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| Elemicin Basic information |
Product Name: | Elemicin | Synonyms: | 5-ALLYL-1,2,3-TRIMETHOXYBENZENE;ELIMICIN;ELEMICIN;1,2,3-trimethoxy-5-(2-propenyl)-benzen;1,2,3-trimethoxy-5-allylbenzene (elemicin);3,4,5-Trimethoxyallylbenzene;4-allyl-1,2,6-trimethoxybenzene;5-allyl-1,2,3-trimethoxy-benzen | CAS: | 487-11-6 | MF: | C12H16O3 | MW: | 208.25 | EINECS: | 207-649-0 | Product Categories: | Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals | Mol File: | 487-11-6.mol | |
| Elemicin Chemical Properties |
Boiling point | 152-156 °C | density | 1.0630 g/cm3 | storage temp. | Amber Vial, -20°C Freezer | solubility | Chloroform (Slightly), Ethyl Acetate (Slightly) | form | Oil | color | Colourless | Odor | at 100.00 %. spice flower | Odor Type | spicy | Stability: | Light Sensitive | LogP | 2.298 (est) | NIST Chemistry Reference | Benzene, 1,2,3-trimethoxy-5-(2-propenyl)-(487-11-6) |
| Elemicin Usage And Synthesis |
Description | Elemicin is a trioxygenated phenylpropane that has been found in A. dracunculus. It is active against S. aureus, B. subtilis, and C. albicans (MICs = 600, 2,500, and 1,000 mg/L, respectively) but not E. coli, K. pneumoniae, P. aeruginosa (MICs = >8,000 mg/L for all), or L. monocytogenes (MIC = >3,000 mg/L). Elemicin is toxic to mice following metabolic activation to 1’-hydroxyelemicin by the cytochrome P450 (CYP) isoforms CYP1A1 and CYP1A2. It increases plasma and hepatic triglyceride levels, decreases stearoyl-CoA desaturase 1 (Scd1) expression, and induces hepatomegaly in mice when administered at a dose of 500 mg/kg per day for three weeks. | Chemical Properties | Clear Colorless Oil | Uses | A constituent of the essential oil of nutmeg and is responsible for the psychoactive effects of nutmeg. Also a minor constituent of the oleoresin and essential oil of Manila elemi (Canarium luzonicum). Exhibits anticholinergic-like effects in humans. | Definition | ChEBI: Elemicin is an olefinic compound. | target | Antifection |
| Elemicin Preparation Products And Raw materials |
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