6,7-Dimethoxy-1-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline is a chemical compound characterized by its complex structure, which includes a tetrahydroisoquinoline core substituted with methoxy groups and a benzyl moiety. This compound features two methoxy groups at the 6 and 7 positions of the isoquinoline ring, enhancing its lipophilicity and potentially influencing its biological activity. The presence of the 4-methoxybenzyl group adds to its molecular complexity and may contribute to its pharmacological properties. Typically, compounds of this class are studied for their potential effects in various biological systems, including neuropharmacological activities. The molecular structure suggests that it may interact with neurotransmitter systems, although specific biological activities would require empirical investigation. Additionally, the compound's solubility, stability, and reactivity can be influenced by the methoxy substituents, which may also affect its synthesis and purification processes. Overall, 6,7-dimethoxy-1-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline represents a class of compounds of interest in medicinal chemistry and pharmacology.

6,7-dimethoxy-1-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

41498-37-7: 6,7-Dimethoxy-1-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline is a chemical compound characterized by its complex structure, which includes a tetrahydroisoquinoline core substituted with methoxy groups and a benzyl moiety. This compound features two methoxy groups at the 6 and 7 positions of the isoquinoline ring, enhancing its lipophilicity and potentially influencing its biological activity. The presence of the 4-methoxybenzyl group adds to its molecular complexity and may contribute to its pharmacological properties. Typically, compounds of this class are studied for their potential effects in various biological systems, including neuropharmacological activities. The molecular structure suggests that it may interact with neurotransmitter systems, although specific biological activities would require empirical investigation. Additionally, the compound's solubility, stability, and reactivity can be influenced by the methoxy substituents, which may also affect its synthesis and purification processes. Overall, 6,7-dimethoxy-1-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline represents a class of compounds of interest in medicinal chemistry and pharmacology.

<p>GS 389, a tetrahydroisoquinoline, relaxes blood vessels by inhibiting brain PDE and raising aorta cGMP.</p>

CAS 41498-37-7

6,7-dimethoxy-1-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

GS 389

Ref: TM-T27436