Safety of N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Like 14215-68-0, Name is N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide. In a document type is Article, introducing its new discovery.
A chitin-binding hemagglutinin was purified about 50-fold from the culture filtrate of Conidiobolus lamprauges.Hemolytic factor(s) and beta-N-acetylglucosaminidase coexisting with the hemagglutinin were removed by treating the culture filtrate with CM Sephadex and formalinized human erythrocytes.Purified hemagglutinin formed large aggregates upon ultrafiltration.The hemagglutinin had a major and a minor band in sodium dodecyl sulfate polyacrylamide gel electrophoresis.The major band of this hemagglutinin was a protein containing a small amount of sugar, and its molecular weight was approximately 86,000.The hemagglutinin was strongly inhibited by N-acetyl chitobi, tri and tetraose; moderately inhibited by phenyl and p-nitrophenyl beta-N-acetyl-D-glucosaminides; and weakly inhibited by D-glucosamine and N-acetyl-D-glucosamine. beta-Configuration was required for inhibition.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide. In my other articles, you can also check out more blogs about 14215-68-0
Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics