ol). Synthesis of 4-((8-bromooctyl)oxy)-2-alkoxy-1-nitrobenzenes (21a-c).Writer Manuscript Writer Manuscript Writer Manuscript Writer ManuscriptCompounds 21a-c were synthesized

ol). Synthesis of 4-((8-bromooctyl)oxy)-2-alkoxy-1-nitrobenzenes (21a-c).Writer Manuscript Writer Manuscript Writer Manuscript Writer ManuscriptCompounds 21a-c were synthesized from 20a-c (one.32.06 mmol) following the general synthesis of compounds 6a-i. 4-((8-Bromooctyl)oxy)-2-methoxy-1-nitrobenzene (21a). Yellow JAK…

Reports | Vol:.(1234567890)(2021) 11:24494 |doi/10.1038/s41598-021-03569-www.nature.com/scientificreports/FigureReports | Vol:.(1234567890)(2021) 11:24494 |doi/10.1038/s41598-021-03569-www.nature.com/scientificreports/Figure 8. Net MM/GBSA binding totally free

Reports | Vol:.(1234567890)(2021) 11:24494 |doi/10.1038/s41598-021-03569-www.nature.com/scientificreports/FigureReports | Vol:.(1234567890)(2021) 11:24494 |doi/10.1038/s41598-021-03569-www.nature.com/scientificreports/Figure 8. Net MM/GBSA binding totally free energy and energy dissociation components (kcal/mol) calculated for the docked poses (orange color) and MD…