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1 INNClassRoute (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 complexTargets from DrugCentral Links
FENTANYL

FENTANYL


ATC N01AH01
ATC N02AB03
ATC N01AH51

NERVOUS SYSTEM
ANALGESIC
ANESTHETICS
NARCOTICS
MU-TYPE OPIOID RECEPTOR AGONISTS

INJECTION TRANSDERMAL ORAL TRANSMUCOSAL IONTOPHORESIS BUCCAL SUBLINGUAL NASAL

Cmax 7.4 NANOMOLAR

Tmax 0.33 HOUR

F 50 PERCENT

VD 260 LITER (65 KILOGRAM)

PPB 82 PERCENT

Cl 32.5 LITER / HOUR (65 KILOGRAM)

HT 7 HOUR

SOLUBILITY SPARINGLY SOLUBLE IN WATER

MU-TYPE OPIOID RECEPTOR

PDB 5TZO (COMPUTATIONALLY DESIGNED FENTANYL BINDER - FEN49*-COMPLEX)

LIGAND CODE = 7V7 (link to the list of PDB complexes)

Download experimental 3D coordinates of 7V7 with added hydrogens

MU OPIOID RECEPTOR AGONIST CHEMBL233 MU OPIOID RECEPTOR P35372 MU-TYPE OPIOID RECEPTOR HOMO SAPIENS MEMBRANE RECEPTOR 7TM1 PEPTIDE SHORT PEPTIDE OPIOID RECEPTORANSM (in French)

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