Facile green diversity-oriented synthesis, molecular docking, and cytotoxicity evaluation of quinoline -triazole appended peptidomimetics as inhibitors of human breast cancer cell line MCF-7

The synthesis of quinoline-based drugs has significant interest from researchers due to their broad spectrum of biological activities. In this context, a concise approach for the synthesis of quinoline-functionalized hybrid peptidomimetics is described. The peptidomimetics are constructed based on a...

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Main Authors: K. Ramya, Seena Chakko, V.S. Shinu, Davis Varghese, Ron Joy Pullukkara, S. Arun
Format: Article
Language:English
Published: Elsevier 2025-05-01
Series:Results in Chemistry
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Online Access:http://www.sciencedirect.com/science/article/pii/S2211715625001559
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author K. Ramya
Seena Chakko
V.S. Shinu
Davis Varghese
Ron Joy Pullukkara
S. Arun
author_facet K. Ramya
Seena Chakko
V.S. Shinu
Davis Varghese
Ron Joy Pullukkara
S. Arun
author_sort K. Ramya
collection DOAJ
description The synthesis of quinoline-based drugs has significant interest from researchers due to their broad spectrum of biological activities. In this context, a concise approach for the synthesis of quinoline-functionalized hybrid peptidomimetics is described. The peptidomimetics are constructed based on a recombinant approach via Iqbal multicomponent coupling strategy and click chemistry and were linked via copper (I) catalysed [3 + 2] azide-alkyne cycloaddition. The peptidomimetics showed exceptional inhibitory properties for CDK2 protein which is responsible for many malignancies and also showed remarkable cytotoxicity against human breast cancer cell line MCF-7. The IC50 value (8 μM) and binding affinity (−10.2 Kcal/mol) found for 4b against MCF-7 cells are hopeful for the development of potential anticancer drugs based on these new scaffolds.
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series Results in Chemistry
spelling doaj-art-eb7bdc0f988b4029bb80ac8489f7add32025-08-20T03:46:50ZengElsevierResults in Chemistry2211-71562025-05-011510217210.1016/j.rechem.2025.102172Facile green diversity-oriented synthesis, molecular docking, and cytotoxicity evaluation of quinoline -triazole appended peptidomimetics as inhibitors of human breast cancer cell line MCF-7K. Ramya0Seena Chakko1V.S. Shinu2Davis Varghese3Ron Joy Pullukkara4S. Arun5Research & Post Graduate Department of Chemistry, Christ College (Autonomous) Irinjalakuda, 680125, Affiliated to the University of Calicut, Kerala, IndiaResearch & Post Graduate Department of Chemistry, Christ College (Autonomous) Irinjalakuda, 680125, Affiliated to the University of Calicut, Kerala, IndiaResearch & Post Graduate Department of Chemistry, St. Joseph's College, Devagiri (Autonomous), Kozhikode 673008, Affiliated to the University of Calicut, Kerala, IndiaDepartment of Physics, Loyola College, Chennai 600034, Affiliated to the University of Madras, IndiaDepartment of General Surgery, Jubilee Mission Medical College and Research Institute, Thrissur 680005, Affiliated to Kerala University of Health Sciences, Kerala, IndiaResearch & Post Graduate Department of Chemistry, Christ College (Autonomous) Irinjalakuda, 680125, Affiliated to the University of Calicut, Kerala, India; Corresponding author.The synthesis of quinoline-based drugs has significant interest from researchers due to their broad spectrum of biological activities. In this context, a concise approach for the synthesis of quinoline-functionalized hybrid peptidomimetics is described. The peptidomimetics are constructed based on a recombinant approach via Iqbal multicomponent coupling strategy and click chemistry and were linked via copper (I) catalysed [3 + 2] azide-alkyne cycloaddition. The peptidomimetics showed exceptional inhibitory properties for CDK2 protein which is responsible for many malignancies and also showed remarkable cytotoxicity against human breast cancer cell line MCF-7. The IC50 value (8 μM) and binding affinity (−10.2 Kcal/mol) found for 4b against MCF-7 cells are hopeful for the development of potential anticancer drugs based on these new scaffolds.http://www.sciencedirect.com/science/article/pii/S2211715625001559PeptidomimeticsClick chemistryTriazoleMulticomponent reactionsQuinoline
spellingShingle K. Ramya
Seena Chakko
V.S. Shinu
Davis Varghese
Ron Joy Pullukkara
S. Arun
Facile green diversity-oriented synthesis, molecular docking, and cytotoxicity evaluation of quinoline -triazole appended peptidomimetics as inhibitors of human breast cancer cell line MCF-7
Results in Chemistry
Peptidomimetics
Click chemistry
Triazole
Multicomponent reactions
Quinoline
title Facile green diversity-oriented synthesis, molecular docking, and cytotoxicity evaluation of quinoline -triazole appended peptidomimetics as inhibitors of human breast cancer cell line MCF-7
title_full Facile green diversity-oriented synthesis, molecular docking, and cytotoxicity evaluation of quinoline -triazole appended peptidomimetics as inhibitors of human breast cancer cell line MCF-7
title_fullStr Facile green diversity-oriented synthesis, molecular docking, and cytotoxicity evaluation of quinoline -triazole appended peptidomimetics as inhibitors of human breast cancer cell line MCF-7
title_full_unstemmed Facile green diversity-oriented synthesis, molecular docking, and cytotoxicity evaluation of quinoline -triazole appended peptidomimetics as inhibitors of human breast cancer cell line MCF-7
title_short Facile green diversity-oriented synthesis, molecular docking, and cytotoxicity evaluation of quinoline -triazole appended peptidomimetics as inhibitors of human breast cancer cell line MCF-7
title_sort facile green diversity oriented synthesis molecular docking and cytotoxicity evaluation of quinoline triazole appended peptidomimetics as inhibitors of human breast cancer cell line mcf 7
topic Peptidomimetics
Click chemistry
Triazole
Multicomponent reactions
Quinoline
url http://www.sciencedirect.com/science/article/pii/S2211715625001559
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