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Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonist

Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonist

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_osti_scitechconnect_1355830

Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonist

About this item

Full title

Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonist

Publisher

United States: American Association for the Advancement of Science

Journal title

Science (American Association for the Advancement of Science), 2015-12, Vol.350 (6267), p.1491-1491

Language

English

Formats

Publication information

Publisher

United States: American Association for the Advancement of Science

More information

Scope and Contents

Contents

Voltage-gated sodium (Nav) channels propagate action potentials in excitable cells. Accordingly, Nav channels are therapeutic targets for many cardiovascular and neurological disorders. Selective inhibitors have been challenging to design because the nine mammalian Nav channel isoforms share high sequence identity and remain recalcitrant to high-re...

Alternative Titles

Full title

Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonist

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_osti_scitechconnect_1355830

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_osti_scitechconnect_1355830

Other Identifiers

ISSN

0036-8075

E-ISSN

1095-9203

DOI

10.1126/science.aac5464

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