Carbohydrate-binding small molecules with antiviral activity

Pending Publication Date: 2021-08-26
RES FOUND THE CITY UNIV OF NEW YORK +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

[0012]This brief description of the invention is intended only to provide a brief overview of subject matter disclosed herein according to one or more illustrative embodiments, and does not serve as a guide to interpreting the claims or to define or limit the scope of the invention, which is defined only by the appended claims. This brief description is provided to introduce an illustrative selection of concepts

Problems solved by technology

Since its arrival in Brazil in 2014, infecting millions of people, it has rapidly spread throughout the Americas, causing an expanding pandemic.
Although great strides have been made since 2016 in the search for drugs for the treatment of ZIKV, there is to date no vaccine or antiviral therap

Method used

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  • Carbohydrate-binding small molecules with antiviral activity
  • Carbohydrate-binding small molecules with antiviral activity
  • Carbohydrate-binding small molecules with antiviral activity

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Embodiment Construction

[0065]This disclosure provides a series of small molecule SCRs that preferentially bind mannosides and glucosides. The binding of some of these SCRs with a series of monosaccharides was studied by 1H NMR in chloroform and dichloromethane, and their association constants (Kas) toward a series of biologically relevant monosaccharides were reported, with selectivities as high as 103:1 β Man:β Gal. This preference for binding mannosides is driven by cooperative binding modes that arise from the flexible and multivalent structures of the SCRs. As association between glycan binding proteins on the envelope of ZIKV and glycans on the cell surface is an important part of viral entry into the host cell, the SCRs may disrupt this process.

[0066]This disclosure describes the ability of small-molecule SCRs to mitigate ZIKV infection in Vero and HeLa cells using a ZIKV reporter virus-based infection assay. The capsid-premembrane-envelope (C-prM-E) gene construct of ZIKV is used to generate reporter

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Abstract

Compounds with anti-viral properties are provided that are based on the following structures:
A variety of heteroaromatic groups have been found to be biologically active against viral infections. In some embodiments, a dimeric compound is provided with each monomer linked by a repeating glycol linking group.

Description

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Claims

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Application Information

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Owner RES FOUND THE CITY UNIV OF NEW YORK
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