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In Silico Discovery of Natural Products Against Dengue RNA-Dependent RNA Polymerase Drug Target
被引:2
|作者:
Billones, Junie B.
[1
]
Clavio, Nina Abigail B.
[1
]
机构:
[1] Univ Philippines, Dept Phys Sci & Math, Coll Arts & Sci, Manila 1000, Philippines
关键词:
Dengue virus (DENV);
RNA-dependent RNA polymerase (RdRp);
molecular docking;
in silico ADMET;
natural products;
MOLECULAR DOCKING;
ANTIINFLAMMATORY CONSTITUENTS;
CRYSTAL-STRUCTURE;
VIRUS;
INHIBITORS;
PREDICTION;
ANTITUBERCULOSIS;
DERIVATIVES;
DITERPENES;
INITIATION;
D O I:
10.1273/cbij.21.11
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The viral infection caused by the dengue virus (DENV) is one of the most challenging diseases in the tropical regions of the world. The absence of drugs for dengue to this date calls for intense efforts to discover and develop the much coveted therapeutics for this mosquito-borne disease. One of the most attractive antiviral targets is the DENV RNA-dependent RNA polymerase (RdRp), which catalyzes the de novo initiation as well as elongation of the flavivirus RNA genome. In this work, almost 5000 natural products were docked to DENV RdRp. The top 197 molecules with greater binding energies than the known ligand of the target were further clustered down to furnish 35 classes of molecular structures. These compounds with satisfactory predicted drug properties and with known natural origin can be further explored to pave the way for the first anti-dengue drug.
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页码:11 / 27
页数:17
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