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

Stem definitionDrug idCAS RN
863 97-23-4

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • dichlorophen
  • dichlorofen
  • dichlorophene
  • dichlorphen
  • diclorofen
  • didroxan
  • didroxane
Nontoxic laxative vermicide effective for taenia infestation. It tends to produce colic and nausea. It is also used as a veterinary fungicide, anthelmintic, and antiprotozoan. (From Merck, 11th ed.)
  • Molecular weight: 269.12
  • Formula: C13H10Cl2O2
  • CLOGP: 4.80
  • LIPINSKI: 0
  • HAC: 2
  • HDO: 2
  • TPSA: 40.46
  • ALOGS: -3.94
  • ROTB: 2

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 4.733 Moderate 0.65
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.446 Moderate 0.65
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 34.198 10^-6 cm/s Moderate 0.65
dh-clint Dog hepatocyte intrinsic clearance 248.886 uL/min/10^6 cells Moderate 0.65
dppb Dog plasma protein binding (% unbound) 0.050 % Moderate 0.65
fcs-ppb Fetal calf serum protein binding (% unbound) 0.270 % Moderate 0.65
herg hERG pIC50 4.952 pIC50 Moderate 0.65
hh-clint Human hepatocyte intrinsic clearance 2223.310 uL/min/10^6 cells Moderate 0.65
hlm-clint Human liver microsomal intrinsic clearance 36.644 uL/min/mg protein Moderate 0.65
hppb Human plasma protein binding (% unbound) 0.210 % Moderate 0.65
kinase-safety-class ACVR2A,ACVR2B,AKT2,AKT3,AURKA,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK4,CDK5,CDK9,DDR1,DYRK1B,EGFR,EIF2AK3,EPHB4,ERBB2,FLT3,GRK2,GSK3B,IKBKB,ITK,JAK1,JAK2,JAK3,MAP2K6,MAP3K14,MAP3K21,MAP3K7,MAPK10,MAPK12,MAPK14,MAPK7,MAPK8,MAPK9,MAPKAPK2,MTOR,NTRK2,PDK1,PDK2,PDK4,PDPK1,PIK3CA,PIK3CB,PIK3CD,PIK3CG,PIM2,PRKCD,PRKDC,SIK2,SIK3,STK33,SYK,TEK,TGFBR1,TTK,ZAP70 59
kinase-selectivity-class AXL,EIF2AK3,GRK2,MAP2K6,MAPK8,TEK 6
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 1.528 Moderate 0.65
mh-clint Mouse hepatocyte intrinsic clearance 500.035 Moderate 0.65
mppb Mouse plasma protein binding (% unbound) 0.140 Moderate 0.65
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 0.560 Moderate 0.65
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 0.280 % Moderate 0.65
rh-clint Rat hepatocyte intrinsic clearance 353.183 uL/min/10^6 cells Moderate 0.65
rh-fuinc Rat hepatocyte fraction unbound in incubation 5.110 % Moderate 0.65
rppb Rat plasma protein binding (% unbound) 0.120 % Moderate 0.65
solubility-dd Solubility at pH 7.4 in DMSO 20.989 uM Moderate 0.65

Approvals:

DateAgencyCompanyOrphan
None FDA

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 P02DX02 ANTIPARASITIC PRODUCTS, INSECTICIDES AND REPELLENTS
ANTHELMINTICS
ANTICESTODALS
Other anticestodals
MeSH PA D000871 Anthelmintics
MeSH PA D000890 Anti-Infective Agents
MeSH PA D000923 Anticestodal Agents
MeSH PA D000935 Antifungal Agents
MeSH PA D000977 Antiparasitic Agents
MeSH PA D000980 Antiplatyhelmintic Agents
MeSH PA D000981 Antiprotozoal Agents
CHEBI has role CHEBI:35443 anthelminthic drug

Related Drugs by ATC class:

