Antiviral activity evaluation and action mechanism of chalcone derivatives containing phenoxypyridine
Tóm tắt
Từ khóa
Tài liệu tham khảo
Wylie S (2023) Tobamoviruses: special issue editorial. Viruses 15:2174. https://doi.org/10.3390/v15112174
Verhage L (2021) How tobacco mosaic virus goes the distance. Plant J 106:894–895. https://doi.org/10.1111/tpj.15268
Su B, Cai CL, Deng M, Wang QM (2016) Spatial configuration and three-dimensional conformation directed design, synthesis, antiviral activity, and structure–activity relationships of phenanthroindolizidine analogues. J Agric Food Chem 64:2039–2045. https://doi.org/10.1021/acs.jafc.5b06112
Qian XH, Lee PW, Cao S (2010) China: forward to the green pesticides via a basic research program. J Agric Food Chem 58:2613–2623. https://doi.org/10.1021/jf904098w
Seiber JN (2011) Sustainability and agricultural and food chemistry. J Agric Food Chem 59:1–21. https://doi.org/10.1021/jf1046078
Wu ZJ, Ouyang MA, Wang CZ, Zhang ZK, Shen JG (2007) Anti-tobacco mosaic virus (TMV) triterpenoid saponins from the leaves of Ilex oblonga. J Agric Food Chem 55:1712–1717. https://doi.org/10.1021/jf062421r
Elkanzi NAA, Hrichi H, Alolayan RA, Derafa W, Zahou FM, Bakr RB (2022) Synthesis of chalcones derivatives and their biological activities: a review. ACS Omega 7:27769–27786. https://doi.org/10.1021/acsomega.2c01779
Guo T, Xia RJ, Liu TT, Peng F, Tang XM, Zhou Q, Luo H, Xue W (2020) Synthesis, biological activity and action mechanism study of novel chalcone derivatives containing malonate. Chem Biodivers 17:e2000025. https://doi.org/10.1002/cbdv.202000025
Liu YT, Sun XM, Yin DW, Yuan F (2013) Syntheses and biological activity of chalcones-imidazole derivatives. Res Chem Intermed 39:1037–1048. https://doi.org/10.1007/s11164-012-0665-z
Sayed M, El-Dean AMK, Ahmed M, Hassanien R (2018) Synthesis, characterization, and screening for anti-inflammatory and antimicrobial activity of novel indolyl chalcone derivatives synthesis, characterization, and screening for anti-inflammatory and antimicrobial activity of novel indolyl chalcone derivatives. J Heterocyclic Chem 55:1166. https://doi.org/10.1002/jhet.3149
Fu Y, Liu D, Zeng HN, Ren XL, Song BA, Hu DY, Gan XH (2020) New chalcone derivatives: synthesis, antiviral activity and mechanism of action. RSC Adv 10:24483–24490. https://doi.org/10.1039/d0ra03684f
Wang YJ, Zhou DG, He FC, Chen JX, Chen YZ, Gan XH, Hu DY, Song BA (2018) Synthesis and antiviral bioactivity of novel chalcone derivatives containing purine moiety. Chin Chem Lett 29:127–130. https://doi.org/10.1016/j.cclet.2017.07.006
Bale AT, Salar U, Khan KM, Chigurupati S, Fasina T, Ali F, Ali M, Nanda SS, Taha M, Perveen S (2021) Chalcones and bis-chalcones analogs as DPPH and ABTS radical scavengers. Lett Drug Des Discov 18:249–257. https://doi.org/10.2174/1570180817999201001155032
Ouyang Y, Li JJ, Chen XY, Fu XY, Sun S, Wu Q (2021) Chalcone derivatives: role in anticancer therapy. Biomolecules 11:894. https://doi.org/10.3390/biom11060894
Guan YF, Liu XJ, Yuan XY, Liu WB, Li YR, Yu GX, Tian XY, Zhang YB, Song J, Li W, Zhang SY (2021) Design, synthesis, and anticancer activity studies of novel quinoline-chalcone derivatives. Molecules 26:4899. https://doi.org/10.3390/molecules26164899
