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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 | |||
| TENAPANOR
| TENAPANOR | NERVOUS SYSTEM | ORAL | PPB 99 PERCENT SOLUBILITY PRACTICALLY INSOLUBLE IN WATER | SODIUM/HYDROGEN EXCHANGER 3 (NHE3) | transporter Sodium/hydrogen exchanger 3 inhibitor P48764 SL9A3_HUMAN | EMA | |||
