E. V. Koroleva, A. L. Ermolinskaya, Zh. V. Ignatovich, O. V. Panibrat, Thi-Kim-Dung Hoang, Thi-Kim-Chi Huynh, Thi-Cam-Thu Nguyen
{"title":"作为潜在蛋白激酶抑制剂的4-(1h -苯并咪唑-2-基)- n-{3-[(嘧啶-2-基)氨基]苯基}苯酰胺的合成及抗增殖活性","authors":"E. V. Koroleva, A. L. Ermolinskaya, Zh. V. Ignatovich, O. V. Panibrat, Thi-Kim-Dung Hoang, Thi-Kim-Chi Huynh, Thi-Cam-Thu Nguyen","doi":"10.1134/S1070428024604679","DOIUrl":null,"url":null,"abstract":"<p>The results of studying the synthesis and antiproliferative activity of new 4-(1<i>H</i>-benzimidazol-2-yl)benzamides containing pharmacophoric 2aminopyrimidine and pyridine moieties are reported. The target compounds were obtained by the acylation of <i>N</i>-(pyrimidin-2-yl)-<i>m</i>-phenylenediamines with 4-(1<i>H</i>-benzimidazol-2-yl)benzoyl chloride or by the aminolysis 4-(1<i>H</i>-benzimidazol-2-yl)benzoic acid with the same amines. The synthesized compounds were evaluated for their in vitro antiproliferative activity against stable human tumor cell lines K562, HL-60, RPMI 1788, and HeLa.</p>","PeriodicalId":766,"journal":{"name":"Russian Journal of Organic Chemistry","volume":"61 3","pages":"378 - 384"},"PeriodicalIF":0.8000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and Antiproliferative Activity of 4-(1H-Benzimidazol-2-yl)-N-{3-[(pyrimidin-2-yl)amino]phenyl}benzamides as Potential Protein Kinase Inhibitors\",\"authors\":\"E. V. Koroleva, A. L. Ermolinskaya, Zh. V. Ignatovich, O. V. Panibrat, Thi-Kim-Dung Hoang, Thi-Kim-Chi Huynh, Thi-Cam-Thu Nguyen\",\"doi\":\"10.1134/S1070428024604679\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The results of studying the synthesis and antiproliferative activity of new 4-(1<i>H</i>-benzimidazol-2-yl)benzamides containing pharmacophoric 2aminopyrimidine and pyridine moieties are reported. The target compounds were obtained by the acylation of <i>N</i>-(pyrimidin-2-yl)-<i>m</i>-phenylenediamines with 4-(1<i>H</i>-benzimidazol-2-yl)benzoyl chloride or by the aminolysis 4-(1<i>H</i>-benzimidazol-2-yl)benzoic acid with the same amines. The synthesized compounds were evaluated for their in vitro antiproliferative activity against stable human tumor cell lines K562, HL-60, RPMI 1788, and HeLa.</p>\",\"PeriodicalId\":766,\"journal\":{\"name\":\"Russian Journal of Organic Chemistry\",\"volume\":\"61 3\",\"pages\":\"378 - 384\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-05-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1070428024604679\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1070428024604679","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Synthesis and Antiproliferative Activity of 4-(1H-Benzimidazol-2-yl)-N-{3-[(pyrimidin-2-yl)amino]phenyl}benzamides as Potential Protein Kinase Inhibitors
The results of studying the synthesis and antiproliferative activity of new 4-(1H-benzimidazol-2-yl)benzamides containing pharmacophoric 2aminopyrimidine and pyridine moieties are reported. The target compounds were obtained by the acylation of N-(pyrimidin-2-yl)-m-phenylenediamines with 4-(1H-benzimidazol-2-yl)benzoyl chloride or by the aminolysis 4-(1H-benzimidazol-2-yl)benzoic acid with the same amines. The synthesized compounds were evaluated for their in vitro antiproliferative activity against stable human tumor cell lines K562, HL-60, RPMI 1788, and HeLa.
期刊介绍:
Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.