Literature DB >> 21756287

Synthesis of aryl aldimines and their activity against fungi of clinical interest.

Cleiton M da Silva1, Danielle L da Silva, Cleide V B Martins, Maria A de Resende, Esther S Dias, Thais F F Magalhães, Letícia P Rodrigues, Adão A Sabino, Rosemeire B Alves, Ângelo de Fátima.   

Abstract

Aldimines are aldehyde-derived compounds that contain a C=N group. Besides its broad industrial applications, this class of non-naturally occurring compounds are found to possess antibacterial, antifungal, antimalarial, antiproliferative, anti-inflammatory, antiviral, and antipyretic properties. Based on this, six aryl aldimines were synthesized from the condensation of aromatic amines with benzaldehydes. The antifungal activities of synthesized compounds were evaluated against nineteen fungal strains that included Candida and Aspergillus species, Cryptococcus neoformans. The aryl aldimines 2-(benzylideneamino)phenol (3) and 4-(benzylideneamino)phenol (8) were the most active compounds against the fungi studied. Compounds 3 and 8 efficiently inhibited the metabolism of C. neoformans mature biofilm.
© 2011 John Wiley & Sons A/S.

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Year:  2011        PMID: 21756287     DOI: 10.1111/j.1747-0285.2011.01185.x

Source DB:  PubMed          Journal:  Chem Biol Drug Des        ISSN: 1747-0277            Impact factor:   2.817


  8 in total

1.  2-(benzylideneamino)phenol: a promising hydroxyaldimine with potent activity against dermatophytoses.

Authors:  Alan Kiill Gasparto; Ludmila Matos Baltazar; Ludmila Ferreira Gouveia; Cleiton Moreira da Silva; Ricardo Martins Duarte Byrro; Milene Alvarenga Rachid; Armando da Silva Cunha Júnior; Maria Aparecida de Resende-Stoianoff; Angelo de Fátima; Daniel Assis Santos
Journal:  Mycopathologia       Date:  2014-12-17       Impact factor: 2.574

2.  Synthesis, spectral studies, antioxidant and antibacterial evaluation of aromatic nitro and halogenated tetradentate Schiff bases.

Authors:  Bhagwat Vhanale; Digambar Kadam; Avinash Shinde
Journal:  Heliyon       Date:  2022-06-05

3.  Virulence Factors and Antifungal Susceptibility in Candida Species Isolated from Dermatomycosis Patients.

Authors:  Victor Galvão Mello; Heloisa Escudeiro; Ana Carolina Villas Bôas Weckwerth; Maria Izilda Andrade; Ana Elisa Fusaro; Eloise Brasil de Moraes; Luciana da Silva Ruiz; Ida Maria Foschiani Dias Baptista
Journal:  Mycopathologia       Date:  2020-11-20       Impact factor: 2.574

4.  4-[(E)-(4-Eth-oxy-benzyl-idene)amino]-phenol.

Authors:  Narissara Kaewmanee; Suchada Chantrapromma; Nawong Boonnak; Hoong-Kun Fun
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-05-18

5.  Crystal structure of (E)-2-hy-droxy-4'-meth-oxy-aza-stilbene.

Authors:  Suchada Chantrapromma; Narissara Kaewmanee; Nawong Boonnak; Kan Chantrapromma; Hazem A Ghabbour; Hoong-Kun Fun
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-05-07

6.  Photophysical, photostability, and ROS generation properties of new trifluoromethylated quinoline-phenol Schiff bases.

Authors:  Inaiá O Rocha; Yuri G Kappenberg; Wilian C Rosa; Clarissa P Frizzo; Nilo Zanatta; Marcos A P Martins; Isadora Tisoco; Bernardo A Iglesias; Helio G Bonacorso
Journal:  Beilstein J Org Chem       Date:  2021-12-01       Impact factor: 2.883

7.  (E)-2-[(2,4,6-Tri-meth-oxy-benzyl-idene)amino]-phenol.

Authors:  Narissara Kaewmanee; Suchada Chantrapromma; Nawong Boonnak; Ching Kheng Quah; Hoong-Kun Fun
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-12-14

8.  Butenafine and analogues: An expeditious synthesis and cytotoxicity and antifungal activities.

Authors:  Ana María Garzón Porras; Bruna Silva Terra; Taniris Cafiero Braga; Thais Furtado Ferreira Magalhães; Cleide Viviane Buzanello Martins; Danielle Letícia da Silva; Ludmila Matos Baltazar; Ludmila Ferreira Gouveia; Gustavo José Cota de Freitas; Daniel Assis Santos; Maria Aparecida Resende-Stoianoff; Beth Burgwyn Fuchs; Eleftherios Mylonakis; Rossimiriam Pereira de Freitas; Ângelo de Fátima
Journal:  J Adv Res       Date:  2018-06-21       Impact factor: 10.479

  8 in total

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