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10.1016/j.molstruc.2020.129829

http://scihub22266oqcxt.onion/10.1016/j.molstruc.2020.129829
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suck abstract from ncbi


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pmid33390613      J+Mol+Struct 2021 ; 1229 (ä): 129829
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  • Synthesis of novel indolo 3,2-c isoquinoline derivatives bearing pyrimidine, piperazine rings and their biological evaluation and docking studies against COVID-19 virus main protease #MMPMID33390613
  • Verma VA; Saundane AR; Meti RS; Vennapu DR
  • J Mol Struct 2021[Apr]; 1229 (ä): 129829 PMID33390613show ga
  • A series of hybrid indolo[3,2-c]isoquinoline (delta-carboline) analogs incorporating two pyrimidine and piperizine ring frameworks were synthesized. Intending biological activities and SAR we propose replacements of fluorine, methyl and methoxy of synthetic compounds for noteworthy antimicrobial, antioxidant, anticancer and anti-tuberculosis activities. Among these compounds 3a, 4a and 5e were progressively strong against E. coli and K. pneumonia. Whereas, compounds 4a, 5a and 6a with addition of various functional groups (OCH(3), CH(3)) were excellent against S. aureus and B. subtilis. Compound 5c exhibited strong RSA and dynamic ferrous ion (Fe(2+)) metal chelating impact with IC(50) of 7.88 +/- 0.93 and 4.06 +/- 0.31 microg/mL, respectively. Compound 5e was considerably cytotoxic against all cancer cells displaying activity better than the standard drug. Compounds 6b and 6e inhibited M. tuberculosis (MIC 1.0 mg/L) considerably. Molecular docking studies indicate that compounds 4d, 5a, 5b, 6b and 6f exhibited good interactions with 6LZE (COVID-19) and 6XFN (SARS-CoV-2) at active sites. The structure of the synthesized compounds were elementally analyzed using IR, (1)H, (13)C NMR and mass spectral information.
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