Zaprinast| CAS 37762-06-4|DC Chemicals

Cas No.:	37762-06-4
Chemical Name:	7H-1,2,3-Triazolo[4,5-d]pyrimidin-7-one,3,6-dihydro-5-(2-propoxyphenyl)-
Synonyms:	7H-1,2,3-Triazolo[4,5-d]pyrimidin-7-one,3,6-dihydro-5-(2-propoxyphenyl)-;Zaprinast;1,4-Dihydro-5-(2-propoxyphenyl)-7H-1,2,3-triazolo(4,5-d)pyrimidin-7-one;2-(2-Propoxyphenyl)-8-azahypoxanthine;2-(2-PROPYLOXYPHENYL)-8-AZAPURIN-6-ONE;2-o-propoxyphenyl-8-azapurin-6-one;3,6-dihydro-5-(2-propoxyphenyl);8-Aza-2-(2-propoxyphenyl)-6-purinone;B 22,948;Phenylaza purinon;Potassium phosphate monobasic
SMILES:	CCCOC1=CC=CC=C1C1=NC(=O)C2=NNNC2=N1
Formula:	C₁₃H₁₃N₅O₂
M.Wt:	271.274621725082
Purity:	>98%
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Description:	Zaprinast (M&B 22948) is an inhibitor of cGMP-selective Phosphodiesterases(PDEs)[1]. Zaprinast is a G protein-coupled receptor (GPR) 35 agonist which activates rat GPR35 strongly and activates human GPR35 moderately[2]. Zaprinast reduces vessel remodeling through antiproliferative and proapoptotic effects[3].
Target:	PDE[1], GPR35[2]
References:	[1]. Choi SH , et al. Zaprinast, an inhibitor of cGMP-selective phosphodiesterases, enhances the secretion of TNF-alpha and IL-1beta and the expression of iNOS and MHC class II molecules in rat microglial cells. J Neurosci Res. 2002 Feb 1;67(3):411-21. [2]. Taniguchi Y, et al. Zaprinast, a well-known cyclic guanosine monophosphate-specific phosphodiesterase inhibitor, is an agonist for GPR35. FEBS Lett. 2006 Sep 18;580(21):5003-8. Epub 2006 Aug 17. [3]. Keswani AN , et al The cyclic GMP modulators YC-1 and zaprinast reduce vessel remodeling through antiproliferative and proapoptotic effects. J Cardiovasc Pharmacol Ther. 2009 Jun;14(2):116-24.

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