Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H21ClFN3O3 |
Molecular Weight | 405.85 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12CN(C[C@@]1([H])NCCC2)C3=C(Cl)C4=C(C=C3F)C(=O)C(=CN4C5CC5)C(O)=O
InChI
InChIKey=VRXORHRXNRJZCQ-ZUZCIYMTSA-N
InChI=1S/C20H21ClFN3O3/c21-16-17-12(19(26)13(20(27)28)8-25(17)11-3-4-11)6-14(22)18(16)24-7-10-2-1-5-23-15(10)9-24/h6,8,10-11,15,23H,1-5,7,9H2,(H,27,28)/t10-,15+/m0/s1
Molecular Formula | C20H21ClFN3O3 |
Molecular Weight | 405.85 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Comparative in-vitro activities of the new quinolone, Bay y 3118, and ciprofloxacin, sparfloxacin, tosufloxacin, CI-960 and CI-990. | 1993 Apr |
|
In vitro antibacterial activity of the new quinolone Bay y3118 against clinical isolates. | 1994 Dec |
|
Development of a firefly luciferase-based assay for determining antimicrobial susceptibility of Mycobacterium avium subsp. paratuberculosis. | 1999 Feb |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:37:31 GMT 2023
by
admin
on
Sat Dec 16 05:37:31 GMT 2023
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Record UNII |
08VLU38WTI
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Record Status |
Validated (UNII)
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Record Version |
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-
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08VLU38WTI
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119375
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151213-16-0
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admin on Sat Dec 16 05:37:31 GMT 2023 , Edited by admin on Sat Dec 16 05:37:31 GMT 2023
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DTXSID40164736
Created by
admin on Sat Dec 16 05:37:31 GMT 2023 , Edited by admin on Sat Dec 16 05:37:31 GMT 2023
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |