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Details

Stereochemistry ACHIRAL
Molecular Formula C12H9NO6
Molecular Weight 263.203
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MILOXACIN

SMILES

CON1C=C(C(O)=O)C(=O)C2=C1C=C3OCOC3=C2

InChI

InChIKey=ABQYZRZVRIPTPI-UHFFFAOYSA-N
InChI=1S/C12H9NO6/c1-17-13-4-7(12(15)16)11(14)6-2-9-10(3-8(6)13)19-5-18-9/h2-4H,5H2,1H3,(H,15,16)

HIDE SMILES / InChI

Molecular Formula C12H9NO6
Molecular Weight 263.203
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Miloxacin, an antibacterial agent that was used in veterinary. This drug was also studied for the treatment of acute intestinitis. Experiments in vitro have shown that this compound exhibited significant activities against Escherichia coli, Klebsiella pneumonia, Proteus mirabilis, Proteus vulgaris, and less active against a Pseudomonas aeruginosa infection and inactive at the maximum test doses against a Streptococcus pyogenes infection. Information about the current use of miloxacin is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Clinical studies of miloxacin for acute intestinitis (author's transl)].
1981-11
Determination of miloxacin and metabolites in human serum and urine by high-pressure liquid chromatography.
1980-07
[Antimicrobial susceptibility patterns of clinical isolates of Pseudomonas cepacia (author's transl)].
1979-10
[Determination of a new antibacterial agent miloxacin by high performance liquid chromatography and ultraviolet spectrophotometry (author's transl)].
1979-07
Studies on quinoline derivatives and related compounds. 5. Synthesis and antimicrobial activity of novel 1-alkoxy-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids.
1977-06
Patents

Patents

Sample Use Guides

healthy volunteers receiving 500 mg of miloxacin orally after the morning meal.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:26:03 GMT 2025
Edited
by admin
on Mon Mar 31 18:26:03 GMT 2025
Record UNII
VM4W7043SN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MILOXACIN [MI]
Preferred Name English
MILOXACIN
INN   MI  
INN  
Official Name English
5,8-DIHYDRO-5-METHOXY-8-OXO-1,3-DIOXOLO(4,5-G)QUINOLINE-7-CARBOXYLIC ACID
Systematic Name English
miloxacin [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C258
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
Code System Code Type Description
EVMPD
SUB08967MIG
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID70190563
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
FDA UNII
VM4W7043SN
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
DRUG CENTRAL
3360
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
CAS
37065-29-5
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
MERCK INDEX
m7547
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY Merck Index
INN
4524
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
PUBCHEM
37614
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
MESH
C023981
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
ChEMBL
CHEMBL339309
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
SMS_ID
100000080635
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
NCI_THESAURUS
C66154
Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY