Details
Stereochemistry | RACEMIC |
Molecular Formula | C21H27NO.ClH |
Molecular Weight | 345.906 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCC(=O)C(CC(C)N(C)C)(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=FJQXCDYVZAHXNS-UHFFFAOYSA-N
InChI=1S/C21H27NO.ClH/c1-5-20(23)21(16-17(2)22(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19;/h6-15,17H,5,16H2,1-4H3;1H
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 |
Molecular Formula | C21H27NO |
Molecular Weight | 309.4452 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:13:19 UTC 2023
by
admin
on
Fri Dec 15 15:13:19 UTC 2023
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Record UNII |
229809935B
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C1506
Created by
admin on Fri Dec 15 15:13:19 UTC 2023 , Edited by admin on Fri Dec 15 15:13:19 UTC 2023
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DEA NO. |
9250
Created by
admin on Fri Dec 15 15:13:19 UTC 2023 , Edited by admin on Fri Dec 15 15:13:19 UTC 2023
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NCI_THESAURUS |
C67413
Created by
admin on Fri Dec 15 15:13:19 UTC 2023 , Edited by admin on Fri Dec 15 15:13:19 UTC 2023
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Code System | Code | Type | Description | ||
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CHEMBL651
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14184
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218337
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PRIMARY | RxNorm | ||
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70181-39-4
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SUPERSEDED | |||
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DBSALT000346
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70172-45-1
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DTXSID2020501
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100000091446
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1095-90-5
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214-140-7
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229809935B
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19600
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229809935B
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SUB03203MIG
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50140
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1398009
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125-56-4
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m7286
Created by
admin on Fri Dec 15 15:13:19 UTC 2023 , Edited by admin on Fri Dec 15 15:13:19 UTC 2023
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PRIMARY | Merck Index | ||
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C638
Created by
admin on Fri Dec 15 15:13:19 UTC 2023 , Edited by admin on Fri Dec 15 15:13:19 UTC 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE | |||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (TITRATION)
EP
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (TITRATION)
USP
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Related Record | Type | Details | ||
---|---|---|---|---|
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METABOLITE INACTIVE -> PARENT |
Cytochrome P450 enzymes, primarily CYP3A4, CYP2B6, and CYP2C19 and to a lesser extent CYP2C9 and CYP2D6, are responsible for conversion of methadone to EDDP and other inactive metabolites, which are excreted mainly in the urine.
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Related Record | Type | Details | ||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (GC)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (GC)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (GC)
EP
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||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (GC)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (GC)
EP
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Related Record | Type | Details | ||
---|---|---|---|---|
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ACTIVE MOIETY |