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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 | |||
| BEXAGLIFLOZIN
| BEXAGLIFLOZIN | METABOLISM | ORAL | Cmax 288 NANOMOLAR Tmax 3 HOUR VD 262 LITER PPB 93 PERCENT Cl 19.1 LITER / HOUR HT 12 HOUR SOLUBILITY SLIGHTLY SOLUBLE IN WATER | SODIUM-GLUCOSE CO-TRANSPORTER 2 SGLT2 | sodium-glucose co-transporter 2 UNIPROT P31639 more at DrugCentral | EMA | |||
