<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao LX</submitter><funding>the &amp;amp;quot;Academic Backbone&amp;amp;quot; Project of Northeast Agricultural University</funding><funding>the Research Science Foundation in Technology Innovation of Harbin</funding><funding>Natural Science Foundation of Heilongjiang Province of China</funding><funding>National Natural Science Foundation of China</funding><pagination>E514</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6843476</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(10)</volume><pubmed_abstract>The herbicide fomesafen has the advantages of low toxicity and high selectivity, and the target of this compound is protoporphyrinogen IX oxidase (PPO, EC 1.3.3.4). However, this herbicide has a long residual period and can have phytotoxic effects on succeeding crops. To protect maize from fomesafen, a series of thiazole phenoxypyridines were designed based on structure-activity relationships, active substructure combinations, and bioisosterism. Bioassays showed that thiazole phenoxypyridines could improve maize tolerance under fomesafen toxicity stress to varying degrees at a dose of 10 mg·kg&lt;sup>-1&lt;/sup>. Compound &lt;b>4i&lt;/b> exhibited the best effects. After being treated by compound &lt;b>4i&lt;/b>, average recovery rates of growth index exceeded 72%, glutathione content markedly increased by </pubmed_abstract><journal>Biomolecules</journal><pubmed_title>Novel Thiazole Phenoxypyridine Derivatives Protect Maize from Residual Pesticide Injury Caused by PPO-Inhibitor Fomesafen.</pubmed_title><pmcid>PMC6843476</pmcid><funding_grant_id>31572042</funding_grant_id><funding_grant_id>2017RAQXJ017</funding_grant_id><funding_grant_id>16XG24</funding_grant_id><funding_grant_id>ZD2017002</funding_grant_id><pubmed_authors>Zhao LX</pubmed_authors><pubmed_authors>Zou YL</pubmed_authors><pubmed_authors>Yin ML</pubmed_authors><pubmed_authors>Fu Y</pubmed_authors><pubmed_authors>Ye F</pubmed_authors><pubmed_authors>Ren T</pubmed_authors><pubmed_authors>Gao S</pubmed_authors><pubmed_authors>Wang QR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Novel Thiazole Phenoxypyridine Derivatives Protect Maize from Residual Pesticide Injury Caused by PPO-Inhibitor Fomesafen.</name><description>The herbicide fomesafen has the advantages of low toxicity and high selectivity, and the target of this compound is protoporphyrinogen IX oxidase (PPO, EC 1.3.3.4). However, this herbicide has a long residual period and can have phytotoxic effects on succeeding crops. To protect maize from fomesafen, a series of thiazole phenoxypyridines were designed based on structure-activity relationships, active substructure combinations, and bioisosterism. Bioassays showed that thiazole phenoxypyridines could improve maize tolerance under fomesafen toxicity stress to varying degrees at a dose of 10 mg·kg&lt;sup>-1&lt;/sup>. Compound &lt;b>4i&lt;/b> exhibited the best effects. After being treated by compound &lt;b>4i&lt;/b>, average recovery rates of growth index exceeded 72%, glutathione content markedly increased by </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Sep</publication><modification>2026-04-08T00:27:59.206Z</modification><creation>2020-05-21T20:01:35Z</creation></dates><accession>S-EPMC6843476</accession><cross_references><pubmed>31547161</pubmed><doi>10.3390/biom9100514</doi></cross_references></HashMap>