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通过构效关系 (SAR) 研究对新型喹诺酮查尔酮化合物进行先导优化,以提高疗效和代谢稳定性。

Lead optimization of novel quinolone chalcone compounds by a structure-activity relationship (SAR) study to increase efficacy and metabolic stability.

机构信息

Health Science North Research Institute, 56 Walford Road, Sudbury, ON, P3E 2H3, Canada.

Department of Chemistry and Biochemistry, Laurentian University, 935 Ramsey Lake Road, Sudbury, ON, P3E 2C6, Canada.

出版信息

Sci Rep. 2021 Nov 3;11(1):21576. doi: 10.1038/s41598-021-01058-z.

Abstract

Many agents targeting the colchicine binding site in tubulin have been developed as potential anticancer agents. However, none has successfully made it to the clinic, due mainly to dose limiting toxicities and the emergence of multi-drug resistance. Chalcones targeting tubulin have been proposed as a safe and effective alternative. We have shown previously that quinolone chalcones target tubulin and maintain potent anti-proliferative activity vis-à-vis colchicine, while also having high tolerability and low toxicity in mouse models of cancer and refractivity to multi-drug resistance mechanisms. To identify the most effective anticancer chalcone compound, we synthesized 17 quinolone-chalcone derivatives based on our previously published CTR-17 and CTR-20, and then carried out a structure-activity relationship study. We identified two compounds, CTR-21 [((E)-8-Methoxy-3-(3-(2-methoxyphenyl)-3-oxoprop-1-enyl) quinolin-2(1H)-one)] and CTR-32 [((E)-3-(3-(2-ethoxyphenyl)-3-oxoprop-1-enyl) quinolin-2(1H)-one)] as potential leads, which contain independent moieties that play a significant role in their enhanced activities. At the nM range, CTR-21 and CTR-32 effectively kill a panel of different cancer cells originated from a variety of different tissues including breast and skin. Both compounds also effectively kill multi-drug resistant cancer cells. Most importantly, CTR-21 and CTR-32 show a high degree of selectivity against cancer cells. In silico, both of them dock near the colchicine-binding site with similar energies. Whereas both CTR-21 and CTR-32 effectively prevents tubulin polymerization, leading to the cell cycle arrest at G2/M, CTR-21 has more favorable metabolic properties. Perhaps not surprisingly, the combination of CTR-21 and ABT-737, a Bcl-2 inhibitor, showed synergistic effect in killing cancer cells, since we previously found the "parental" CTR-20 also exhibited synergism. Taken together, CTR-21 can potentially be a highly effective and relatively safe anticancer drug.

摘要

许多靶向微管中秋水仙素结合位点的药物已被开发为潜在的抗癌药物。然而,由于剂量限制毒性和多药耐药性的出现,没有一种药物成功进入临床。靶向微管的查耳酮已被提议作为一种安全有效的替代药物。我们之前已经表明,喹诺酮查耳酮靶向微管,保持对秋水仙素的有效抗增殖活性,同时在癌症的小鼠模型中具有高耐受性和低毒性,并且对多药耐药机制具有耐药性。为了确定最有效的抗癌查尔酮化合物,我们基于之前发表的 CTR-17 和 CTR-20 合成了 17 种喹诺酮-查尔酮衍生物,并进行了构效关系研究。我们确定了两种化合物,CTR-21[((E)-8-甲氧基-3-(3-(2-甲氧基苯基)-3-氧代丙-1-烯基)喹啉-2(1H)-酮)]和 CTR-32[((E)-3-(3-(2-乙氧基苯基)-3-氧代丙-1-烯基)喹啉-2(1H)-酮)],它们是潜在的先导化合物,其中包含独立的部分,在其增强的活性中起着重要作用。在纳摩尔范围内,CTR-21 和 CTR-32 有效地杀死了来自多种不同组织的一系列不同癌症细胞,包括乳腺和皮肤。这两种化合物也能有效地杀死多药耐药的癌细胞。最重要的是,CTR-21 和 CTR-32 对癌细胞表现出高度的选择性。在计算机模拟中,它们都在靠近秋水仙素结合位点的地方结合,能量相似。虽然 CTR-21 和 CTR-32 都能有效地阻止微管聚合,导致细胞周期停滞在 G2/M 期,但 CTR-21 具有更好的代谢特性。也许并不奇怪,CTR-21 和 Bcl-2 抑制剂 ABT-737 的联合使用在杀死癌细胞方面显示出协同作用,因为我们之前发现“母体”CTR-20 也表现出协同作用。总之,CTR-21 有可能成为一种高效、相对安全的抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f16/8566451/136620733bc4/41598_2021_1058_Fig1_HTML.jpg

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