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Total synthesis and herbicidal activity of natural rubrolides C, E and F.
Gong, Mengqiang; Cai, Jinlong; Lu, Xingliang; Zhou, Xudong; Li, Junkai; Wu, Qinglai; Wu, Jianfeng.
Affiliation
  • Gong M; School of Agriculture, Yangtze University, Jingzhou, PRChina.
  • Cai J; Department of Environment and Life Science, Beijing University of Technology, Beijing, PRChina.
  • Lu X; School of Chemical and Biological Engineering, Lanzhou Jiaotong University, Lanzhou, PRChina.
  • Zhou X; TCM and Ethnomedicine Innovation and Development Laboratory, School of Pharmacy, Hunan University of Chinese Medicine, Changsha, PRChina.
  • Li J; School of Agriculture, Yangtze University, Jingzhou, PRChina.
  • Wu Q; School of Agriculture, Yangtze University, Jingzhou, PRChina.
  • Wu J; State Key Laboratory of Toxicology and Medical Countermeasures and Laboratory of Toxicant Analysis, Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing, PRChina.
Nat Prod Res ; : 1-10, 2024 May 02.
Article in En | MEDLINE | ID: mdl-38695089
ABSTRACT
Rubrolides are natural butyrolactones isolated from the tunicate Ritterella rubra, shows antibacterial, antiviral and plant photosynthesis inhibitory activities. In this study, a facile total synthetic method for preparing the rubrolides from benzaldehyde by a Darzens reaction, aldol reaction and vinylogous aldol condensation in five steps is presented. Three natural rubrolides (E, C and F) were synthesised in the total yields of 25-40%. The bioassay results indicate that rubrolides E, C and F exhibit some herbicidal inhibitory effect against rapeseed, in particular, rubrolide F shows the best herbicidal activities against rapeseed root with the growth inhibitory rate of 72.8%. At greenhouse treatment concentrations of 100 and 500 mg/L, rubrolide F show a positive dose-toxicity correlation towards abutilon plants. Collectively, facile total Synthesis strategy provided the base for further bioactivities study of rubrolides family. Rubrolide F may be act as inhibitor of photosynthesis, and this could be lead structure of new herbicide.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nat Prod Res / Nat. prod. res. (Online) / Natural product research (Online) Year: 2024 Document type: Article Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nat Prod Res / Nat. prod. res. (Online) / Natural product research (Online) Year: 2024 Document type: Article Country of publication: Reino Unido