IndraLab

Statements


3 1 | 5

reach
"Meanwhile, disopyramide was demonstrated to block I hERG1 at clinically relevant concentrations (IC 50 < 10 muM), and this action was proposed to constitute the molecular basis of its proarrhythmic effect."

reach
"Stereoselective block of the hERG potassium channel by the Class Ia antiarrhythmic drug disopyramide."

reach
"In this regard, disopyramide inhibition of hERG appears similar to the drug's open-channel inhibition of Kv1.5, which depends on drug–channel interaction with the S6 helix but for which residues at th[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

reach
"Considered collectively, therefore, our mutagenesis and docking data support a scheme in which disopyramide inhibition of hERG occurs via inner cavity interactions with F656 and Y652 on channel openin[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

reach
"Recently, McPate et al. suggested that hERG block by the class I antiarrhythmic disopyramide is only slightly attenuated by the N588K mutation, suggesting that it may be worth investigating disopyramide as a clinical adjunct for SQT1 [90]."