Schwarzinicine A inhibits transient receptor potential canonical channels and exhibits overt vasorelaxation effects-Reference-Cited by-同舟云学术

Schwarzinicine A inhibits transient receptor potential canonical channels and exhibits overt vasorelaxation effects

Published:2022-05-10 Issue:7 Volume:36 Page:2952-2963
ISSN:0951-418X
Container-title:Phytotherapy Research
language:en
Short-container-title:Phytotherapy Research

Author:

Mak Yin‐Ying¹,Loong Bi‐Juin¹,Millns Paul²,Bauer Claudia C.³,Bon Robin S.³,Mbaki Yvonne²,Lee Fong‐Kai¹,Lim Kuan‐Hon¹,Kong Cin¹,Then Sue‐Mian¹,Ting Kang‐Nee¹^ORCID

Affiliation:

1. School of Pharmacy University of Nottingham Malaysia Semenyih Malaysia

2. School of Life Sciences University of Nottingham Nottingham UK

3. Department of Discovery and Translational Science, Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds Leeds UK

Funder

British Heart Foundation

British Pharmacological Society

Malaysia Toray Science Foundation

Ministry of Education – Kingdom of Saudi Arabi

University of Nottingham

Publisher

Wiley

Subject

Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ptr.7489

Reference48 articles.

1. (−)-Englerin A is a Potent and Selective Activator of TRPC4 and TRPC5 Calcium Channels

2. Differences in TRPC3 and TRPC6 channels assembly in mesenteric vascular smooth muscle cells in essential hypertension

3. Mechanisms and significance of Ca2+ entry through TRPC channels

4. Structural basis for pharmacological modulation of the TRPC6 channel

5. Xanthine-based photoaffinity probes allow assessment of ligand engagement by TRPC5 channels

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