Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H18ClN3O3 |
| Molecular Weight | 335.785 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC=C(C=C1)C2CN(CC(=O)N3CCNC(=O)C3)C(=O)C2
InChI
InChIKey=QPKMIYNBZGPJAR-UHFFFAOYSA-N
InChI=1S/C16H18ClN3O3/c17-13-3-1-11(2-4-13)12-7-15(22)20(8-12)10-16(23)19-6-5-18-14(21)9-19/h1-4,12H,5-10H2,(H,18,21)
| Molecular Formula | C16H18ClN3O3 |
| Molecular Weight | 335.785 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Fast systematic approach for the determination of drugs in biological fluids by fully automated high-performance liquid chromatography with on-line solid-phase extraction and automated cartridge exchange. Application to cebaracetam in human urine. | 1992-06-10 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:21:48 GMT 2025
by
admin
on
Mon Mar 31 18:21:48 GMT 2025
|
| Record UNII |
Q25MNP6OC1
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C1509
Created by
admin on Mon Mar 31 18:21:48 GMT 2025 , Edited by admin on Mon Mar 31 18:21:48 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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SUB06160MIG
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PRIMARY | |||
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100000081374
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PRIMARY | |||
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6861
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PRIMARY | |||
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113957-09-8
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PRIMARY | |||
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65919
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PRIMARY | |||
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CHEMBL2105942
Created by
admin on Mon Mar 31 18:21:48 GMT 2025 , Edited by admin on Mon Mar 31 18:21:48 GMT 2025
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PRIMARY | |||
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DTXSID70869580
Created by
admin on Mon Mar 31 18:21:48 GMT 2025 , Edited by admin on Mon Mar 31 18:21:48 GMT 2025
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PRIMARY | |||
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Q25MNP6OC1
Created by
admin on Mon Mar 31 18:21:48 GMT 2025 , Edited by admin on Mon Mar 31 18:21:48 GMT 2025
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PRIMARY | |||
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C78115
Created by
admin on Mon Mar 31 18:21:48 GMT 2025 , Edited by admin on Mon Mar 31 18:21:48 GMT 2025
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PRIMARY | |||
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CEBARACETAM
Created by
admin on Mon Mar 31 18:21:48 GMT 2025 , Edited by admin on Mon Mar 31 18:21:48 GMT 2025
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PRIMARY | |||
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C077252
Created by
admin on Mon Mar 31 18:21:48 GMT 2025 , Edited by admin on Mon Mar 31 18:21:48 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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|
ENANTIOMER -> RACEMATE | |||
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|
ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |