Na+ currents in cardioprotection: Better to be late
We report the discovery of a selective, potent inhibitor of the late current mediated by the cardiac isoform of the sodium channel (Na V1.5). The compound, 3,4-dihydro-N-[(2S)-3-[(2-hydroxy-3- methylphenyl) thio]-2-methylpropyl]-2H-(3R)-1,5-ben
Le Grand, Bruno,Pignier, Christophe,Létienne, Robert,Colpaert, Francis,Cuisiat, Florence,Rolland, Fran?oise,Mas, Agnes,Borras, Maud,Vacher, Bernard
supporting information; experimental part
p. 4149 - 4160
(2010/03/02)
More Articles about upstream products of 1169760-04-6