Literature DB >> 31356740

Design, Herbicidal Activity, and QSAR Analysis of Cycloalka[d]quinazoline-2,4-dione-Benzoxazinones as Protoporphyrinogen IX Oxidase Inhibitors.

Da-Wei Wang1, Rui-Bo Zhang1, Ismail Ismail1, Zhi-Yuan Xue1, Lu Liang1, Shu-Yi Yu1, Xin Wen1, Zhen Xi1.   

Abstract

In continuation of our search for potent protoporphyrinogen IX oxidase (PPO, EC 1.3.3.4) inhibitors, we designed and synthesized a series of novel herbicidal cycloalka[d]quinazoline-2,4-dione-benzoxazinones. The bioassay results of these synthesized compounds indicated that most of the compounds exhibited very strong Nicotiana tabacum PPO (NtPPO) inhibition activity. More than half of the 37 synthesized compounds displayed over 80% control of all three tested broadleaf weeds at 37.5-150 g ai/ha by postemergent application, and a majority of them showed no phytotoxicity toward at least one kind of crop at 150 g ai/ha. Promisingly, 17i (Ki = 6.7 nM) was 6 and 4 times more potent than flumioxazin (Ki = 46 nM) and trifludimoxazin (Ki = 31 nM), respectively. Moreover, 17i displayed excellent, broad-spectrum herbicidal activity, even at levels as low as 37.5 g ai/ha, and it was determined to be safe for wheat at 150 g ai/ha in postemergent application, indicating the great potential for 17i development as a herbicide for weed control in wheat fields.

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Keywords:  benzoxazinone; cycloalka[]quinazoline-2,4-dione; herbicide; protoporphyrinogen IX oxidase; weed control

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Year:  2019        PMID: 31356740     DOI: 10.1021/acs.jafc.9b02996

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  2 in total

1.  In Silico Structure-Guided Optimization and Molecular Simulation Studies of 3-Phenoxy-4-(3-trifluoromethylphenyl)pyridazines as Potent Phytoene Desaturase Inhibitors.

Authors:  Lijun Yang; Dawei Wang; Dejun Ma; Di Zhang; Nuo Zhou; Jing Wang; Han Xu; Zhen Xi
Journal:  Molecules       Date:  2021-11-19       Impact factor: 4.411

2.  Para-Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes.

Authors:  Michael Berger; Marola S Lenhard; Siegfried R Waldvogel
Journal:  Chemistry       Date:  2022-06-07       Impact factor: 5.020

  2 in total

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