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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 | |||
| ETIDRONATE DISCONTINUED
| ETIDRONATE | METABOLISM | ORAL INJECTION | F 3 PERCENT HT 3.5 HOUR SOLUBILITY HIGHLY SOLUBLE IN WATER | FARNESYL PYROPHOSPHATE SYNTHASE PDB 3SDV (STRUCTURE OF A THREE-DOMAIN SESQUITERPENE SYNTHASE: A PROSPECTIVE TARGET FOR ADVANCED BIOFUELS PRODUCTION) LIGAND CODE = 911 (link to the list of PDB complexes) Download experimental 3D coordinates of 911 with added hydrogens | Type IV secretion-like conjugative transfer relaxase protein TraI UNIPROT B1LRJ1 traI more at DrugCentral | EMA | |||
