Literature DB >> 30597328

N,N'-diaryl-bishydrazones in a biphenyl platform: Broad spectrum antifungal agents.

Nishad Thamban Chandrika1, Emily K Dennis1, Sanjib K Shrestha1, Huy X Ngo1, Keith D Green1, Stefan Kwiatkowski2, Agripina Gabriela Deaciuc1, Linda P Dwoskin1, David S Watt3, Sylvie Garneau-Tsodikova4.   

Abstract

N,N'-Diaryl-bishydrazones of [1,1'-biphenyl]-3,4'-dicarboxaldehyde, [1,1'-biphenyl]-4,4'-dicarboxaldehyde, and 4,4'-bisacetyl-1,1-biphenyl exhibited excellent antifungal activity against a broad spectrum of filamentous and non-filamentous fungi. These N,N'-diaryl-bishydrazones displayed no antibacterial activity in contrast to previously reported N,N'-diamidino-bishydrazones and N-amidino-N'-aryl-bishydrazones. The leading candidate, 4,4'-bis((E)-1-(2-(4-fluorophenyl)hydrazono)ethyl)-1,1'-biphenyl, displayed less hemolysis of murine red blood cells at concentrations at or below that of a control antifungal agent (voriconazole), was fungistatic in a time-kill study, and possessed no mammalian cytotoxicity and no toxicity with respect to hERG inhibition.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Aspergillus sp.; Candida albicans; Cytotoxicity; Hemolysis; Non-albicans Candida; hERG channel

Mesh:

Substances:

Year:  2018        PMID: 30597328      PMCID: PMC6351225          DOI: 10.1016/j.ejmech.2018.12.042

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  1 in total

1.  Visible Light-Driven, Gold(I)-Catalyzed Preparation of Symmetrical (Hetero)biaryls by Homocoupling of Arylazo Sulfones.

Authors:  Lorenzo Di Terlizzi; Simone Scaringi; Carlotta Raviola; Riccardo Pedrazzani; Marco Bandini; Maurizio Fagnoni; Stefano Protti
Journal:  J Org Chem       Date:  2022-03-22       Impact factor: 4.354

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.