Details
Stereochemistry | RACEMIC |
Molecular Formula | C24H30N2O4 |
Molecular Weight | 410.506 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(C=C1)C=C(N(C)C2=O)C3=CC=C(OCC(O)CNC(C)(C)C)C=C3
InChI
InChIKey=MZELTXWHFDTAOO-UHFFFAOYSA-N
InChI=1S/C24H30N2O4/c1-24(2,3)25-14-18(27)15-30-19-9-6-16(7-10-19)22-12-17-8-11-20(29-5)13-21(17)23(28)26(22)4/h6-13,18,25,27H,14-15H2,1-5H3
Molecular Formula | C24H30N2O4 |
Molecular Weight | 410.506 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2883988
Single dose - 400 mg
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:27:27 GMT 2023
by
admin
on
Fri Dec 15 16:27:27 GMT 2023
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Record UNII |
K3B3L3Q0GV
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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 |
C29576
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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Code System | Code | Type | Description | ||
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CHEMBL1742429
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K3B3L3Q0GV
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admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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67793-71-9
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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10070156
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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C65479
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admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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SUB06397MIG
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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DTXSID301024412
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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5869
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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126522-41-6
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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SUPERSEDED | |||
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100000080817
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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Draquinolol
Created by
admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
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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 |