Key result
A database of 655 small-molecule NS5B inhibitors of bovine viral diarrhea virus was constructed with structural parameters and physicochemical properties to aid in the discovery of anti-BVDV drugs.
The constructed database provides an accessible platform of molecular information to aid in the discovery and screening of anti-BVDV drugs and related viral inhibitors.
Database of NS5B inhibitors may aid antiviral screening; leaves open whether specific scaffolds yield effective BVDV therapies.
Bovine viral diarrhea virus (BVDV) is a major pathogen that may be one of the main reasons for economic losses in the livestock industry. BVDV is a well-characterized member of Flaviviridae family with plus-stranded RNA viruses. Non-structural NS5B protein is RNA-dependent RNA polymerase, which is responsible for viral RNA synthesis and genome replication of BVDV. Therefore, the NS5B polymerase is a key target for the discovery of anti-BVDV drugs. A number of small-molecule inhibitors against the NS5B polymerase have been reported in literature of which we collected series molecules having various scaffold with their biological data determined by evident experimental conditions, methods and procedures. Then, we constructed database of 655 small-molecule NS5B inhibitors having definitive activity values, structural parameters, and physicochemical properties (such as molecular hydrophobicity, hydrophilicity, polarity, Hbond donors and H-bond acceptors) associated with their absorption and permeability through a cheminformatics approach. The database was opened to provide insight for allosteric NS5B inhibitors of BVDV with an accessible platform on the web (http://nabic.rda.go.kr/chemical genomic database/BVDV RNA dependent RNA polymerase inhibitors). This molecular information in the database would be useful in attempting to identify features and decision factors that enhance anti-BVDV activity or increase selectivity of the allosteric inhibitor. These anti-BVDV molecules could also be screening for the purpose of exploiting potent NS5B inhibitors in the same family (e.g., HCV, CSFV, YFV, WNV, and DENV).
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Chai et al. (2017) studied Bovine viral diarrhea virus (BVDV) infection (n=655). Cheminformatics database construction was evaluated on Construction of a database with structural parameters and physicochemical properties. A database of 655 small-molecule NS5B inhibitors of bovine viral diarrhea virus was constructed with structural parameters and physicochemical properties to aid in the discovery of anti-BVDV drugs.
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