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Pyrazolyl Thioureas and Carbothioamides with an NNSN Motif against MSSA and MRSA.
Delpe-Acharige, Anjana; Zhang, Man; Eschliman, Kayla; Dalecki, Alex; Covarrubias-Zambrano, Obdulia; Minjarez-Almeida, Azriel; Shrestha, Tejaswi; Lewis, Tanji; Al-Ibrahim, Fatimah; Leonard, Sophia; Roberts, Riana; Tebeje, Anteneh; Malalasekera, Aruni P; Wang, Hongwang; Kalubowilage, Madumali; Wolschendorf, Frank; Kutsch, Olaf; Bossmann, Stefan H.
Afiliação
  • Delpe-Acharige A; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Zhang M; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Eschliman K; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Dalecki A; Department of Medicine, University of Alabama at Birmingham, 845 19th Street S, Birmingham, Alabama 35294, United States.
  • Covarrubias-Zambrano O; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Minjarez-Almeida A; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Shrestha T; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Lewis T; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Al-Ibrahim F; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Leonard S; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Roberts R; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Tebeje A; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Malalasekera AP; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Wang H; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Kalubowilage M; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
  • Wolschendorf F; Department of Medicine, University of Alabama at Birmingham, 845 19th Street S, Birmingham, Alabama 35294, United States.
  • Kutsch O; Department of Medicine, University of Alabama at Birmingham, 845 19th Street S, Birmingham, Alabama 35294, United States.
  • Bossmann SH; Department of Chemistry, Kansas State University, Manhattan, Kansas 66506, United States.
ACS Omega ; 6(9): 6088-6099, 2021 Mar 09.
Article em En | MEDLINE | ID: mdl-33718700
ABSTRACT
A novel series of copper-activatable drugs intended for use against methicillin-sensitive Staphylococcus aureus (MSSA) and methicillin-resistant S. aureus (MRSA) were synthesized, characterized, and tested against the MSSA strain Newman and the MRSA Lac strain (a USA300 strain), respectively. These drugs feature an NNSN structural motif, which enables the binding of copper. In the absence of copper, no activity against MSSA and MRSA at realistic drug concentrations was observed. Although none of the novel drug candidates exhibits a stereocenter, sub-micromolar activities against SA Newman and micromolar activities against SA Lac were observed in the presence, but not in the absence, of bioavailable copper. Copper influx is a component of cellular response to bacterial infections, which is often described as nutritional immunity.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article