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
METABOLISM ANTIPERISTALTIC ANTIDIARRHEAL AGENT CHEMICALLY RELATED TO THE NARCOTIC MEPERIDINE INHIBIT NET FLUID SECRETION BY INDIRECT MECHANISMS (PMID8386327)
ORAL
Cmax 377 NANOMOLAR
Tmax 0.83 HOUR
HT 13 HOUR
MU-TYPE OPIOID RECEPTOR
MU OPIOID RECEPTOR AGONIST CHEMBL233 MU OPIOID RECEPTOR P35372 MU-TYPE OPIOID RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE OPIOID RECEPTOR
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