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10.1016/j.molstruc.2020.129649 http://scihub22266oqcxt.onion/10.1016/j.molstruc.2020.129649 33223566!7668221!33223566     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=33223566&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       J+Mol+Struct 2021 ; 1230 (?): 129649 Nephropedia Template TP {{tp|p=33223566|t=2021. Synthesis of potentially new schiff bases of N-substituted-2-quinolonylacetohydrazides as anti-COVID-19 agents |pdf=|usr=}}{{33223566}} gab.com Text Synthesis of potentially new schiff bases of N-substituted-2-quinolonylacetohydrazides as anti-COVID-19 agents JO: J Mol Struct http://www.kidney.de/pget.php?&tw=1&pmid=33223566 #FOAvip We report herein a new series of synthesized N-substituted-2-quinolonylacetohydrazides aiming to evaluate their activity towards SARS-CoV-2. The structures of the obtained products were fully confirmed by NMR, mass, IR spectra and elemental analysis as well. Molecular docking calculations showed that most of the tested compounds possessed good binding affinity to the SARS-CoV-2 main protease (M(pro)) comparable toRemdesivir. Twit Text FOAVip Synthesis of potentially new schiff bases of N-substituted-2-quinolonylacetohydrazides as anti-COVID-19 agents ????J Mol Struct http://www.kidney.de/pget.php?&tw=1&pmid=33223566 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33223566 #FOAvip English Wikipedia <ref>{{Cite pmid|33223566}}</ref> Synthesis of potentially new schiff bases of N-substituted-2-quinolonylacetohydrazides as anti-COVID-19 agents #MMPMID33223566 Alshammari MB; Ramadan M; Aly AA; El-Sheref EM; Bakht MA; Ibrahim MAA; Shawky AM J Mol Struct 2021[Apr]; 1230 (?): 129649 PMID33223566show ga We report herein a new series of synthesized N-substituted-2-quinolonylacetohydrazides aiming to evaluate their activity towards SARS-CoV-2. The structures of the obtained products were fully confirmed by NMR, mass, IR spectra and elemental analysis as well. Molecular docking calculations showed that most of the tested compounds possessed good binding affinity to the SARS-CoV-2 main protease (M(pro)) comparable toRemdesivir. ?Synthesis of potentially new schiff bases of N-substituted-2-quinolon(epmc).pdf DeepDyve Pubget Overpricing