CT-5252
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CT-5252
CT-5252 is a substituted tryptamine, tryptamine-like non-rigid structure, less-rigid structural analogue, analogue of lysergic acid diethylamide (LSD). It is a 10,11-secoergoline; that is, an substituted ergoline, ergoline in which the covalent bond between the 10 and 11 positions of the ergoline ring system (chemistry), ring system has been broken to conformational constraint, unconstrain the chemical structure, structure. The drug produces specific LSD-like behavioral changes in guinea pigs but with only about 1/48th the potency (pharmacology), potency of LSD. It also causes seizures at slightly higher doses than those that cause LSD-like effects. CT-5252 was first described in the scientific literature in 1969. The structural analog, analogue of CT-5252 with an ''N'',''N''-diethyl-carboxamide moiety (chemistry), moiety on the tetrahydropyridine ring (chemistry), ring instead of the carboxylate functional group, group (i.e., more analogous to LSD) has also been assessed and descr ...
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N-DEAOP-NMT
''N''-(3-Diethylamino-3-oxopropyl)-''N''-methyltryptamine (''N''-DEAOP-NMT) is a substituted tryptamine, tryptamine chemical derivative, derivative and a "partial" or simplified ergoline which is closely related to the highly potency (pharmacology), potent serotonergic psychedelic lysergic acid diethylamide (LSD). It is the structural analog, analogue of LSD in which two of LSD's carbon atoms in the ergoline ring (chemistry), ring, those at positions 9 and 10, have been removed. This in turn renders the ''N''-DEAOP-NMT molecule flexible and makes it a conformational constraint, non-rigid tryptamine rather than an ergoline. The compound is pharmacology, pharmacologically active, as are a number of its analogues and derivatives, with activities of the compounds including serotonin 5-HT2A receptor, 5-HT2A receptor agonist, agonism and LSD- or hallucinogen-like effects. Pharmacology ''N''-DEAOP-NMT has been found to produce quantifiable oxytocic effects in animals. However, in co ...
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