3195-01-5

Usage

Uses

Used in Pharmaceutical Industry:
NorarMepavine is used as a therapeutic agent for respiratory disorders due to its bronchodilator and smooth muscle relaxant properties, making it a potential treatment for conditions such as asthma and chronic obstructive pulmonary disease.
Used in Cardiovascular Medicine:
NorarMepavine is utilized as a vasodilator, which may aid in the treatment of cardiovascular diseases by improving blood flow and reducing the workload on the heart.
Used in Neurological Applications:
NorarMepavine is employed as a cognitive enhancer and memory improver, suggesting its potential use in addressing neurological conditions that affect cognitive function and memory.
Used in Anti-Inflammatory and Antioxidant Therapies:
Due to its potential anti-inflammatory and antioxidant properties, NorarMepavine is used as a therapeutic agent to combat inflammation and oxidative stress, which are implicated in various diseases and conditions.

Upstream product

• 10214-84-3 N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(4-hydroxyphenyl)acetamide 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 156-38-7 4-hydroxyphenylacetate 
• 123285-94-9 (3R,10bS)-8,9-dimethoxy-3-phenyl-2,3,5,6-tetrahydro-10bH-oxazolo<2.3-a>isoquinoline 
• 47626-99-3 1-(4-(benzyloxy)benzyl)-6,7-dimethoxy-3,4-dihydroisoquinoline 
• 5884-31-1 2-(4-benzyloxyphenyl)-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide 
• 56441-69-1 2-<4-(phenylmethoxy)phenyl>acetic acid ethyl ester 
• 655245-11-7 1-(4-benzyloxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 836-42-0 4-benzyloxybenzyl chloride 

Relevant academic research and scientific papers

Total Synthesis of (S, S)-Tetramethylmagnolamine via Aerobic Desymmetrization

We describe a concise synthesis of the pseudodimeric tetrahydroisoqunoline alkaloid (S,S)-tetramethylmagnolamine by a catalytic aerobic desymmetrization of phenols. Desymmetrization reactions increase molecular complexity with high levels of efficiency, b

Enantioselective synthesis of the tetrahydrobenzyl-isoquinoline alkaloid (-)-norarmepavine using polymer supported reagents

We describe, in full, the enantioselective synthesis of the tetrahydrobenzylisoquinoline alkaloid (-)-norarmepavine (1) in 77% e.e. This compound was prepared using solid-supported reagents and scavengers in multi-step sequences of reactions to give mater

Asymmetric synthesis of 1-benzyltetrahydroisoquinolines using chiral oxazolo[2,3-a]tetrahydroisoquinolines

A novel synthetic route to enantiomerically pure 1-benzyltetrahydroisoquinolines (1) was developed via the reaction of oxazolo[2,3-a]tetrahydroisoquinoline (5) with benzyltriisopropoxytitanium compounds (10). This method was applied to the synthesis of (S)-trimetoquinol (1c; a bronchodilator).