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Synthesis and evaluation of 1,5-dithialaminaribiose and -triose tetravalent constructs.
Ahiadorme, Daniil; Ande, Chennaiah; Fernandez-Botran, Rafael; Crich, David.
Afiliação
  • Ahiadorme D; Department of Chemistry, University of Georgia, 302 East Campus Road, Athens, GA, 30602, United States; Department of Pharmaceutical and Biomedical Sciences, University of Georgia, 250 West Green Street, Athens, GA, 30602, United States.
  • Ande C; Department of Pharmaceutical and Biomedical Sciences, University of Georgia, 250 West Green Street, Athens, GA, 30602, United States.
  • Fernandez-Botran R; Department of Pathology and Laboratory Medicine, University of Louisville, 511 South Floyd Street, Louisville, KY, 40292, United States.
  • Crich D; Department of Chemistry, University of Georgia, 302 East Campus Road, Athens, GA, 30602, United States; Department of Pharmaceutical and Biomedical Sciences, University of Georgia, 250 West Green Street, Athens, GA, 30602, United States; Complex Carbohydrate Research Center, University of Georgia, 3
Carbohydr Res ; 525: 108781, 2023 Mar.
Article em En | MEDLINE | ID: mdl-36898263
ABSTRACT
We report the synthesis of novel tetravalent glucoclusters containing 1,5-dithia mimetics of laminaribiose and triose. The new constructs were evaluated for their ability to inhibit anti-CR3 fluorescent staining of human neutrophils, for which they showed moderate affinity. Evaluation of the synthesized glycoclusters for their ability to inhibit anti-Dectin-1 fluorescent staining of mouse macrophages revealed little to no affinity for Dectin-1.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lectinas Tipo C Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lectinas Tipo C Idioma: En Ano de publicação: 2023 Tipo de documento: Article