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Three new 16-membered macrolide compounds from a genetically engineered strain S. avermitilis MHJ1011.
Pan, Jun-Jie; Wan, Xu; Zhang, Shao-Yong; Huang, Jun; Zhang, Hui; Chen, An-Liang; Wang, Ji-Dong.
Afiliação
  • Pan JJ; Provincial Joint Engineering Laboratory of Biopesticide Preparation, School of Forestry & Biotechnology, Zhejiang Agricultural and Forestry University, Lin'An 311300, PR China.
  • Wan X; Provincial Joint Engineering Laboratory of Biopesticide Preparation, School of Forestry & Biotechnology, Zhejiang Agricultural and Forestry University, Lin'An 311300, PR China.
  • Zhang SY; Provincial Joint Engineering Laboratory of Biopesticide Preparation, School of Forestry & Biotechnology, Zhejiang Agricultural and Forestry University, Lin'An 311300, PR China.
  • Huang J; Department of New Drug Screening, Zhejiang Hisun Pharmaceutical Co., Ltd, Taizhou 318000, PR China.
  • Zhang H; Department of New Drug Screening, Zhejiang Hisun Pharmaceutical Co., Ltd, Taizhou 318000, PR China.
  • Chen AL; Provincial Joint Engineering Laboratory of Biopesticide Preparation, School of Forestry & Biotechnology, Zhejiang Agricultural and Forestry University, Lin'An 311300, PR China. Electronic address: anlchen@126.com.
  • Wang JD; Provincial Joint Engineering Laboratory of Biopesticide Preparation, School of Forestry & Biotechnology, Zhejiang Agricultural and Forestry University, Lin'An 311300, PR China; Department of New Drug Screening, Zhejiang Hisun Pharmaceutical Co., Ltd, Taizhou 318000, PR China. Electronic address:
Bioorg Med Chem Lett ; 26(14): 3376-3379, 2016 07 15.
Article em En | MEDLINE | ID: mdl-27246617
ABSTRACT
Three new 16-membered macrolide compounds, 13α-O-α-l-oleandrosyl milbemycin ß3 (1), 13α-O-α-l-oleandrosyl-25-ethyl milbemycin ß3 (2), 13α-O-α-l-oleandrosyl-25-isopropyl milbemycin ß3 (3), were isolated from the genetically engineered strains Streptomyces avermitilis MHJ1011. Their structures were determined on the basis of spectroscopic analysis, including 1D and 2D NMR techniques as well as ESI-MS and comparison with data from the literature. Both compounds 1-3 displayed impressive acaricidal activity against larval mites with the IC50 values of 0.0327, 0.0276 and 0.0235mg/L, respectively, which are higher than those of 13α-hydroxy milbemycin ß3 and 13α-hydroxy-25-ethyl milbemycin ß3.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Streptomyces / Engenharia Genética / Macrolídeos / Ácaros Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Streptomyces / Engenharia Genética / Macrolídeos / Ácaros Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article