This review focuses on the advances in the development of N-type calcium channel blockers as analgesic agents over the last 2 years. Firstly, it highlights the clinical progress with SNX-111 (Ziconotide; Elan Pharmaceuticals, Smithfield, RI) and then secondly, it outlines the various approaches being taken by researchers to design orally active, selective, small molecule modulators without the perceived disadvantages associated with SNX-111
AbstractWe previously reported the small organic N-type calcium channel blocker NP078585 that while ...
Ziconotide is a selective and potent blocker of N-type voltage-gated calcium channels. It was approv...
© 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article dis...
N-type calcium channels are located at presynaptic termini throughout the central nervous system (CN...
Highly selective Cav2.2 voltage-gated calcium channel (VGCC) inhibitors have emerged as a new class ...
Significance of the study: The clinical management of severe and chronic pain relies heavily on opio...
Neuropathic pain remains poorly treated for large numbers of patients and little progress has been m...
Chronic pain affects approximately 20% of people worldwide and places a large economic and social bu...
Crown Copyright © 2018 Published by Elsevier Ltd. This manuscript version is made available under t...
The T-type Ca2+ channel is a low-voltage-activated Ca2+ channel related to nociceptive stimuli. Incr...
ABSTRACT: Low-voltage-activated (T-type) calcium chan-nels are important regulators of the transmiss...
International audienceBackgroundT‐type calcium channels have been shown to play an important role in...
Pain is the most common and debilitating medical problem for which patients seek medical care. Opioi...
The discovery of a novel peripherally acting and selective Ca<sub>v</sub>3.2 T-type calcium channel ...
Abstract Background N-type Ca2+ channels (Cav2.2) play an important role in the transmission of pain...
AbstractWe previously reported the small organic N-type calcium channel blocker NP078585 that while ...
Ziconotide is a selective and potent blocker of N-type voltage-gated calcium channels. It was approv...
© 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article dis...
N-type calcium channels are located at presynaptic termini throughout the central nervous system (CN...
Highly selective Cav2.2 voltage-gated calcium channel (VGCC) inhibitors have emerged as a new class ...
Significance of the study: The clinical management of severe and chronic pain relies heavily on opio...
Neuropathic pain remains poorly treated for large numbers of patients and little progress has been m...
Chronic pain affects approximately 20% of people worldwide and places a large economic and social bu...
Crown Copyright © 2018 Published by Elsevier Ltd. This manuscript version is made available under t...
The T-type Ca2+ channel is a low-voltage-activated Ca2+ channel related to nociceptive stimuli. Incr...
ABSTRACT: Low-voltage-activated (T-type) calcium chan-nels are important regulators of the transmiss...
International audienceBackgroundT‐type calcium channels have been shown to play an important role in...
Pain is the most common and debilitating medical problem for which patients seek medical care. Opioi...
The discovery of a novel peripherally acting and selective Ca<sub>v</sub>3.2 T-type calcium channel ...
Abstract Background N-type Ca2+ channels (Cav2.2) play an important role in the transmission of pain...
AbstractWe previously reported the small organic N-type calcium channel blocker NP078585 that while ...
Ziconotide is a selective and potent blocker of N-type voltage-gated calcium channels. It was approv...
© 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article dis...