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Details

Stereochemistry ABSOLUTE
Molecular Formula 2C18H20FN3O4.H2O
Molecular Weight 740.7503
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOFLOXACIN

SMILES

O.C[C@H]1COC2=C3N1C=C(C(O)=O)C(=O)C3=CC(F)=C2N4CCN(C)CC4.C[C@H]5COC6=C7N5C=C(C(O)=O)C(=O)C7=CC(F)=C6N8CCN(C)CC8

InChI

InChIKey=SUIQUYDRLGGZOL-RCWTXCDDSA-N
InChI=1S/2C18H20FN3O4.H2O/c2*1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21;/h2*7-8,10H,3-6,9H2,1-2H3,(H,24,25);1H2/t2*10-;/m00./s1

HIDE SMILES / InChI

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 15:30:28 UTC 2023
Edited
by admin
on Fri Dec 15 15:30:28 UTC 2023
Record UNII
6GNT3Y5LMF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOFLOXACIN
MART.   ORANGE BOOK   USAN   USP-RS   VANDF  
USAN  
Official Name English
OFLOXACIN S-(-)-FORM HEMIHYDRATE [MI]
Common Name English
(-)-(S)-9-FLUORO-2,3-DIHYDRO-3-METHYL-10-(4-METHYL-1-PIPERAZINYL)-7-OXO-7H-PYRIDO(1,2,3-DE)-1,4-BENZOXAZINE-6-CARBOXYLIC ACID, HEMIHYDRATE
Common Name English
LEVOFLOXACIN [VANDF]
Common Name English
LEVOFLOXACIN HYDRATE [JAN]
Common Name English
LEVOFLOXACIN HYDRATE
JAN  
Common Name English
LEVOFLOXACIN [ORANGE BOOK]
Common Name English
CRAVIT
Brand Name English
LEVOFLOXACIN [USP MONOGRAPH]
Common Name English
VOLEQUIN
Brand Name English
QUINSAIR
Brand Name English
IQUIX
Brand Name English
QUIXIN
Brand Name English
LEVOFLOXACIN HEMIHYDRATE
WHO-DD  
Common Name English
LEVAQUIN
Brand Name English
RWJ-25213
Code English
TAVANIC
Brand Name English
LEVOFLOXACIN HEMIHYDRATE [EP MONOGRAPH]
Common Name English
L-OFLOXACIN
Common Name English
DR-3355
Code English
7H-PYRIDO(1,2,3-DE)-1,4-BENZOXAZINE-6-CARBOXYLIC ACID, 9-FLUORO-2,3-DIHYDRO-3-METHYL-10-(4-METHYL-1-PIPERAZINYL)-7-OXO-HYDRATE (2:1), (S)-
Common Name English
LEVOFLOXACIN (AS HEMIHYDRATE)
Common Name English
Levofloxacin hemihydrate [WHO-DD]
Common Name English
OFLOXACIN, (S)-
Common Name English
LEVOFLOXACIN [USP-RS]
Common Name English
LEVOFLOXACIN [USAN]
Common Name English
NOFAXIN
Brand Name English
LEVOFLOXACIN [MART.]
Common Name English
Classification Tree Code System Code
WHO-ATC S01AE05
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
WHO-ATC A02BD10
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
NDF-RT N0000007606
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
FDA ORPHAN DRUG 253707
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
WHO-ATC J01MA12
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
LIVERTOX NBK548357
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
NDF-RT N0000175937
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
NCI_THESAURUS C795
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
EU-Orphan Drug EU/3/08/566
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
WHO-VATC QS01AE05
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
WHO-VATC QJ01RA05
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
WHO-ATC J01RA05
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
EMA ASSESSMENT REPORTS QUINSAIR (AUTHORIZED: CYSTIC FIBROSIS)
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
WHO-VATC QJ01MA12
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C1586
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
RS_ITEM_NUM
1362103
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
FDA UNII
6GNT3Y5LMF
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
DAILYMED
6GNT3Y5LMF
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
WIKIPEDIA
LEVOFLOXACIN
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
EPA CompTox
DTXSID60160533
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
DRUG CENTRAL
1569
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
CHEBI
63598
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
USAN
II-30
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
EVMPD
SUB21640
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
CAS
138199-71-0
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
MERCK INDEX
m8133
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
SMS_ID
100000091529
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
PUBCHEM
3033924
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
LACTMED
Levofloxacin
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
DRUG BANK
DB01137
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
RXCUI
82122
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY RxNorm
ChEMBL
CHEMBL33
Created by admin on Fri Dec 15 15:30:29 UTC 2023 , Edited by admin on Fri Dec 15 15:30:29 UTC 2023
PRIMARY
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Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
MIC PHARMACOKINETIC SUSCEPTIBILITY: RESISTANT

PATHOGEN: ENTEROBACTERIACEAE, E. FAECALIS, STAPHYLOCOCCUS SPECIES, P. AERUGINOSA, S. PNEUMONIAE, S. PYOGENES

MIC BIOLOGICAL SUSCEPTIBILITY: SUSCEPTIBLE

PATHOGEN: ENTEROBACTERIACEAE, E. FAECALIS, STAPHYLOCOCCUS SPECIES, P. AERUGINOSA, H. INFLUENZAE, H. PARAINFLUENZAE, S. PNEUMONIAE, S. PYOGENES

Volume of Distribution PHARMACOKINETIC POPULATION: INFANTS ≥ 6 MONTHS, CHILDREN, AND ADOLESCENTS ≤ 16 YEARS

Biological Half-life PHARMACOKINETIC POPULATION: CHILDREN 12-16 YEARS

Biological Half-life PHARMACOKINETIC POPULATION: CHILDREN 5-10 YEARS

Tmax PHARMACOKINETIC
MIC PHARMACOKINETIC SUSCEPTIBILITY: SUSCEPTIBLE

PATHOGEN: YERSINIA PESTIS, BACILLUS ANTHRACIS

Biological Half-life PHARMACOKINETIC POPULATION: ADULTS WITH RENAL IMPAIRMENT (CrCL < 20 ML/MIN)

Biological Half-life PHARMACOKINETIC POPULATION: CHILDREN 10-12 YEARS

ORAL BIOAVAILABILITY PHARMACOKINETIC ROUTE OF ADMINISTRATION: ORAL

Biological Half-life PHARMACOKINETIC POPULATION: ADULTS WITH RENAL IMPAIRMENT (CrCL 20-49 ML/MIN)

Volume of Distribution PHARMACOKINETIC POPULATION: ADULTS

Biological Half-life PHARMACOKINETIC POPULATION: INFANTS ≥ 6 MONTHS AND CHILDREN ≤ 5 YEARS

Biological Half-life PHARMACOKINETIC POPULATION: ADULTS

MIC PHARMACOKINETIC SUSCEPTIBILITY: INTERMEDIATE

PATHOGEN: ENTEROBACTERIACEAE, E. FAECALIS, STAPHYLOCOCCUS SPECIES, P. AERUGINOSA, S. PNEUMONIAE, S. PYOGENES