Synthesis of an Inhibitor of Human Immunodeficiency Virus Infection
Author(s) -
Hatanaka Kenichi,
Yoshida Takashi,
Uryu Toshiyuki,
Yoshida Osamu,
Nakashima Hideki,
Yamamoto Naoki,
Mimura Toru,
Kaneko Yutaro
Publication year - 1989
Publication title -
japanese journal of cancer research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.035
H-Index - 141
eISSN - 1349-7006
pISSN - 0910-5050
DOI - 10.1111/j.1349-7006.1989.tb02272.x
Subject(s) - lentinan , sulfation , chemistry , sulfate , pyridinium , in vitro , biochemistry , polysaccharide , medicinal chemistry , organic chemistry
Anti‐HIV effects of lentinan sulfate were investigated by using an HTLV‐I‐carrying cell line, MT–4, in vitro. Lentinan, a fungal branched (1→3)‐β‐ d ‐glucan, was sulfated to various degrees by means of two kinds of procedures using piperidine N‐sulfonic acid in dimetbyl sulfoxide or chlorosulfonic acid in pyridine. Lentinan sulfate with a sulfur content of more than 13.9% effectively prevented HIV‐induced cytopathic effects (CPE) at concentrations of more than 3.3 μg/ml. However, low‐substituted lentinan sulfate did not prevent HIV‐induced CPE at any concentration tested. When the counter‐cation was 50% Na ± and 50% pyridinium ion, the inhibitory capacity was low. Anticoagulant activity of the lentinan sulfate was also assessed.
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