About: Enzymatic synthesis of new C-6-acylated derivatives of NAG-thiazoline and evaluation of their inhibitor activities towards fungal beta-N-acetylhexosaminidase     Goto   Sponge   NotDistinct   Permalink

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  • beta-N-Acetylhexosaminidases (EC 3.2.1.52) from the CAZy glycoside hydrolase families 20 and 84 are two distinct enzyme groups with similar reactivity and different physiological functions, thus selective inhibition of these enzymes is of crucial importance. Here, we report on the lipase-catalyzed synthesis of a set of novel monomeric and dimeric C-6-acylated derivatives of NAG-thiazoline, which is a typical competitive inhibitor of both these enzyme classes. The prepared compounds were tested as potential inhibitors of a fungal GH20 beta-N-acetylhexosaminidase from Talaromyces flavus, however, the results of the inhibition tests were quite ambiguous. The observed inhibition was generally weak with some features of competitive inhibition (increase of K-M), but the overall pattern appeared indecisive
  • beta-N-Acetylhexosaminidases (EC 3.2.1.52) from the CAZy glycoside hydrolase families 20 and 84 are two distinct enzyme groups with similar reactivity and different physiological functions, thus selective inhibition of these enzymes is of crucial importance. Here, we report on the lipase-catalyzed synthesis of a set of novel monomeric and dimeric C-6-acylated derivatives of NAG-thiazoline, which is a typical competitive inhibitor of both these enzyme classes. The prepared compounds were tested as potential inhibitors of a fungal GH20 beta-N-acetylhexosaminidase from Talaromyces flavus, however, the results of the inhibition tests were quite ambiguous. The observed inhibition was generally weak with some features of competitive inhibition (increase of K-M), but the overall pattern appeared indecisive (en)
Title
  • Enzymatic synthesis of new C-6-acylated derivatives of NAG-thiazoline and evaluation of their inhibitor activities towards fungal beta-N-acetylhexosaminidase
  • Enzymatic synthesis of new C-6-acylated derivatives of NAG-thiazoline and evaluation of their inhibitor activities towards fungal beta-N-acetylhexosaminidase (en)
skos:prefLabel
  • Enzymatic synthesis of new C-6-acylated derivatives of NAG-thiazoline and evaluation of their inhibitor activities towards fungal beta-N-acetylhexosaminidase
  • Enzymatic synthesis of new C-6-acylated derivatives of NAG-thiazoline and evaluation of their inhibitor activities towards fungal beta-N-acetylhexosaminidase (en)
skos:notation
  • RIV/61388971:_____/13:00395403!RIV14-MSM-61388971
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  • I, P(GAP207/11/0629), P(LD13042), P(OC09045), Z(MSM6046137305)
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  • MAR
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  • 73078
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  • RIV/61388971:_____/13:00395403
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  • NAG-thiazoline; Lipase; Vinyl ester (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [25606F6D56AF]
http://linked.open...i/riv/nazevZdroje
  • Journal of Molecular Catalysis B-Enzymatic
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  • 87
http://linked.open...iv/tvurceVysledku
  • Křen, Vladimír
  • Pelantová, Helena
  • Riva, S.
  • Slámová, Kristýna
  • Vavříková, Eva
  • Spiwok, V.
  • Šimon, Petr
  • Krejzová, Jana
http://linked.open...ain/vavai/riv/wos
  • 000314012900019
http://linked.open...n/vavai/riv/zamer
issn
  • 1381-1177
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.molcatb.2012.10.016
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