• Molecular NameDeflazacort
  • SynonymNA
  • Weight441.524
  • Drugbank_IDN/A
  • ACS_NO14484-47-0
  • Show 2D model
  • LogP (experiment)N/A
  • LogP (predicted, AB/LogP v2.0)3.05
  • pkaN/A
  • LogD (pH=7, predicted)3.05
  • Solubility (experiment)N/A
  • LogS (predicted, ACD/Labs)(ph=7)-4.12
  • LogSw (predicted, AB/LogsW2.0)0.01
  • Sw (mg/ml) (predicted, ACD/Labs)0.03
  • No.of HBond Donors1
  • No.of HBond Acceptors7
  • No.of Rotatable Bonds4
  • TPSA102.26
  • StatusN/A
  • AdministrationN/A
  • PharmacologyA glucocorticoid used as an anti-inflammatory and immunosuppressant.
  • Absorption_valueN/A
  • Absorption (description)Deflazacort is well absorbed from the gastro-intestinal tract
  • Caco_2N/A
  • Bioavailability68.0
  • Protein binding40.0
  • Volume of distribution (VD)Deflazacort-6-beta-hydroxide, 83 L.
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmImmediately converted by plasma esterases to its active metabolite, 21-desacetyldeflazacort with further metabolism to deflazacort-6-β-hydroxide.
  • Half life2.1 h
  • ExcretionElimination is mainly via the kidneys, with 70% of the administrated dose recovered in the urine and the remaining 30% in faeces.
  • Urinary ExcretionN/A
  • Clerance83.9 ± 24.5 (36 mg dose) to 97.1 ± 47.7 L/h (3 mg dose).
  • ToxicityN/A
  • LD50 (rat)N/A
  • LD50 (mouse)N/A