2-(Dimethylamino)oxazoline-4-carboxylic acids 5 were compounds 8 were expected to have inhibitory activity towards chitinases. Enzyme assays showed that glycosyl prepared by condensation of binucleophilic amino acids 4 and O-ethyl-N,N-dimethylisourea 3. New heterocyclic N-amides 8 indeed were modera
ChemInform Abstract: Synthesis of N-Acetylglucosaminyl and Diacetylchitobiosyl Amides of Heterocyclic Carboxylic Acids as Potential Chitinase Inhibitors.
β Scribed by Antje Rottmann; Bjoernar Synstad; Vincent Eijsink; Martin G. Peter
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Synthesis of N-Acetylglucosaminyl and Diacetylchitobiosyl Amides of Heterocyclic Carboxylic Acids as Potential Chitinase Inhibitors.
-A series of new compounds are synthesized, consisting of a 1-acylamino-2acetamido-1,2-dideoxy-Ξ²-D-glucose unit, where the 1-N-acyl group is derived from a heterocyclic carboxylic acid. Enzyme assays show that these compounds are moderate inhibitors of chitinases. -(ROTTMANN, ANTJE; SYNSTAD,
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