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Synthesis and docking study of benzimidazole–triazolothiadiazine hybrids as aromatase inhibitors

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Aromatase, Chemistry, Benzimidazole, Docking (animal), Stereochemistry, Enzyme, Active site, Cytotoxicity, Bromide, Aromatase inhibitor, Cell culture, MTT assay, Substituent, Structure–activity relationship, In vitro, Biochemistry, Biology, Cancer, Breast cancer, Organic chemistry

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