flumequine 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | PK/Tox | Related Drugs | BioActivity |

Stem definitionDrug idCAS RN
quinoline derivatives 1197 42835-25-6

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • flumequine
  • flumigal
  • (+/-)-Flumequine
  • apurone
  • Molecular weight: 261.25
  • Formula: C14H12FNO3
  • CLOGP: 2.43
  • LIPINSKI: 0
  • HAC: 4
  • HDO: 1
  • TPSA: 57.61
  • ALOGS: -2.32
  • ROTB: 1

Drug dosage:

DoseUnitRoute
1.20 g O

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 0.875 High 1
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.612 High 1
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 94.406 10^-6 cm/s High 1
dh-clint Dog hepatocyte intrinsic clearance 9.616 uL/min/10^6 cells High 1
dppb Dog plasma protein binding (% unbound) 27.230 % High 1
fcs-ppb Fetal calf serum protein binding (% unbound) 26.190 % High 1
herg hERG pIC50 4.416 pIC50 High 1
hh-clint Human hepatocyte intrinsic clearance 1.096 uL/min/10^6 cells High 1
hlm-clint Human liver microsomal intrinsic clearance 6.966 uL/min/mg protein High 1
hppb Human plasma protein binding (% unbound) 14.660 % High 1
kinase-safety-class ACVR2B,AXL,EIF2AK3,GRK2,MAPK7,PDK1,PDK2,PDK4,PIK3CD,PIK3CG,PRKDC 11
kinase-selectivity-class ACVR2B,AXL,BRAF,CDK9,DYRK1B,EIF2AK3,GRK2,MAP2K6,MAPK7,PDK4,PIK3CB,PIK3CD,PRKDC,STK33,TEK,TGFBR1,TTK 17
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 1.742 High 1
mh-clint Mouse hepatocyte intrinsic clearance 19.055 High 1
mppb Mouse plasma protein binding (% unbound) 23.730 High 1
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 3.048 High 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 19.280 % High 1
rh-clint Rat hepatocyte intrinsic clearance 6.887 uL/min/10^6 cells High 1
rh-fuinc Rat hepatocyte fraction unbound in incubation 86.720 % High 1
rppb Rat plasma protein binding (% unbound) 10.690 % High 1
solubility-dd Solubility at pH 7.4 in DMSO 885.116 uM High 1

Approvals:

None

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC J01MB07 ANTIINFECTIVES FOR SYSTEMIC USE
ANTIBACTERIALS FOR SYSTEMIC USE
QUINOLONE ANTIBACTERIALS
Other quinolones
MeSH PA D000890 Anti-Infective Agents
MeSH PA D000892 Anti-Infective Agents, Urinary
MeSH PA D000970 Antineoplastic Agents
MeSH PA D004791 Enzyme Inhibitors
MeSH PA D059003 Topoisomerase Inhibitors
MeSH PA D059005 Topoisomerase II Inhibitors
CHEBI has role CHEBI:33281 antimicrobial agent
CHEBI has role CHEBI:33282 antibacterial agent
CHEBI has role CHEBI:35703 xenobiotic
CHEBI has role CHEBI:50750 EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor
CHEBI has role CHEBI:53559 topoisomerase IV inhibitor
CHEBI has role CHEBI:78298 environmental contaminant

Related Drugs by ATC class:

J01MB Other quinolones 7 drugs

Drug Use | Suggest Off label Use Form| |View source of the data|

None




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 6.03 acidic
pKa2 1.31 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
D02302 KEGG_DRUG
C0060493 UMLSCUI
CHEBI:85267 CHEBI
CHEMBL370252 ChEMBL_ID
DB08972 DRUGBANK_ID
C012976 MESH_SUPPLEMENTAL_RECORD_UI
3374 PUBCHEM_CID
13650 IUPHAR_LIGAND_ID
3776 INN_ID
UVG8VSP2SJ UNII
25112 RXNORM
005327 NDDF
765389005 SNOMEDCT_US

Pharmaceutical products:

None