Discovery of Selective Inhibitors of NaV1.7 Templated on Saxitoxin as Therapeutics for Pain
The voltage-gated sodium channel isoform NaV1.7 has drawn widespread interest as a target for non-opioid, investigational new drugs to treat pain. Selectivity over homologous, off-target sodium channel isoforms, which are expressed in peripheral motor neurons, the central nervous system, skeletal mu...
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Published in | ACS medicinal chemistry letters Vol. 13; no. 11; pp. 1763 - 1768 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
10.11.2022
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Subjects | |
Online Access | Get full text |
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