Literature DB >> 16377034

Synthesis, structure and anticancer activity of novel 2,4-diamino-1,3,5-triazine derivatives.

F Saczewski1, A Bułakowska, P Bednarski, R Grunert.   

Abstract

A series of 2-(4,6-diamino-1,3,5-triazin-2-yl)-2-{[4-(dimethylamino)-phenyl]imino}acetonitriles 19-27 have been synthesized by the reaction of 2-(4-amino-6-alkylamino-1,3,5-triazin-2-yl)acetonitriles 10-15 with p-nitrosodimethylaniline. Unexpectedly, a similar reaction of acetonitriles 10, 14, 15, 17 and 18 with nitrosobenzene led to the formation of 4,6-diamino-N-phenyl-1,3,5-triazine-2-carboxamides 28-32. The in vitro antitumor activity of the compounds obtained has been tested and 2-[4-Amino-6-(4-phenylpiperazin-1-yl)-1,3,5-triazin-2-yl]-2{[4-(dimethylamino)phenyl]imino}acetonitrile (19) having remarkable activity against melanoma MALME-3 M cell line (GI(50)=3.3 x 10(-8) M, TGI=1.1 x 10(-6) M) is a leading candidate for further development.

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Year:  2005        PMID: 16377034     DOI: 10.1016/j.ejmech.2005.10.013

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  8 in total

1.  Synthesis and cytotoxic activity of novel poly-substituted imidazo[2,1-c][1,2,4]triazin-6-amines.

Authors:  Tahmineh Akbarzadeh; Saeedeh Noushini; Somayeh Taban; Mohammad Mahdavi; Mahsima Khoshneviszadeh; Mina Saeedi; Saeed Emami; Mohammad Eghtedari; Yaghoub Sarrafi; Mehdi Khoshneviszadeh; Maliheh Safavi; Kouros Divsalar; Mohammad Hassan Moshafi; Ali Asadipour; Reyhaneh Sabourian; Najmeh Edraki; Omidreza Firouzi; Ramin Miri; Abbas Shafiee; Alireza Foroumadi
Journal:  Mol Divers       Date:  2015-01-23       Impact factor: 2.943

2.  Novel inhibitors of Rad6 ubiquitin conjugating enzyme: design, synthesis, identification, and functional characterization.

Authors:  Matthew A Sanders; Ghali Brahemi; Pratima Nangia-Makker; Vitaly Balan; Matteo Morelli; Hend Kothayer; Andrew D Westwell; Malathy P V Shekhar
Journal:  Mol Cancer Ther       Date:  2013-01-21       Impact factor: 6.261

3.  Synthesis, molecular docking, ctDNA interaction, DFT calculation and evaluation of antiproliferative and anti-Toxoplasma gondii activities of 2,4-diaminotriazine-thiazole derivatives.

Authors:  Krzysztof Z Łączkowski; Joanna Anusiak; Marta Świtalska; Katarzyna Dzitko; Joanna Cytarska; Angelika Baranowska-Łączkowska; Tomasz Plech; Agata Paneth; Joanna Wietrzyk; Joanna Białczyk
Journal:  Med Chem Res       Date:  2018-02-06       Impact factor: 1.965

4.  Hybrid Molecules Composed of 2,4-Diamino-1,3,5-triazines and 2-Imino-Coumarins and Coumarins. Synthesis and Cytotoxic Properties.

Authors:  Anna Makowska; Franciszek Sączewski; Patrick J Bednarski; Jarosław Sączewski; Łukasz Balewski
Journal:  Molecules       Date:  2018-07-03       Impact factor: 4.411

5.  Synthesis and anticancer activity of new benzensulfonamides incorporating s-triazines as cyclic linkers for inhibition of carbonic anhydrase IX.

Authors:  Abdelrahman I Zain-Alabdeen; Tarek F El-Moselhy; Nabaweya Sharafeldin; Andrea Angeli; Claudiu T Supuran; Mervat H El-Hamamsy
Journal:  Sci Rep       Date:  2022-10-06       Impact factor: 4.996

6.  1,3,5-Triazine Nitrogen Mustards with Different Peptide Group as Innovative Candidates for AChE and BACE1 Inhibitors.

Authors:  Dawid Maliszewski; Agnieszka Wróbel; Beata Kolesińska; Justyna Frączyk; Danuta Drozdowska
Journal:  Molecules       Date:  2021-06-28       Impact factor: 4.411

7.  Synthesis and Characterization of New Series of 1,3-5-Triazine Hydrazone Derivatives with Promising Antiproliferative Activity.

Authors:  Hessa H Al H Al Rasheed; Azizah M M Malebari; Kholood A A Dahlous; Ayman El-Faham
Journal:  Molecules       Date:  2020-06-11       Impact factor: 4.411

8.  Microwave-assisted efficient one-pot synthesis of N 2-(tetrazol-5-yl)-6-aryl/heteroaryl-5,6-dihydro-1,3,5-triazine-2,4-diamines.

Authors:  Moustafa Sherief Moustafa; Ramadan Ahmed Mekheimer; Saleh Mohammed Al-Mousawi; Mohamed Abd-Elmonem; Hesham El-Zorba; Afaf Mohamed Abdel Hameed; Tahany Mahmoud Mohamed; Kamal Usef Sadek
Journal:  Beilstein J Org Chem       Date:  2020-07-16       Impact factor: 2.883

  8 in total

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