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10.1111/cbdd.13812

http://scihub22266oqcxt.onion/10.1111/cbdd.13812
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33289334!ä!33289334
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suck abstract from ncbi

pmid33289334
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  • Repurposing potential of FDA-approved and investigational drugs for COVID-19 targeting SARS-CoV-2 spike and main protease and validation by machine learning algorithm #MMPMID33289334
  • Verma AK; Aggarwal R
  • Chem Biol Drug Des 2021[Apr]; 97 (4): 836-853 PMID33289334show ga
  • The present study aimed to assess the repurposing potential of existing antiviral drug candidates (FDA-approved and investigational) against SARS-CoV-2 target proteins that facilitates viral entry and replication into the host body. To evaluate molecular affinities between antiviral drug candidates and SARS-CoV-2 associated target proteins such as spike protein (S) and main protease (M(pro) ), a molecular interaction simulation was performed by docking software (MVD) and subsequently the applicability score was calculated by machine learning algorithm. Furthermore, the STITCH algorithm was used to predict the pharmacology network involving multiple pathways of active drug candidate(s). Pharmacophore features of active drug(s) molecule was also determined to predict structure-activity relationship (SAR). The molecular interaction analysis showed that cordycepin has strong binding affinities with S protein (-180) and M(pro) proteins (-205) which were relatively highest among other drug candidates used. Interestingly, compounds with low IC50 showed high binding energy. Furthermore, machine learning algorithm also revealed high applicability scores (0.42-0.47) of cordycepin. It is worth mentioning that the pharmacology network depicted the involvement of cordycepin in different pathways associated with bacterial and viral diseases including tuberculosis, hepatitis B, influenza A, viral myocarditis, and herpes simplex infection. The embedded pharmacophore features with cordycepin also suggested strong SAR. Cordycepin's anti-SARS-CoV-2 activity indicated 65% (E-gene) and 42% (N-gene) viral replication inhibition after 48h of treatment. Since, cordycepin has both preclinical and clinical evidences on antiviral activity, in addition the present findings further validate and suggest repurposing potential of cordycepin against COVID-19.
  • |*Drug Repositioning[MESH]
  • |*Machine Learning[MESH]
  • |Antiviral Agents/chemistry/metabolism/pharmacology/*therapeutic use[MESH]
  • |Binding Sites[MESH]
  • |COVID-19/*drug therapy/pathology/virology[MESH]
  • |Cell Line[MESH]
  • |Cell Survival/drug effects[MESH]
  • |Deoxyadenosines/chemistry/metabolism[MESH]
  • |Humans[MESH]
  • |Molecular Docking Simulation[MESH]
  • |Protease Inhibitors/chemistry/metabolism[MESH]
  • |SARS-CoV-2/isolation & purification/metabolism[MESH]
  • |Spike Glycoprotein, Coronavirus/antagonists & inhibitors/metabolism[MESH]
  • |Structure-Activity Relationship[MESH]
  • |Viral Matrix Proteins/antagonists & inhibitors/metabolism[MESH]


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  • suck abstract from ncbi

    836 4.97 2021