Name | D-Tetrahydropalmatine |
---|---|
Synonyms |
6H-Dibenzo[a,g]quinolizine, 5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-, (13aS)-
levo-tetrahydropalmatine 6H-Dibenzo[a,g]quinolizine, 5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-, (13aR)- (S)-tetrahydropalmatine (13aS)-2,3,9,10-Tetramethoxy-5,8,13,13a-tetrahydro-6H-isoquinolino[3,2-a]isoquinoline Tetrahydropalmatine (+)-Tetrahydropalmatine (13aS)-2,3,9,10-Tetramethoxy-5,8,13,13a-tetrahydro-6H-isoquino[3,2-a]isoquinoline d-Tetrahydropalmatine l-Tetrahydropalmatine (-)-Tetrahydropalmatine (R)-(+)-tetrahydropalmatine D-Tetrahydropalmatin (13aR)-2,3,9,10-Tetramethoxy-5,8,13,13a-tetrahydro-6H-isoquinolino[3,2-a]isoquinoline |
Description | D-Tetrahydropalmatine is an isoquinoline alkaloid, mainly in the genus Corydalis[1]. D-Tetrahydropalmatine is a Dopamine (DA) receptor antagonist with preferential affinity toward the D1 receptors[2]. D-Tetrahydropalmatine is a potent organic cation transporter 1 (OCT1) inhibitor[3]. |
---|---|
Related Catalog | |
Target |
DA[2], OCT1[3] |
References |
Density | 1.2±0.1 g/cm3 |
---|---|
Boiling Point | 482.9±45.0 °C at 760 mmHg |
Molecular Formula | C21H25NO4 |
Molecular Weight | 355.427 |
Flash Point | 138.7±25.9 °C |
Exact Mass | 355.178345 |
PSA | 40.16000 |
LogP | 3.70 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.609 |
Hazard Codes | Xi |
---|
~% 3520-14-7 |
Literature: Journal of Organic Chemistry, , vol. 70, # 23 p. 9486 - 9494 |
Precursor 1 | |
---|---|
DownStream 2 | |