• Molecular NameDalfopristin
  • SynonymDalfopristina [inn-spanish]; Dalfopristine [inn-french]; Dalfopristinum [inn-latin]
  • Weight690.859
  • Drugbank_IDDB01764
  • ACS_NO112362-50-2
  • Show 3D model
  • LogP (experiment)N/A
  • LogP (predicted, AB/LogP v2.0)1.27
  • pkaN/A
  • LogD (pH=7, predicted)0.44
  • Solubility (experiment)N/A
  • LogS (predicted, ACD/Labs)(ph=7)-0.94
  • LogSw (predicted, AB/LogsW2.0)0.67
  • Sw (mg/ml) (predicted, ACD/Labs)0.99
  • No.of HBond Donors2
  • No.of HBond Acceptors13
  • No.of Rotatable Bonds7
  • TPSA184.8
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyA streptogramin antibiotic derived from pristinamycin IIA.
  • Absorption_valueN/A
  • Absorption (description)N/A
  • Caco_2N/A
  • BioavailabilityN/A
  • Protein binding53.0
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmIn vitro, the transformation of the parent drugs into their major active metabolites occurs by non-enzymatic reactions and is not dependent on cytochrome-P450 or glutathione-transferase enzyme activities. Fecal excretion constitutes the main elimination route for both parent drugs and their metabolites (75-77% of dose). Urinary excretion accounts for approximately 15% of the quinupristin and 19% of the dalfopristin dose. Preclinical data in rats have demonstrated that approximately 80% of the dose is excreted in the bile and suggest that in man, biliary excretion is probably the principal route for fecal elimination.
  • Half life1 h
  • ExcretionN/A
  • Urinary ExcretionN/A
  • Clerance0.67
  • ToxicityAdverse reactions with an incidence of more than 1% and possibly or probably related to Synercid administration include: infusion site reactions, nausea, vomiting, diarrhea, trombophlebitis, rash, headache, pruritis, pain.
  • LD50 (rat)N/A
  • LD50 (mouse)N/A