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

Stem definitionDrug idCAS RN
2532 14759-06-9

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • sulforidazine
  • imagotan
  • inofal
  • psychoson
  • sulphoridazine
  • thioridazine-2-sulfone
  • Molecular weight: 402.57
  • Formula: C21H26N2O2S2
  • CLOGP: 4.62
  • LIPINSKI: 0
  • HAC: 4
  • HDO: 0
  • TPSA: 40.62
  • ALOGS: -4.65
  • ROTB: 4

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 1.855 Moderate 0.72
caco2-efflux Caco-2 efflux ratio (BA/AB) 2.004 Moderate 0.72
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 18.155 10^-6 cm/s Moderate 0.72
dh-clint Dog hepatocyte intrinsic clearance 38.371 uL/min/10^6 cells Moderate 0.72
dppb Dog plasma protein binding (% unbound) 13.630 % Moderate 0.72
fcs-ppb Fetal calf serum protein binding (% unbound) 24.150 % Moderate 0.72
herg hERG pIC50 6.170 pIC50 Moderate 0.72
hh-clint Human hepatocyte intrinsic clearance 10.839 uL/min/10^6 cells Moderate 0.72
hlm-clint Human liver microsomal intrinsic clearance 48.529 uL/min/mg protein Moderate 0.72
hppb Human plasma protein binding (% unbound) 13.650 % Moderate 0.72
kinase-safety-class ACVR2B,AKT2,AKT3,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK5,CDK9,DYRK1B,EIF2AK3,EPHB4,ERBB2,FLT3,GRK2,ITK,JAK2,JAK3,MAP3K7,MAPK10,MAPK7,MET,NTRK2,PDK2,PDK4,PIK3CA,PIK3CB,PIM2,PRKDC,SIK2,SIK3,STK33,TEK,TTK 35
mdck-mdr1-bcrp-efflux MDCK-MDR1-BCRP efflux ratio 3.289 Moderate 0.70
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 4.446 Moderate 0.72
mh-clint Mouse hepatocyte intrinsic clearance 124.451 Moderate 0.72
mppb Mouse plasma protein binding (% unbound) 15.280 Moderate 0.72
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 26.182 Moderate 0.72
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 28.570 % Moderate 0.72
rat-kpuu-brain Rat brain Kpuu 0.059 % Moderate 0.70
rh-clint Rat hepatocyte intrinsic clearance 144.212 uL/min/10^6 cells Moderate 0.72
rh-fuinc Rat hepatocyte fraction unbound in incubation 46.380 % Moderate 0.72
rppb Rat plasma protein binding (% unbound) 16.070 % Moderate 0.72
solubility-dd Solubility at pH 7.4 in DMSO 963.829 uM Moderate 0.72

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 D000928 Antidepressive Agents
MeSH PA D002491 Central Nervous System Agents
MeSH PA D002492 Central Nervous System Depressants
MeSH PA D011619 Psychotropic Drugs
MeSH PA D014149 Tranquilizing Agents
MeSH PA D014150 Antipsychotic Agents

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 9.22 Basic
pKa2 3.45 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
D(2) dopamine receptor GPCR Ki 9.61 PDSP
D(3) dopamine receptor GPCR Ki 9.16 PDSP

External reference:

IDSource
C0075591 UMLSCUI
CHEBI:135644 CHEBI
CHEMBL2107268 ChEMBL_ID
C040634 MESH_SUPPLEMENTAL_RECORD_UI
31765 PUBCHEM_CID
C476405 MESH_SUPPLEMENTAL_RECORD_UI
2394 INN_ID
B7599I244X UNII
725620001 SNOMEDCT_US

Pharmaceutical products:

None