A Novel of Azo-Thiazole Moiety Alternative for Benzidine-Based Pigments: Design, Synthesis, Characterization, Biological Evaluation, and Molecular Docking Study

A new series of coloring compounds (pigments) based on 5-(2-aminothiazol-5-yl)thiazol-2-amine and 5-(4-aminophenyl)thiazol-2-amine as heterocyclic alternatives for benzidine based on disazo dyestuffs were synthesized. All the newly synthesized pigments are characterized based on their physical, spectral, and analytical data. The antimicrobial activity showed that introducing the heterocyclic analogues thiazole (mono or bis) exhibited less toxic and resisted antimicrobial (five gram-positive strain, three gram-negative, and three fungal species). Thus, derivatives demonstrated moderate to good activity compared with Gentamycin and Ketoconazole. Furthermore, the pigments screened for their in vitro antioxidant properties by the DPPH method, and the newly designed pigments PG4-PG11 with thiazole moiety causes increase antioxidant properties with IC50 values ranged between (0.054-0.192 mu M) compared with PG1, PG2, and PG3 (IC50 = 0.712, 0.239, and 0.191 mu M) as well as Ascorbic acid (IC50 = 2.532 mu M). Further, the synthesized pigments' cytotoxicity activity evaluated against HepG-2 and showed IC50 values ranged between (53.52-94.05 mu M) compared with PG1-PG3 (IC50 =216.04-393.58 mu M) and doxorubicin (IC50 = 8.17 mu M). Molecular docking study concluded that thiazole moiety might be made one or more binding mode as critical hydrogen bonding through the nitrogen of thiazole, as well as arene-cation and/or arene-arene interaction with dihydrofolate reductase (DHFR) active site in 1DLS protein.

Automated summary

A new series of coloring compounds based on heterocyclic analogues thiazole were synthesized and characterized. These compounds exhibited less toxic and resisted antimicrobial activity, as well as increased antioxidant properties. Additionally, they showed lower cytotoxicity against HepG-2 cells compared to existing compounds.