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TH-PVP is a substituted cathinone derivative which has been sold as a designer drug. It was first identified by a forensic laboratory in Hungary in 2015, but has subsequently been found in numerous other countries around the world including Spain, Belgium, Poland, Turkey and Brazil. Pharmacological studies in vitro showed it to inhibit reuptake and promote the release of monoamine neurotransmitters with some selectivity for serotonin, but it failed to produce stimulant effects in animals, and has a pharmacological profile more comparable to that of sedating empathogens such as MDAI and 5-Methyl-MDA.

AttributesValues
rdf:type
rdfs:label
  • TH-PVP (en)
rdfs:comment
  • TH-PVP is a substituted cathinone derivative which has been sold as a designer drug. It was first identified by a forensic laboratory in Hungary in 2015, but has subsequently been found in numerous other countries around the world including Spain, Belgium, Poland, Turkey and Brazil. Pharmacological studies in vitro showed it to inhibit reuptake and promote the release of monoamine neurotransmitters with some selectivity for serotonin, but it failed to produce stimulant effects in animals, and has a pharmacological profile more comparable to that of sedating empathogens such as MDAI and 5-Methyl-MDA. (en)
foaf:name
  • TH-PVP (en)
foaf:depiction
  • http://commons.wikimedia.org/wiki/Special:FilePath/TH-PVP.svg
dcterms:subject
Wikipage page ID
Wikipage revision ID
Link from a Wikipage to another Wikipage
sameAs
dbp:wikiPageUsesTemplate
thumbnail
ATC prefix
  • None (en)
c
CAS number
ChemSpiderID
drug name
  • TH-PVP (en)
H
IUPAC name
legal DE
  • NpSG (en)
legal UK
  • PSA (en)
n
O
PubChem
SMILES
  • CCCCN3CCCC3 (en)
StdInChI
StdInChIKey
  • MMIKQWIZKBYLKZ-UHFFFAOYSA-N (en)
UNII
  • S5MU9GV87C (en)
width
has abstract
  • TH-PVP is a substituted cathinone derivative which has been sold as a designer drug. It was first identified by a forensic laboratory in Hungary in 2015, but has subsequently been found in numerous other countries around the world including Spain, Belgium, Poland, Turkey and Brazil. Pharmacological studies in vitro showed it to inhibit reuptake and promote the release of monoamine neurotransmitters with some selectivity for serotonin, but it failed to produce stimulant effects in animals, and has a pharmacological profile more comparable to that of sedating empathogens such as MDAI and 5-Methyl-MDA. (en)
legal CA
  • Schedule I (en)
prov:wasDerivedFrom
page length (characters) of wiki page
CAS number
  • 2304915-07-7
FDA UNII code
  • S5MU9GV87C
PubChem
  • 132989549
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is Link from a Wikipage to another Wikipage of
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