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This suggests that there is a similar basis of their mechanism of action that is the allosteric modulation of GABA (neurotransmitter gamma-aminobutyric acid) receptors

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Oral bioavailability has not been characterized, and the compound's heptapeptide structure (773.89 Da) makes oral activity less likely than for the smaller Dihexa (504.66 Da), though not impossible given its modified sequence

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