Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H11NO3 |
| Molecular Weight | 193.1992 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(N)C(=O)C1=CC=C2OCOC2=C1
InChI
InChIKey=XDEZOLVDJWWXRG-UHFFFAOYSA-N
InChI=1S/C10H11NO3/c1-6(11)10(12)7-2-3-8-9(4-7)14-5-13-8/h2-4,6H,5,11H2,1H3
| Molecular Formula | C10H11NO3 |
| Molecular Weight | 193.1992 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
BK-MDA (also known as3,4-methylenedioxycathinone or normethylone), a centrally active metabolite that contributes to overall effects of the drug methylone in vivo. Methylone is a new psychoactive substance that possesses anti-depressant and anti-Parkinson properties and is a frequently abused synthetic cathinone derivative.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Metabolites of the ring-substituted stimulants MDMA, methylone and MDPV differentially affect human monoaminergic systems. | 2019-07 |
|
| Identification of three new phase II metabolites of a designer drug methylone formed in rats by N-demethylation followed by conjugation with dicarboxylic acids. | 2018-06 |
|
| Cathinone: an investigation of several N-alkyl and methylenedioxy-substituted analogs. | 1997-12 |
Patents
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 23:08:42 GMT 2025
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Mon Mar 31 23:08:42 GMT 2025
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K0XHQ9FYT3
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Validated (UNII)
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80535-73-5
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METHYLENEDIOXYCATHINONE
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PARENT -> METABOLITE |
