| Weight | 146.193 g/mol |
|---|---|
| Formula | C9H10N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Myosmine (532-12-7)
Score:
#1876 in Biochemistry
,
#4029 in Biology
,
#5078 in Chemistry
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- Chemical studies on tobacco smoke XXIII. Synthesis of carbon14 labelled myosmine, nornicotine and Nnitrosonornicotine (Journal of Labelled Compounds and Radiopharmaceuticals, 1974)
- New Sources of Dietary Myosmine Uptake from Cereals, Fruits, Vegetables, and Milk (Journal of Agricultural and Food Chemistry, 2002)
- Infrared Diagnosis of the Hydrochlorides of Organic Bases. II.1The Structure of Myosmine (Journal of the American Chemical Society, 1954)
- Synthesis of myosmine and nornicotine, using an acylcarbanion equivalent as an intermediate (Journal of Organic Chemistry, 1972)
- Genotoxic effects of myosmine in human lymphocytes and upper aerodigestive tract epithelial cells (Toxicology, 2003)
- Nitrosation of dietary myosmine as risk factor of human cancer. (Food and Chemical Toxicology, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC(=NC1)C2=CN=CC=C2
-
InChIKeyDPNGWXJMIILTBS-UHFFFAOYSA-N
- Pubchem - Myosmine
- Wikipedia - myosmine
Myosmine is an alkaloid found in tobacco and other plants. Chemically, it is closely related to nicotine.
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