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phenyl-2-acetamido-2-deoxy-1-thio-α-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1228577-52-3

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1228577-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1228577-52-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,7 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1228577-52:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*7)+(3*7)+(2*5)+(1*2)=173
173 % 10 = 3
So 1228577-52-3 is a valid CAS Registry Number.

1228577-52-3Downstream Products

1228577-52-3Relevant academic research and scientific papers

The α-Thioglycoligase Derived from a GH89 α-N-Acetylglucosaminidase Synthesises α-N-Acetylglucosamine-Based Glycosides of Biomedical Interest

Tshililo, Ndivhuwo Olga,Strazzulli, Andrea,Cobucci-Ponzano, Beatrice,Maurelli, Luisa,Iacono, Roberta,Bedini, Emiliano,Corsaro, Maria Michela,Strauss, Erick,Moracci, Marco

, p. 663 - 676 (2017)

We report here on the preparation of a novel α-thioglycoligase that can be used for the fast and efficient synthesis of α-N-acetylglucosamine-based glycosides. Using the α-N-acetyl-glucosaminidase from Clostridium perfringens of family GH89 (according to the Carbohydrate Active Enzymes classification) as starting point, we prepared mutants in the acid/base residue glutamic acid 483 that were found to have different synthetic efficiencies (maximal yields >80% after 24 h) in the presence of an activated donor and suitable acceptors. The synthetic potential of the Glu483 alanine mutant as an α-thioglycoligase – only the third biocatalyst with this stereospecificity reported to date, and the first selective for the N-acetylglucosamine moiety – was demonstrated by producing for the first time N-acetyl-α-d-glucosaminyl azide and N-acetylglucosamine α-thioglycosides in high yields. To showcase the application of such compounds, we show that they offer the wild-type CpGH89 protection from thermal unfolding, demonstrating their potential as pharmacological chaperones for the treatment of mucopolysaccharidosis IIIB (Sanfilippo syndrome). (Figure presented.).

Conjugates of plumbagin and phenyl-2-amino-1-thioglucoside inhibit MshB, a deacetylase involved in the biosynthesis of mycothiol

Gammon, David W.,Steenkamp, Daniel J.,Mavumengwana, Vuyo,Marakalala, Mohlopheni J.,Mudzunga, Theophilus T.,Hunter, Roger,Munyololo, Muganza

experimental part, p. 2501 - 2514 (2010/06/21)

N-Acetylglucosaminylinositol (GlcNAc-Ins)-deacetylase (MshB) and mycothiol-S-conjugate amidase (Mca), structurally related amidases present in mycobacteria and other Actinomycetes, are involved in the biosynthesis of mycothiol and in the detoxification of

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