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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 | |||
| LORCASERIN
| LORCASERIN | METABOLISM | ORAL | Tmax 1.75 HOUR PPB 70 PERCENT HT 11 HOUR SOLUBILITY SOLUBILITY IN WATER GREATER THAN 400 MILLIGRAM / MILLILITER | SEROTONIN 2C RECEPTOR (5-HT2C) | 5-hydroxytryptamine receptor 2C UNIPROT P28335 HTR2C more at DrugCentral | EMA | |||
