Drug intelligence / Profile preview

kindolor

Development stage
Unknown
Lead developer
Lohocla Research Corporation
Modality
Small Molecules
Administration
Oral
01

Overview

Kindolor is a novel, non-opiate, non-addicting small molecule developed to treat chronic pain and diabetic neuropathic pain. It was designed using a network pharmacology approach to simultaneously target multiple key nodes in the peripheral nociceptive sensory pathway. Specifically, Kindolor inhibits voltage-sensitive sodium channels Nav1.7 and Nav1.8, blocks NMDA receptors (particularly those containing the NR2B subunit), and acts as an agonist of the delta opioid receptor. The compound is engineered to act primarily in the periphery with minimal penetration into the central nervous system, aiming to reduce side effects associated with CNS-active analgesics and avoid addiction potential seen with opioids[1][3][4][5][6].

Brand names
kindolor
Other names
kindolor tosylateLohocla 201Lohocla201Lohocla-201
02

Targets

DOR (Opioid Receptor Delta 1)GRIN2B (N-methyl-D-aspartate Receptor Subunit Combination: NR1a/NR2B)SCN10A (Sodium channel protein type X alpha subunit)SCN9A (Sodium channel protein type 9 subunit alpha)

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