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Synthesis of sulfonate derivatives of carvacrol and thymol as anti-oomycetes agents.
Chen, Gen-Qiang; Sun, Di; Yang, Jin-Ming; Zhang, Song; Tian, Yue-E; Che, Zhi-Ping; Liu, Sheng-Ming; Jiang, Jia; Lin, Xiao-Min.
Afiliação
  • Chen GQ; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
  • Sun D; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
  • Yang JM; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
  • Zhang S; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
  • Tian YE; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
  • Che ZP; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
  • Liu SM; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
  • Jiang J; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
  • Lin XM; Laboratory of Pesticidal Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471023, China.
J Asian Nat Prod Res ; 23(7): 692-702, 2021 Jul.
Article em En | MEDLINE | ID: mdl-32406756
ABSTRACT
Two series of sulfonate derivatives of carvacrol and thymol were synthesized and screened in vitro for their anti-oomycete activity against Phytophthora capsici, respectively. Among all of 32 derivatives, five compounds 3a, 4a, 4k, 3n, and 4n exhibited more potent anti-oomycete activity against P. capsici with EC50 values of 66.66, 62.94, 68.65, 61.24, and 52.91 mg/L, respectively. This suggested that introduction of different substitutions at the hydroxyl position of 1/2 could have remarkable effect on anti-oomycete activity. Overall, when R1 = isopropyl and R2 = methyl, the anti-oomycete activities of the compounds were higher than that of the corresponding compounds of R1 = methyl and R2 = isopropyl.[Formula see text].
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Timol / Monoterpenos Idioma: En Revista: J Asian Nat Prod Res Assunto da revista: BOTANICA / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Timol / Monoterpenos Idioma: En Revista: J Asian Nat Prod Res Assunto da revista: BOTANICA / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China