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182 related items for PubMed ID: 32223563

  • 1. Combined 3D-quantitative structure-activity relationships and topomer technology-based molecular design of human 4-hydroxyphenylpyruvate dioxygenase inhibitors.
    Liu YX, Gao S, Ye T, Li JZ, Ye F, Fu Y.
    Future Med Chem; 2020 May; 12(9):795-811. PubMed ID: 32223563
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  • 3. Pyrazole-Isoindoline-1,3-dione Hybrid: A Promising Scaffold for 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors.
    He B, Dong J, Lin HY, Wang MY, Li XK, Zheng BF, Chen Q, Hao GF, Yang WC, Yang GF.
    J Agric Food Chem; 2019 Oct 02; 67(39):10844-10852. PubMed ID: 31525997
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  • 7. New Research for Quinazoline-2,4-diones as HPPD Inhibitors Based on 2D-MLR and 3D-QSAR Models.
    Fu Y, Sun YN, Cao HF, Yi KH, Zhao LX, Li JZ, Ye F.
    Comb Chem High Throughput Screen; 2017 Oct 02; 20(9):748-759. PubMed ID: 28637410
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  • 9. Hydrophobicity-oriented drug design (HODD) of new human 4-hydroxyphenylpyruvate dioxygenase inhibitors.
    Ndikuryayo F, Kang WM, Wu FX, Yang WC, Yang GF.
    Eur J Med Chem; 2019 Mar 15; 166():22-31. PubMed ID: 30684868
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  • 10. Computer-Aided and AILDE Approaches to Design Novel 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors.
    Shi J, Gao S, Wang JY, Ye T, Yue ML, Fu Y, Ye F.
    Int J Mol Sci; 2022 Jul 15; 23(14):. PubMed ID: 35887168
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  • 13. 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors: From Molecular Design to Synthesis.
    Ma T, Gao S, Zhao LX, Ye F, Fu Y.
    J Agric Food Chem; 2024 Aug 07; 72(31):17125-17137. PubMed ID: 39047218
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  • 14. 3D-QSAR studies on 4-hydroxyphenylpyruvate dioxygenase inhibitors by comparative molecular field analysis (CoMFA).
    Huang M, Yang DY, Shang Z, Zou J, Yu Q.
    Bioorg Med Chem Lett; 2002 Sep 02; 12(17):2271-5. PubMed ID: 12161114
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  • 15. Synthesis and herbicidal activity of novel pyrazole aromatic ketone analogs as HPPD inhibitor.
    Fu Q, Cai PP, Cheng L, Zhong LK, Tan CX, Shen ZH, Han L, Xu TM, Liu XH.
    Pest Manag Sci; 2020 Mar 02; 76(3):868-879. PubMed ID: 31429196
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  • 16. Design, synthesis and herbicidal activity of new iron chelating motifs for HPPD-inhibitors.
    Witschel M.
    Bioorg Med Chem; 2009 Jun 15; 17(12):4221-9. PubMed ID: 19028100
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  • 19. Structural basis for herbicidal inhibitor selectivity revealed by comparison of crystal structures of plant and mammalian 4-hydroxyphenylpyruvate dioxygenases.
    Yang C, Pflugrath JW, Camper DL, Foster ML, Pernich DJ, Walsh TA.
    Biochemistry; 2004 Aug 17; 43(32):10414-23. PubMed ID: 15301540
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  • 20. Discovery of N-Aroyl Diketone/Triketone Derivatives as Novel 4-Hydroxyphenylpyruvate Dioxygenase Inhibiting-Based Herbicides.
    Fu Y, Zhang D, Zhang SQ, Liu YX, Guo YY, Wang MX, Gao S, Zhao LX, Ye F.
    J Agric Food Chem; 2019 Oct 30; 67(43):11839-11847. PubMed ID: 31589436
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