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Buy α-Pyrrolidinovalerophenone (α-PVP) Cas 14530-33-7

Pyrrolidinovalerophenone (α-PVP), also known as α-pyrrolidinopentiophenone , O-2387, β-keto-prolintane, prolintanone,^[5][6] or desmethylpyrovalerone, or colloquially as flakka or gravel,^[7][8] is a synthetic stimulant of the cathinone class developed in the 1960s that has been sold as a designer drug and often consumed for recreational reasons.^[9][10][11] α-PVP is chemically related to pyrovalerone and is the ketone analog of prolintane.^[12] α-PVP is used by a variety of different routes of administration, including oral, insufflation, injection, vaporization, sublingual, and rectal.^[9] The dose range of α-PVP for therapeutic purposes was originally defined as 10 to 50 mg, with a most-suitable dose of 20 mg, whereas the recreational dose range is typically between 10 and 300 mg.^[9] The effects of α-PVP onset after 10 minutes, peak after 10 to 40 minutes, and last 2 to 3 hours.^[9] The effects of α-PVP include cocaine-like psychostimulant effects, euphoria, elevated mood, alertness, pleasurable rush, feeling "sped up", mania-like symptoms, enhanced energy, motivation and productivity, enhanced music enjoyment, mild sexual stimulation, insomnia, paranoia, hallucinations, and increased aggression and violence.^[9] In emergency settings, commonly observed effects have included psychosis-like state, agitation, aggression, hallucinations, abnormal heart rate, and vomiting.^[9] It also produces sympathomimetic effects, such as increased heart rate and blood pressure.^[9] α-PVP, like other stimulants, can cause hyperstimulation, paranoia, and hallucinations.^[13] α-PVP has been reported to be the cause, or a significant contributory cause of death in suicides and overdoses caused by combinations of drugs.^{[14][15][16][17]} α-PVP has also been linked to at least one death with pulmonary edema and moderately advanced atherosclerotic coronary artery disease when it was combined with pentedrone.^[18] According to Craig Crespi in the journal Case Reports in Psychiatry, "symptoms are known to easily escalate into frightening delusions, paranoid psychosis, extreme agitation, and a multitude of other altered mental states." These common adverse effects of α-PVP are in line with other stimulants.^[19]

Pharmacological Receptor Activity Profile of Novel Pyrovalerones Compared to Reference Amphetamines ^[20]

Drug	NET	DAT	SERT	DAT/SERT Ratio
⍺-PVP	0.02 (0.01‒0.05)	0.03 (0.02‒0.04)	279 (209‒372)	>1000
⍺-PHP	0.06 (0.03‒0.12)	0.06 (0.05‒0.08)	245 (173‒348)	>1000
MDMA	0.41 (0.33‒0.52)	13 (11‒16)	1.6 (1.2‒2.2)	0.12 (0.08‒0.20)
Amphetamine	0.07 (0.05‒0.1)	1.3 (0.8‒2.0)	45 (24‒85)	35 (12‒106)

α-PVP acts as a potent norepinephrine–dopamine reuptake inhibitor (NDRI), similarly to other NDRIs like methylphenidate, cocaine, and methylenedioxypyrovalerone (MDPV).^[9][21] Its IC₅₀Tooltip half-maximal inhibitory concentration values have been found to be 14 to 70 nM for norepinephrine reuptake inhibition and 13 to 80 nM for dopamine reuptake inhibition in rat brain synaptosomes and human embryonic kidney 293 (HEK293) cells expressing the monoamine transporters (MATs).^{[22][23][24][25]} In contrast to its effects on catecholamine reuptake, α-PVP has negligible effects on serotonin reuptake.^[9] The drug is much more potent than amphetamine as an NDRI in in vitro, with 46-fold greater potency in terms of dopamine reuptake inhibition and 7-fold greater potency in terms of norepinephrine reuptake inhibition in HEK293 cells.^[26] It is one of the most potent dopamine reuptake inhibitors in vitro known.^[21] Similarly to other cathinone, α-PVP has been shown to have stimulant-like effects (i.e., hyperlocomotion), reinforcing effects, and sympathomimetic effects in rodents.^{[9][27][28][29]} The absorption of α-PVP is very rapid.^[9] In humans, the effects of the drug onset after 10 minutes, peak between 10 and 40 minutes, and last 2 to 3 hours.^[9] α-PVP is said to be highly lipophilic due to its pyrrolidine ring, which in turn is said to markedly enhance its ability to permeate the blood–brain barrier relative to other cathinones.^[9] The distribution, metabolism, and elimination of α-PVP have been studied.^[9] α-PVP gives no reaction with the Marquis reagent. It gives a grey/black reaction with the Mecke reagent.^[30]