N-Aryl Indoles as a Novel Class of Potent NaV1.7 Inhibitors
Author:
Affiliation:
1. Daiichi Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan
2. Daiichi Sankyo RD Novare Co., Ltd., 1-16-13, Kitakasai, Edogawa-ku, Tokyo 134-8630, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acsmedchemlett.3c00079
Reference16 articles.
1. An SCN9A channelopathy causes congenital inability to experience pain
2. Distinct Nav1.7-dependent pain sensations require different sets of sensory and sympathetic neurons
3. Efficacy of the Nav1.7 blocker PF-05089771 in a randomised, placebo-controlled, double-blind clinical study in subjects with painful diabetic peripheral neuropathy
4. Inhibition of NaV1.7: the possibility of ideal analgesics
5. Challenges and Opportunities for Therapeutics Targeting the Voltage-Gated Sodium Channel Isoform NaV1.7
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