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. 2006 Mar 28;395(Pt 2):233–238. doi: 10.1042/BJ20051002

Figure 6. Pharmacological properties of the intracellular Ca2+ channels mediated by IP3, cADPR and NAADP.

Figure 6

The 45Ca2+ release by supramaximal concentrations of IP3, cADPR and NAADP (all 10 μM) was challenged in the presence of heparin (100 μg/ml), ryanodine (5 μM), Ruthenium Red (5 μM), verapamil (100 μM) and diltiazem (100 μM).