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Updated: Jun 28, 2026

Constructing Thioether/Vinyl Sulfide-tethered Helical Peptides Via Photo-induced Thiol-ene/yne Hydrothiolation
Published on: August 1, 2018
Functionalized analogues of an unnatural amino acid that mimics a tripeptide beta-strand
Tatyana V Khasanova1, Omid Khakshoor, James S Nowick
1Department of Chemistry, University of California, Irvine, Irvine, California 92697-2025, USA.
Abstract:
This paper introduces polar and hydrophobic variants of the unnatural amino acid Hao, which mimics the hydrogen-bonding functionality of one edge of a beta-strand. In these variants, the methyl side chain of Hao is replaced with acidic, basic, and hydrophobic groups. These modifications can impart improved solubility and additional side-chain interactions to peptides containing Hao.
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