| Literature DB >> 32556804 |
Ronak Haj Ersan1, Mehmet Abdullah Alagoz2, Tugba Ertan-Bolelli3, Nizami Duran4, Serdar Burmaoglu5, Oztekin Algul6.
Abstract
In the present work, a series of bisbenzazole derivatives were designed and synthesized as antiproliferative agents. The antiproliferative activity of these compounds was investigated using MTT assay. Bisbenzazole derivatives showed significant antiproliferative activity against all the four tested cancer cell lines. Among the various bisbenzazole derivatives, bisbenzoxazole derivatives exhibited the most promising anticancer activity followed by bisbenzimidazole and bisbenzothiazole derivatives. All the derivatives were found to be less toxic as compared to methotrexate (positive control) in normal human cells, indicating selective and efficient antiproliferative activity of these bisbenzazole derivatives. The structure-activity relationships of heteroaromatic systems and linkers present in bisbenzazole derivatives were analyzed in detail. In silico ADMET prediction revealed that bisbenzazole is a drug-like small molecule with a favorable safety profile. Compound 31 is a potential antiproliferative hit compound that exhibits unique cytotoxic activity distinct from methotrexate. Twenty-one bisbenzoxazole derivatives have been designed synthesized and evaluated to be an antiproliferative activity against four human tumor cell lines.Entities:
Keywords: ADMET; Antiproliferative activity; Bisbenzimidazole; Bisbenzothiazole; Bisbenzoxazole; SAR
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Year: 2020 PMID: 32556804 DOI: 10.1007/s11030-020-10115-0
Source DB: PubMed Journal: Mol Divers ISSN: 1381-1991 Impact factor: 2.943