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New maleimide 1,2,3-triazole hybrids: design, synthesis, anticancer, and antimicrobial activities

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Abstract

A new series of maleimide triazole hybrid compounds namely 3-chloro-1-[(1-aryl-1H-1,2,3-triazol-4-yl)methyl]-4-(arylamino)-1H-pyrrole-2,5-dione have been prepared. Our synthetic strategy starts via the reaction of 2,3-dichloromaleic anhydride with propargyl amine followed by chlorine displacement with arylamine and subsequent formation of a triazole utilizing copper(I) catalyzed azide-alkyne cycloaddition reaction, that generates the designed triazole nucleus. The produced hybrid compounds were identified using various physicochemical properties of the pure compounds. The synthesized compounds were screened for antimicrobial activities against Escherichia coli, Pseudomonas aeruginosa, and Bacillus spizizenii. While selected compounds were tested for their anticancer activities against T47D, HCT 116, and VERO cell lines.

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References

  1. Beller M, Lukas J, Frech M, Junghanss C, Rolfs A, Pews-Davtyan, A (2015) Use of maleimide derivatives for preventing and treating cancer. US Patent 20150313882A1, Nov 5, 2015; (2016) Chem Abstr 167:375003

  2. Wang J-J, Wang S-S, Leeb C-F, Chung M-An, Chern Y-Te (1997) J Chemother 43:182

  3. Bykov VJN, Issaeva N, Zache N, Shilov A, Hultcrantz M, Bergman J, Selivanova G, Wiman KG (2005) J Biol Chem 280:30384

    Article  CAS  Google Scholar 

  4. Stewart SG, Polomska ME, Lim RW (2007) Tetrahedron Lett 48:2241

    Article  CAS  Google Scholar 

  5. Ferri N, Beccalli EM, Contini A, Corsini A, Antonino M, Radice T, Pratesi G, Tinelli S, Zunino F, Gelmi ML (2008) Bioorg Med Chem 16:1691

    Article  CAS  Google Scholar 

  6. Kawabe T, Ishigaki M, Sato T, Yamamoto S, Hasegawa Y (2008) Preparation of pyridinylaminopyrrolinediones and related compounds for treatment of cell proliferation disorders. US Patent 20080275057A1, Nov 6, 2008; (2008) Chem Abstr 149:534065

  7. Cashman JR, MacDonald M, Ghirmai S, Okolotowicz KJ, Sergienko E, Brown B, Garcia X, Zhai D, Dahl R, Reed JC (2010) Bioorg Med Chem Lett 20:6560

    Article  CAS  Google Scholar 

  8. Suzuki T, Tanaka R, Hamada S, Nakagawa H, Miyata N (2010) Bioorg Med Chem Lett 20:1124

    Article  CAS  Google Scholar 

  9. Dou Y (2018) Preparation of amide compound as HSP90 inhibitor for treating tumor. CN Patent 107857758A; Mar 30, 2018; (2018) Chem Abstr 168:387314

  10. Winfield HJ, Cahill MM, O’Shea KD, Pierce LT, Robert T, Ruchaud S, Bach S, Marchand P, McCarthy FO (2018) Bioorg Med Chem 26:4209

    Article  CAS  Google Scholar 

  11. Liu X, Hu Y, Gao A, Xu M, Gao L, Xu L, Zhou Y, Gao J, Ye Q, Li J (2019) Bioorg Med Chem 27:589

    Article  CAS  Google Scholar 

  12. Salameh BA, Abu-Safieh KA, Al-Kaabenah SRA, Al-Qawasmeh RA (2014) Res Chem Intermed 40:3001

    Article  CAS  Google Scholar 

  13. Panov AA, Simonov AY, Lavrenov SN, Lakatosh SA, Trenin AS (2018) Chem Hetrocycl Comp 54:103

    Article  CAS  Google Scholar 

  14. Muus U, Hose C, Yao W, Kosakowska-Cholody T, Farnsworth D, Dyba M, Lountos GT, Waugh DS, Monks A, Burke TR Jr, Michejda CJ (2010) Bioorg Med Chem 18:4535

    Article  CAS  Google Scholar 

  15. Wilke KE, Fihn CA, Carlson EE (2018) Bioorg Med Chem 26:5322

    Article  CAS  Google Scholar 

  16. Panov AA, Lavrenov SN, Simonov AY, Mirchink EP, Isakova EB, Trenin AS (2019) J Antibiot 72:122

    Article  CAS  Google Scholar 

  17. Bellandi P, Gusmeroli M, Mormile S, Badaracco C, Vazzola M (2017) Derivatives of pyrrole-2,5-diones having a fungicidal activity, their agronomical compositions and use thereof. WO Patent 2017168368A1, Oct 5, 2017; (2017) Chem Abstr 167:457095

  18. Rostovtsev VV, Green LG, Fokin VV, Sharpless KB (2002) Angew Chem Int Ed 41:2596

    Article  CAS  Google Scholar 

  19. Tornøe CW, Christensen C, Meldal M (2002) J Org Chem 67:3057

    Article  Google Scholar 

  20. Kolb HC, Sharpless KB (2003) Drug Discov Today 8:1128

    Article  CAS  Google Scholar 

  21. Meldal M, Tornøe CW (2008) Chem Rev 108:2952

    Article  CAS  Google Scholar 

  22. Katritzky AR, Rees CW (1984) Comprehensive heterocyclic chemistry. Pergamon Press, Oxford

    Google Scholar 

  23. Salameh BA, Leffler H, Nilsson UJ (2005) Bioorg Med Chem Lett 15:3344

    Article  CAS  Google Scholar 

  24. Delaine T, Collins P, MacKinnon A, Sharma G, Stegmayr J, Rajput VK, Mandal S, Cumpstey I, Larumbe A, Salameh BA, Kahl-Knutsson B, van Hattum H, van Scherpenzeel M, Pieters RJ, Sethi T, Schambye H, Oredsson S, Leffler H, Blanchard H, Nilsson UJ (2016) ChemBioChem 17:1759

    Article  CAS  Google Scholar 

  25. Leffler H, Salameh BAB, Nilsson U (2010) 3-Triazolyl-galactoside inhibitors of galectins. US Patent 7,700,763, Apr 20, 2010; (2005) Chem Abstr 144:7029

  26. Shafi S, Alam MM, Mulakayala N, Mulakayala C, Vanaja G, Kalle AM, Pallu R, Alam MS (2012) Eur J Med Chem 49:324

    Article  CAS  Google Scholar 

  27. Hanaineh-Abdelnour L, Salameh BA (1999) Heterocycles 51:2931

    Article  CAS  Google Scholar 

  28. Talib WH (2017) Nutrition 43:89

    Article  Google Scholar 

  29. Talib WH, Zarga MHA, Mahasneh AM (2012) Molecules 17:3291

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We wish to thank The Hashemite University for financial support. RAA thanks Research institute for Science and Engineering (RISE) and the funded project 1902142080.

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Correspondence to Bader A. Salameh.

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Salameh, B.A., Abu-Safieh, K., Al-Hushki, E.H. et al. New maleimide 1,2,3-triazole hybrids: design, synthesis, anticancer, and antimicrobial activities. Monatsh Chem 151, 1609–1619 (2020). https://doi.org/10.1007/s00706-020-02685-4

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