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Safety of m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact 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 or concate me.

An article Synthesis, anti-oomycete activity, and SAR studies of paeonol derivatives WOS:000512395000001 published article about PHYTOPHTHORA-CAPSICI; BOTRYTIS-CINEREA; TREE PEONY; ANALOGS; RESISTANCE; SEED in [Tian, Yue-E; Sun, Di; Han, Xiao-Xiao; Yang, Jin-Ming; Zhang, Song; Feng, Nan-Nan; Zhu, Li-Na; Xu, Zhong-Yuan; Che, Zhi-Ping; Liu, Sheng-Ming; Lin, Xiao-Min; Jiang, Jia; Chen, Gen-Qiang] Henan Univ Sci & Technol, Coll Forestry, Dept Plant Protect, Lab Pharmaceut Design & Synth, Luoyang 471023, Peoples R China in 2021.0, Cited 25.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6. Safety of m-Methoxyphenol

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. [GRAPHICS] .

Safety of m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact 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 or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles