Related references
Note: Only part of the references are listed.Quaternary Lidocaine Derivatives: Past, Present, and Future
Qi Wang et al.
DRUG DESIGN DEVELOPMENT AND THERAPY (2021)
The E15R Point Mutation in Scorpion Toxin Cn2 Uncouples Its Depressant and Excitatory Activities on Human Na(v)1.6
Mathilde R. Israel et al.
JOURNAL OF MEDICINAL CHEMISTRY (2018)
Selective cold pain inhibition by targeted block of TRPM8-expressing neurons with quaternary lidocaine derivative QX-314
Serra Ongun et al.
COMMUNICATIONS BIOLOGY (2018)
Quaternary Lidocaine Derivative QX-314 Activates and Permeates Human TRPV1 and TRPA1 to Produce Inhibition of Sodium Channels and Cytotoxicity
Thomas Stueber et al.
ANESTHESIOLOGY (2016)
Analgesic Effects of GpTx-1, PF-04856264 and CNV1014802 in a Mouse Model of NaV1.7-Mediated Pain
Jennifer R. Deuis et al.
TOXINS (2016)
Inhibition of mechanical allodynia in neuropathic pain by TLR5-mediated A-fiber blockade
Zhen-Zhong Xu et al.
NATURE MEDICINE (2015)
Structural Basis for Pharmacology of Voltage-Gated Sodium and Calcium Channels
William A. Catterall et al.
MOLECULAR PHARMACOLOGY (2015)
Bupivacaine-induced cellular entry of QX-314 and its contribution to differential nerve block
C. Brenneis et al.
BRITISH JOURNAL OF PHARMACOLOGY (2014)
Chemical Engineering and Structural and Pharmacological Characterization of the α-Scorpion Toxin OD1
Thomas Durek et al.
ACS CHEMICAL BIOLOGY (2013)
Ciguatoxins activate specific cold pain pathways to elicit burning pain from cooling
Irina Vetter et al.
EMBO JOURNAL (2012)
The Quaternary Lidocaine Derivative, QX-314, Exerts Biphasic Effects on Transient Receptor Potential Vanilloid Subtype 1 Channels In Vitro
Ricardo E. Rivera-Acevedo et al.
ANESTHESIOLOGY (2011)
Extracellular Proton Modulation of the Cardiac Voltage-Gated Sodium Channel, Nav1.5
D. K. Jones et al.
BIOPHYSICAL JOURNAL (2011)
TRPA1 acts as a cold sensor in vitro and in vivo
Yuji Karashima et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
General Anesthetics Sensitize the Capsaicin Receptor Transient Receptor Potential V1
Paul M. Cornett et al.
MOLECULAR PHARMACOLOGY (2008)
General anesthetics activate a nociceptive ion channel to enhance pain and inflammation
Jose A. Matta et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Inhibition of nociceptors by TRPV1-mediated entry of impermeant sodium channel blockers
Alexander M. Binshtok et al.
NATURE (2007)
An SCN9A channelopathy causes congenital inability to experience pain
James J. Cox et al.
NATURE (2006)
International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels
WA Catterall et al.
PHARMACOLOGICAL REVIEWS (2005)
The principle of temperature-dependent gating in cold- and heat-sensitive TRP channels
T Voets et al.
NATURE (2004)