Synthesis and cytotoxicity studies of 1-propenyl-1,3-dihydro-benzimidazol-2-one.

Journal of Chemical Biology Pub Date : 2015-04-17 eCollection Date: 2015-07-01 DOI:10.1007/s12154-015-0130-8
Biswadip Banerji, Sumit Kumar Pramanik
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引用次数: 4

Abstract

A heterocyclic compound 1-propenyl-1,3-dihydro-benzimidazol-2-one was synthesized by a palladium-catalyzed rearrangement reaction. Anticancer activities were confirmed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay against Neura 2a (neuroblastoma cell), HEK 293 (kidney cancer) and MCF-7 (breast cancer) cell lines at low micromolar range. Furthermore, clear images from phase-contrast and fluorescence microscopes and confocal images unambiguously confirm the cancer cell death. The single X-ray crystal structure of the compound unambiguously proves the structure of the benzimidazolone compound.

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1-丙烯-1,3-二氢苯并咪唑-2-酮的合成及细胞毒性研究。
采用钯催化重排反应合成了杂环化合物1-丙烯-1,3-二氢苯并咪唑-2-酮。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)在低微摩尔范围内对神经母细胞瘤细胞Neura 2a、肾癌细胞HEK 293和乳腺癌细胞MCF-7的抑癌活性证实。此外,相衬显微镜、荧光显微镜和共聚焦显微镜的清晰图像明确证实了癌细胞的死亡。该化合物的单x射线晶体结构明确地证明了苯并咪唑酮化合物的结构。
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Last issue of journal of chemical biology. JOCB Bulletin. Design, synthesis, and characterization of 2,2-bis(2,4-dinitrophenyl)-2-(phosphonatomethylamino)acetate as a herbicidal and biological active agent. Design and synthesis of an indol derivative as antibacterial agent against Staphylococcus aureus. Amphotericin B potentiates the anticancer activity of doxorubicin on the MCF-7 breast cancer cells.
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