Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H12N2O |
| Molecular Weight | 176.2151 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H]1N=C(N)O[C@@H]1C2=CC=CC=C2
InChI
InChIKey=LJQBMYDFWFGESC-APPZFPTMSA-N
InChI=1S/C10H12N2O/c1-7-9(13-10(11)12-7)8-5-3-2-4-6-8/h2-7,9H,1H3,(H2,11,12)/t7-,9+/m1/s1
| Molecular Formula | C10H12N2O |
| Molecular Weight | 176.2151 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Levamisole: a dangerous new cocaine adulterant. | 2010-09 |
|
| Rewarding properties of the stereoisomers of 4-methylaminorex: involvement of the dopamine system. | 2005-08 |
|
| Pharmacokinetics and tissue distribution of the stereoisomers of 4-methylaminorex in the rat. | 2004-06 |
|
| Acute neurochemical and behavioral effects of stereoisomers of 4-methylaminorex in relation to brain drug concentrations. | 2002-02 |
|
| Detection and assay of cis- and trans-isomers of 4-methylaminorex in urine, plasma and tissue samples. | 2001-09-15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:59:58 GMT 2025
by
admin
on
Mon Mar 31 21:59:58 GMT 2025
|
| Record UNII |
II4E31003P
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| Record Status |
Validated (UNII)
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| Record Version |
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II4E31003P
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10189-63-6
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15560173
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DTXSID40574154
Created by
admin on Mon Mar 31 21:59:58 GMT 2025 , Edited by admin on Mon Mar 31 21:59:58 GMT 2025
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