Details
Stereochemistry | RACEMIC |
Molecular Formula | C19H22FN3O4 |
Molecular Weight | 375.3941 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(N2CCNC(C)C2)C(F)=CC3=C1N(C=C(C(O)=O)C3=O)C4CC4
InChI
InChIKey=XUBOMFCQGDBHNK-UHFFFAOYSA-N
InChI=1S/C19H22FN3O4/c1-10-8-22(6-5-21-10)16-14(20)7-12-15(18(16)27-2)23(11-3-4-11)9-13(17(12)24)19(25)26/h7,9-11,21H,3-6,8H2,1-2H3,(H,25,26)
Molecular Formula | C19H22FN3O4 |
Molecular Weight | 375.3941 |
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 15:44:07 UTC 2023
by
admin
on
Fri Dec 15 15:44:07 UTC 2023
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Record UNII |
81485Y3A9A
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Record Status |
Validated (UNII)
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Record Version |
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-
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Common Name | English | ||
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Systematic Name | English | ||
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Brand Name | English | ||
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Common Name | English | ||
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Code | English |
Classification Tree | Code System | Code | ||
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WHO-ATC |
J01MA16
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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WHO-ATC |
S01AX21
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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NDF-RT |
N0000007606
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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NDF-RT |
N0000175937
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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LIVERTOX |
NBK547840
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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Code System | Code | Type | Description | ||
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7423
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PRIMARY | |||
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SUB13952MIG
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DTXSID5045704
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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758701
Created by
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PRIMARY | |||
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DB01044
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY | |||
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81485Y3A9A
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY | |||
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81485Y3A9A
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY | |||
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1546025
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY | RxNorm | ||
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C175722
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY | |||
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5379
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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100000090510
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY | |||
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m5679
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY | Merck Index | ||
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112811-59-3
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY | |||
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Gatifloxacin
Created by
admin on Fri Dec 15 15:44:07 UTC 2023 , Edited by admin on Fri Dec 15 15:44:07 UTC 2023
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PRIMARY |
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SOLVATE->ANHYDROUS |
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT |
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TARGET ORGANISM->INHIBITOR |
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SOLVATE->ANHYDROUS |
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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TARGET ORGANISM->INHIBITOR |
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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