Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/54782
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSerbian, Immo-
dc.contributor.authorPrell, Erik-
dc.contributor.authorFischer, Claudia-
dc.contributor.authorDeigner, Hans-Peter-
dc.contributor.authorCsuk, René-
dc.date.accessioned2022-01-13T10:32:55Z-
dc.date.available2022-01-13T10:32:55Z-
dc.date.issued2021-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/56734-
dc.identifier.urihttp://dx.doi.org/10.25673/54782-
dc.description.abstractA convenient route has been developed for the synthesis of novel 6-amino-2,2-(or 3,3-difluoro)-2-(or 3),6-dideoxy-hexopyranoses. Biological screening showed these compounds as good inhibitors for several glycosidases. Especially n-propyl 6-amino-2,6-dideoxy-2,2-difluoro-β-d-glucopyranoside (8) was an excellent competitive inhibitor for the β-galactosidase from E. coli holding a Ki of 0.50 μM.eng
dc.description.sponsorshipPublikationsfonds MLU-
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc547-
dc.titlen-Propyl 6-amino-2,6-dideoxy-2,2-difluoro-β-d-glucopyranoside is a good inhibitor for the β-galactosidase from E. colieng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleMedicinal Chemistry Research-
local.bibliographicCitation.volume30-
local.bibliographicCitation.pagestart1099-
local.bibliographicCitation.pageend1107-
local.bibliographicCitation.publishernameBirkhäuser Boston-
local.bibliographicCitation.publisherplaceCambridge, Mass. [u.a.]-
local.bibliographicCitation.doi10.1007/s00044-021-02715-8-
local.openaccesstrue-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

Files in This Item:
File Description SizeFormat 
Serbian2021_Article_N-Propyl6-amiNo-26-DiDeoxy-22-.pdf851.42 kBAdobe PDFThumbnail
View/Open