3767-40-6 Usage
Explanation
The compound's full chemical name, which describes its structure and composition.
Explanation
An alternative name for the compound, which is often used in scientific literature.
Explanation
The molecular formula represents the number of atoms of each element in a molecule of the compound.
Explanation
The compound's structure, which is characterized by a tetrahydroisoquinolinium core with specific functional groups attached.
Explanation
The compound has been studied for its potential therapeutic effects, including cancer treatment, pain relief, and reducing inflammation.
Explanation
The compound's ability to inhibit the growth of cancer cells is one of its key properties, making it a potential anti-cancer agent.
Explanation
The compound's unique structure and molecular properties have made it a promising candidate for further research in the medical field.
Explanation
The compound belongs to the isoquinolinium class of chemicals, which are known for their diverse biological activities.
Explanation
The solubility of the compound in various solvents is not mentioned in the provided material.
Explanation
The stability of the compound under different conditions is not provided in the material.
Structure
Tetrahydroisoquinolinium with a 3,4-dimethoxybenzyl group and two methoxy groups on the 6th and 7th positions
Potential Pharmaceutical Properties
Anti-cancer, analgesic, and anti-inflammatory
Mechanism of Action
Inhibition of cancer cell growth
Research Status
Investigated for further development in medicine and drug discovery
Chemical Class
Isoquinolinium
Solubility
Unknown
Stability
Unknown
Check Digit Verification of cas no
The CAS Registry Mumber 3767-40-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3767-40:
(6*3)+(5*7)+(4*6)+(3*7)+(2*4)+(1*0)=106
106 % 10 = 6
So 3767-40-6 is a valid CAS Registry Number.
3767-40-6Relevant academic research and scientific papers
ALKALOIDS FROM THE ROOTS OF Papaver pseudo-orientale (FEDDE) MEDW.
Veznik, Frantisek,Taborska, Eva,Sedmera, Petr,Dolejs, Ladislav,Slavik, Jiri
, p. 1752 - 1763 (2007/10/02)
Two new alkaloids, pseudorine (Ia) (quaternary benzyltetrahydroisoquinoline type) and pseudoronine (II) (benzil type), were isolated from the roots of Papaver pseudo-orientale (FEDDE) MEDW.This is a first occurence of this type of alkaloids in Papaveraceae.The main component of the tertiary alkaloid fraction was isothebaine accompanied by smaller amounts of orientalidine, mecambridine, bracteoline, nuciferine, protopine, and allocryptopine.The presence of salutaridine and papaverrubine D was established.Traces of coptisine and palmatine were also found in some samples.Strongly polar portion of the extract was converted to iodides.N-Methylisothebainium iodide (IIIa) (major component), pseudorine iodide (Ia), and corytuberine hydriodide (IV) (significant amounts), a minor alkaloids such as alborine iodide (alkaloid PO-5), pseudoronine (II), and magnoflorine iodide (IIIb) were isolated from this source.Structure of pseudorine was determined by UV, IR, 1H, and 13C NMR spectroscopy and using the correlation with laudanosine and codamine.Proposed structure of pseudoronine is based on the mass spectra comparison.
