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

Stem definitionDrug idCAS RN
antibacterials, nalidixic acid derivatives 2024 14698-29-4

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • oxolinic acid
  • dioxacin
  • nidantin
  • prodoxal
Synthetic antimicrobial related to NALIDIXIC ACID and used in URINARY TRACT INFECTIONS.
  • Molecular weight: 261.23
  • Formula: C13H11NO5
  • CLOGP: 1.66
  • LIPINSKI: 0
  • HAC: 6
  • HDO: 1
  • TPSA: 76.07
  • ALOGS: -2.14
  • ROTB: 2

Drug dosage:

DoseUnitRoute
1 g O

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 0.383 High 1
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.798 High 1
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 82.604 10^-6 cm/s High 1
dh-clint Dog hepatocyte intrinsic clearance 5.794 uL/min/10^6 cells High 1
dppb Dog plasma protein binding (% unbound) 46.090 % High 1
fcs-ppb Fetal calf serum protein binding (% unbound) 54.360 % High 1
herg hERG pIC50 4.456 pIC50 High 1
hh-clint Human hepatocyte intrinsic clearance 1.387 uL/min/10^6 cells High 1
hlm-clint Human liver microsomal intrinsic clearance 3.945 uL/min/mg protein High 1
hppb Human plasma protein binding (% unbound) 26.770 % High 1
kinase-safety-class ACVR2A,ACVR2B,AURKA,AXL,BRAF,CAMK2D,CDK5,CDK9,DDR1,DYRK1B,EIF2AK3,ERBB2,GRK2,MAP3K21,MAPK7,NTRK2,PDK1,PDK2,PIK3CB,PIK3CG,PRKDC,SIK2,STK33,TEK,TGFBR1 25
kinase-selectivity-class ACVR2B,AXL,BRAF,CDK9,DYRK1B,EIF2AK3,GRK2,MAP2K6,MAPK7,PDK4,PRKDC,STK33,TGFBR1,TTK 14
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 3.656 High 1
mh-clint Mouse hepatocyte intrinsic clearance 14.191 High 1
mppb Mouse plasma protein binding (% unbound) 36.100 High 1
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 4.786 High 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 33.490 % High 1
rh-clint Rat hepatocyte intrinsic clearance 5.188 uL/min/10^6 cells High 1
rh-fuinc Rat hepatocyte fraction unbound in incubation 85.400 % High 1
rppb Rat plasma protein binding (% unbound) 12.330 % High 1
solubility-dd Solubility at pH 7.4 in DMSO 582.103 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 J01MB05 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 D000900 Anti-Bacterial Agents
MeSH PA D000970 Antineoplastic Agents
MeSH PA D004791 Enzyme Inhibitors
MeSH PA D059005 Topoisomerase II Inhibitors
CHEBI has role CHEBI:23924 enzyme inhibitor
CHEBI has role CHEBI:33281 antimicrobial agent
CHEBI has role CHEBI:33282 antibacterial agent
CHEBI has role CHEBI:35441 antiinfective agent
CHEBI has role CHEBI:35718 antifungal agent
CHEBI has role CHEBI:36047 antibacterial drug

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 6.23 acidic
pKa2 2.58 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
N0000166914 NUI
D02301 KEGG_DRUG
C0030031 UMLSCUI
CHEBI:138856 CHEBI
OXI PDB_CHEM_ID
CHEMBL416755 ChEMBL_ID
DB13627 DRUGBANK_ID
D010093 MESH_DESCRIPTOR_UI
4628 PUBCHEM_CID
12999 IUPHAR_LIGAND_ID
1866 INN_ID
L0A22B22FT UNII
7798 RXNORM
002871 NDDF
66653008 SNOMEDCT_US
L0A22B22FT INXIGHT DRUGS

Pharmaceutical products:

None