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Three derivatives of the D-Nle-X-Ile-(6)amino- hexanoic amide, where X is: Cys, Trp, or Met were examined to determine whether the percent of inhibition of dimerization and the binding affinity for each compound for HGF could be correlated to in vitro cellular activity, namely inhibition of MDCK cell scattering

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Further understanding the mechanisms underlying OMM permeabilization may provide novel strategies to regulate cytochrome c and control apoptosis

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