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Design, Structure–Activity Relationships, and Computational Modeling Studies of a Series of α-Helix Biased, Ultra-Short Glucagon-like Peptide-1 Receptor Agonists.

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Title: Design, Structure–Activity Relationships, and Computational Modeling Studies of a Series of α-Helix Biased, Ultra-Short Glucagon-like Peptide-1 Receptor Agonists.
Authors: Sawyer, Jonathon R.1,2,3 (AUTHOR) hruby@arizona.edu, Audie, Joseph A.4 (AUTHOR) jon@chemmodeling.com, Swanson, Jon4 (AUTHOR) djrdiller@gmail.com, Diller, David4 (AUTHOR), Santiago, Solimar1 (AUTHOR) gribkoffv@aol.com, Gribkoff, Valentin K.1 (AUTHOR) aackerman26@gmail.com, Ackerman, Allison1 (AUTHOR) bpentelute@gmail.com, Hruby, Victor J.2 (AUTHOR), Gobbo, Gianpaolo5 (AUTHOR) gadelio1984@gmail.com, Bellucci, Michael A.5 (AUTHOR) michael.bellucci@xtalpi.com, Glauser, William A.5 (AUTHOR) william.glauser@xtalpi.com, Pentelute, Brad L.1 (AUTHOR) tomi.sawyer@maestrotherapeutics.com, Sawyer, Tomi K.1,6 (AUTHOR)
Source: Molecules. Jan2025, Vol. 30 Issue 1, p12. 29p.
Database: Academic Search Ultimate
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  Data: Design, Structure–Activity Relationships, and Computational Modeling Studies of a Series of α-Helix Biased, Ultra-Short Glucagon-like Peptide-1 Receptor Agonists.
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  Data: <searchLink fieldCode="JN" term="%22Molecules%22">Molecules</searchLink>. Jan2025, Vol. 30 Issue 1, p12. 29p.
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              Text: Jan2025
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