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Details

Stereochemistry RACEMIC
Molecular Formula C11H15NO3.ClH
Molecular Weight 245.703
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MMDA hydrochloride

SMILES

Cl.COC1=CC(CC(C)N)=CC2=C1OCO2

InChI

InChIKey=HULCPMREEFWFRE-UHFFFAOYSA-N
InChI=1S/C11H15NO3.ClH/c1-7(12)3-8-4-9(13-2)11-10(5-8)14-6-15-11;/h4-5,7H,3,6,12H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula C11H15NO3
Molecular Weight 209.2417
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P28223
Gene ID: 3356.0
Gene Symbol: HTR2A
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:18:28 GMT 2025
Edited
by admin
on Mon Mar 31 22:18:28 GMT 2025
Record UNII
LYE581JI1D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(3,4-METHYLENEDIOXY-5-METHOXYPHENYL)ISOPROPYLAMINE HYDROCHLORIDE
Preferred Name English
MMDA hydrochloride
Common Name English
1,3-BENZODIOXOLE-5-ETHANAMINE, 7-METHOXY-.ALPHA.-METHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
5-methoxy-MDA hydrochloride
Common Name English
1,3-BENZODIOXOLE-5-ETHANAMINE, 7-METHOXY-.ALPHA.-METHYL-, HYDROCHLORIDE
Systematic Name English
MMDA (drug) hydrochloride
Common Name English
MMDA (PSYCHEDELIC) hydrochloride
Common Name English
3-methoxy-4,5-methylenedioxyamphetamine hydrochloride
Systematic Name English
1-(7-METHOXY-1,3-BENZODIOXOL-5-YL)PROPAN-2-AMINE HYDROCHLORIDE
Systematic Name English
1-(3,4-METHYLENEDIOXY-5-METHOXYPHENYL)-2-AMINOPROPANE HYDROCHLORIDE
Systematic Name English
5-METHOXY-3,4-METHYLENEDIOXYAMPHETAMINE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
43398
Created by admin on Mon Mar 31 22:18:28 GMT 2025 , Edited by admin on Mon Mar 31 22:18:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID0048890
Created by admin on Mon Mar 31 22:18:28 GMT 2025 , Edited by admin on Mon Mar 31 22:18:28 GMT 2025
PRIMARY
CAS
60676-84-8
Created by admin on Mon Mar 31 22:18:28 GMT 2025 , Edited by admin on Mon Mar 31 22:18:28 GMT 2025
PRIMARY
CAYMAN
17658
Created by admin on Mon Mar 31 22:18:28 GMT 2025 , Edited by admin on Mon Mar 31 22:18:28 GMT 2025
PRIMARY
FDA UNII
LYE581JI1D
Created by admin on Mon Mar 31 22:18:28 GMT 2025 , Edited by admin on Mon Mar 31 22:18:28 GMT 2025
PRIMARY
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