| | ||||||||||
| 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 | |||
| EMEDASTINE DISCONTINUED
| EMEDASTINE | ALLERGIC CONJUNCTIVITIS | OPHTHALMIC | Cmax 1.6 NANOMOLAR (MAXIMUM QUANTIFIED) HT 3.5 HOUR SOLUBILITY WATER SOLUBLE FINE POWDER | HISTAMINE H1 RECEPTOR (KI=1.3 NANOMOLAR) | Histamine H1 receptor UNIPROT P35367 HRH1 more at DrugCentral | EMA | |||
