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| 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 | |||
| FOSPROPOFOL DISCONTINUED (has an active metabolite)
| FOSPROPOFOL | NERVOUS SYSTEM | INTRAVENOUS | Cmax 732.6 MICROMOLAR (18 MILLIGRAM/KG) VD 21.4 LITER (65 KILOGRAM) PPB 98 PERCENT Cl 18.2 LITER / HOUR (65 KILOGRAM) HT 0.81 HOUR (18 MILLIGRAM/KG) SOLUBILITY WATER SOLUBLE PRODRUG OF PROPOFOL | GAMMA-AMINOBUTYRIC-ACID RECEPTOR SUBUNIT ALPHA-1 (GABA(A)) BETA-ADRENOCEPTOR (BETA-AR) (PMID21793316) | GABA-A RECEPTOR O14764 GAMMA-AMINOBUTYRIC ACID RECEPTOR SUBUNIT DELTA HOMO SAPIENS ION CHANNEL LGIC GABAA | EMA | |||
