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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 | |||
| TEGASEROD DISCONTINUED
| TEGASEROD | METABOLISM | ORAL | Tmax 1 HOUR F 10 PERCENT VD 368 LITER PPB 98 PERCENT Cl 77 LITER / HOUR HT 11 HOUR SOLUBILITY VERY SLIGHTLY SOLUBLE IN WATER | 5-HYDROXYTRYPTAMINE 4 RECEPTOR | 5-hydroxytryptamine receptor 4 UNIPROT Q13639 HTR4 more at DrugCentral | EMA | |||
