Literature DB >> 29171934

Design, Synthesis, and Evaluation of ω-(Isothiocyanato)alkylphosphinates and Phosphine Oxides as Antiproliferative Agents.

Łukasz Janczewski1, Mateusz Psurski2, Marta Świtalska2, Anna Gajda1, Tomasz M Goszczyński2, Józef Oleksyszyn3, Joanna Wietrzyk2, Tadeusz Gajda1.   

Abstract

A series of 21 novel, structurally diverse ω-(isothiocyanato)alkylphosphinates and phosphine oxides (ITCs) were designed and synthesized in moderate to good yields. The synthesized compounds were evaluated for in vitro antiproliferative activity using LoVo and LoVo/DX cancer cell lines. The biological activity of the synthesized compounds was higher than that of natural isothiocyanates such as benzyl isothiocyanate or sulforaphane. The antiproliferative activity of selected ITCs was also tested on selected cancer cell lines: A549, MESSA and MESSA/DX-5, HL60 and HL60MX2, BALB/3T3, and 4T1. These compounds were assessed for their mechanism of action as inducers of cell-cycle arrest and apoptosis. Ethyl (6-isothiocyanatohexyl)(phenyl)phosphinate (71) was tested in vivo on the 4T1 cell line and demonstrated moderate antitumor activity, similar to that benzyl isothiocyanate and cyclophosphamide.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  apoptosis; cell cycle; isothiocyanates; isothiocyanatoalkyl phosphinates; isothiocyanatoalkyl phosphine oxides

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Year:  2017        PMID: 29171934     DOI: 10.1002/cmdc.201700619

Source DB:  PubMed          Journal:  ChemMedChem        ISSN: 1860-7179            Impact factor:   3.466


  5 in total

1.  RASS-Enabled S/P-C and S-N Bond Formation for DEL Synthesis.

Authors:  Dillon T Flood; Xuejing Zhang; Xiang Fu; Zhenxiang Zhao; Shota Asai; Brittany B Sanchez; Emily J Sturgell; Julien C Vantourout; Paul Richardson; Mark E Flanagan; David W Piotrowski; Dominik K Kölmel; Jinqiao Wan; Mei-Hsuan Tsai; Jason S Chen; Phil S Baran; Philip E Dawson
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-11       Impact factor: 15.336

2.  The Anti-Tumoral Potential of Phosphonate Analog of Sulforaphane in Zebrafish Xenograft Model.

Authors:  Magdalena Rudzinska-Radecka; Łukasz Janczewski; Anna Gajda; Marlena Godlewska; Malgorzata Chmielewska-Krzesinska; Krzysztof Wasowicz; Piotr Podlasz
Journal:  Cells       Date:  2021-11-18       Impact factor: 6.600

Review 3.  Sulforaphane and Its Bifunctional Analogs: Synthesis and Biological Activity.

Authors:  Łukasz Janczewski
Journal:  Molecules       Date:  2022-03-07       Impact factor: 4.411

4.  Isothiocyanates (ITCs) 1-(Isothiocyanatomethyl)-4-phenylbenzene and 1-Isothiocyanato-3,5-bis(trifluoromethyl)benzene-Aldehyde Dehydrogenase (ALDH) Inhibitors, Decreases Cisplatin Tolerance and Migratory Ability of NSCLC.

Authors:  Jolanta Kryczka; Jakub Kryczka; Łukasz Janczewski; Anna Gajda; Andrzej Frączyk; Joanna Boncela; Beata Kolesińska; Ewa Brzeziańska-Lasota
Journal:  Int J Mol Sci       Date:  2022-08-03       Impact factor: 6.208

5.  Synthesis of Isothiocyanates Using DMT/NMM/TsO- as a New Desulfurization Reagent.

Authors:  Łukasz Janczewski; Dorota Kręgiel; Beata Kolesińska
Journal:  Molecules       Date:  2021-05-06       Impact factor: 4.411

  5 in total

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