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Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes

Compared to the numerous X-ray crystal structures of protein-carbohydrate complexes, the successful elucidation of the crystal structures of complexes between artificial receptors and carbohydrates has been very rarely reported in the literature. In this work, we describe the binding modes of two co...

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Autores principales: Köhler, Linda, Hübler, Conrad, Seichter, Wilhelm, Mazik, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034237/
https://www.ncbi.nlm.nih.gov/pubmed/35480817
http://dx.doi.org/10.1039/d1ra03390e
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author Köhler, Linda
Hübler, Conrad
Seichter, Wilhelm
Mazik, Monika
author_facet Köhler, Linda
Hübler, Conrad
Seichter, Wilhelm
Mazik, Monika
author_sort Köhler, Linda
collection PubMed
description Compared to the numerous X-ray crystal structures of protein-carbohydrate complexes, the successful elucidation of the crystal structures of complexes between artificial receptors and carbohydrates has been very rarely reported in the literature. In this work, we describe the binding modes of two complexes formed between methyl α-d-glucopyranoside and an artificial receptor belonging to the class of compounds consisting of a 1,3,5-trisubstituted 2,4,6-trialkylbenzene scaffold. It is particularly noteworthy that these two complexes are present in one crystal structure, as was observed by us for the first time in the case of the recently reported three crystal structures of the complexes with methyl β-d-glucopyranoside, each containing two different receptor–carbohydrate complexes. The noncovalent interactions stabilizing the new complexes are compared with those observed in the aforementioned crystalline complexes with methyl β-d-glucopyranoside.
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spelling pubmed-90342372022-04-26 Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes Köhler, Linda Hübler, Conrad Seichter, Wilhelm Mazik, Monika RSC Adv Chemistry Compared to the numerous X-ray crystal structures of protein-carbohydrate complexes, the successful elucidation of the crystal structures of complexes between artificial receptors and carbohydrates has been very rarely reported in the literature. In this work, we describe the binding modes of two complexes formed between methyl α-d-glucopyranoside and an artificial receptor belonging to the class of compounds consisting of a 1,3,5-trisubstituted 2,4,6-trialkylbenzene scaffold. It is particularly noteworthy that these two complexes are present in one crystal structure, as was observed by us for the first time in the case of the recently reported three crystal structures of the complexes with methyl β-d-glucopyranoside, each containing two different receptor–carbohydrate complexes. The noncovalent interactions stabilizing the new complexes are compared with those observed in the aforementioned crystalline complexes with methyl β-d-glucopyranoside. The Royal Society of Chemistry 2021-06-24 /pmc/articles/PMC9034237/ /pubmed/35480817 http://dx.doi.org/10.1039/d1ra03390e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Köhler, Linda
Hübler, Conrad
Seichter, Wilhelm
Mazik, Monika
Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes
title Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes
title_full Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes
title_fullStr Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes
title_full_unstemmed Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes
title_short Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes
title_sort binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034237/
https://www.ncbi.nlm.nih.gov/pubmed/35480817
http://dx.doi.org/10.1039/d1ra03390e
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