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Its medicinal-chemistry program, described in detail by Kruse and colleagues, introduced several deliberate substitutions into the amylin backbone: residues borrowed from rat amylin (which does not readily form fibrils) to blunt the aggregation tendency, an engineered salt bridge to stabilize the central helix, and a C 20 fatty-diacid moiety attached through a linker to promote reversible binding to serum albumin

PMID: 27517151 Citations are provided for research reference

N-Acetyl Semax & Selank Blend pairs two N-acetylated, C-amidated heptapeptide analogs: N-Acetyl Semax Amidate (an ACTH(4-10) analog) and N-Acetyl Selank Amidate (a tuftsin-derived analog)

It has also been studied for wound healing and angiogenesis through the VEGFR2 pathway

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