Evaluation of the biological potencies of newly synthesized berberine derivatives bearing benzothiazole moieties with substituted functionalities

الملخص EN

Benzothiazole moieties substituted with various functional groups were utilized to link with the isoquinoline alkaloid berberine through a pentyl side chain.

Entitled analogs were screened for antioxidant potency using the DPPH and ABTS bioassays and for their in vitro anticancer activities against HeLa, CaSki (cervical cancer), and SK-OV-3 (ovarian cancer) cell lines using the SRB bioassay.

The compounds were evaluated for their toxicity to the Madin–Darby canine kidney (MDCK) cell line.

The final compounds demonstrated significant antioxidant potency with IC50 levels of 13.03–24.50 lg/mL and 4.958–7.570 lg/mL in the DPPH and ABTS radical scavenging bioassays, respectively.

The 5e analog with a methoxy functional group and the 5m analog with a cyano functional group had the most significant DPPH and ABTS radical scavenging activities, respectively.

Moreover, the 5m cyano-based analog had the highest potency against all cancer cell lines, with IC50 levels of 5.474, 5.311, and 32.61 lg/mL against the HeLa, CaSki, and SK-OV-3 cell lines, respectively.

All the synthesized compounds were characterized by IR, 1H NMR, 13C NMR spectroscopy and elemental analysis.