Abstract

We report the synthesis and biological activity of a new glucagon analog that was designed as a glucagon receptor antagonist by appropriate modifications in the N-terminal region of glucagon. The structure of the new analog is [des His 1, des Phe 6, Glu 9]glucagon amide , and its binding potency IC 50 value of 48 nM. The compound was found to be a pure antagonist in a new much more sensitive assay for glucagon stimulated cAMP accumulation activity and showed a pA 2 value of 8.20 in this assay. We report the sythesis and biological activity of a new glucagon analog that was designed as a glucagon receptor antagonist. The new analog, [ des His 1, des Phe 6, Glu 9]glucagon, amide , was found to be a pure antagonist in a new more sensitive assay for partial agonist activity, with a binding potency IC 50 of 48 nM and a pA 2 valueof 8.20.

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