Design, synthesis, and anticancer activity of novel 4,6-dimorpholinyl-1,3,5-triazine compounds

The chalcone structure was introduced into the 4,6-dimorpholinyl-1,3,5-triazine molecule through the C-N bond, and a series of new compounds were obtained. Among them, the pyridyl-containing 6o exhibits anti-proliferation activity similar to that of cisplatin on SW620. Interestingly, the phenyl-cont...

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Main Authors: Li Jinjing, Li Linbo, Liu Yuxiao, Zhang Jie, Shi Chengyang, Zhou Shujing, Qiu Hongbin
Format: Article
Language:English
Published: De Gruyter 2023-06-01
Series:Heterocyclic Communications
Subjects:
Online Access:https://doi.org/10.1515/hc-2022-0152
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author Li Jinjing
Li Linbo
Liu Yuxiao
Zhang Jie
Shi Chengyang
Zhou Shujing
Qiu Hongbin
author_facet Li Jinjing
Li Linbo
Liu Yuxiao
Zhang Jie
Shi Chengyang
Zhou Shujing
Qiu Hongbin
author_sort Li Jinjing
collection DOAJ
description The chalcone structure was introduced into the 4,6-dimorpholinyl-1,3,5-triazine molecule through the C-N bond, and a series of new compounds were obtained. Among them, the pyridyl-containing 6o exhibits anti-proliferation activity similar to that of cisplatin on SW620. Interestingly, the phenyl-containing 6a exhibits a certain selectivity for the anti-proliferation activity of SW620.
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spelling doaj.art-a4336f0d34eb47478d787580abcdae7f2023-08-14T07:06:12ZengDe GruyterHeterocyclic Communications2191-01972023-06-01291673610.1515/hc-2022-0152Design, synthesis, and anticancer activity of novel 4,6-dimorpholinyl-1,3,5-triazine compoundsLi Jinjing0Li Linbo1Liu Yuxiao2Zhang Jie3Shi Chengyang4Zhou Shujing5Qiu Hongbin6College of Pharmacy, Jiamusi University, Jiamusi, 154007, ChinaCollege of Pharmacy, Jiamusi University, Jiamusi, 154007, ChinaCollege of Pharmacy, Jiamusi University, Jiamusi, 154007, ChinaCollege of Pharmacy, Jiamusi University, Jiamusi, 154007, ChinaCollege of Pharmacy, Jiamusi University, Jiamusi, 154007, ChinaInstitute of Pharmacy in Heilongjiang Province, Jiamusi, 154007, ChinaJiamusi University, Jiamusi, 154007, ChinaThe chalcone structure was introduced into the 4,6-dimorpholinyl-1,3,5-triazine molecule through the C-N bond, and a series of new compounds were obtained. Among them, the pyridyl-containing 6o exhibits anti-proliferation activity similar to that of cisplatin on SW620. Interestingly, the phenyl-containing 6a exhibits a certain selectivity for the anti-proliferation activity of SW620.https://doi.org/10.1515/hc-2022-0152chalcones4,6-dimorpholinyl-1,3,5-triazineanticancer activity
spellingShingle Li Jinjing
Li Linbo
Liu Yuxiao
Zhang Jie
Shi Chengyang
Zhou Shujing
Qiu Hongbin
Design, synthesis, and anticancer activity of novel 4,6-dimorpholinyl-1,3,5-triazine compounds
Heterocyclic Communications
chalcones
4,6-dimorpholinyl-1,3,5-triazine
anticancer activity
title Design, synthesis, and anticancer activity of novel 4,6-dimorpholinyl-1,3,5-triazine compounds
title_full Design, synthesis, and anticancer activity of novel 4,6-dimorpholinyl-1,3,5-triazine compounds
title_fullStr Design, synthesis, and anticancer activity of novel 4,6-dimorpholinyl-1,3,5-triazine compounds
title_full_unstemmed Design, synthesis, and anticancer activity of novel 4,6-dimorpholinyl-1,3,5-triazine compounds
title_short Design, synthesis, and anticancer activity of novel 4,6-dimorpholinyl-1,3,5-triazine compounds
title_sort design synthesis and anticancer activity of novel 4 6 dimorpholinyl 1 3 5 triazine compounds
topic chalcones
4,6-dimorpholinyl-1,3,5-triazine
anticancer activity
url https://doi.org/10.1515/hc-2022-0152
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