- Molecular NameRepaglinide
- SynonymAG-EE 388 ZW; AG-EE 623 ZW; Repaglinida [INN-Spanish]; repaglinide; Repaglinidum [INN-Latin]
- Weight452.595
- Drugbank_IDDB00912
- ACS_NO135062-02-1
- Show 3D model
- LogP (experiment)N/A
- LogP (predicted, AB/LogP v2.0)5.45
- pkaN/A
- LogD (pH=7, predicted)2.33
- Solubility (experiment)N/A
- LogS (predicted, ACD/Labs)(ph=7)-3.63
- LogSw (predicted, AB/LogsW2.0)0.01
- Sw (mg/ml) (predicted, ACD/Labs)0.01
- No.of HBond Donors2
- No.of HBond Acceptors6
- No.of Rotatable Bonds10
- TPSA78.87
- StatusFDA approved
- AdministrationN/A
- PharmacologyA drug is used for the treatment of type II diabetes.
- Absorption_value100.0
- Absorption (description)N/A
- Caco_2N/A
- Bioavailability56.0
- Protein binding97.4
- Volume of distribution (VD)0.41 L/kg
- Blood/Plasma Partitioning ratio (D_blood)N/A
- MetabollsmUndergoes extensive oxidative and conjugative metabolism; CYP3A4 has been implicated in the formation of the major (60% of dose) metabolite.
- Half life0.8 h
- ExcretionFecal (90%) and renal (8%)
- Urinary Excretion0.3~2.6
- Clerance9.3 ml/min/kg
- ToxicityLD50 >1 g/kg (rat) (W. Grell)
- LD50 (rat)N/A
- LD50 (mouse)N/A