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

Stem definitionDrug idCAS RN
3761 303-14-0

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • isopromethazine
  • isomethazine
  • isophenergan
  • prothiazin
  • Molecular weight: 284.42
  • Formula: C17H20N2S
  • CLOGP: 4.60
  • LIPINSKI: 0
  • HAC: 2
  • HDO: 0
  • TPSA: 6.48
  • ALOGS: -4.11
  • ROTB: 3

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 3.249 Moderate 0.71
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.313 Moderate 0.71
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 35.892 10^-6 cm/s Moderate 0.71
dh-clint Dog hepatocyte intrinsic clearance 80.353 uL/min/10^6 cells Moderate 0.71
dppb Dog plasma protein binding (% unbound) 6.430 % Moderate 0.71
fcs-ppb Fetal calf serum protein binding (% unbound) 11 % Moderate 0.71
herg hERG pIC50 5.572 pIC50 Moderate 0.71
hh-clint Human hepatocyte intrinsic clearance 14.521 uL/min/10^6 cells Moderate 0.71
hlm-clint Human liver microsomal intrinsic clearance 41.591 uL/min/mg protein Moderate 0.71
hppb Human plasma protein binding (% unbound) 5.240 % Moderate 0.71
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 0.449 Moderate 0.71
mh-clint Mouse hepatocyte intrinsic clearance 198.153 Moderate 0.71
mppb Mouse plasma protein binding (% unbound) 6.260 Moderate 0.71
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 1.213 Moderate 0.71
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 12.630 % Moderate 0.71
rh-clint Rat hepatocyte intrinsic clearance 306.196 uL/min/10^6 cells Moderate 0.71
rh-fuinc Rat hepatocyte fraction unbound in incubation 41.790 % Moderate 0.71
rppb Rat plasma protein binding (% unbound) 5.500 % Moderate 0.71
solubility-dd Solubility at pH 7.4 in DMSO 653.131 uM Moderate 0.71

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 D000982 Antipruritics
MeSH PA D003879 Dermatologic Agents
MeSH PA D006633 Histamine Antagonists
MeSH PA D006634 Histamine H1 Antagonists
MeSH PA D018377 Neurotransmitter Agents
MeSH PA D018926 Anti-Allergic 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 8.93 Basic
pKa2 3.55 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
C0022232 UMLSCUI
D011398 MESH_DESCRIPTOR_UI
110669 PUBCHEM_CID
044033O3TY UNII
CHEBI:135176 CHEBI

Pharmaceutical products:

None