Melatonin
Melatonin | |
| 5-methoxy-N-acetyltryptamine | |
| Empiric formula | C13H16N2O2 |
| Molecular weight | 232.28 |
| Bioavailability | 30 - 50% |
| Metabolism | Liver |
| Elimination half life | 32 - 40 minutes |
| Excretion | Urine |
| Pregnancy category | ? |
| Delivery |
1mg, 2.5mg, 3mg, and 5mg capsules; 1mg/mL or 1mg/4mL liquid; .5mg and 3mg lozenges; 2.5mg sublingual tablets; 1mg, 2mg, and 3mg timed-release tablets |
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Indicated for: | |
Melatonin helps regulate sleep-wake or circadian rhythms. Normally, production of melatonin by the pineal gland is stimulated by darkness and inhibited by light.
In recent times, melatonin has become available as a drug and a dietary supplement. It appears to have some use against insomnia and jet lag. It has been studied for the treatment of cancer, immune disorders, cardiovascular diseases, depression, seasonal affective disorder, and sexual dysfunction; no apparent benefit in these has been found.
To synthesize melatonin, serotonin is converted to N-acetylserotonin by the enzyme 5-HT N-acetyltransferase. N-acetylserotonin is then converted to melatonin by the enzyme 5-hydroxyindole-O-methyltransferase. See serotonin for details on how tryptophan is converted to serotonin.
Commercial melatonin may be extracted from bovine pineal glands. There may be a risk of contracting mad cow disease. [1]
Evidence shows that melatonin can be responsible for vivid dreaming. This may be because melatonin releases naturally produced dimethyltryptamine from the pineal gland.
| Tryptamines |
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| {Alpha-ethyltryptamine} {Alphamethyltryptamine} {Bufotenine} {Diethyltryptamine} {Diisopropyltryptamine} {Dimethyltryptamine} {Dipropyltryptamine} {Melatonin} {5-MeO-AMT} {5-MeO-DMT} {N-ethyltryptamine} {Psilocin} {Psilocybin} {Serotonin} {Tryptamine} |
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