reporter assay.1 It increases inositol phosphate accumulation in 1321N1 astrocytoma cells expressing human P2Y1 receptors (EC50 = 51 nM).2 2-Methylthioadenosine triphosphate inhibits uroguanylin-induced increases in urine flow and sodium excretion in rats.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Pollatzek, E., Hitzel, N., Ott, D., et alFunctional expression of P2 purinoceptors in a primary neuroglial cell culture of the rat arcuate nucleus. Neuroscience 327, 95-114 (2016).

    2. Schachter, J.B., and Harden, T.K. An examination of deoxyadenosine 5'(α-thio)triphosphate as a ligand to define P2Y receptors and its selectivity as a low potency partial agonist of the P2Y1 receptor. Br. J. Pharmacol. 121(2), 338-334 (1997).

    3. Parkinson, S.J., Carrithers, S.L., and Waldman, S.A. Opposing adenine nucleotide-dependent pathways regulate guanylyl cyclase C in rat intestine. The Journal of Biological Chemisty 269(36), 22683-22690 (1994).

    4. Zeng, C., Xia, T., Zheng, S., et alSynergistic effect of uroguanylin and D1 dopamine receptors on sodium excretion in hypertension. J. Am. Heart Assoc. 11(6), e022827 (2022).