In a global context, weed management has emerged as a significant challenge in agricultural production, causing substantial economic losses annually. Consequently, the development of innovative and efficient herbicides is crucial. Natural products serve as important sources for discovering novel herbicides. Through chemical synthesis and structural modification of natural compounds, novel herbicides can be developed. Protoporphyrinogen oxidase (PPO, EC 1.3.3.4) catalyzes the oxidation of protoporphyrinogen IX to protoporphyrin IX, a critical step in the biosynthesis of porphyrins. PPO inhibitors target protoporphyrinogen oxidase, inhibiting its activity and thereby blocking porphyrin biosynthesis, ultimately leading to plant death. In this research, protoporphyrinogen oxidase was targeted, and monomeric compounds were extracted from natural rice husks, followed by selective manipulation to design and synthesize 33 new compounds. Weed control assays (37.5-300 g ai/ha) showed that most of the new compounds exhibited significant herbicidal activity against dicot weeds, but less effectiveness against monocot weeds. In particular, compound I-c4 demonstrated excellent post-emergence herbicidal activity on six weed species, comparable to the commercial herbicide oxyfluorfen. Activity experiments showed that compound I-c4 significantly reduced PPO levels in weeds. Molecular docking results indicated that compound I-c4 effectively occupies the substrate pocket of PPO enzymes, demonstrating strong inhibitory effects on receptor protein activity. Thus, compound I-c4 shows promise as a novel PPO herbicide for effective weed control.
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http://dx.doi.org/10.1016/j.pestbp.2025.106312 | DOI Listing |
Pestic Biochem Physiol
March 2025
Department of Chemistry, College of Arts and Sciences, Northeast Agricultural University, Harbin 150030, China; Key Laboratory of Agricultural Functional Molecule Design and Utilization of Heilongjiang Province, Northeast Agricultural University, Harbin 150030, China. Electronic address:
In a global context, weed management has emerged as a significant challenge in agricultural production, causing substantial economic losses annually. Consequently, the development of innovative and efficient herbicides is crucial. Natural products serve as important sources for discovering novel herbicides.
View Article and Find Full Text PDFJ Med Chem
August 2024
State Key Laboratory of Esophageal Cancer Prevention and Treatment; Key Laboratory of Advanced Pharmaceutical Technology, Ministry of Education of China; School of Pharmaceutical Science and Institute of Pharmaceutical Science, Zhengzhou University, Zhengzhou 450001, China.
Cardiotoxicity associated with chemotherapy has gradually become the major cause of death in cancer patients. The development of bifunctional drugs with both cardioprotective and antitumor effects has become the future direction. HDAC6 plays important roles in the progression, treatment, and prognosis of cancer and cardiovascular diseases, but bifunctional inhibitors have not been reported.
View Article and Find Full Text PDFJ Phys Chem A
September 2018
College of Chemistry and Molecular Sciences , Wuhan University, Wuhan , 430072 , People's Republic of China.
Heptafluoroisobutyronitrile (C4) has been utilized as a dielectric compound to replace sulfur hexafluoride for the sake of environmental concern. Energetic profiles of the potential energy surface for the unimolecular reaction of C4 were calculated using density functional theory (M06-2X), quadratic complete basis set (CBS-QB3), Gaussian-4, multireference Rayleigh-Schrodinger perturbation theory (RS2, RS2C), and state-averaged multiconfiguration self-consistent-field (SA-MCSCF) ab initio methods. Among 38 production channels, the most energetically accessible reaction path is the three-centered rearrangement of cyanide to isocyanide.
View Article and Find Full Text PDFCancer Res
May 1994
Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan.
7-N-((2-([2-(gamma-L-Glutamylamino)ethyl]dithio)ethyl))mitomycin C (KW-2149) is an analogue of mitomycin C (MMC) and has prominent activities against various tumors. We studied the antitumor effects of KW-2149 in MMC-resistant variants of human colon carcinoma HT-29 (HT-29/MMC) and mouse hepatoma Hepa-I (C4, B13NBii1) cells, which are deficient in DT-diaphorase and cytochrome P450 reductase, respectively. These enzymes mediate the reductive activation of MMC in the cells.
View Article and Find Full Text PDFMutagenesis
March 1994
Institute of Medicine, Chung Shan Medical and Dental College, Taichung, Taiwan, ROC.
The antimutagenicity of 19 naturally occurring flavonoids and their derivatives including flavones, flavonols, flavanones, isoflavones and flavanols were determined using Salmonella typhimurium TA98 against 2-amino-3-methylimidazo[4,5-f] quinoline (IQ) in the presence of Aroclor 1254-induced rat hepatic S9. In general, a relationship between the chemical structure of flavonoids and their antimutagenicity was found for compounds containing one or more of the following features: (i) C4 keto group, (ii) aglycone, (iii) double bond at positions C2 and C3, (iv) phenyl group at position C2, and (v) three hydroxy substituents at positions C4', C5 and C7. The inhibitory effects of flavonoids on activities of 7-ethoxycoumarin deethylase (ECD) and 7-ethoxyresorufin deethylase (ESD) of Aroclor 1254-induced hepatic microsomes were also examined.
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