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• W3186392652 abstract "• PGLC ROBB, PGLCROMBT, and PGLCROB synthesized by Mizoroki-Heck reaction. • Synthesized compounds characterized by 1H, 13C-NMR, IR, and mass spectrometry. • PGLCROB showed promising activity against A549 (lung cancer) cell lines. • From QTAIM and NCI-RDG analysis used to identify molecular interactions. • From FMO, PGLCROMBT (7.331 eV) have low HOMO-LUMO energy gap. In the current research work synthesis of novel steroids, PGLCROBB, PGLCROMBT , and PGLCROB are being reported employing palladium catalyzed Mizoroki-Heck reaction. Structure elucidation of all the synthesized compounds was done by 1 H NMR, 13 C NMR, IR, and mass spectrometry. These prodrugs PGL, PGLCRO, PGLCROBB, PGLCROMBT , and PGLCROB were tested on human lung cancer cell line (A549). The results were very promising as PGLCROB has shown significant anticancer activity against lung cancer cells. In order to look into the structural stability and electronic feature analyses, quantum chemical calculations have been performed using the DFT approach. To spot, describe, and estimate competently the weak C-H⋯O H-bonding and H⋯H (conventional) as well as C⋯H (unconventional) non-covalent interactions (NCIs) involved therein, the Bader's QTAIM and NCI-plot have also been executed. The H⋯H bond paths range from 2.021 Å to 2.039 Å however the C⋯H bond paths fall between 2.806 Å and 2.871 Å and such type of interactions demonstrate all the characteristics of a closed-shell interaction. The analyzed chemical reactivity mainly emphasized for PGLCRO, PGLCROB, PGLCROBB and PGLCROMBT systems shows that the PGLCROB (with a very marginal difference with the PGLCROBB ) is chemically more reactive (highly sensitive) species among all steroids. This work represents another instance of the utilization and successful application of the concept of bond path and the QTAIM." @default.
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• W3186392652 date "2021-12-01" @default.
• W3186392652 modified "2023-10-16" @default.
• W3186392652 title "Experimental and theoretical investigation of synthesized pregnenolone derivatives via palladium catalyzed cross coupling reactions, their anticancer activity against lung cancer cells" @default.
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• W3186392652 doi "https://doi.org/10.1016/j.molstruc.2021.131115" @default.
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