1990
DOI: 10.1021/ma00218a001
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Synthesis and structural analysis of curdlan sulfate with a potent inhibitory effect in vitro of AIDS virus infection

Abstract: The inhibitory effects against a human immunodeficiency virus (HIV) in vitro and the structural studies on curdlan sulfate were investigated. Curdlan, a natural linear (l-*-3)-/8-D-glucan, was sulfated by piperidine-N-sulfonic acid in dimethyl sulfoxide to give curdlan sulfates with several molecular sizes and different sulfur contents. Curdlan sulfate with a sulfur content of 14.4% completely inhibited the infection of HIV in the drug concentration of as low as 3.3 pg/mh. This is one of the most potent anti-A… Show more

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Cited by 110 publications
(51 citation statements)
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“…It is known that the modification of the OH group with sulfate in glucosyl compounds entails both a strong downfield shift of the carbon bearing the OH group itself (a-effect) and an upfield shift of the adjacent carbon (b-effect) with respect to carbons with unsubstituted OH groups. Thus, in combination with published data on sulfated polysaccharides, 29,30) the above peaks were assigned as follows: at d 69.8 to the carbons C6(6) (bearing a sulfate group) and thus reflecting an a-effect; at d 76.1 to the carbons C5(6) adjacent to substituted C-6 carbons (reflecting a b-effect); at d 81.6 to the C2(2) carbons (a-effect); at d 71.9 to the C4(2) carbons (g-effect); at d 79.3 to the C4(4) carbons (a-effect); at d 78.1 to the C2(4) carbons (g-effect); and at d 103.7 to the C1(2) carbons (b-effect). Theoretically, position 3 of the terminal glucosyl side chains could also be substituted, although the signal of O-substituted C-3 was not distinct, mainly because of its low content and steric hindrance.…”
Section: Resultsmentioning
confidence: 55%
“…It is known that the modification of the OH group with sulfate in glucosyl compounds entails both a strong downfield shift of the carbon bearing the OH group itself (a-effect) and an upfield shift of the adjacent carbon (b-effect) with respect to carbons with unsubstituted OH groups. Thus, in combination with published data on sulfated polysaccharides, 29,30) the above peaks were assigned as follows: at d 69.8 to the carbons C6(6) (bearing a sulfate group) and thus reflecting an a-effect; at d 76.1 to the carbons C5(6) adjacent to substituted C-6 carbons (reflecting a b-effect); at d 81.6 to the C2(2) carbons (a-effect); at d 71.9 to the C4(2) carbons (g-effect); at d 79.3 to the C4(4) carbons (a-effect); at d 78.1 to the C2(4) carbons (g-effect); and at d 103.7 to the C1(2) carbons (b-effect). Theoretically, position 3 of the terminal glucosyl side chains could also be substituted, although the signal of O-substituted C-3 was not distinct, mainly because of its low content and steric hindrance.…”
Section: Resultsmentioning
confidence: 55%
“…In 1990, we carried out the sulfation of curdlan which is a natural polysaccharide with a linear (1→3)-β-D-glucopyranosidic structure produced by a fungus. Curdlan sulfate was found to have potent anti-HIV activity below 3.3 μg/ml and the lowest cytotoxicity at more than 1000 μg/ml (1).…”
Section: Sulfated Polysaccharides With Antiviral Activitymentioning
confidence: 97%
“…In addition to bacterial and fungal resistance, 1,3--glucans have also demonstrated promising results against malaria [78], herpes simplex virus [79] and human immunodeficiency virus (HIV) [80][81][82]. Expanding on HIV research, various complexes have been synthesized with curdlan sulfate in order to enhance the efficacy of the polysaccharide.…”
Section: Infection Preventionmentioning
confidence: 99%