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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 the equation t1/2 = VD / Cl * 0.693 was used | Primary Target and PDB code of Protein-Drug complex | Targets from DrugCentral | Links | |||
| DIAZOXIDE
| DIAZOXIDE | CARDIOVASCULAR | INJECTION ORAL | Tmax 1 HOUR VD 13.6 LITER (65 KILOGRAM) PPB 94 PERCENT Cl 0.23 LITER / HOUR (65 KILOGRAM) HT 48 HOUR SOLUBILITY SPARINGLY SOLUBLE IN WATER | MITOCHONDRIAL KATP-CHANNEL (PMID9400389) PDB 4LV9 (FRAGMENT-BASED IDENTIFICATION OF AMIDES DERIVED FROM TRANS-2-(PYRIDIN-3-YL)CYCLOPROPANECARBOXYLIC ACID AS POTENT INHIBITORS OF HUMAN NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT)) LIGAND CODE = 20J (link to the list of PDB complexes) Download experimental 3D coordinates of 20J with added hydrogens | Sulfonylurea receptor 1, Kir6.2 UNIPROT Q09428 ABCC8_HUMAN -- Nicotinamide phosphoribosyltransferase UNIPROT P43490 NAMPT_HUMAN more at DrugCentral | EMA | |||
