3195-01-5 Usage
Description
NorarMepavine, a chemical compound belonging to the benzylisoquinoline alkaloids, is derived from the plant Stephania glabra. It exhibits a range of pharmacological properties, such as bronchodilator, smooth muscle relaxant, and vasodilator effects, along with potential anti-inflammatory and antioxidant capabilities. NorarMepavine demonstrates promise as a multifunctional compound with a variety of potential therapeutic applications.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 3195-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,9 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3195-01:
(6*3)+(5*1)+(4*9)+(3*5)+(2*0)+(1*1)=75
75 % 10 = 5
So 3195-01-5 is a valid CAS Registry Number.
3195-01-5Relevant articles and documents
Total Synthesis of (S, S)-Tetramethylmagnolamine via Aerobic Desymmetrization
Huang, Zheng,Ji, Xiang,Lumb, Jean-Philip
supporting information, p. 9194 - 9197 (2019/11/14)
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
Asymmetric synthesis of 1-benzyltetrahydroisoquinolines using chiral oxazolo[2,3-a]tetrahydroisoquinolines
Hashigaki,Kan,Qais,Takeuchi,Yamato
, p. 1126 - 1131 (2007/10/02)
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).
