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Names

O-2574
3,4-Dihydroxy-α-pyrrolidinovalerophenone
HHPV

IUPAC name

1-(3,4-Dihydroxyphenyl)-2-(pyrrolidin-1-yl)pentan-1-one

ID 1417 · Formula C₁₅H₂₁NO₃ · Molecular weight 263.332

InChI InChI=1S/C15H21NO3/c1-2-5-12(16-8-3-4-9-16)15(19)11-6-7-13(17)14(18)10-11/h6-7,10,12,17-18H,2-5,8-9H2,1H3

InChI Key KKTUFJIEHNEGDF-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES CCCC(C(=O)c1ccc(c(c1)O)O)N1CCCC1

ChemSpider 9394303
PubChem 11219249

Meltzer, PC; Butler, D; Deschamps, JR; Madras, BK. 1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (pyrovalerone) analogues: A promising class of monoamine uptake inhibitors. J. Med. Chem., 23 Feb 2006, 49 (4), 1420–1432. 179 kB. https://doi.org/10.1021/jm050797a

Anizan, S; Ellefsen, K; Concheiro, M; Suzuki, M; Rice, KC; Baumann, MH; Huestis, MA. 3,4-Methylenedioxypyrovalerone (MDPV) and metabolites quantification in human and rat plasma by liquid chromatography–high resolution mass spectrometry. Anal. Chim. Acta, 1 May 2014, 827, 54-63. 1.4 MB. https://doi.org/10.1016/j.aca.2014.04.015 #3,4-Catechol-PV

Luethi, D; Kolaczynska, KE; Walter, M; Suzuki, M; Rice, KC; Blough, BE; Hoener, MC; Baumann, MH; Liechti, ME. Metabolites of the ring-substituted stimulants MDMA, methylone and MDPV differentially affect human monoaminergic systems. J. Psychopharmacol., 1 Jul 2019, 33 (7), 831–841. 492 kB. https://doi.org/10.1177/0269881119844185 #HHPV

MDDEBP

MDPVP

MDIPVP

MDDMHP

ED-mor-A

α,N-Butenyl-M

N,N-Butenyl-M

4-MeO-DOM-FLY

742

4-MeO-MPH

Hydroxypethidine

N-Butanoyl-MDMA

N-Ethyl-hexylone

CPe-2-en · Cyclopent-2-enscaline

CPe-3-en · Cyclopent-3-enscaline

N-Butyl-norbutylone

7 Dec 2019 · · Isomer Design