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
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
| 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
| 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 22:18:28 GMT 2025
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admin
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Mon Mar 31 22:18:28 GMT 2025
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LYE581JI1D
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ACTIVE MOIETY |
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