9,10-Dihydro-LSD, or 9,10-DH-LSD, also known simply as dihydro-LSD (DH-LSD) or as 9,10-dihydrolysergic acid diethylamide, is a non-hallucinogenic serotonin receptor modulator of the lysergamide family related to lysergic acid diethylamide (LSD). It is the analogue of LSD in which the 9,10- double bond in the D ring of the ergoline ring system has been hydrogenated.
Use and effects 9,10-Dihydro-LSD has been found to be inactive in terms of psychedelic effects in humans. Whereas LSD is active at an oral dose of 1μg/kg (70μg for a 70-kg person), 9,10-dihydro-LSD was said to be inactive orally at doses of up to 50μg/kg (3.5mg for a 70-kg person). As such, 9,10-dihydro-LSD does not appear to produce psychedelic effects at doses of up to 50times the effective doses of LSD, demonstrating less than 2% of the potency of LSD in this regard. Another source stated it to have 0% of the psychedelic potency of LSD. Despite its lack of psychedelic effects however, 9,10-dihydro-LSD at doses of 100 to 200μg orally has nonetheless been reported to produce strong autonomic effects in humans, including nausea, emesis, tachycardia, shivering, polyuria, headache, and paresthesias.
Toxicity The of 9,10-dihydro-LSD given intravenously in mice is 56mg/kg.
Pharmacology Pharmacodynamics 9,10-Dihydro-LSD has been shown to bind to the serotonin 5-HT2A, 5-HT2C, and 5-HT1A receptors. It acts as a partial agonist of the serotonin 5-HT2A receptor similarly to LSD, whereas functional activities at the other serotonin receptors were not reported. At the serotonin 5-HT2A receptor, 9,10-dihydro-LSD's affinity (K0.5) was 2.9nM (compared to 1.08nM for LSD), whereas its activational potency () in terms of calcium release was 3,840nM and its intrinsic activity () was 58% (relative to 595nM and 55% for LSD, respectively). Hence, 9,10-dihydro-LSD had about 2.7-fold lower affinity and 6-fold lower activational potency at the receptor compared to LSD, whereas its activational efficacy in terms of calcium release was about the same. At the serotonin 5-HT2C and 5-HT1A receptors, 9,10-dihydro-LSD showed 4.6-fold and 26-fold lower affinities than those of LSD, respectively.
In earlier studies, 9,10-dihydro-LSD showed 52% of the serotonin antagonist activity of LSD in the isolated rat uterus in vitro. It was reported to have failed to produce the autonomic or sympathomimetic effects typical of LSD and related psychedelics in animals, such as mydriasis, piloerection, and hyperthermia, although it did produce hypothermia.
Chemistry Synthesis The chemical synthesis of 9,10-dihydro-LSD has been described.
Analogues A number of analogues and derivatives of 9,10-dihydro-LSD are known, for instance dihydroergotoxine, a mixture of dihydroergocornine, dihydroergocristine, and dihydroergocryptine, and dihydroergotamine. Various 9,10-dihydrolysergamides are known to be very potent α-adrenergic antagonists, to have almost no effects on the uterus (i.e., no oxytocic activity), and to have markedly reduced central effects. Dihydroergotoxine has been used to treat vascular disorders and essential hypertension, but has largely been discontinued. Other 9,10-Dihydrolysergamides have shown emetic activity. They often have comparable antiserotonergic activity relative to the saturated analogues. In general, 9,10-dihydrolysergamides are said to be devoid of hallucinogenic activity.
History 9,10-Dihydro-LSD was first described in the scientific literature by at least the 1950s.
See also Substituted lysergamide AWD 52-39 2,3-Dihydro-LSD Lumi-LSD (10-hydroxy-9,10-dihydro-LSD)
References
External links 9,10-Dihydro-LSD - Isomer Design