Literature DB >> 19751208

An update on peptide drugs for voltage-gated calcium channels.

Lei Gao1.   

Abstract

Voltage-gated calcium channels are one of the major ion channels distributed in the human central nervous system, and mediate an influx of extracellular Ca(2+) in response to membrane depolarization. Calcium channels are of particular interest in a broad range of cellular functions including cell proliferation and differentiation, gene expression, neurite outgrowth, transmitter and hormone release, and brain plasticity. The dysfunction of calcium channels is related to a variety of clinical disorders such as migraine, hemiplegia, and epilepsy. Therefore, calcium channels have gained great pharmaceutical interest as a privileged target class for the treatment of a wide range of human diseases. This review will examine the known marketed peptide drugs for calcium channels and address the development of some important patented peptide molecules targeting calcium channels.

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Year:  2010        PMID: 19751208     DOI: 10.2174/157488910789753558

Source DB:  PubMed          Journal:  Recent Pat CNS Drug Discov        ISSN: 1574-8898


  2 in total

1.  Post-treatment with voltage-gated Na(+) channel blocker attenuates kainic acid-induced apoptosis in rat primary hippocampal neurons.

Authors:  Arabinda Das; Misty McDowell; Casey M O'Dell; Megan E Busch; Joshua A Smith; Swapan K Ray; Naren L Banik
Journal:  Neurochem Res       Date:  2010-12-03       Impact factor: 3.996

2.  The Concise Guide to PHARMACOLOGY 2013/14: ion channels.

Authors:  Stephen P H Alexander; Helen E Benson; Elena Faccenda; Adam J Pawson; Joanna L Sharman; William A Catterall; Michael Spedding; John A Peters; Anthony J Harmar
Journal:  Br J Pharmacol       Date:  2013-12       Impact factor: 8.739

  2 in total

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