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Alongside studies of GIP(7-30)NH 2 , other truncated forms: GIP(10-30), GIP(6-30)NH 2 and GIP(7-30) were characterised as GIP receptor antagonists with the ability to block GIPs activation of the GIP receptor in vitro

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Correspondingly, the importance of hydrogen bonding and dipoledipole interactions in the pure alcohol decreases, while the importance of London dispersion forces increases, which leads to progressively fewer favorable electrostatic interactions with water