start work on Lysergic acid diethylamide table:


Lysergic acid diethylamide[1] [2] [3] [4]
Site Ki (nM) Species Ref
SERTTooltip Serotonin transporter >30,000 Human [3][4]
NETTooltip Norepinephrine transporter >30,000 Human [3]
DATTooltip Dopamine transporter >10,000 Human [4][3]
5-HT1A >10,000 Human
5-HT1B >10,000 Human
5-HT1D >10,000 Human
5-HT1E >10,000 Human
5-HT2A >10,000 Human
5-HT2B >10,000 Human
5-HT2C >10,000 Human
5-HT3 >10,000 Human
5-HT5A >10,000 Human
5-HT6 >10,000 Human
5-HT7 0.39 - 199.5 (8.7) Rat
Guinea Pig
α1A 670.0 Human [3]
α2A 12.0 Human [3]
β1 140.0 Human [5]
β2 740.0 Human [5]
D1 273.0 - 310.0
30.0
180.0
Human
Calf
Rat
[4][3]
[2]
[5]
D2 25.0 - 38.8
120.0
Human
Rat
[4][3]
[5]
D3 27.1 - 96.0
27.0
Human
Rat
[4][3]
[5]
D4 330.0
56.0
Human
Rat
[4]
[5]
D5 340.0 Rat [5]
H1 1,100
1,300 - 1,540
Human
Rat (brain)
[3]
[6] [5]
TARR >10,000
450
Mouse
Rat
[3]
[3]
Values are Ki (nM), unless otherwise noted. The smaller the value, the more strongly the drug interacts with the site.
  1. ^ Roth, BL; Driscol, J. "PDSP Ki Database". Psychoactive Drug Screening Program (PDSP). University of North Carolina at Chapel Hill and the United States National Institute of Mental Health. {{cite web}}: |access-date= requires |url= (help); Missing or empty |url= (help)
  2. ^ a b Burt, DR; Creese, I; Snyder, SH (September 1976). "Properties of [3H]haloperidol and [3H]dopamine binding associated with dopamine receptors in calf brain membranes". Molecular pharmacology. 12 (5): 800–12. PMID 995128.
  3. ^ a b c d e f g h i j k l Rickli, Anna; Luethi, Dino; Reinisch, Julian; Buchy, Danièle; Hoener, Marius C.; Liechti, Matthias E. (December 2015). "Receptor interaction profiles of novel N-2-methoxybenzyl (NBOMe) derivatives of 2,5-dimethoxy-substituted phenethylamines (2C drugs)". Neuropharmacology. 99: 546–553. doi:10.1016/j.neuropharm.2015.08.034.
  4. ^ a b c d e f g Janowsky, Aaron; Eshleman, Amy J.; Johnson, Robert A.; Wolfrum, Katherine M.; Hinrichs, David J.; Yang, Jongtae; Zabriskie, T. Mark; Smilkstein, Martin J.; Riscoe, Michael K. (July 2014). "Mefloquine and psychotomimetics share neurotransmitter receptor and transporter interactions in vitro". Psychopharmacology. 231 (14): 2771–2783. doi:10.1007/s00213-014-3446-0.
  5. ^ a b c d e f g h Nichols, David E.; Frescas, Stewart; Marona-Lewicka, Danuta; Kurrasch-Orbaugh, Deborah M. (1 September 2002). "Lysergamides of Isomeric 2,4-Dimethylazetidines Map the Binding Orientation of the Diethylamide Moiety in the Potent Hallucinogenic Agent N , N -Diethyllysergamide (LSD)". Journal of Medicinal Chemistry. 45 (19): 4344–4349. doi:10.1021/jm020153s.
  6. ^ Tran, V T; Chang, R S; Snyder, S H (December 1978). "Histamine H1 receptors identified in mammalian brain membranes with [3H]mepyramine". Proceedings of the National Academy of Sciences. 75 (12): 6290–6294. doi:10.1073/pnas.75.12.6290.