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Synthesis and bioactivities of novel piperazine-containing 1,5-Diphenyl-2-penten-1-one analogues from natural product lead.
Xu, Gaofei; Yang, Xinling; Jiang, Biaobiao; Lei, Peng; Liu, Xili; Wang, Qingmin; Zhang, Xuebo; Ling, Yun.
Afiliação
  • Xu G; Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.
  • Yang X; Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.
  • Jiang B; Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.
  • Lei P; Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.
  • Liu X; Department of Plant Pathology, College of Agronomy and Biotechnology, China Agricultural University, 100193, China.
  • Wang Q; State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China.
  • Zhang X; Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.
  • Ling Y; Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.
Bioorg Med Chem Lett ; 26(7): 1849-53, 2016 Apr 01.
Article em En | MEDLINE | ID: mdl-26906636
A series of novel 1,5-Diphenyl-2-penten-1-one analogues (7a-h, 8a-h) with piperazine moiety have been designed and synthesized on the basis of natural product 1,5-Diphenyl-2-penten-1-one (I). All the synthesized compounds were evaluated in vitro for anti-plant pathogenic fungi activities and insecticidal activities. The results indicated that most of these analogues exhibited moderate antifungal activities and moderate to good insecticidal activities. Amongst them, the most potent 7c, 7e and 7h keep a mortality of 100% against larva of mosquito at the concentration of 1mg/L. Initial structure-activity relationship (SAR) analysis showed that, a methyl group can influence the biological activities of these compounds significantly, the compounds with N'-unsubstituted piperazine showed much better antifungal activities and larvicidal activity against mosquito than the compounds with N'-methylated piperazine. In addition, the larvicidal activity against mosquito had sharply decline when the substituent on benzene ring was changed from 4-position to 2 or 3-position.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pentanonas / Piperazinas / Inseticidas Limite: Animals / Humans Idioma: En Revista: Bioorg Med Chem Lett Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pentanonas / Piperazinas / Inseticidas Limite: Animals / Humans Idioma: En Revista: Bioorg Med Chem Lett Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China