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

Stem definitionDrug idCAS RN
anti-inflammatory, anilinonicotinic acid derivatives 705 17737-65-4

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • clonixin
  • chlonixin
  • clonixic acid
  • clonixine
  • clonixin lysinate
Anti-inflammatory analgesic.
  • Molecular weight: 262.69
  • Formula: C13H11ClN2O2
  • CLOGP: 5.03
  • LIPINSKI: 1
  • HAC: 4
  • HDO: 2
  • TPSA: 62.22
  • ALOGS: -3.69
  • ROTB: 3

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 0.690 Moderate 0.66
caco2-efflux Caco-2 efflux ratio (BA/AB) 1.104 Moderate 0.66
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 106.660 10^-6 cm/s Moderate 0.66
dh-clint Dog hepatocyte intrinsic clearance 11.194 uL/min/10^6 cells Moderate 0.66
dppb Dog plasma protein binding (% unbound) 1.290 % Moderate 0.66
fcs-ppb Fetal calf serum protein binding (% unbound) 1.400 % Moderate 0.66
herg hERG pIC50 4.379 pIC50 Moderate 0.66
hh-clint Human hepatocyte intrinsic clearance 14.125 uL/min/10^6 cells Moderate 0.66
hlm-clint Human liver microsomal intrinsic clearance 4.121 uL/min/mg protein Moderate 0.66
hppb Human plasma protein binding (% unbound) 0.510 % Moderate 0.66
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 3.214 Moderate 0.66
mh-clint Mouse hepatocyte intrinsic clearance 32.659 Moderate 0.66
mppb Mouse plasma protein binding (% unbound) 2.470 Moderate 0.66
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 1.186 Moderate 0.66
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 1.490 % Moderate 0.66
rh-clint Rat hepatocyte intrinsic clearance 44.157 uL/min/10^6 cells Moderate 0.66
rh-fuinc Rat hepatocyte fraction unbound in incubation 69.030 % Moderate 0.66
rppb Rat plasma protein binding (% unbound) 0.510 % Moderate 0.66
solubility-dd Solubility at pH 7.4 in DMSO 905.733 uM Moderate 0.66

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
MeSH PA D000700 Analgesics
MeSH PA D000893 Anti-Inflammatory Agents
MeSH PA D000894 Anti-Inflammatory Agents, Non-Steroidal
MeSH PA D018501 Antirheumatic Agents
MeSH PA D018689 Sensory System Agents
MeSH PA D018712 Analgesics, Non-Narcotic
CHEBI has role CHEBI:35475 non-steroidal anti-inflammatory drug
CHEBI has role CHEBI:35481 non-narcotic analgesic
CHEBI has role CHEBI:35493 antipyretic
CHEBI has role CHEBI:35544 EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor
CHEBI has role CHEBI:35620 vasodilator agent
CHEBI has role CHEBI:35856 lipoxygenase inhibitor
CHEBI has role CHEBI:50427 platelet aggregation inhibitor

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 1.96 acidic
pKa2 5.45 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Dihydroorotate dehydrogenase (quinone), mitochondrial Enzyme IC50 4.89 CHEMBL

External reference:

IDSource
N0000167333 NUI
D03555 KEGG_DRUG
2601 RXNORM
C0009018 UMLSCUI
CHEBI:76200 CHEBI
6J3 PDB_CHEM_ID
CHEMBL1332971 ChEMBL_ID
DB09218 DRUGBANK_ID
D003002 MESH_DESCRIPTOR_UI
28718 PUBCHEM_CID
2718 INN_ID
V7DXN0M42R UNII
004344 NDDF
006033 NDDF
414111000221106 SNOMEDCT_US
455741000221101 SNOMEDCT_US
V7DXN0M42R INXIGHT DRUGS

Pharmaceutical products:

None