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Details

Stereochemistry RACEMIC
Molecular Formula C11H15NO3
Molecular Weight 209.2417
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MMDA

SMILES

COC1=C2OCOC2=CC(CC(C)N)=C1

InChI

InChIKey=YQYUWUKDEVZFDB-UHFFFAOYSA-N
InChI=1S/C11H15NO3/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

HIDE SMILES / InChI

Approval Year

Unknown
139594
Targets

Targets

Primary TargetPharmacologyConditionPotency
5-hydroxytryptamine receptor 2A
69
Target ID: P28223
Gene ID: 3356.0
Gene Symbol: HTR2A
Target Organism: Homo sapiens (Human)
Agonist
2678
PubMed

PubMed

TitleDatePubMed
Patents

Patents

20110159100
6
Name Type Language
MMDA
Common Name English
5-methoxy-MDA
Common Name English
MMDA (drug)
Common Name English
1,3-BENZODIOXOLE-5-ETHANAMINE, 7-METHOXY-ALPHA-METHYL
Systematic Name English
5-METHOXY-3,4-METHYLENEDIOXYAMPHETAMINE
Systematic Name English
MMDA (PSYCHEDELIC)
Common Name English
(±)-5-METHOXY-3,4-METHYLENEDIOXYAMPHETAMINE
Systematic Name English
3-METHOXY-METHYLENEDIOXYAMPHETAMINE
Systematic Name English
3-methoxy-4,5-methylenedioxyamphetamine
Systematic Name English
(±)-MMDA
Common Name English
BETA-METHOXY-ALPHA-METHYL-4,5-(METHYLENEDIOXY)PHENETHYL AMINE
Systematic Name English
.BETA.-METHOXY-.ALPHA.-METHYL-4,5-(METHYLENEDIOXY)PHENETHYL AMINE
Common Name English
3-METHOXY-.ALPHA.-METHYL-4,5-(METHYLENEDIOXY)PHENETHYLAMINE
Common Name English
3-METHOXY-ALPHA-METHYL-4,5-(METHYLENEDIOXY)PHENETHYLAMINE
Common Name English
Classification Tree Code System Code
WIKIPEDIA PiHKAL
Created by admin on Fri Dec 15 15:22:55 GMT 2023 , Edited by admin on Fri Dec 15 15:22:55 GMT 2023
WIKIPEDIA Designer-drugs-MMDA
Created by admin on Fri Dec 15 15:22:55 GMT 2023 , Edited by admin on Fri Dec 15 15:22:55 GMT 2023
Code System Code Type Description
DRUG BANK
DB01442
Created by admin on Fri Dec 15 15:22:55 GMT 2023 , Edited by admin on Fri Dec 15 15:22:55 GMT 2023
PRIMARY
CAS
13674-05-0
Created by admin on Fri Dec 15 15:22:55 GMT 2023 , Edited by admin on Fri Dec 15 15:22:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID50860757
Created by admin on Fri Dec 15 15:22:55 GMT 2023 , Edited by admin on Fri Dec 15 15:22:55 GMT 2023
PRIMARY
WIKIPEDIA
MMDA (DRUG)
Created by admin on Fri Dec 15 15:22:55 GMT 2023 , Edited by admin on Fri Dec 15 15:22:55 GMT 2023
PRIMARY
FDA UNII
RG7FY73ZAA
Created by admin on Fri Dec 15 15:22:55 GMT 2023 , Edited by admin on Fri Dec 15 15:22:55 GMT 2023
PRIMARY
PUBCHEM
26175
Created by admin on Fri Dec 15 15:22:55 GMT 2023 , Edited by admin on Fri Dec 15 15:22:55 GMT 2023
PRIMARY
ACTIVE MOIETY
Structure of MMDA
PARENT (METABOLITE)
Structure of MYRISTICIN
SALT/SOLVATE (PARENT)
Structure of MMDA hydrochloride
NIH
NCATS
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DISCLAIMER
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