Details
Stereochemistry | RACEMIC |
Molecular Formula | C21H23NO4S |
Molecular Weight | 385.477 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)SCC(CC1=CC=CC=C1)C(=O)NCC(=O)OCC2=CC=CC=C2
InChI
InChIKey=ODUOJXZPIYUATO-UHFFFAOYSA-N
InChI=1S/C21H23NO4S/c1-16(23)27-15-19(12-17-8-4-2-5-9-17)21(25)22-13-20(24)26-14-18-10-6-3-7-11-18/h2-11,19H,12-15H2,1H3,(H,22,25)
Molecular Formula | C21H23NO4S |
Molecular Weight | 385.477 |
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 16:27:17 UTC 2023
by
admin
on
Fri Dec 15 16:27:17 UTC 2023
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Record UNII |
76K53XP4TO
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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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WHO-ATC |
A07XA04
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admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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FDA ORPHAN DRUG |
732920
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admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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WHO-VATC |
QA07XA04
Created by
admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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Code System | Code | Type | Description | ||
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RACECADOTRIL
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DTXSID8045513
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60
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76K53XP4TO
Created by
admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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m9477
Created by
admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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PRIMARY | Merck Index | ||
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SUB12435MIG
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100000089968
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CHEMBL2103772
Created by
admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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7378
Created by
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81110-73-8
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16738
Created by
admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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PRIMARY | RxNorm | ||
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C049331
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107751
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C66503
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DB11696
Created by
admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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PRIMARY | |||
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759828
Created by
admin on Fri Dec 15 16:27:17 UTC 2023 , Edited by admin on Fri Dec 15 16:27:17 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
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METABOLITE ACTIVE -> PRODRUG |
bulk of its inhibitory actions on enkephalinase.
MAJOR
PLASMA
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Related Record | Type | Details | ||
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IMPURITY -> PARENT |
REFERENCE SOLUTION USED
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
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IMPURITY -> PARENT |
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity F = 0.7
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
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|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity E = 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
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IMPURITY -> PARENT |
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity C = 1.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|