Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4)

Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4) Suppliers list
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
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Products Intro: Product Name:2-Chloroadenosine 5-triphosphate (sodium salt)
CAS:301334-89-4
Purity:95% Package:500μg;1mg
Company Name: Changzhou Bojia Biomedical Technology Co., Ltd.  
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Products Intro: Product Name:Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4)
CAS:301334-89-4
Purity:98% HPLC Package:1KG;10KG;100KG
Company Name: Cayman Chemical Company  
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Products Intro: Product Name:2-Chloroadenosine 5-triphosphate (sodium salt)
CAS:301334-89-4
Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4) Basic information
Product Name:Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4)
Synonyms:Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4);2-Chloroadenosine 5-triphosphate (sodium salt)
CAS:301334-89-4
MF:C10H16ClN5NaO13P3
MW:565.62
EINECS:
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Mol File:301334-89-4.mol
Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4) Structure
Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4) Chemical Properties
storage temp. -20°C
solubility Water: soluble
Water Solubility Water: soluble
Safety Information
MSDS Information
Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4) Usage And Synthesis
Biological Activity2-Chloroadenosine 5-triphosphate (2-chloro ATP) is an adenine nucleotide and analog of ATP .1,2 It is an antagonist of the purinergic P2Y1 receptor, inhibiting intracellular calcium mobilization induced by ADP in Jurkat cells expressing the human receptor (Ki = 2.3 μM).3 2-chloro ATP is an agonist of purinergic P2X receptors, inducing inward currents in HEK293 cells expressing the human bladder smooth muscle or rat PC12 forms of the receptor (EC50s = 0.5 and 2.5 μM, respectively).4 It induces relaxation of precontracted isolated guinea pig taenia caeci strips in a concentration-dependent manner.1 It has been used to study the substrate specificity of cyclic nucleotide-dependent protein kinases, such as protein kinase A (PKA) and PKG.2
References1.Satchell, G., and Maguire, M.H.Inhibitory effects of adenine nucleotide analogs on the isolated guinea-pig taenia coliJ. Pharmacol. Exp. Ther.195(3)540-548(1975) 2.Flockhart, D.A., Freist, W., Hoppe, J.O., et al.ATP analog specificity of CAMP-dependent protein kinase, cGMP-dependent protein kinase, and phosphorylase kinaseEur. J. Biochem.140(2)289-295(1984) 3.Hechler, B., Vigne, P., Léon, C., et al.ATP derivatives are antagonists of the P2Y1 receptor: Similarities to the platelet ADP receptorMol. Pharmacol.53(4)727-733(1997) 4.Evans, R.J., Lewis, C., Buell, G., et al.Pharmacological characterization of heterologously expressed ATP-gated cation channels (P2x purinoceptors)Mol. Pharmacol.48(2)178-183(1995)
Adenosine 5'-(tetrahydrogen triphosphate), 2-chloro-, sodium salt (1:4) Preparation Products And Raw materials
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