| | ||||||||||
| 1 | INN | Class | Route (list) | PK parameters= Cmax; Tmax; F: bioavailability; t1/2: half-life; VD: volume of distribution; Cl: clearance; PPB: plasma protein binding;(EQN means that value was calculated using VD=(Cl*t1/2)/0.693) | Primary Target and PDB code of Protein-Drug complex | Targets from DrugCentral | Links | |||
| RANITIDINE
| RANITIDINE | METABOLISM | ORAL INJECTION | Cmax 1.56 MICROMOLAR Tmax 2.5 HOUR F 50 PERCENT VD 91 LITER (65 KILOGRAM) PPB 15 PERCENT Cl 45.6 LITER / HOUR HT 2.75 HOUR SOLUBILITY SOLUBLE IN WATER | HISTAMINE H2 RECEPTOR | HISTAMINE H2 RECEPTOR ANTAGONIST CHEMBL1941 HISTAMINE H2 RECEPTOR P25021 HISTAMINE H2 RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 SMALLMOL MONOAMINE RECEPTOR HISTAMINE RECEPTOR | ANSM (in French) | |||
