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J

James Herrington

bristol-myers squibb
H指数:36
被引数:4,311
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Defining the structure-activity relationship for a novel class of allosteric MKP5 inhibitors
2022-12-012
OAAI
An allosteric site on MKP5 reveals a strategy for small-molecule inhibition
2020-08-2514
OAAI
Discovery of Indole- and Indazole-acylsulfonamides as Potent and Selective Nav1.7 Inhibitors for the Treatment of Pain (vol 62, pg 831, 2019)
2019-02-080
PREAI
Discovery of Indole- and Indazole-acylsulfonamides as Potent and Selective NaV1.7 Inhibitors for the Treatment of Pain

吲哚-和吲唑-酰基磺酰胺作为治疗疼痛的有效和选择性NaV1.7抑制剂的发现

2018-12-2124
PREAI
Discovery of non-zwitterionic aryl sulfonamides as Nav1.7 inhibitors with efficacy in preclinical behavioral models and translational measures of nociceptive neuron activation

发现非两性离子芳基磺酰胺作为Nav1.7抑制剂,在临床前行为模型和疼痛神经元激活的转化措施中具有功效

2017-10-0122
PREAI
A Functional NaV1.7-NaVAb Chimera with a Reconstituted High-Affinity ProTx-II Binding Site
2017-09-0111
OAAI
Effects of BMS-902483, an α7 nicotinic acetylcholine receptor partial agonist, on cognition and sensory gating in relation to receptor occupancy in rodents
2017-07-0122
PREAI
Development of New Benzenesulfonamides As Potent and Selective Nav1.7 Inhibitors for the Treatment of Pain
2017-03-1044
PREAI
B-973, a novel piperazine positive allosteric modulator of the α7 nicotinic acetylcholine receptor

B-973,α7烟碱型乙酰胆碱受体的新型哌嗪正变构调节剂

2017-03-0118
PREAI
Discovery of GluN2A-Selective NMDA Receptor Positive Allosteric Modulators (PAMs): Tuning Deactivation Kinetics via Structure-Based Design
2016-03-0888
PREAI
A KV2.1 gating modifier binding assay suitable for high throughput screening
2014-10-2711
OAAI
Improved Cav2.2 Channel Inhibitors through a gem-Dimethylsulfone Bioisostere Replacement of a Labile Sulfonamide
2013-09-1317
OA
The Role of Voltage-Gated Potassium Channels Kv2.1 and Kv2.2 in the Regulation of Insulin and Somatostatin Release from Pancreatic Islets
2013-02-0165
PREAI
Aminopiperidine Sulfonamide Cav2.2 Channel Inhibitors for the Treatment of Chronic Pain
2012-11-1227
PREAI
Characterization of the Substituted N-Triazole Oxindole TROX-1, a Small-Molecule, State-Dependent Inhibitor of Cav2 Calcium Channels
2012-03-0151
PREAI
Identification of Novel and Selective KV2 Channel Inhibitors
2011-12-0128
PREAI
Analgesic Effects of a Substituted N-Triazole Oxindole (TROX-1), a State-Dependent, Voltage-Gated Calcium Channel 2 Blocker
2010-08-0186
PREAI
Blockers of the delayed-rectifier potassium current in pancreatic β-cells enhance glucose-dependent insulin secretion
2006-04-01157
OAAI
Block of peripheral nerve sodium channels selectively inhibits features of neuropathic pain in rats
2006-03-0157
PREAI