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Details

Stereochemistry RACEMIC
Molecular Formula C12H17NO2
Molecular Weight 207.2689
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EDMA

SMILES

CNC(C)CC1=CC2=C(OCCO2)C=C1

InChI

InChIKey=UJKWLAZYSLJTKA-UHFFFAOYSA-N
InChI=1S/C12H17NO2/c1-9(13-2)7-10-3-4-11-12(8-10)15-6-5-14-11/h3-4,8-9,13H,5-7H2,1-2H3

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
117.0 nM [EC50]
325.0 nM [EC50]
PubMed

PubMed

TitleDatePubMed
Ethylenedioxy homologs of N-methyl-(3,4-methylenedioxyphenyl)-2-aminopropane (MDMA) and its corresponding cathinone analog methylenedioxymethcathinone: Interactions with transporters for serotonin, dopamine, and norepinephrine.
2015 Sep 1
Name Type Language
EDMA
Common Name English
1-(2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)-N-METHYLPROPAN-2-AMINE
Systematic Name English
ETHYLENEDIOXYMETHYLAMPHETAMINE
Systematic Name English
1,4-BENZODIOXIN-6-ETHANAMINE, 2,3-DIHYDRO-N,.ALPHA.-DIMETHYL-
Systematic Name English
(±)-EDMA
Common Name English
3,4-ETHYLENEDIOXY-N-METHYLAMPHETAMINE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-EDMA
Created by admin on Sat Dec 16 10:41:44 GMT 2023 , Edited by admin on Sat Dec 16 10:41:44 GMT 2023
Code System Code Type Description
CAS
133787-66-3
Created by admin on Sat Dec 16 10:41:44 GMT 2023 , Edited by admin on Sat Dec 16 10:41:44 GMT 2023
PRIMARY
PUBCHEM
24257269
Created by admin on Sat Dec 16 10:41:44 GMT 2023 , Edited by admin on Sat Dec 16 10:41:44 GMT 2023
PRIMARY
FDA UNII
UJ7UU2C6E6
Created by admin on Sat Dec 16 10:41:44 GMT 2023 , Edited by admin on Sat Dec 16 10:41:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID501027143
Created by admin on Sat Dec 16 10:41:44 GMT 2023 , Edited by admin on Sat Dec 16 10:41:44 GMT 2023
PRIMARY
WIKIPEDIA
EDMA
Created by admin on Sat Dec 16 10:41:44 GMT 2023 , Edited by admin on Sat Dec 16 10:41:44 GMT 2023
PRIMARY 3,4-Ethylenedioxy-N-methylamphetamine (EDMA) is an entactogen drug of the amphetamine class. It is an analogue of MDMA where the methylenedioxy ring has been replaced by an ethylenedioxy ring. EDMA was first synthesized by Alexander Shulgin.[1] In his book PiHKAL, the dosage is listed as 150?250 mg, and the duration listed as 3?5 hours. According to Shulgin, EDMA produces a bare threshold consisting of paresthesia, nystagmus, and hypnogogic imagery, with few to no other effects.