U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H20FN3O4
Molecular Weight 361.3675
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOFLOXACIN ANHYDROUS

SMILES

C[C@H]1COC2=C3N1C=C(C(O)=O)C(=O)C3=CC(F)=C2N4CCN(C)CC4

InChI

InChIKey=GSDSWSVVBLHKDQ-JTQLQIEISA-N
InChI=1S/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/t10-/m0/s1

HIDE SMILES / InChI

Molecular Formula C18H20FN3O4
Molecular Weight 361.3675
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:44:23 UTC 2023
Edited
by admin
on Fri Dec 15 15:44:23 UTC 2023
Record UNII
RIX4E89Y14
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOFLOXACIN ANHYDROUS
Common Name English
OFLOXACIN S-(-)-FORM [MI]
Common Name English
OFLOXACIN S-(-)-FORM
MI  
Common Name English
Levofloxacin [WHO-DD]
Common Name English
NSC-758709
Code English
levofloxacin [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC J01MA12
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
WHO-ATC S01AX19
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
Code System Code Type Description
HSDB
8028
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
SMS_ID
100000089067
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
EVMPD
SUB08471MIG
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
NSC
758709
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
FDA UNII
RIX4E89Y14
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
CHEBI
63598
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
DRUG BANK
DB01137
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
NCI_THESAURUS
C170539
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
CAS
100986-85-4
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
RXCUI
1546009
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY RxNorm
INN
6708
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
PUBCHEM
149096
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
EVMPD
SUB127353
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
MERCK INDEX
m8133
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID0041060
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
DAILYMED
RIX4E89Y14
Created by admin on Fri Dec 15 15:44:23 UTC 2023 , Edited by admin on Fri Dec 15 15:44:23 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TRANSPORTER -> INHIBITOR
IC50
TARGET ORGANISM->INHIBITOR
18 STRAINS; LESS THE 8 ng/mL for some strains; MIC range listed
MIC90
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
TRANSPORTER -> INHIBITOR
IC50
SALT/SOLVATE -> PARENT
SUBSTANCE->BASIS OF STRENGTH
SOLVATE->ANHYDROUS
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METABOLITE LESS ACTIVE -> PARENT
Less than 5% of an administered dose was recovered in the urine as the desmethyl and N-oxide metabolites
URINE
METABOLITE -> PARENT
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ACTIVE MOIETY