Pranidipine

Pranidipine

Names
IUPAC name methyl (2E)-phenylprop-2-en-1-yl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
Other names 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid O^5-methyl O^3-[(E)-3-phenylprop-2-enyl] ester
Identifiers
CAS Number	99522-79-9
3D model (Jmol)	Interactive image
ChEMBL	ChEMBL1096842
ChemSpider	4940726
MeSH	C048161
PubChem	6436048
UNII	9DES9QVH58
InChI InChI=1S/C25H24N2O6/c1-16-21(24(28)32-3)23(19-12-7-13-20(15-19)27(30)31)22(17(2)26-16)25(29)33-14-8-11-18-9-5-4-6-10-18/h4-13,15,23,26H,14H2,1-3H3/b11-8+ Key: XTFPDGZNWTZCMF-DHZHZOJOSA-N InChI=1/C25H24N2O6/c1-16-21(24(28)32-3)23(19-12-7-13-20(15-19)27(30)31)22(17(2)26-16)25(29)33-14-8-11-18-9-5-4-6-10-18/h4-13,15,23,26H,14H2,1-3H3/b11-8+ Key: XTFPDGZNWTZCMF-DHZHZOJOBA
SMILES CC1=C(C(C(=C(N1)C)C(=O)OCC=CC2=CC=CC=C2)C3=CC(=CC=C3)[N+](=O)[O-])C(=O)OC
Properties
Chemical formula	C25H24N2O6
Molar mass	448.46786
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Pranidipine is a calcium channel blocker. It is a long acting calcium channel antagonist of the dihydropyridine group.^[1]

References

1. Jin Yang; Keisuke Fukuo; Shigeto Morimoto; Tadaaki Niinobu; Toshimitsu Suhara; Toshio Ogihara (2000). "Pranidipine Enhances the Action of Nitric Oxide Released From Endothelial Cells". Hypertension. 35: 82–85. doi:10.1161/01.hyp.35.1.82.