
tatM2NX is a novel мощный, селективный, клетка permeable, peptide TRPM2 channel антагонист с IC50 of 396 nM, IC90 of 2 uM (TRPM2 channel currents), prevents лиганд связывание and TRPM2 activation.tatM2NX interacts with the ADPR связывание site on the NUT9-H domain of TRPM2 channel. tatM2NX inhibits TRPM2-mediated dephosphorylation of GSK3β (activation), tatM2NX demonstrated селективный neuroprotective effects in a mouse model of focal ischemia (stroke).
tatM2NX is a novel potent, selective, cell permeable, peptide TRPM2 channel antagonist with IC50 of 396 nM, IC90 of 2 uM (TRPM2 channel currents), prevents ligand binding and TRPM2 activation.tatM2NX interacts with the ADPR binding site on the NUT9-H domain of TRPM2 channel. tatM2NX inhibits TRPM2-mediated dephosphorylation of GSK3β (activation), tatM2NX demonstrated selective neuroprotective effects in a mouse model of focal ischemia (stroke).
Только для научно-исследовательского применения. Не предназначено для использования у пациентов или в качестве лекарственного средства.