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3,4-Methylenedioxy-N-propylamphetamine

Field	Value
verifiedrevid	379537419
drug_name	MDPR
image	Methylenedioxypropylamphetamine.svg
image_class	skin-invert-image
width	250px
routes_of_administration	Oral
class	Psychoactive drug
ATC_prefix	None
duration_of_action	Unknown
CAS_number_Ref
CAS_number	74698-36-5
PubChem	559375
ChemSpiderID	486273
UNII_Ref
UNII	B4W69BKX3L
ChEMBL	197038
IUPAC_name	N-[1-(2H-1,3-benzodioxol-5-yl)propan-2-yl]propan-1-amine
C	13	H=19	N=1	O=2
SMILES	CC(NCCC)Cc1ccc2OCOc2c1	StdInChI = 1S/C13H19NO2/c1-3-6-14-10(2)7-11-4-5-12-13(8-11)16-9-15-12/h4-5,8,10,14H,3,6-7,9H2,1-2H3
StdInChIKey	LBXMQBTXOLBCCA-UHFFFAOYSA-N

| Drugs.com =

| elimination_half-life =

3,4-Methylenedioxy-N-propylamphetamine (MDPR) is a lesser-known psychoactive drug and a substituted amphetamine. MDPR was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 200 mg, and the duration unknown. MDPR is described as a "promoter"; by itself it has almost no effects on the mind, but it promotes the effects of hallucinogens, similarly to the closely related MDPH.

Shulgin reported that 160 mg of MDPR strongly enhanced the effects of a small (60 μg) dose of LSD, and that similar enhancement of hallucinogenic effect was noted when mixing MDPR with other drugs such as psilocybin, mescaline, 2C-B, and 2C-T-7. The reason for this synergistic action of MDPR has not been elucidated. Very little data exists about the pharmacological properties, metabolism, and toxicity of MDPR other than what is written in PiHKAL.

References

[http://www.erowid.org/library/books_online/pihkal/pihkal118.shtml MDPR entry in ''PiHKAL'']

Info: Wikipedia Source

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methylenedioxyphenethylamines pihkal propyl-compounds substituted-amphetamines

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