e-Drug3D

1865

LOFEXIDINE


INN
LOFEXIDINE

cas 31036-80-3
CLASS

NERVOUS SYSTEM
CENTRAL ALPHA-2 ADRENERGIC AGONIST
INDICATED FOR MITIGATION OF OPIOID WITHDRAWAL SYMPTOMS TO FACILITATE ABRUPT OPIOID DISCONTINUATION IN ADULTS

ROUTE (list)

ORAL

ATC code

N07BC04

PK parameters

F 72 PERCENT (0.36 MILLIGRAM)
Tmax 4 HOUR
VD 480 LITER
Cl 17.6 LITER / HOUR
PPB 55 PERCENT
t1/2 12 HOUR

Solubility

FREELY SOLUBLE IN WATER


Target

TARGET ALPHA-2 ADRENERGIC RECEPTOR

DrugCentral

Alpha-2A adrenergic receptor UNIPROT P08913 ADRA2A

Download SDF file 1H-Imidazole, 2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-

Formula:
C11H12Cl2N2O

Calculated chemical properties:

MW 259.13
NB_atoms 16
XLogP 2.76
PSA 33.24
NB_HD 1
NB_HA 3
fsp3 0.36
Lipinski(0=no;1=yes) 1

FDA
NDA 209229 (label) INN (LOFEXIDINE HYDROCHLORIDE) LUCEMYRA (BIOCORRX PHARMS) APPROVAL= AP YEAR= 2018 NEWMOLECULARENTITY
NDA 218613 (pdf not found) INN (LOFEXIDINE HYDROCHLORIDE) LOFEXIDINE HYDROCHLORIDE (INDOCO) APPROVAL= AP YEAR= 2024
NDA 218699 (pdf not found) INN (LOFEXIDINE HYDROCHLORIDE) LOFEXIDINE HYDROCHLORIDE (MSN) APPROVAL= AP YEAR= 2025

Other links:

PubChem
ChemicalProbes

U.S. repository of Clinical Trials

VigiAccess
SIDER side effects

ChemSynthesis
Patent@SureChEMBL