Selective activation of vascular Kv7.4/Kv7.5 K+ channels by fasudil contributes to its vasorelaxant effect

. 2016 Nov 1;173(24):3480–3491. doi: 10.1111/bph.13639

TARGETS
GPCRs ^a	Voltage‐gated ion channels ^b
α₁‐Adrenoceptors	K_v7.1/KCNE1 channel
M₂ receptor	K_v7.2 channel
	K_v7.3 channel
	K_v7.4 channel
	K_v7.5 channel

LIGANDS
ACh	Retigabine
Fasudil	XE991
Phenylephrine

These Tables list key protein targets and ligands in this article which are hyperlinked to corresponding entries in http://www.guidetopharmacology.org, the common portal for data from the IUPHAR/BPS Guide to PHARMACOLOGY (Southan et al., 2016) and are permanently archived in the Concise Guide to PHARMACOLOGY 2015/16 (^a,bAlexander et al., 2015a,b).