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[1] 6-Hydroxymelatonin is produced as a result of the enzymatic conversion of melatonin through hydroxylation. [2] Similar to melatonin, 6-OHM is a full agonist of the MT 1 and MT 2 receptors. [3] [4] It is also an antioxidant and neuroprotective, and is even more potent in this regard relative to melatonin. [5] [6]
The bioavailability of melatonin is between 2.5 and 50%. [6] [7] Melatonin is rapidly absorbed and distributed, reaching peak plasma concentrations after 60 minutes of administration, and is then eliminated. [6] Usual doses of exogenous melatonin of 1 to 12 mg produce melatonin concentrations 10 to 100 times higher than endogenous peak levels. [7]
5-Methoxytryptamine (5-MT, 5-MeO-T, or 5-OMe-T), also known as serotonin methyl ether or O-methylserotonin and as mexamine, is a tryptamine derivative closely related to the neurotransmitters serotonin and melatonin. [3] It has been shown to occur naturally in the body in low levels, especially in the pineal gland.
Cyclic 3-hydroxymelatonin (3-OHM) is a metabolite of melatonin and an antioxidant more potent than melatonin. [1] It is a non-radical species and does not further propagate the radical chain reaction It is a footprint product of the reaction between melatonin and hydroxyl radical. [2]
6-MeO-DMT, or 6-methoxy-N,N-dimethyltryptamine, also known as 6-OMe-DMT, is a serotonergic drug of the tryptamine family. [ 1 ] [ 2 ] It is the 6- methoxy derivative of the serotonergic psychedelic N , N -dimethyltryptamine (DMT) and is a positional isomer of the serotonergic psychedelic 5-MeO-DMT .
5-MeT is known to act as a potent serotonin 5-HT 2A receptor full agonist, with an EC 50 Tooltip half-maximal effective concentration of 6.00 nM and an E max Tooltip maximal efficacy of 100%. [1] In addition, it is known to be a ligand of the serotonin 5-HT 1A [ 3 ] and 5-HT 2B receptors [ 2 ] and an agonist of the serotonin 5-HT 1D [ 4 ] [ 5 ...
5,6-Dihydroxytryptamine (5,6-DHT) is a monoaminergic neurotoxin and tryptamine derivative related to serotonin (5-hydroxytryptamine) and 5,7-dihydroxytryptamine (5,7-DHT). [ 1 ] [ 2 ] [ 3 ] It is a relatively selective serotonergic neurotoxin , but also acts as a dopaminergic and noradrenergic neurotoxin at higher doses.
[3] [5] [6] The drug does not substitute for serotonergic psychedelics in animal drug discrimination tests and does not produce the head-twitch response, a behavioral of psychedelic effects, at any dose. [1] [3] [5] [7] [6] Hence, it appears to be non-hallucinogenic. [3] [5] [6] On the other hand, 5-MeO-isoDMT has comparable psychoplastogenic ...