FHATHBIN
FHATHBIN, also known as 5-hydroxy-11-aminotetrahydrobenzindole, is a serotonin receptor agonist of the partial ergoline group.\ It is a cyclized tryptamine and tricyclic compound, tricyclic chemical derivative, derivative of serotonin (5-hydroxytryptamine) as well as a simplified structural analog, analogue of LSD. The drug is known to act on the serotonin 5-HT1A receptor, 5-HT1A receptor. FHATHBIN was first reported in the scientific literature by 1984. See also * Partial ergoline * RU-27849 * Bay R 1531 (LY-197206) * FAEFHI * O-Methylnordehydrobufotenine, ''O''-Methylnordehydrobufotenine References

5-Hydroxytryptamines Alpha-Alkyltryptamines Partial ergolines Phenethylamines Serotonin receptor agonists Tricyclic compounds {{Nervous-system-drug-stub ...
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FAEFHI
FAEFHI, also known as 4-(2-aminoethyl)-5-hydroxyindole, is a serotonin receptor modulator of the indole group related to serotonin and other substituted tryptamine, tryptamines. It is a positional isomer of serotonin in which the ethyl group, ethylamine side chain at the 3 position of the indole ring system (chemistry), ring system has been moved to the 4 position. FAEFHI can also be thought of as a greatly simplified structural analog, analogue of LSD and hence partial ergoline. Although FAEFHI shows significant affinity (pharmacology), affinity for serotonin receptors, it had much lower affinity than serotonin or tryptamine (171-fold lower than serotonin and 5-fold lower than tryptamine). In addition, it did not show serotonin-like activity (i.e., serotonin receptor agonism) even at very high concentrations ''in vitro''. FAEFHI was first described in the scientific literature by 1984. See also * Partial ergoline * FHATHBIN * RU-27251 * DEIMDHPCA * WXVL_BT0793LQ2118 References
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