Deciphering the conformation of C-linked α-D-mannopyranosides and their application toward the synthesis of low nanomolar E. Coli FimH ligands

Mousavifar, Leila; Vergoten, Gérard et Roy, René (2018). Deciphering the conformation of C-linked α-D-mannopyranosides and their application toward the synthesis of low nanomolar E. Coli FimH ligands ARKIVOC: Free Online Journal of Organic Chemistry , vol. 2018 , nº 7. pp. 384-397. DOI: 10.24820/ark.5550190.p010.783.

Prévisualisation

PDF - Version publiée Disponible sous licence Creative Commons Attribution. Télécharger (1MB) | Prévisualisation

Résumé

Some symboles could not be reproduce. For the full abstract, please consult the original article

C-Allyl –D-mannopyranosideswere preparedvia a variety of routesto determine an optimal route to the -anomers. The relative conformational energies of the key intermediate was evaluated by molecular modelingwhich showed the conventional 4C1chair conformation to be the lowest energy conformer. This finding was also confirmed by NMR and X-ray crystallography. The perbenzoylated C-allyl mannoside was also converted into 1,1’-biphenyl analogues using a palladium-catalyzed Heck reaction. Two of the resulting minor reaction products were co-crystallized with the uropathogenic E. coliFimH. Alternatively, the KDof the major and expected Heck product was in the low nM range as measured by SPR. Crystal data showed that the C-linked derivatives efficiently bind in the FimH binding cavity near the so-called hydrophobic tyrosine gate.

Type de document:	Article
Mots-clés libres:	-
Centre:	Centre INRS-Institut Armand Frappier
Date de dépôt:	08 août 2019 01:28
Dernière modification:	07 déc. 2020 16:32
URI:	https://espace.inrs.ca/id/eprint/8151

Gestion Actions (Identification requise)

Modifier la notice