In this paper we report an IC50 value for 1,6-epi-cyclophellitol (compound 7, JJB307) as a human lysosomal α-glucosidase (GAA) inhibitor of 54.1 ± 4.9 nM in vitro and 97.6 ± 14.5 nM in situ (Figure 3a). We re-evaluated these data and now find that compound 7 is actually a low micromolar GAA inhibitor with an IC50 of 14.6 ± 1.6 μM in vitro and >50 μM in situ.
. 2017 May 18;3(6):673. doi: 10.1021/acscentsci.7b00185
Correction to “Detection of Active Mammalian GH31 α-Glucosidases in Health and Disease Using In-Class, Broad-Spectrum Activity-Based Probes”
Jianbing Jiang
, Chi-Lin Kuo
, Liang Wu
, Christian Franke
, Wouter W Kallemeijn
, Bogdan I Florea
, Eline van Meel
, Gijsbert A van der Marel
, Jeroen D C Codée
, Rolf G Boot
, Gideon J Davies
, Herman S Overkleeft
✉, Johannes M F G Aerts
✉
Jianbing Jiang
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Chi-Lin Kuo
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Liang Wu
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Christian Franke
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Wouter W Kallemeijn
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Bogdan I Florea
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Eline van Meel
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Gijsbert A van der Marel
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Jeroen D C Codée
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Rolf G Boot
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Gideon J Davies
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Herman S Overkleeft
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Johannes M F G Aerts
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Corresponding author.
Received 2017 Apr 28; Issue date 2017 Jun 28.
Copyright © 2017 American Chemical
Society
This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
PMCID: PMC5492415 PMID: 28691081
This corrects the article "Detection of Active Mammalian GH31 α-Glucosidases
in Health and Disease Using
In-Class, Broad-Spectrum Activity-Based Probes" in volume 2 on page 351.