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Identification of a Novel, Small Molecule Inhibitor of KCNQ2 Channels

Haibo Yu, Kaiping Xu, Beiyan Zou, Meng Wu, Owen B. McManus, Julie Le Engers, Yiu-Yin Cheung, James M. Salovich, Corey R. Hopkins, Craig W. Lindsley, Min Li

PMID: 23658963

Abstract:

A high-throughput screen (HTS) of the Molecular Libraries Probe Centers Network (MLPCN) library was performed using a thallium influx assay in order to identify inhibitors of potassium voltage-gated channel, KQT-like subfamily, member 2 (KCNQ2) channels. Structure activity relationship (SAR) studies of active compounds yielded ML252, a potent (IC50 = 69 nM) inhibitor of KCNQ2 channels in electrophysiological assays. ML252 displayed more than forty-fold selectivity for blocking KCNQ2 channels compared with KCNQ1 channels. SAR studies revealed a site on ML252 at which small structural changes caused a functional shift from antagonist to agonist activity, suggesting that ML252 interacted with a critical site for controlling gating of KCNQ2 channels. ML252 represents a novel and potent inhibitor of KCNQ2 channels with a selectivity profile that enables use of the probe for investigating the role of KCNQ2 channels in neuronal function.

Chemicals Related in the Paper:

Catalog Number Product Name Structure CAS Number Price
AP1392494642 ML252 ML252 1392494-64-2 Price
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