Literature DB >> 10476861

Synthesis and cytotoxic activity of N-(2-pyridylsulfenyl)urea derivatives. A new class of potential antineoplastic agents.

M J Gil1, M A Mañú, C Arteaga, M Migliaccio, I Encío, A González, V Martínez-Merino.   

Abstract

Starting from a 3D-model for the antineoplastic activity of diarylsulfonylureas several new features were proposed and tested. Both types of assayed compounds, the N-(2-pyridylsulfonyl)urea and N-(2-pyridylsulfenyl)urea derivatives, inhibited by 50% the growth of the CCRF-CEM cell line at a dosage near to 1 microM. The N -(2-pyrimidinyl) derivative of the sulfenylurea 6c showed a better profile against HT-29, K-562 and HTB-54 tumor cell lines than the corresponding sulfonylurea 6b. Structural modifications on aryl systems affected differently to the cytotoxic activity shown by the compounds against each cell line.

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Year:  1999        PMID: 10476861     DOI: 10.1016/s0960-894x(99)00373-x

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

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Authors:  Man Yee Mallory Leung; Nils P Carlsson; Graham A Colditz; Su-Hsin Chang
Journal:  Value Health       Date:  2016-11-04       Impact factor: 5.725

2.  Benzo[b]thiophenesulphonamide 1,1-dioxide derivatives inhibit tNOX activity in a redox state-dependent manner.

Authors:  I Encío; D J Morré; R Villar; M J Gil; V Martínez-Merino
Journal:  Br J Cancer       Date:  2005-02-28       Impact factor: 7.640

  2 in total

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