Synthesis and Biological Activity of N-Acyl O-Indolylalkyl Ethanolamines

• JIANG Shaoliang

  College of Pharmaceutical Science, Zhejiang University of Technology

• GAO Jianrong

  State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, Zhejiang University of Technology

• HAN Liang

  State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, Zhejiang University of Technology

Bibliographic Information

Other Title

• Synthesis and Biological Activity of<i>N</i>-Acyl<i>O</i>-Indolylalkyl Ethanolamines

Abstract

The plant-growth regulators, indole-3-carboxylic acids, were introduced into N-acyl ethanolamines, and a series of N-acyl O-indolylalkyl ethanolamines were prepared. Their biological activities to regulate rape hypocotyl elongation, cucumber cotyledon expansion and common wheat coleoptile growth were tested. The results indicate that the title compounds inhibited rape hypocotyl elongation, especially the indole-3-propionic acid derivatives, whose bioactivity was better than that of indole-3-acetic acid.

Journal

• Bioscience, Biotechnology, and Biochemistry

  Bioscience, Biotechnology, and Biochemistry 75 (4), 768-770, 2011

  Japan Society for Bioscience, Biotechnology, and Agrochemistry

Keywords

• indole carboxylic acid
• <I>N</I>-acylethanolamine
• <I>N</I>-acyl <I>O</I>-indolylalkyl ethanolamine
• synthesis
• plant growth bioactivity

Details

• CRID: 1390282681454358912
• NII Article ID: 10028271886
• NII Book ID: AA10824164
• DOI: 10.1271/bbb.100804
• ISSN: 13476947
• ISSN: 09168451
• NDL BIB ID: 11071123
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I11071123
• Web Site: http://www.tandfonline.com/doi/pdf/10.1271/bbb.100804
• Text Lang: en
• Data Source:
  • JaLC
  • NDL
  • Crossref
  • CiNii Articles
• Abstract License Flag: Disallowed