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pubmed-article:8324766pubmed:abstractTextNephritogenoside has been prepared by coupling of the acyl azide derivative of a N-triglycosyl dipeptide, derived from the corresponding hydrazide derivative of O-(2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl)-(1-->6)-O-(2,3,4-tri-O -acetyl - beta-D-glucopyranosyl)-(1-->6)-2,3-di-O-benzyl-1-N-[N-(tert-butoxycarbon yl)- L-aspart-1-oyl-(L-proline methyl ester)-4-oyl]-alpha-D-glucopyranosylamine, with a nonadecapeptide, followed by deprotection of the desired protected nephritogenoside. The N-triglycosyl pentapeptide also has been prepared as a model compound.lld:pubmed
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pubmed-article:8324766pubmed:year1993lld:pubmed
pubmed-article:8324766pubmed:articleTitleSyntheses of nephritogenoside and related compounds.lld:pubmed
pubmed-article:8324766pubmed:affiliationFaculty of Pharmaceutical Sciences, Nagoya City University, Japan.lld:pubmed
pubmed-article:8324766pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8324766pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed