Design, Synthesis, and Biological Evaluation of 2‐(2‐Bromo‐3‐nitrophenyl)‐5‐phenyl‐1, 3, 4‐oxadiazole Derivatives as Possible Anti‐Breast Cancer Agents. Issue 2 (29th January 2020)

• Record Type: Journal Article
• Authors: Ananth, Arjun H.; Manikandan, Natarajan; Rajan, Ravi Kumar; Elancheran, Ramakrishnan; Lakshmithendral, Kunasekaran; Ramanathan, Muthiah; Bhattacharjee, Atanu; Kabilan, Senthamaraikannan
• Is Part Of: Chemistry & biodiversity. Volume 17:Issue 2(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-01-29
• Subjects: 1, 3, 4-oxadiazole -- breast cancer -- estrogen receptor -- single-crystal XRD -- molecular dynamics -- ADMET -- cytotoxicity; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Biodiversity -- Periodicals; 572
• DOI: 10.1002/cbdv.201900659
• Languages: English
• ISSNs: 1612-1872

Abstract

Abstract: Breast Cancer (BCa) is the most often diagnosed cancer among women who were in the late 1940's. Breast cancer growth is largely dependent on the expression of estrogen and progesterone receptor. Breast cancer cells may have one, both, or none of these receptors. The treatment for breast cancer may involve surgery, hormonal therapy (Tamoxifen, an aromatase inhibitor, etc.) and oral chemotherapeutic drugs. The molecular docking technique reported the findings on the potential binding modes of the 2‐(2‐bromo‐3‐nitrophenyl)‐5‐phenyl‐1, 3, 4‐oxadiazole derivatives with the estrogen receptor (PDB ID: 3ERT). The 1, 3, 4‐oxadiazole derivatives 4a –4j have been synthesized and described by spectroscopic method. 2‐(2‐Bromo‐6‐nitrophenyl)‐5‐(4‐bromophenyl)‐1, 3, 4‐oxadiazole (4c ) was reconfirmed by single‐crystal XRD. All the compounds have been tested in combination with generic Imatinib pharmaceutical drug against breast cancer cell lines isolated from Caucasian woman MCF‐7, MDA‐MB‐453 and MCF‐10A non‐cancer cell lines. The compounds with the methoxy (in 4c ) and methyl (in 4j ) substitution were shown to have significant cytotoxicity, with 4c showing dose‐dependent activation and decreased cell viability. The mechanism of action was reported by induced apoptosis and tested by a DNA enzyme inhibitor experiment (ELISA) for Methyl Transferase. Molecular dynamics simulations were made for hit molecule 4c to study the stability and interaction of the protein−ligand complex. The toxicity properties of ADME were calculated for all the compounds. All these results provide essential information for further clinical trials. Abstract :