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Volumn 119, Issue 46, 1997, Pages 11137-11146

Combined chemical and enzymatic synthesis of a C-glycopeptide and its inhibitory activity toward glycoamidases

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLGLUCOSAMINIDASE; AMIDASE; ENZYME INHIBITOR; GLYCOPEPTIDE;

EID: 0030670057     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9712027     Document Type: Article
Times cited : (90)

References (89)
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    • note
    • In this paper, we prefer to name and number the compounds as C-glycosyl derivatives because the systematic heptitol nomenclature may not invoke synthetically and biochemically relevant analogies. Moreover, the heptitol nomenclature will be very tedious especially when the substituents become large and complex.
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    • Recently, an endo-β-N-acetylglucosaminidase from Mucor hiemalis (called Endo-M) was shown to be able to transfer disialo complex-type oligosaccharide to the terminal GlcNAc residue in glycopeptides, see: (a) Haneda, K.; Inazu, T.; Yamamoto, K.; Kumagai, H.; Nakahara, Y.; Kobata, A. Carbohydr. Res. 1996, 292, 61. (b) Yamamoto, K.; Kadowaki, S.; Watanabe, J.; Kumagai, H. Biochem. Biophys. Res. Commun. 1994, 203, 244.
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