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10.3390/computation8020053 http://scihub22266oqcxt.onion/10.3390/computation8020053 32661494!7357730!32661494     free     free     free Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Computation+(Basel) 2020 ; 8 (2): ä Nephropedia Template TP {{tp|p=32661494|t=2020. Computational View toward the Inhibition of SARS-CoV-2 Spike Glycoprotein and the 3CL Protease |pdf=|usr=}}{{32661494}} gab.com Text Computational View toward the Inhibition of SARS-CoV-2 Spike Glycoprotein and the 3CL Protease JO: Computation (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=32661494 #FOAvip Since the outbreak of the 2019 novel coronavirus disease (COVID-19), the medical research community is vigorously seeking a treatment to control the infection and save the lives of severely infected patients. The main potential candidates for the control of viruses are virally targeted agents. In this short letter, we report our calculations on the inhibitors for the SARS-CoV-2 3CL protease and the spike protein for the potential treatment of COVID-19. The results show that the most potent inhibitors of the SARS-CoV-2 3CL protease include saquinavir, tadalafil, rivaroxaban, sildenafil, dasatinib, etc. Ergotamine, amphotericin b, and vancomycin are most promising to block the interaction of the SARS-CoV-2 S-protein with human ACE-2. Twit Text FOAVip Computational View toward the Inhibition of SARS-CoV-2 Spike Glycoprotein and the 3CL Protease ????Computation (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=32661494 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32661494 #FOAvip English Wikipedia <ref>{{Cite pmid|32661494}}</ref> Computational View toward the Inhibition of SARS-CoV-2 Spike Glycoprotein and the 3CL Protease #MMPMID32661494 Qiao Z; Zhang H; Ji HF; Chen Q Computation (Basel) 2020[Jun]; 8 (2): ä PMID32661494show ga Since the outbreak of the 2019 novel coronavirus disease (COVID-19), the medical research community is vigorously seeking a treatment to control the infection and save the lives of severely infected patients. The main potential candidates for the control of viruses are virally targeted agents. In this short letter, we report our calculations on the inhibitors for the SARS-CoV-2 3CL protease and the spike protein for the potential treatment of COVID-19. The results show that the most potent inhibitors of the SARS-CoV-2 3CL protease include saquinavir, tadalafil, rivaroxaban, sildenafil, dasatinib, etc. Ergotamine, amphotericin b, and vancomycin are most promising to block the interaction of the SARS-CoV-2 S-protein with human ACE-2. äComputational View toward the Inhibition of SARS-CoV-2 Spike Glycoprot(epmc).pdf DeepDyve Pubget Overpricing