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
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
| 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 | ( + / - ) |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: P28223 Gene ID: 3356.0 Gene Symbol: HTR2A Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/17203365 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Identification of compounds in the essential oil of nutmeg seeds (Myristica fragrans Houtt.) that inhibit locomotor activity in mice. | 2010-11-23 |
|
| Rediscovering MDMA (ecstasy): the role of the American chemist Alexander T. Shulgin. | 2010-08 |
|
| Interactions of amphetamine analogs with human liver CYP2D6. | 1997-06-01 |
Patents
| Substance Class |
Chemical
Created
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admin
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Mon Mar 31 17:55:49 GMT 2025
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Mon Mar 31 17:55:49 GMT 2025
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| Record UNII |
RG7FY73ZAA
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| Record Status |
Validated (UNII)
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PiHKAL
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Designer-drugs-MMDA
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DB01442
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13674-05-0
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DTXSID50860757
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MMDA (DRUG)
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RG7FY73ZAA
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26175
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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TARGET -> AGONIST |
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METABOLIC ENZYME -> INHIBITOR |
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METABOLIC ENZYME -> INHIBITOR |
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PARENT -> METABOLITE |
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ACTIVE MOIETY |
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