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3,4-Methylenedioxy-N-methylphentermine


FieldValue
drug_nameMDMP
imageMDMP.svg
image_classskin-invert-image
width250px
routes_of_administrationOral
ATC_prefixNone
duration_of_action"Perhaps 6 hours"
CAS_number81262-69-3
PubChem44366836
ChemSpiderID21106335
UNIIP556669V7S
ChEMBL347779
synonymsMDMP; MDMPH; 3,4-Methylenedioxy-α,α,N-trimethylphenethylamine
IUPAC_name1-(2H-1,3-benzodioxol-5-yl)-N,2-dimethylpropan-2-amine
C12H=17N=1O=2
SMILESCC(C)(NC)Cc1ccc2OCOc2c1
StdInChI1S/C12H17NO2/c1-12(2,13-3)7-9-4-5-10-11(6-9)15-8-14-10/h4-6,13H,7-8H2,1-3H3
StdInChIKeyCRFWCCGPRXKZSM-UHFFFAOYSA-N

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3,4-Methylenedioxy-N-methylphentermine (MDMP or MDMPH), also known as 3,4-methylenedioxy-α,α,N-trimethylphenethylamine, is a lesser-known drug.

Use and effects

MDMP was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dose is listed as 110 mg, and the duration is listed as approximately 6 hours. MDMP produces few to no effects, and is slightly similar to MDMA.

Pharmacology

Pharmacodynamics

MDMP failed to act as a serotonin releasing agent in rat brain synaptosomes in vitro.

Society and culture

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.

References

References

  1. {{CitePiHKAL [http://www.erowid.org/library/books_online/pihkal/pihkal113.shtml MDMP entry]
  2. (1989). "Structure-activity relationships of MDMA-like substances". NIDA Research Monograph.
  3. (1990). "Ecstasy: The Clinical, Pharmacological and Neurotoxicological Effects of the Drug MDMA". Springer US.
  4. (May 1982). "Effects of certain hallucinogenic amphetamine analogues on the release of [3H]serotonin from rat brain synaptosomes". Journal of Medicinal Chemistry.
  5. "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design.
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