Details
Stereochemistry | RACEMIC |
Molecular Formula | C17H26FNO2 |
Molecular Weight | 295.3922 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C(CCCCCC(O)=O)NCC1=CC=C(F)C=C1
InChI
InChIKey=YZYKBQUWMPUVEN-UHFFFAOYSA-N
InChI=1S/C17H26FNO2/c1-13(2)16(6-4-3-5-7-17(20)21)19-12-14-8-10-15(18)11-9-14/h8-11,13,16,19H,3-7,12H2,1-2H3,(H,20,21)
Molecular Formula | C17H26FNO2 |
Molecular Weight | 295.3922 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Zafuleptine is an antidepressant drug developed in the 1970s by Science Union & Cie. The compound was reported to have anti-aggressive activity without having other effects on the central nervous system. The mode of action of the compound is similar to that found with the Thyrotropin-Releasing Hormone.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:58:59 GMT 2023
by
admin
on
Fri Dec 15 15:58:59 GMT 2023
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Record UNII |
E697IIC25J
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C265
Created by
admin on Fri Dec 15 15:58:59 GMT 2023 , Edited by admin on Fri Dec 15 15:58:59 GMT 2023
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Code System | Code | Type | Description | ||
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C66679
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Zafuleptine
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5844
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SUB00129MIG
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E697IIC25J
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CHEMBL2106479
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admin on Fri Dec 15 15:58:59 GMT 2023 , Edited by admin on Fri Dec 15 15:58:59 GMT 2023
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59209-97-1
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admin on Fri Dec 15 15:58:59 GMT 2023 , Edited by admin on Fri Dec 15 15:58:59 GMT 2023
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261-658-4
Created by
admin on Fri Dec 15 15:58:59 GMT 2023 , Edited by admin on Fri Dec 15 15:58:59 GMT 2023
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68789
Created by
admin on Fri Dec 15 15:58:59 GMT 2023 , Edited by admin on Fri Dec 15 15:58:59 GMT 2023
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100000079366
Created by
admin on Fri Dec 15 15:58:59 GMT 2023 , Edited by admin on Fri Dec 15 15:58:59 GMT 2023
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DTXSID60866745
Created by
admin on Fri Dec 15 15:58:59 GMT 2023 , Edited by admin on Fri Dec 15 15:58:59 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE |
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ENANTIOMER -> RACEMATE |
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Related Record | Type | Details | ||
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ACTIVE MOIETY |