P02DX Other anticestodals 1 drug

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

DiseaseRelationSNOMED_IDDOID
Open-angle glaucoma indication 84494001 DOID:1067
Secondary glaucoma indication 95717004
Angle-closure glaucoma indication 392291006 DOID:13550
Malignant glaucoma off-label use 10100008
Renal tubular acidosis contraindication 1776003 DOID:14219
Respiratory acidosis contraindication 12326000
Hyperkalemia contraindication 14140009
Metabolic acidosis, normal anion gap, acidifying salts contraindication 18104000
Diabetes mellitus type 2 contraindication 44054006 DOID:9352
Diabetes mellitus type 1 contraindication 46635009 DOID:9744
Acute nephropathy contraindication 58574008
Hepatic failure contraindication 59927004
Decreased respiratory function contraindication 80954004
Hyponatremia contraindication 89627008
Gout contraindication 90560007 DOID:13189
Kidney disease contraindication 90708001 DOID:557
Disease of blood AND/OR blood-forming organ contraindication 191124002 DOID:74
Disease of liver contraindication 235856003 DOID:409
Disorder of electrolytes contraindication 237840007
Primary adrenocortical insufficiency contraindication 373662000
Recurrent Calcium Renal Calculi contraindication




🐶 Veterinary Drug Use

SpeciesUseRelation
Cats Removal of ascarids, Toxocara canis Indication
Cats Removal of hookworms, Ancylostoma caninum Indication
Cats Removal of tapeworms, Taenia pisiformis Indication
Cats Removal of tapeworms, Dipylidium caninum Indication
Cats Removal of tapeworms, Echinococcus granulosus Indication
Cats Removal of hookworms, Uncinaria stenocephala Indication
Cats Removal of ascarids, Toxascaris leonina Indication
Dogs Removal of ascarids, Toxocara canis Indication
Dogs Removal of hookworms, Ancylostoma caninum Indication
Dogs Removal of tapeworms, Taenia pisiformis Indication
Dogs Removal of tapeworms, Dipylidium caninum Indication
Dogs Removal of tapeworms, Echinococcus granulosus Indication
Dogs Removal of hookworms, Uncinaria stenocephala Indication
Dogs Removal of ascarids, Toxascaris leonina Indication

🐶 Veterinary products

ProductApplicantIngredients
Vermiplex Intervet Inc. 2
Happy Jack Tapeworm Tablets Happy Jack Inc. 1
Anaplex Caps, Canine and Feline Wormer Caps Cronus Pharma Specialities India Private Limited 2
Difolin No. 1 Capsules, Difolin No. 2.5 Capsules, Difolin No. 25 Capsules, Difolin No. 40 Capsules, Difolin No. 5 Capsules Zoetis Inc. 2
Tri-Plex Worm Capsules Intervet Inc. 2
Trivermicide Worm Capsules Happy Jack Inc. 2
Worm Capsules Farnam Companies Inc. 2
D & T Worm Capsules Cronus Pharma Specialities India Private Limited 2

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 8.56 acidic
pKa2 11.34 acidic

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
Indoleamine 2,3-dioxygenase 1 Enzyme IC50 4.15 CHEMBL
Solute carrier family 22 member 1 Transporter IC50 5.08 CHEMBL
78 kDa glucose-regulated protein Cytosolic other IC50 4 CHEMBL

External reference:

IDSource
N0000166606 NUI
3351 RXNORM
C0012082 UMLSCUI
CHEBI:34689 CHEBI
JAL PDB_CHEM_ID
CHEMBL33845 ChEMBL_ID
DB11396 DRUGBANK_ID
D004003 MESH_DESCRIPTOR_UI
3037 PUBCHEM_CID
674 INN_ID
T1J0JOU64O UNII
004478 NDDF
255999002 SNOMEDCT_US
411343001 SNOMEDCT_US
T1J0JOU64O INXIGHT DRUGS

Pharmaceutical products:

None