Synthesis, anti-oomycete activity, and SAR studies of paeonol derivatives.

Abstract:

:Three series of sulfonate derivatives of paeonol were synthesized and screened in vitro for their anti-oomycete activity against P. capsici, respectively. Among all the compounds, 4m displayed the best promising and pronounced anti-oomycete activity against P. capsici than zoxamide, with the EC50 values of 24.51 and 26.87 mg/L, respectively. The results show that acetyl and 4-OCH3 are two necessary groups. The existence of these two sites is closely related to the anti-oomycete activity. Relatively speaking, hydroxyl group is well tolerated, and the results showed that after modification of hydroxyl group with sulfonyl, the anti-oomycete activity was significantly increased. [Formula: see text].

journal_name

J Asian Nat Prod Res

authors

Tian YE,Sun D,Han XX,Yang JM,Zhang S,Feng NN,Zhu LN,Xu ZY,Che ZP,Liu SM,Lin XM,Jiang J,Chen GQ

doi

10.1080/10286020.2020.1718116

subject

Has Abstract

pub_date

2020-02-03 00:00:00

pages

1-12

eissn

1028-6020

issn

1477-2213

pub_type

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