Extracellular loop C of NPC1L1 is important for binding to ezetimibe
…, W Schmalhofer, B Williams… - Proceedings of the …, 2008 - National Acad Sciences
Niemann–Pick C1-like protein (NPC1L1) mediates the absorption of dietary cholesterol in
the proximal region of the intestine, a process that is blocked by cholesterol absorption …
the proximal region of the intestine, a process that is blocked by cholesterol absorption …
Ivermectin and Nodulisporic Acid Receptors in Drosophila melanogaster Contain Both γ-Aminobutyric Acid-Gated Rdl and Glutamate-Gated GluClα Chloride …
SW Ludmerer, VA Warren, BS Williams, Y Zheng… - Biochemistry, 2002 - ACS Publications
35 S-labeled derivatives of the insecticides nodulisporic acid and ivermectin were synthesized
and demonstrated to bind with high affinity to a population of receptors in Drosophila …
and demonstrated to bind with high affinity to a population of receptors in Drosophila …
Discovery of a novel class of benzazepinone Nav1. 7 blockers: potential treatments for neuropathic pain
…, A Ritter, MHM Smith, VA Warren, BS Williams… - Bioorganic & medicinal …, 2007 - Elsevier
A series of benzodiazepines and benzazepinones were synthesized and evaluated as
potential sodium channel blockers in a functional, membrane potential-based assay. One …
potential sodium channel blockers in a functional, membrane potential-based assay. One …
Analgesic effects of a substituted N-triazole oxindole (TROX-1), a state-dependent, voltage-gated calcium channel 2 blocker
…, AM Swensen, VA Warren, B Williams… - … of Pharmacology and …, 2010 - ASPET
Voltage-gated calcium channel (Ca v )2.2 (N-type calcium channels) are key components in
nociceptive transmission pathways. Ziconotide, a state-independent peptide inhibitor of Ca …
nociceptive transmission pathways. Ziconotide, a state-independent peptide inhibitor of Ca …
Functional assay of voltage-gated sodium channels using membrane potential-sensitive dyes
JP Felix, BS Williams, BT Priest, RM Brochu… - Assay and drug …, 2004 - liebertpub.com
The discovery of novel therapeutic agents that act on voltage-gated sodium channels requires
the establishment of high-capacity screening assays that can reliably measure the activity …
the establishment of high-capacity screening assays that can reliably measure the activity …
Characterization of a new class of potent inhibitors of the voltage-gated sodium channel Nav1. 7
BS Williams, JP Felix, BT Priest, RM Brochu, K Dai… - Biochemistry, 2007 - ACS Publications
Voltage-gated sodium channels (Nav1) transmit pain signals from peripheral nociceptive
neurons, and blockers of these channels have been shown to ameliorate a number of pain …
neurons, and blockers of these channels have been shown to ameliorate a number of pain …
Benzazepinone Nav1. 7 blockers: potential treatments for neuropathic pain
…, R Tschirret-Guth, VA Warren, BS Williams… - Bioorganic & medicinal …, 2007 - Elsevier
… Williams, DP McHale, JN Wood, FM Gribble, CG Woods … Ritter, MM Smith, VA Warren,
BS Williams, GJ Kaczorowski, WH Parsons … JP Felix, BS Williams, BT Priest, RM Brochu …
BS Williams, GJ Kaczorowski, WH Parsons … JP Felix, BS Williams, BT Priest, RM Brochu …
Asymmetric synthesis and evaluation of a hydroxyphenylamide voltage-gated sodium channel blocker in human prostate cancer xenografts
…, A Cordova, OB McManus, BS Williams… - Bioorganic & medicinal …, 2012 - Elsevier
Voltage-gated sodium channels are known to be expressed in neurons and other excitable
cells. Recently, voltage-gated sodium channels have been found to be expressed in human …
cells. Recently, voltage-gated sodium channels have been found to be expressed in human …
Imidazopyridines: a novel class of hNav1. 7 channel blockers
C London, SB Hoyt, WH Parsons, BS Williams… - Bioorganic & medicinal …, 2008 - Elsevier
A series of imidazopyridines were evaluated as potential sodium channel blockers for the
treatment of neuropathic pain. Several members were identified with good hNa v 1.7 potency …
treatment of neuropathic pain. Several members were identified with good hNa v 1.7 potency …
A disubstituted succinamide is a potent sodium channel blocker with efficacy in a rat pain model
Sodium channel blockers are used clinically to treat a number of neuropathic pain conditions,
but more potent and selective agents should improve on the therapeutic index of currently …
but more potent and selective agents should improve on the therapeutic index of currently …