Literature DB >> 22632793

Morita-Baylis-Hillman adducts: biological activities and potentialities to the discovery of new cheaper drugs.

Claudio G Lima-Junior1, Mário L A A Vasconcellos.   

Abstract

This review aims to present by the first time the Morita-Baylis-Hillman adducts (MBHA) as a new class of bioactive compounds and highlight its potentialities to the discovery of new cheaper and efficient drugs. Now, most these compounds can be prepared fast and on a single synthetic step (one-pot reaction) in high yields and using ecofriendly synthetic protocols. We highlight here the aromatic MBHA, which have shown diverse biological activities as anti-Leishmania chagasi and Leishmania amazonensis (parasites that cause cutaneous and visceral leishmaniasis), anti-Trypanosoma cruzi (parasite that cause Chagas disease), anti-Plasmodium falciparum and Plasmodium berghei (parasites that cause malaria), lethal against Biomphalaria glabrata (the snail transmitter of schistosomiasis), antibacterial, antifungal, herbicide and actives against some human tumor cell lines. Understanding of the biological mechanisms of action of this new class of molecules is still in the infancy stage. However, we report here which has been described to date on the possibilities of biological mechanisms of action, and we present new analyzes based on literature in this area. The academic and industrial interest in selecting green and cheaper experiments to the drugs development has been the prime mover of the growth on the subject.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22632793     DOI: 10.1016/j.bmc.2012.04.061

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  12 in total

1.  Synthesis, anti-proliferative activity, theoretical and 1H NMR experimental studies of Morita-Baylis-Hillman adducts from isatin derivatives.

Authors:  Vinicius B M Brito; Gilmar F Santos; Thiago D S Silva; Júlia L C Souza; Gardenia C G Militão; Felipe T Martins; Fábio P L Silva; Boaz G Oliveira; Edigenia C C Araújo; Mário L A A Vasconcellos; Claudio G Lima-Júnior; Edilson B Alencar-Filho
Journal:  Mol Divers       Date:  2019-04-06       Impact factor: 2.943

2.  Morita-Baylis-Hillman adducts derived from thymol: synthesis, in silico studies and biological activity against Giardia lamblia.

Authors:  Francisco J S Xavier; Andressa B Lira; Gabriel C Verissimo; Fernanda S de S Saraiva; Abrahão A de Oliveira Filho; Elaine M de Souza-Fagundes; Margareth de F F M Diniz; Maria A Gomes; Aleff C Castro; Fábio P L Silva; Claudio G Lima-Junior; Mário L A A Vasconcellos
Journal:  Mol Divers       Date:  2021-09-05       Impact factor: 3.364

3.  Trypanosoma cruzi cell death induced by the Morita-Baylis-Hillman adduct 3-Hydroxy-2-methylene-3-(4-nitrophenylpropanenitrile).

Authors:  Jana M Sandes; Adriana Fontes; Carlos G Regis-da-Silva; Maria C A Brelaz de Castro; Claudio G Lima-Junior; Fábio P L Silva; Mário L A A Vasconcellos; Regina C B Q Figueiredo
Journal:  PLoS One       Date:  2014-04-08       Impact factor: 3.240

4.  Morita-Baylis-Hillman Adducts Display Anti-Inflammatory Effects by Modulating Inflammatory Mediator Expression in RAW264.7 Cells.

Authors:  Glaucia V Faheina-Martins; Jacqueline Alves Leite; Bruna Braga Dantas; Cláudio G Lima-Júnior; Mário L A A Vasconcellos; Sandra Rodrigues-Mascarenhas; Demetrius A M Araújo
Journal:  Mediators Inflamm       Date:  2017-07-12       Impact factor: 4.711

5.  Synthesis of 16 New Hybrids from Tetrahydropyrans Derivatives and Morita-Baylis-Hillman Adducts: In Vitro Screening against Leishmania donovani.

Authors:  Suervy Canuto de Oliveira Sousa; Juliana da Câmara Rocha; Tatjana de Souza Lima Keesen; Everton da Paz Silva; Priscilla Anne Castro de Assis; João Paulo Gomes de Oliveira; Saulo Luís Capim; Francisco José Seixas Xavier; Bruno Guimarães Marinho; Fábio Pedrosa Lins Silva; Claudio Gabriel Lima-Junior; Mário Luiz Araújo de Almeida Vasconcellos
Journal:  Molecules       Date:  2017-01-30       Impact factor: 4.411

6.  Synthesis and Evaluation of Baylis-Hillman Reaction Derived Imidazole and Triazole Cinnamates as Antifungal Agents.

Authors:  Grady L Nelson; Michael J Williams; Shirisha Jonnalagadda; Mohammad A Alam; Gautam Mereddy; Joseph L Johnson; Sravan K Jonnalagadda
Journal:  Int J Med Chem       Date:  2018-10-16

7.  Dihydroquinolines, Dihydronaphthyridines and Quinolones by Domino Reactions of Morita-Baylis-Hillman Acetates.

Authors:  Joel K Annor-Gyamfi; Ebenezer Ametsetor; Kevin Meraz; Richard A Bunce
Journal:  Molecules       Date:  2021-02-08       Impact factor: 4.411

8.  Determination of the absolute configuration of compounds bearing chiral quaternary carbon centers using the crystalline sponge method.

Authors:  Shiho Sairenji; Takashi Kikuchi; Mohamed Ahmed Abozeid; Shinobu Takizawa; Hiroaki Sasai; Yuichiro Ando; Kohsuke Ohmatsu; Takashi Ooi; Makoto Fujita
Journal:  Chem Sci       Date:  2017-05-16       Impact factor: 9.825

9.  One-Electron Reduction Potentials: Calibration of Theoretical Protocols for Morita⁻Baylis⁻Hillman Nitroaromatic Compounds in Aprotic Media.

Authors:  Amauri Francisco da Silva; Antonio João da Silva Filho; Mário L A A Vasconcellos; Otávio Luís de Santana
Journal:  Molecules       Date:  2018-08-24       Impact factor: 4.411

10.  Naphthalenes and Quinolines by Domino Reactions of Morita-Baylis-Hillman Acetates.

Authors:  Joel K Annor-Gyamfi; Ebenezer Ametsetor; Kevin Meraz; Richard A Bunce
Journal:  Molecules       Date:  2020-11-06       Impact factor: 4.411

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