Name | Etripamil |
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Synonyms |
MSP-2017
UNII:S82A18Y42P (-)-MSP-2017 Methyl 3-(2-{[(4S)-4-cyano-4-(3,4-dimethoxyphenyl)-5-methylhexyl](methyl)amino}ethyl)benzoate Benzoic acid, 3-[2-[[(4S)-4-cyano-4-(3,4-dimethoxyphenyl)-5-methylhexyl]methylamino]ethyl]-, methyl ester Etripamil |
Description | Etripamil (MSP-2017) is a short-acting L-type calcium-channel antagonist with a rapid onset of action designed for intranasal administration, used to treat Paroxysmal Supraventricular Tachycardia (PSVT). Etripamil (MSP-2017) slows atrioventricular nodal conduction and prolongs atrioventricular nodal refractory periods by inhibiting calcium ion influx through the calcium slow channels in the atrioventricular node cells[1][2]. |
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Related Catalog | |
Target |
L-type calcium channel |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 593.8±50.0 °C at 760 mmHg |
Molecular Formula | C27H36N2O4 |
Molecular Weight | 452.59 |
Flash Point | 312.9±30.1 °C |
Exact Mass | 452.267517 |
LogP | 4.14 |
Vapour Pressure | 0.0±1.7 mmHg at 25°C |
Index of Refraction | 1.534 |