CAS 525-74-6
:N-Methylmyosmine
Description:
N-Methylmyosmine is an alkaloid compound that belongs to the class of pyridine derivatives. It is characterized by its molecular structure, which includes a pyridine ring and a methyl group attached to the nitrogen atom. This compound is typically found in tobacco and is a product of the degradation of nicotine. N-Methylmyosmine is known for its potential biological activity, including its role in the formation of DNA adducts, which may have implications for carcinogenicity. The substance is a colorless to pale yellow liquid with a distinctive odor and is soluble in organic solvents. Its chemical formula is C₇H₈N₂, and it has a relatively low molecular weight. Due to its presence in tobacco products, N-Methylmyosmine has garnered interest in studies related to tobacco harm and the health effects of smoking. Safety data indicates that, like many alkaloids, it should be handled with care, as it may pose health risks upon exposure.
Formula:C10H12N2
InChI:InChI=1S/C10H12N2/c1-12-7-3-5-10(12)9-4-2-6-11-8-9/h2,4-6,8H,3,7H2,1H3
InChI key:InChIKey=TVKHGXPZBZKXFM-UHFFFAOYSA-N
SMILES:CN1C(=CCC1)C=2C=CC=NC2
Synonyms:- 3-(1-Methyl-2,3-dihydropyrrol-5-yl)pyridine
- 3-(1-methyl-4,5-dihydro-1H-pyrrol-2-yl)pyridine
- Dihydronicotyrine
- N-Methylmyosmine
- Pyridine, 3-(4,5-dihydro-1-methyl-1H-pyrrol-2-yl)-
- Pyridine, 3-(4,5-dihydro-1-methylpyrrol-2-yl)-
- 3-(4,5-Dihydro-1-methyl-1H-pyrrol-2-yl)pyridine
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Found 3 products.
Dihydro nicotyrine
CAS:<p>Dihydro nicotyrine is an alkaloid that is toxic to plants and microorganisms. It has been shown to inhibit the activity of hydroxylase enzymes, which are involved in the metabolism of aromatic compounds, such as tyrosine and phenylalanine. This inhibition leads to a decrease in the production of dopamine and norepinephrine, which may be involved in the development of Parkinson's disease. Dihydro nicotyrine is also a substrate for hydroxylases that have been sequenced from various strains of bacteria. The enzyme has been cloned from a wild-type strain of Escherichia coli, but not from soil bacteria or other organisms. Dihydro nicotyrine can be synthesized by reacting benzaldehyde with 2-amino-3-hydroxybenzoic acid in an organic solvent.</p>Formula:C10H12N2Purity:Min. 95%Color and Shape:PowderMolecular weight:160.22 g/molRef: 4Z-N-0661
Discontinued product


