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8-pCPT-2-O-Me-cAMP-AM

8-pCPT-2-O-Me-cAMP-AM
8-pCPT-2-O-Me-cAMP-AM
8-pCPT-2-O-Me-cAMP-AM
Catalog Description Size Price (USD) Qty
GBM-2736-100UG8-pCPT-2-O-Me-cAMP-AM100ug$311.00
Epac activator
Bioassays Specification
Bio-Activity Epac activator
Chemical Name 8-(4-Chlorophenylthio)-2’-O-methyladenosine-3’,5’-cyclic monophosphate, acetoxymethyl ester
Function / Pharmacology A potent, cell-permeable Epac (exchange protein directly activated by cAMP) activator1. Induces RAP1 activation and insulin secretion in pancreatic beta cell lines2-5. Induces vascular relaxation in rat mesenteric artery6. The acetoxymethyl ester confers increased cell-permeability and is cleaved by endogenous esterases to yield the active compound, 8-pCPT-2'-O-Me-cAMP. Addition to cell cultures should be done in serum-free media as esterases in serum will cleave the acetoxymethyl ester and reduce cell permeability.
CAS# 1152197-23-3
MW 557.91
Molecular Formula C20H21ClN5O8PS
Solubility Soluble in DMSO (up to 50 mg/ml).
Supplied powder
Storage as supplied -20°C
Ship temp Ambient
References 1) Vliem et al. (2008), 8-pCPT-2’-O-Me-cAMP-AM: an improved Epac-selective cAMP analogue; Chem. Biochem., 9 2052 2) Chepurny et al. (2009), Enhanced Rap1 activation and insulin secretagogue properties of an acetoxymethyl ester of an Epac-selective cyclic AMP analog in rat INS-1 cells: studies with 8-pCPT-2’-O-Me-cAMP-AM; J. Biol. Chem., 284 10728 3) Kelley et al. (2009), Glucose-dependent potentiation of mouse islet insulin secretion by Epac activator 8-pCPT-2’-O-Me-cAMP-AM; Islets, 1 260 4) Chepurny et al. (2010), PKA-dependent potentiation of glucose-stimulated insulin secretion by Epac activator 8-pCPT-2’-O-Me-cAMP-AM in human islets of Langerhans; Am. J. Physiol. Endocrinol. Metab., 298 E622 5) Dzhura et al. (2011), Phospholipase C-ε links EPAC2 activation to the potentiation of glucose stimulated insulin secretion from moused islets of Langerhans; Islets, 3 121 6) Roberts et al. (2013), Exchange protein activated by cAMP (Epac) induces vascular relaxation by activating Ca2+-sensitive K+ channels in rat mesenteric artery; J. Physiol., 591 5107
Protein Specification
Purity >98%

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