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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 | |||
| FLOXURIDINE (has an active metabolite)
| FLOXURIDINE | ANTINEOPLASTIC | INJECTION | SOLUBILITY FREELY SOLUBLE IN WATER | URIDINE 5-MONOPHOSPHATE SYNTHASE (UMP SYNTHASE) PDB 2QCF (CRYSTAL STRUCTURE OF THE OROTIDINE-5-MONOPHOSPHATE DECARBOXYLASE DOMAIN (ASP312ASN MUTANT) OF HUMAN UMP SYNTHASE BOUND TO 5-FLUORO-UMP) LIGAND CODE = 5FU (link to the list of PDB complexes) Download experimental 3D coordinates of 5FU with added hydrogens | Thymidylate synthase UNIPROT P04818 TYMS more at DrugCentral | EMA | |||
