ChemicalBook--->CAS DataBase List--->41498-37-7

41498-37-7

41498-37-7 Structure

41498-37-7 Structure
IdentificationBack Directory
[Synonyms]

GS 389
HIGE-004
6,7-Dimethoxy-1-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline
1,2,3,4-Tetrahydro-1-(4-methoxybenzyl)-6,7-dimethoxyisoquinoline
1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(4-methoxybenzyl)isoquinoline
6,7-diMethoxy-1-(4-Methoxybenzyl)-1,2,3,4-tetrahydroisoquinolin-2-iuM chloride
[MDL Number]

MFCD00914751
Chemical PropertiesBack Directory
[Melting point ]

200-203 °C
[Boiling point ]

454.0±45.0 °C(Predicted)
[density ]

1.108±0.06 g/cm3(Predicted)
[pka]

8.75±0.40(Predicted)
Hazard InformationBack Directory
[Description]

GS 389 is a novel tetrahydroisoquinoline analog. GS-389 significantly increased cGMP levels in the rat aorta and inhibited cGMP phosphodiesterase from the rabbit brain. It has vasorelaxant properties.
[Uses]

GS 389 ((±)-O,O-Dimethylcoclaurine) is a tetrahydroisoquinoline. GS-389 inhibites Cyclic AMP and cyclic AMP dependent phosphodiesterases from rat atrial and ventricular tissue. GS-389 relaxes the contraction induced by phenylephrine and high K+ in rat aortic rings[1].
[References]

[1] Chang KC, et al. Different pharmacological characteristics of structurally similar benzylisoquinoline analogs, papaverine, higenamine, and GS 389, on isolated rat aorta and heart. Can J Physiol Pharmacol. 1994;72(4):327-334. DOI:10.1139/y94-049
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