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Novel hybrid DHPM-fatty acids: synthesis and activity against glioma cell growth in vitro.
Treptow, Tamara G M; Figueiró, Fabrício; Jandrey, Elisa H F; Battastini, Ana M O; Salbego, Christianne G; Hoppe, Juliana B; Taborda, Priscila S; Rosa, Sabrina B; Piovesan, Luciana A; Montes D'Oca, Caroline Da R; Russowsky, Dennis; Montes D'Oca, Marcelo G.
Affiliation
  • Treptow TG; Laboratório Kolbe de Síntese Orgânica, Universidade Federal do Rio Grande, FURG, Rio Grande, RS, Brazil.
  • Figueiró F; Departamento de Bioquímica, ICBS, Universidade Federal do Rio Grande do Sul, UFRGS, Porto Alegre, RS, Brazil.
  • Jandrey EH; Departamento de Bioquímica, ICBS, Universidade Federal do Rio Grande do Sul, UFRGS, Porto Alegre, RS, Brazil.
  • Battastini AM; Departamento de Bioquímica, ICBS, Universidade Federal do Rio Grande do Sul, UFRGS, Porto Alegre, RS, Brazil.
  • Salbego CG; Departamento de Bioquímica, ICBS, Universidade Federal do Rio Grande do Sul, UFRGS, Porto Alegre, RS, Brazil.
  • Hoppe JB; Departamento de Bioquímica, ICBS, Universidade Federal do Rio Grande do Sul, UFRGS, Porto Alegre, RS, Brazil.
  • Taborda PS; Laboratório Kolbe de Síntese Orgânica, Universidade Federal do Rio Grande, FURG, Rio Grande, RS, Brazil.
  • Rosa SB; Laboratório Kolbe de Síntese Orgânica, Universidade Federal do Rio Grande, FURG, Rio Grande, RS, Brazil.
  • Piovesan LA; Laboratório Kolbe de Síntese Orgânica, Universidade Federal do Rio Grande, FURG, Rio Grande, RS, Brazil.
  • Montes D'Oca Cda R; Laboratório de Síntese Orgânica, Universidade Federal do Rio Grande do Sul, UFRGS, Porto Alegre, RS, Brazil.
  • Russowsky D; Laboratório de Síntese Orgânica, Universidade Federal do Rio Grande do Sul, UFRGS, Porto Alegre, RS, Brazil.
  • Montes D'Oca MG; Laboratório Kolbe de Síntese Orgânica, Universidade Federal do Rio Grande, FURG, Rio Grande, RS, Brazil. Electronic address: dqmdoca@furg.br.
Eur J Med Chem ; 95: 552-62, 2015 May 05.
Article in En | MEDLINE | ID: mdl-25863023
We described the first synthesis of fatty acid 3,4-dihydropyrimidinones (DHPM-fatty acids) using the Biginelli multicomponent reaction. Antiproliferative activity on two glioma cell lines (C6 rat and U-138-MG human) was also reported. The novel DHPM-fatty acids reduced glioma cell viability relative to temozolomide. Hybrid oxo-monastrol-palmitic acid was the most potent, reducing U-138-MG human cell viability by ca. 50% at 10 µM. In addition, the DHPM-fatty acids showed a large safety range to neural cells, represented by the organotypic hippocampal culture. These results suggest that the increased lipophilicity of DHPM-fatty acids offer a promising approach to overcoming resistance to chemotherapy and may play an important role in the development of new antitumor drugs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Uridine / Fatty Acids / Glioma / Antineoplastic Agents Limits: Animals / Humans / Male Language: En Journal: Eur J Med Chem Year: 2015 Document type: Article Affiliation country: Brazil Country of publication: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Uridine / Fatty Acids / Glioma / Antineoplastic Agents Limits: Animals / Humans / Male Language: En Journal: Eur J Med Chem Year: 2015 Document type: Article Affiliation country: Brazil Country of publication: France