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Synthesis and biological evaluation of N, N-dialkylcarboxy coumarin-NO donor conjugates as potential anticancer agents.
Nelson, Grady L; Ronayne, Conor T; Solano, Lucas N; Jonnalagadda, Sravan K; Jonnalagadda, Shirisha; Schumacher, Tanner J; Gardner, Zachary S; Palle, Hithardha; Mani, Chinnadurai; Rumbley, Jon; Mereddy, Venkatram R.
Afiliación
  • Nelson GL; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA.
  • Ronayne CT; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA.
  • Solano LN; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA.
  • Jonnalagadda SK; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA.
  • Jonnalagadda S; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA.
  • Schumacher TJ; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA.
  • Gardner ZS; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA.
  • Palle H; Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
  • Mani C; Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
  • Rumbley J; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA; Department of Pharmacy Practice & Pharmaceutical Sciences, University of Minnesota, Duluth, MN 55812, USA.
  • Mereddy VR; Integrated Biosciences Graduate Program, University of Minnesota, Duluth, MN 55812, USA; Department of Pharmacy Practice & Pharmaceutical Sciences, University of Minnesota, Duluth, MN 55812, USA; Department of Chemistry and Biochemistry, University of Minnesota Duluth, Duluth, MN 55812, USA. Ele
Bioorg Med Chem Lett ; 52: 128411, 2021 11 15.
Article en En | MEDLINE | ID: mdl-34626786
ABSTRACT
A series of nitric oxide (NO) donor furoxan conjugates of N, N-dialkylcarboxy coumarins have been synthesized as potential anticancer agents. The synthesized compounds have been tested for their in vitro antiproliferative activities on various cancer and noncancerous cell lines. The candidate derivatives exhibit selectivity towards cancer cells with excellent activities in low nM to µM concentrations. In vitro mechanistic studies indicate that the candidate compounds generate substantial NO, inhibit colony formation, and cause apoptosis in cancer cells. A preliminary in vivo tolerance study of the lead candidate 10 in mice indicates that it is well-tolerated, evidenced by zero mortality and normal body weight gains in treated mice. Further translation of the lead derivative 10 using MDA-MB-231 based tumor xenograft model shows good tumor growth reduction.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cumarinas / Antineoplásicos / Óxido Nítrico Límite: Animals / Female / Humans Idioma: En Revista: Bioorg Med Chem Lett Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cumarinas / Antineoplásicos / Óxido Nítrico Límite: Animals / Female / Humans Idioma: En Revista: Bioorg Med Chem Lett Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos