Aza-Isotryptophan: Synthesis, Pictet–Spengler Chemistry, Incorporation and Conformational Analysis in Peptides, and Activity in Modulators of the Cluster of Differentiation-36 Receptor
Isotryptophan (Itr) is the rare 2-indoyl counterpart of the essential amino acid tryptophan. Considering the potential to explore novel side chain χ-space in a residue prone to adopt backbone turn conformers, azaItr has been effectively synthesized and employed in Pictet-Spengler and peptide chemistry. β-Turn geometry was characterized in model peptides of the Ala-azaItr-d-Phe triad by X-ray and NMR analyses. Moreover, azaItr analogs of growth hormone-releasing peptide 6 (GHRP-6) demonstrated a promising cluster of differentiation-36 receptor (CD36) binding affinity and modulatory effect on the inflammatory response induced by the activated complex composed of the latter coreceptor in the Toll-like receptor-2/6 heterodimer.
Authors
- Sylvain Chemtob (ORCID: https://orcid.org/0000-0001-7923-5221)
- Huy Ong
- Xiaozheng Wei (ORCID: https://orcid.org/0000-0003-4771-4716)
- William D. Lubell (ORCID: https://orcid.org/0000-0002-3080-2712)
- Mukandila Mulumba (ORCID: https://orcid.org/0000-0001-7708-7480)
Institutions
- Université du Québec à Montréal (CA)
- Université de Montréal (CA)
Publication Details
- Journal
- Journal of Medicinal Chemistry
- Published
- 2025-10-28
- DOI
- https://doi.org/10.1021/acs.jmedchem.5c01693
- Primary Topic
- Neuropeptides and Animal Physiology
- Type
- article
- Field-Weighted Citation Impact
- 0.00