Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain.

A series of neoglycoconjugates derived from deoxynojirimycin has been prepared by click connection with functionalised adamantanes. They have been assayed as glycosidase inhibitors, as inhibitors of the glycoenzymes relevant to the treatment of Gaucher disease, as well as correctors of the defective...

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Main Authors: Ardes-Guisot, N, Alonzi, D, Reinkensmeier, G, Butters, T, Norez, C, Becq, F, Shimada, Y, Nakagawa, S, Kato, A, Blériot, Y, Sollogoub, M, Vauzeilles, B
Format: Journal article
Language:English
Published: 2011
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author Ardes-Guisot, N
Alonzi, D
Reinkensmeier, G
Butters, T
Norez, C
Becq, F
Shimada, Y
Nakagawa, S
Kato, A
Blériot, Y
Sollogoub, M
Vauzeilles, B
author_facet Ardes-Guisot, N
Alonzi, D
Reinkensmeier, G
Butters, T
Norez, C
Becq, F
Shimada, Y
Nakagawa, S
Kato, A
Blériot, Y
Sollogoub, M
Vauzeilles, B
author_sort Ardes-Guisot, N
collection OXFORD
description A series of neoglycoconjugates derived from deoxynojirimycin has been prepared by click connection with functionalised adamantanes. They have been assayed as glycosidase inhibitors, as inhibitors of the glycoenzymes relevant to the treatment of Gaucher disease, as well as correctors of the defective ion-transport protein involved in cystic fibrosis. We have demonstrated that it is possible to selectively either strongly inhibit ER-α-glucosidases and ceramide glucosyltransferase or restore the activity of CFTR in CF-KM4 cells by varying the length of the alkyl chain linking DNJ and adamantane.
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spelling oxford-uuid:144012ed-3879-4549-a57e-1b3b9d7f5e5b2022-03-26T10:18:38ZSelection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:144012ed-3879-4549-a57e-1b3b9d7f5e5bEnglishSymplectic Elements at Oxford2011Ardes-Guisot, NAlonzi, DReinkensmeier, GButters, TNorez, CBecq, FShimada, YNakagawa, SKato, ABlériot, YSollogoub, MVauzeilles, BA series of neoglycoconjugates derived from deoxynojirimycin has been prepared by click connection with functionalised adamantanes. They have been assayed as glycosidase inhibitors, as inhibitors of the glycoenzymes relevant to the treatment of Gaucher disease, as well as correctors of the defective ion-transport protein involved in cystic fibrosis. We have demonstrated that it is possible to selectively either strongly inhibit ER-α-glucosidases and ceramide glucosyltransferase or restore the activity of CFTR in CF-KM4 cells by varying the length of the alkyl chain linking DNJ and adamantane.
spellingShingle Ardes-Guisot, N
Alonzi, D
Reinkensmeier, G
Butters, T
Norez, C
Becq, F
Shimada, Y
Nakagawa, S
Kato, A
Blériot, Y
Sollogoub, M
Vauzeilles, B
Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain.
title Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain.
title_full Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain.
title_fullStr Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain.
title_full_unstemmed Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain.
title_short Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain.
title_sort selection of the biological activity of dnj neoglycoconjugates through click length variation of the side chain
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