| Weight | 192.214 g/mol |
|---|---|
| Formula | C11H12O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Myristicin (607-91-0)
asaricin · 5-allyl-1-methoxy-2,3-(methylenedioxy)benzene
Score:
#828 in Biochemistry
,
#2232 in Biology
,
#2745 in Chemistry
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- Synergism between myristicin and xanthotoxin, a naturally cooccurring plant toxicant. (Journal of Chemical Ecology, 1985)
- Hepatoprotective Effect of Myristicin from Nutmeg (Myristica fragrans) on Lipopolysaccharide/d-Galactosamine-Induced Liver Injury (Journal of Agricultural and Food Chemistry, 2003)
- Possible implication of myristicin as a psychotropic substance. (Nature, 1966)
- Myristicin, an insecticide and synergist occurring naturally in the edible parts of parsnips. (Journal of Agricultural and Food Chemistry, 1963)
- Genotoxicity of the alkenylbenzenes and -asarone, myristicin and elemicin as determined by the UDS assay in cultured rat hepatocytes (Food and Chemical Toxicology, 1994)
- Myristicin-induced neurotoxicity in human neuroblastoma SK-N-SH cells (Toxicology Letters, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - asaricin
- 5-allyl-1-methoxy-2,3-(methylenedioxy)benzene
-
SMILESCOC1=CC(=CC2=C1OCO2)CC=C
-
InChIKeyBNWJOHGLIBDBOB-UHFFFAOYSA-N
- Pubchem - Myristicin
- Wikipedia - myristicin
Myristicin is a phenylpropene, a natural organic compound present in small amounts in the essential oil of nutmeg and to a lesser extent in other spices such as parsley and dill. It is insoluble in water, but soluble in ethanol and acetone. Myristicin is a psychoactive drug, acting as an anticholinergic, and is the traditional precursor for the synthesis of the psychedelic and empathogenic drug MMDA.
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Myristicin
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