D-Tetrahydropalmatine

Modify Date: 2024-01-02 12:11:31

D-Tetrahydropalmatine Structure
D-Tetrahydropalmatine structure
Common Name D-Tetrahydropalmatine
CAS Number 3520-14-7 Molecular Weight 355.427
Density 1.2±0.1 g/cm3 Boiling Point 482.9±45.0 °C at 760 mmHg
Molecular Formula C21H25NO4 Melting Point N/A
MSDS N/A Flash Point 138.7±25.9 °C

 Use of D-Tetrahydropalmatine


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].

 Names

Name D-Tetrahydropalmatine
Synonym More Synonyms

 D-Tetrahydropalmatine Biological Activity

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

[1]. Ma ZJ, et al. [Effects of different types and standard of processing vinegaron inherent constituents in rhizoma of Corydalis yanhusuo]. Zhongguo Zhong Yao Za Zhi. 2006 Mar;31(6):465-7.

[2]. Xu SX, et al. Effects of tetrahydroprotoberberines on dopamine receptor subtypes in brain. Zhongguo Yao Li Xue Bao. 1989 Mar;10(2):104-10.

[3]. Tu M, et al. Organic cation transporter 1 mediates the uptake of monocrotaline and plays an important rolein its hepatotoxicity. Toxicology. 2013 Sep 15;311(3):225-30.

 Chemical & Physical Properties

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

 Safety Information

Hazard Codes Xi

 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
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