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

Stem definitionDrug idCAS RN
anorexics 697 14261-75-7

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • oberex
  • cloforex
  • clophorex
  • frenapyl
carbamic ethyl ester of chlorphentermine; structure in Negwer, 5th ed, #2275
  • Molecular weight: 255.74
  • Formula: C13H18ClNO2
  • CLOGP: 3.89
  • LIPINSKI: 0
  • HAC: 3
  • HDO: 1
  • TPSA: 38.33
  • ALOGS: -4.07
  • ROTB: 5

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 3.976 High 1
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.614 High 1
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 74.645 10^-6 cm/s High 1
dh-clint Dog hepatocyte intrinsic clearance 22.131 uL/min/10^6 cells High 1
dppb Dog plasma protein binding (% unbound) 2.490 % High 1
fcs-ppb Fetal calf serum protein binding (% unbound) 3.980 % High 1
herg hERG pIC50 4.908 pIC50 High 1
hh-clint Human hepatocyte intrinsic clearance 25.119 uL/min/10^6 cells High 1
hlm-clint Human liver microsomal intrinsic clearance 50.119 uL/min/mg protein High 1
hppb Human plasma protein binding (% unbound) 1.940 % High 1
kinase-safety-class ACVR2A,ACVR2B,AURKA,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK5,CDK9,DDR1,DYRK1B,EGFR,EIF2AK3,EPHB4,ERBB2,GRK2,GSK3B,ITK,JAK2,MAP3K21,MAP3K7,MAPK12,MAPK7,MAPK9,MAPKAPK2,MET,NTRK2,PDK1,PDK2,PDK4,PDPK1,PIK3CB,PIK3CG,PIM2,PRKCD,PRKDC,SIK2,SIK3,STK33,SYK,TEK,TTK 43
kinase-selectivity-class ACVR2B,AXL,BRAF,GRK2,PDK4 5
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 0.224 High 1
mh-clint Mouse hepatocyte intrinsic clearance 142.233 High 1
mppb Mouse plasma protein binding (% unbound) 2.730 High 1
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 0.579 High 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 3.060 % High 1
rh-clint Rat hepatocyte intrinsic clearance 137.721 uL/min/10^6 cells High 1
rh-fuinc Rat hepatocyte fraction unbound in incubation 36.740 % High 1
rppb Rat plasma protein binding (% unbound) 2.170 % High 1
solubility-dd Solubility at pH 7.4 in DMSO 9.268 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:

None

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 13.68 acidic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
C0614696 UMLSCUI
CHEBI:135049 CHEBI
CHEMBL1697686 ChEMBL_ID
C032205 MESH_SUPPLEMENTAL_RECORD_UI
26602 PUBCHEM_CID
1994 INN_ID
2QJT5ZC1L6 UNII

Pharmaceutical products:

None