Literature DB >> 26306006

LASSBio-1829 Hydrochloride: Development of a New Orally Active N-Acylhydrazone IKK2 Inhibitor with Anti-inflammatory Properties.

Isabella A Guedes1, Rosana H C N Freitas2, Natália M Cordeiro3, Thaís S do Nascimento3, Tayna S Valerio3, Patrícia D Fernandes3, Laurent E Dardenne1, Carlos A M Fraga4.   

Abstract

Inhibitor of nuclear factor κB kinase 2 (IKK2) is suggested to be a potential target for the development of novel anti-inflammatory and anticancer drugs. In this work, we applied structure-based drug design to improve the potency of the inhibitor (E)-N'-(4-nitrobenzylidene)-2-naphthohydrazide (LASSBio-1524, 1 a: IC50 =20 μm). The molecular model built for IKK2 together with the docking methodology employed were able to provide important and consistent information with respect to the structural and chemical inhibitor characteristics that may confer potency to IKK2 inhibitors, providing important guidelines for the development of a new N-acylhydrazone (NAH) derivative. (E)-N'-(4-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzylidene)-2-naphthohydrazide hydrochloride (LASSBio-1829 hydrochloride, 10) is a 7-azaindole NAH able to inhibit IKK2 with an IC50 value of 3.8 μm. LASSBio-1829 hydrochloride was found to be active in several pharmacological inflammation tests in vivo, showing its potential as an anti-inflammatory prototype.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  IKK2; N-acylhydrazones; anti-inflammatory agents; molecular docking; structure-based drug design

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Year:  2015        PMID: 26306006     DOI: 10.1002/cmdc.201500266

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


  2 in total

1.  Discovery of Novel Orally Active Tetrahydro-Naphthyl-N-Acylhydrazones with In Vivo Anti-TNF-α Effect and Remarkable Anti-Inflammatory Properties.

Authors:  Natália M Cordeiro; Rosana H C N Freitas; Carlos A M Fraga; Patricia D Fernandes
Journal:  PLoS One       Date:  2016-05-26       Impact factor: 3.240

2.  Synthesis and pharmacological evaluation of novel isoquinoline N-sulphonylhydrazones designed as ROCK inhibitors.

Authors:  Ramon Guerra de Oliveira; Fabiana Sélos Guerra; Cláudia Dos Santos Mermelstein; Patrícia Dias Fernandes; Isadora Tairinne de Sena Bastos; Fanny Nascimento Costa; Regina Cely Rodrigues Barroso; Fabio Furlan Ferreira; Carlos Alberto Manssour Fraga
Journal:  J Enzyme Inhib Med Chem       Date:  2018-12       Impact factor: 5.051

  2 in total

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