Skip to main content
. Author manuscript; available in PMC: 2018 Mar 16.
Published in final edited form as: Compr Physiol. 2017 Mar 16;7(2):485–581. doi: 10.1002/cphy.c160011

Table 1.

Vascular Voltage-Gated Ca2+ Channels and Their Pharmacology

Channel Gene Alternative
names
Accessory
subunits
Inhibitors/antagonists (IC50) Activators/agonists (EC50)
CaV 1.2 CACNA1C L-type β2 and β3, α2δ1 Nifedipine (10–100 nmol/L) (872) BayK 8644 (6 nmol/L) (1638)
Nimodipine (139 nmol/L) (1563) FPL64176 (211 nmol/L) (1638)
Diltiazem (500 nmol/L) (615)
Verapamil (60 nmol/L) (615)
Mibefradil (1.4–13 µmol/L) (576, 948)
Cd2+ (7 µmol/L) (1054)
Ni2+ (280 µmol/L) (1054)
Kurtoxin (> 10 µmol/L) (251)
ML218 (> 10 µmol/L) (1560)
CaV 3.1 CACNA1G T-type, α1G Mibefradil (0.4–1.2 µmol/L) (576)
Cd2+ (160 µmol/L) (833)
Ni2+ (167–250 µmol/L) (833)
Kurtoxin (15 nmol/L) (251)
ML218 (~300 nmol/L) (1560)
CaV 3.2 CACNA1H T-type, α1H Mibefradil (1.1–1.2 µmol/L) (576)
Cd2+ (160 µmol/L) (833)
Ni2+ (5.7–12 µmol/L) (833)
Kurtoxin (61 nmol/L) (251)
ML218 (310 nmol/L) (1560)