Structure–Activity Relationship Study of Xanthoxyline and Related Small Methyl Ketone Herbicides

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dc.contributor.authorWarot Chotpatiwetchkul
dc.contributor.authorNawasit Chotsaeng
dc.contributor.authorChamroon Laosinwattana
dc.contributor.authorPatchanee Charoenying
dc.date.accessioned2026-05-08T19:15:43Z
dc.date.issued2022-8-11
dc.description.abstract) were found to be the most active methyl ketones that highly suppressed plant growth at low concentrations. The molecular docking on the 4-hydroxyphenylpyruvate dioxygenase (HPPD) enzyme indicated that carbonyl, aromatic, and azaindole were key interactions of HPPD inhibitors. This finding would be useful for the development of small ketone herbicides.
dc.identifier.doi10.1021/acsomega.2c02704
dc.identifier.urihttps://dspace.kmitl.ac.th/handle/123456789/15181
dc.publisherACS Omega
dc.subjectAllelopathy and phytotoxic interactions
dc.subjectWeed Control and Herbicide Applications
dc.subjectFungal Plant Pathogen Control
dc.titleStructure–Activity Relationship Study of Xanthoxyline and Related Small Methyl Ketone Herbicides
dc.typeArticle

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