321125-47-7

Upstream product

• 6346-05-0 3-benzyloxy-4-methoxybenzaldehyde 
• 1064202-02-3 2-benzyloxy-1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene 

Downstream Products

• 60011-91-8 (+/-)-1-(3-benzyloxy-4-methoxyphenyl)propan-2-amine 
• 1064205-62-4 2-(4-ethoxy-3,5-dimethoxybenzoyl)-3-ethyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline 
• 1064205-65-7 2-(4-ethoxy-3,5-dimethoxy-benzyl)-3-ethyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline 
• 1064205-67-9 2-(4-ethoxy-3,5-dimethoxy-benzyl)-3-ethyl-6-hydroxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline 
• 1064205-46-4 2-(2-chloro-5-methoxy-benzyl)-3-methyl-6-benzyloxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline 
• 1064205-47-5 (+/-)-6-benzyloxy-2-(2,5-dimethoxybenzyl)-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline 
• 1064205-58-8 (+/-)-2-(2,5-dimethoxybenzyl)-7-methoxy-3-methyl-6-sulfamoyloxy-1,2,3,4-tetrahydroisoquinoline 
• 1064205-53-3 (+/-)-2-(2,5-dimethoxybenzyl)-6-hydroxy-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline 
• 1064205-39-5 (+/-)-2-(3-ethylbenzyl)-6-hydroxy-7-methoxy-3-methyl-1,2,3,4-tetrahydroisoquinoline 
• 1064202-34-1 (+/-)-7-methoxy-3-methyl-6-sulfamoyloxy-2-(3,4,5-trimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline 
• 1064205-57-7 (±)-7-methoxy-3-methyl-6-sulfamoyloxy-2-(2-chloro-5-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline 
• 1064205-55-5 (+/-)-2-(2-fluoro-5-methoxybenzyl)-7-methoxy-3-methyl-6-sulfamoyloxy-1,2,3,4-tetrahydroisoquinoline 
• 1064202-30-7 (+/-)-2-(3,5-dimethoxybenzyl)-7-methoxy-3-methyl-6-sulfamoyloxy-1,2,3,4-tetrahydroisoquinoline 
• 1602589-27-4 (+/-)-2-(3,4-dimethoxybenzyl)-7-methoxy-3-methyl-6-sulfamoyloxy-1,2,3,4-tetrahydroisoquinoline 

Relevant academic research and scientific papers

Synthesis, antitubulin, and antiproliferative sar of c3/c1-substituted tetrahydroisoquinolines

The syntheses and antiproliferative activities of novel substituted tetrahydroisoquinoline derivatives and their sulfamates are discussed. Biasing of conformational populations through substitution on the tetrahydroisoquinoline core at C1 and C3 has a pro

Steroidomimetic tetrahydroisoquinolines for the design of new microtubule disruptors

Structure-activity relationship translation offers an expeditious means for discovery of new active series. This approach was applied to discover tetrahydroisoquinoline (THIQ)-based steroidomimetic microtubule disruptors. The two A-ring elements of a thre