Chemical modification of the C-6 substituent in the carbohydrate moiety of N-acetylmuramoyl-L-alanyl-D-isoglutamine (MDP), and the immunoadjuvant activity.

DOI: 10.1016/0008-6215(83)88409-2

Source and publish data:

Carbohydrate research p. 87 - 98 (1983)

Update date:2022-08-02

Topics:

Authors:

Okumura Okumura

Tokushima

Saiki Saiki

Azuma Azuma

Kiso Kiso

Hasegawa

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Article abstract of DOI:10.1016/0008-6215(83)88409-2

N-Acetyl-6-O-mesyl-, -6-O-methyl-, and -4,6-di-O-methyl-muramoyl-L-alanyl-D-isoglutamine and N-acetyl-6-chloro-, -6-bromo-, and -6-azido-6-deoxymuramoyl-L-alanyl-D-isoglutamine were synthesized from benzyl 2-acetamido-2-deoxy-3-O-[D-1-(methoxycarbonyl) et

Full text of DOI:10.1016/0008-6215(83)88409-2

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Product name:benzyl 2-acetamido-6-chloro-2,6-dideoxy-3-O--α-D-glucopyranoside

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