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RH-34

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
RH-34
Clinical data
Other namesEZS-8-NBOMe; NBOMe-EZS-8
Routes of
administration
?
ATC code
  • None
Legal status
Legal status
Identifiers
  • 3-[2-(2-methoxybenzylamino)ethyl]-1H-quinazoline-2,4-dione
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H19N3O3
Molar mass325.368 g·mol−1
3D model (JSmol)
  • O=C1C=2C(NC(=O)N1CCNCC3=C(OC)C=CC=C3)=CC=CC2
  • InChI=1S/C18H19N3O3/c1-24-16-9-5-2-6-13(16)12-19-10-11-21-17(22)14-7-3-4-8-15(14)20-18(21)23/h2-9,19H,10-12H2,1H3,(H,20,23) ☒N
  • Key:NUAJBITWGGTZCM-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

RH-34 is acompound which acts as apotent andselectivepartial agonist for the5-HT2Aserotoninreceptor subtype. It was derived by structural modification of the selective 5-HT2Aantagonistketanserin, with the 4-(p-fluorobenzoyl)piperidinemoiety replaced by theN-(2-methoxybenzyl)pharmacophore found in such potent 5-HT2A agonists asNBOMe-2C-B andNBOMe-2C-I. This alteration was found to retain 5-HT2Aaffinity and selectivity, but reversed activity from an antagonist to a moderateefficacy partial agonist.[2][3][4]

Legal status

[edit]

RH-34 is a controlled substance in Hungary[5] and Brazil.[6]

See also

[edit]

References

[edit]
  1. ^Anvisa (2023-07-24)."RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese).Diário Oficial da União (published 2023-07-25).Archived from the original on 2023-08-27. Retrieved2023-08-27.
  2. ^Ralf Heim. Synthese und Pharmakologie potenter 5-HT2A-Rezeptoragonisten mit N-2-Methoxybenzyl-Partialstruktur. Entwicklung eines neuen Struktur-Wirkungskonzepts. (German)
  3. ^Maria Silva. Theoretical study of the interaction of agonists with the 5-HT2A receptor. Universität Regensburg, 2009.
  4. ^Silva ME, Heim R, Strasser A, Elz S, Dove S (January 2011). "Theoretical studies on the interaction of partial agonists with the 5-HT(2A) receptor".Journal of Computer-aided Molecular Design.25 (1):51–66.Bibcode:2011JCAMD..25...51S.CiteSeerX 10.1.1.688.2670.doi:10.1007/s10822-010-9400-2.PMID 21088982.S2CID 3103050.
  5. ^A Magyarországon megjelent, a Kábítószer és Kábítószer-függőség Európai Megfigyelő Központjának Korai Jelzőrendszerébe (EMCDDA EWS) 2005 óta bejelentett ellenőrzött anyagok büntetőjogi vonatkozású besorolása
  6. ^"Anvisa". Archived fromthe original on 2019-02-18. Retrieved2019-02-18.
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres:JRT
Others
Natural sources
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
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