Premium
Comparing Cyclophellitol N ‐Alkyl and N ‐Acyl Cyclophellitol Aziridines as Activity‐Based Glycosidase Probes
Author(s) -
Jiang Jianbing,
Beenakker Thomas J. M.,
Kallemeijn Wouter W.,
van der Marel Gijsbert A.,
van den Elst Hans,
Codée Jeroen D. C.,
Aerts Johannes M. F. G.,
Overkleeft Herman S.
Publication year - 2015
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201501313
Subject(s) - aziridine , alkyl , chemistry , glycoside hydrolase , stereochemistry , hydrolysis , biochemistry , combinatorial chemistry , organic chemistry , ring (chemistry)
The synthesis and evaluation as activity‐based probes (ABPs) of three configurationally distinct, fluorescent N ‐alkyl cyclophellitol aziridine isosteres for profiling GH1 β‐glucosidase (GBA), GH27 α‐galactosidase (GLA) and GH29 α‐fucosidase (FUCA) is described. In comparison with the corresponding acyl aziridine ABPs reported previously, the alkyl aziridine ABPs are synthesized easily and are more stable in mild acidic and basic media, and are thus easier to handle. The β‐glucose‐configured alkyl aziridine ABP proves equally effective in labeling GBA as its N ‐acyl counterpart, whereas the N ‐acyl aziridines targeting GLA and FUCA outperform their N ‐alkyl counterparts. Alkyl aziridines can therefore be an attractive alternative in retaining glycosidase ABP design, but in targeting a new retaining glycosidase both N ‐alkyl and N ‐acyl aziridines are best considered at the onset of a new study.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom