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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 | |||
| CHLORTHALIDONE
| CHLORTHALIDONE |
CARDIOVASCULAR | ORAL | F 64 PERCENT VD 253 LITER (65 KILOGRAM) PPB 76 PERCENT Cl 5.8 LITER / HOUR HT 36 HOUR SOLUBILITY PRACTICALLY INSOLUBLE IN WATER (0.12 MILLIGRAM / MILLILITER) | SODIUM CHLORIDE SYMPORTER PDB 3F4X (CARBONIC ANHYDRASE INHIBITORS. COMPARISON OF CHLORTHALIDONE AND INDAPAMIDE X-RAY CRYSTAL STRUCTURES IN ADDUCTS WITH ISOZYME II: WHEN THREE WATER MOLECULES MAKE THE DIFFERENCE) LIGAND CODE = KLT (link to the list of PDB complexes) Download experimental 3D coordinates of KLT with added hydrogens | Solute carrier family 12 member 3 UNIPROT P55017 SLC12A3 more at DrugCentral | EMA | |||
