Literature DB >> 21986585

A modular approach to trim cellular targets in anticancer drug discovery.

Carla Ríos-Luci1, Raquel Domínguez-Kelly, Leticia G León, Elena Díaz-Rodríguez, Raimundo Freire, Atanasio Pandiella, Inga Cikotiene, José M Padrón.   

Abstract

A Phenotypic Drug Discovery strategy was applied to study a set of pyrimidine analogs prepared by means of intramolecular oxidation-reduction reactions of N-substituted-N-(2,6-disubstituted-5-nitro-4-pyrimidinyl)aminoacetic acid methyl esters in basic media. The combined and rational use of specific assays allowed in short time reducing from all possible cellular targets to those involved in metaphase to anaphase transition.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21986585     DOI: 10.1016/j.bmcl.2011.09.069

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


  2 in total

1.  Three successive and regiocontroled palladium cross-coupling reactions to easily synthesize novel series of 2,4,6-tris(het)aryl pyrido[1',2':1,5]pyrazolo[3,4-d]pyrimidines.

Authors:  R Belaroussi; A Ejjoummany; A El Hakmaoui; M Akssira; G Guillaumet; S Routier
Journal:  RSC Adv       Date:  2018-01-02       Impact factor: 3.361

2.  The first example of the Fischer-Hepp type rearrangement in pyrimidines.

Authors:  Inga Cikotiene; Mantas Jonusis; Virginija Jakubkiene
Journal:  Beilstein J Org Chem       Date:  2013-09-06       Impact factor: 2.883

  2 in total

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