Literature DB >> 24961981

TRPs: modulation by drug-like compounds.

Michael Schaefer1.   

Abstract

Drug-like compounds that exert biological activity towards TRP channels are either being used as cell biological tools or further developed into pharmacological lead structures aiming at therapeutic use in diseased states. Although drug-likeliness is not easy to predict, common rules include a relatively low molecular weight, physicochemical constraints, and the absence of known reactive or otherwise toxic groups. Small molecules that exert a biological activity to block, activate, or modulate TRP channels are intensely sought. Such tool compounds may be useful to assign native currents to a certain TRP channel and to validate the channel as a candidate target for future pharmacological intervention. Depending on the TRP channel isotype, these activities have reached different levels, with only few TRP channels modulators already being clinically tested in humans, whereas other compounds only underwent a preliminary validation. For some TRP channels, reliable low molecular weight inhibitors are not yet available. Hence, further efforts need to be undertaken in order to explore the physiological impact and possible therapeutic potential of TRP channel targeting with drug-like compounds.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24961981     DOI: 10.1007/978-3-319-05161-1_15

Source DB:  PubMed          Journal:  Handb Exp Pharmacol        ISSN: 0171-2004


  6 in total

1.  Location and function of transient receptor potential canonical channel 1 in ventricular myocytes.

Authors:  Qinghua Hu; Azmi A Ahmad; Thomas Seidel; Chris Hunter; Molly Streiff; Linda Nikolova; Kenneth W Spitzer; Frank B Sachse
Journal:  J Mol Cell Cardiol       Date:  2020-01-23       Impact factor: 5.000

Review 2.  Neuroendocrine neoplasia of the gastrointestinal tract revisited: towards precision medicine.

Authors:  Guido Rindi; Bertram Wiedenmann
Journal:  Nat Rev Endocrinol       Date:  2020-08-24       Impact factor: 43.330

3.  Boron-Based Inhibitors of the NLRP3 Inflammasome.

Authors:  Alex G Baldwin; Jack Rivers-Auty; Michael J D Daniels; Claire S White; Carl H Schwalbe; Tom Schilling; Halah Hammadi; Panichakorn Jaiyong; Nicholas G Spencer; Hazel England; Nadia M Luheshi; Manikandan Kadirvel; Catherine B Lawrence; Nancy J Rothwell; Michael K Harte; Richard A Bryce; Stuart M Allan; Claudia Eder; Sally Freeman; David Brough
Journal:  Cell Chem Biol       Date:  2017-09-21       Impact factor: 8.116

Review 4.  Modulators of Transient Receptor Potential (TRP) Channels as Therapeutic Options in Lung Disease.

Authors:  Alexander Dietrich
Journal:  Pharmaceuticals (Basel)       Date:  2019-02-01

Review 5.  TRP channels in schistosomes.

Authors:  Swarna Bais; Robert M Greenberg
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2016-07-27       Impact factor: 4.077

6.  A Precise Microfluidic Assay in Single-Cell Profile for Screening of Transient Receptor Potential Channel Modulators.

Authors:  Xiaoni Ai; Yang Wu; Wenbo Lu; Xinran Zhang; Lin Zhao; Pengfei Tu; KeWei Wang; Yong Jiang
Journal:  Adv Sci (Weinh)       Date:  2020-04-19       Impact factor: 16.806

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.