• Molecular NameAzithromycin
  • SynonymAritromicina [Spanish]; Azithramycine; Azithromycin Dihydrate; Azithromycine [French]; Azithromycinum [Latin]
  • Weight748.996
  • Drugbank_IDDB00207
  • ACS_NO83905-01-5
  • Show 3D model
  • LogP (experiment)4.02
  • LogP (predicted, AB/LogP v2.0)3.36
  • pka8.1 and 8.8
  • LogD (pH=7, predicted)-0.48
  • Solubility (experiment)slightly soluble
  • LogS (predicted, ACD/Labs)(ph=7)0.13
  • LogSw (predicted, AB/LogsW2.0)2.06
  • Sw (mg/ml) (predicted, ACD/Labs)13.72
  • No.of HBond Donors5
  • No.of HBond Acceptors14
  • No.of Rotatable Bonds7
  • TPSA180.08
  • StatusFDA approved
  • AdministrationOral (capsule or suspension), intravenous, ophthalmic
  • PharmacologyAn azalide, a subclass of macrolide antibiotics.
  • Absorption_value37.0
  • Absorption (description)Azithromycin is rapidly absorbed after oral administration with a bioavailability of about 40%.
  • Caco_2N/A
  • Bioavailability34.0
  • Protein binding28.5
  • Volume of distribution (VD)31 L/kg
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmSome demethylation of the drug occurs in the liver
  • Half life14 to >40 h
  • ExcretionIt is excreted in bile as the unchanged drug and its metabolites (approx. 10 with no microbial activity); more than 50% of a dose is excreted in faeces as the unchanged drug. About 12% of an oral dose is excreted in urine over the course of about a week.
  • Urinary Excretion12
  • Clerance9 ml/min/kg
  • ToxicityPotentially serious side effects of angioedema and cholestatic jaundice were reported
  • LD50 (rat)N/A
  • LD50 (mouse)N/A