Stantliff TM, Hill A, Kuo ME, Neal HE, Harrod TC, Goens K, Mashuta M, Christianson AMAM, Krzysiak AJ (2023) Flexibility in the bridge of chalcone derivatives is important for the inhibition of cellular growth. Bioorg Med Chem Lett 95:129467. https://doi.org/10.1016/j.bmcl.2023.129467
Fu DJ, Zhang SY, Song J, Liu YC, Zhang L, Zhao RH, Zi XL, Liu HM, Zhang YB (2016) Design and antiproliferative activity of N-heterocycle-chalcone derivatives. J Chem Res 40:620–623. https://doi.org/10.3184/174751916x14740355883191
Luo L, Liu D, Lan SC, Gan XH (2022) Design, synthesis, and biological activity of novel chalcone derivatives containing an 1,2,4-oxadiazole moiety. Front Chem 10:943062. https://doi.org/10.3389/fchem.2022.943062
Firmino PP, Queiroz JE, Dias LD, Wenceslau PRS, Souza LM, Iermak I, Vaz WF, Custódio JMF, Oliver AG, Aquino GLB, Napolitano HB (2022) Synthesis, molecular structure, thermal and spectroscopic analysis of a novel bromochalcone derivative with larvicidal activity. Crystals 12:440. https://doi.org/10.3390/cryst12040440
Chen T, Xiong H, Yang JF, Zhu XL, Qu RY, Yang GF (2020) Diaryl ether: a privileged scaffold for drug and agrochemical discovery. J Agric Food Chem 68:9839–9877. https://doi.org/10.1021/acs.jafc.0c03369
Guan AY, Liu CL, Sun XF, Xie Y, Wang MA (2015) Discovery of pyridine-based agrochemicals by using intermediate derivatization methods. Bioorganic Med Chem 24:342–353. https://doi.org/10.1016/j.bmc.2015.09.031
Zhao LX, Peng JF, Liu FY, Zou YL, Gao S, Fu Y, Ye F (2022) Discovery of novel phenoxypyridine as promising protoporphyrinogen IX oxidase inhibitors. Pestic Biochem Physiol 184:105102. https://doi.org/10.1016/j.pestbp.2022.105102
Zhao LX, Wang ZX, Peng JF, Zou YL, Hui YZ, Chen YZ, Gao S, Fu Y, Ye F (2021) Design, synthesis, and herbicidal activity of novel phenoxypyridine derivatives containing natural product coumarin. Pest Manag Sci 77:4785–4798. https://doi.org/10.1002/ps.6523
Zhao LX, Wang ZX, Zou YL, Gao S, Fu Y, Ye F (2021) Phenoxypyridine derivatives containing natural product coumarins with allelopathy as novel and promising proporphyrin IX oxidase-inhibiting herbicides: design, synthesis and biological activity study. Pestic Biochem Physiol 177:104897. https://doi.org/10.1016/j.pestbp.2021.104897
Liu YF, Esser L, Bai H, Fu B, Xia D, Zhou YH, Hong S, Yang SH, Xiao YM, Qin ZH (2023) Synthesis and antiphytopathogenic activity of novel oxazolidine 2,4-diones bearing phenoxypyridine moiety. J Agric Food Chem 71:14199–14210. https://doi.org/10.1021/acs.3c034
Wang LZ, Yang ZK, Pan SX, Zhu MN, Guan AY, Sun XF, Zhang JB, Song YQ, Liu CL, Yang XL (2022) A new potential aphicide against Myzus persicae: design, synthesis and 3D-QSAR of novel phenoxypyridine derivatives containing 4-aminopyrimidine. J Mol Struct 1262:132949. https://doi.org/10.1016/j.molstruc.2022.132949
Song BA, Zhang HP, Wang H, Yang S, Jin LH, Hu DY, Pang LL, Xue W (2005) Synthesis and antiviral activity of novel chiral cyanoacrylate derivatives. J Agric Food Chem 53:7886–7891. https://doi.org/10.1021/jf051050w
Peng F, Liu TT, Cao X, Wang QF, Liu F, Liu LW, He M, Xue W (2023) Antiviral activities of novel myricetin derivatives containing 1,3,4-oxadiazole bisthioether. Chem Biodivers 19:e202100939. https://doi.org/10.1002/cbdv.202100939
Peng F, Liu TT, Zhu YY, Liu F, Cao X, Wang QF, Liu LW, Xue W (2023) Novel 1,3,4-oxadiazole sulfonate/carboxylate flavonoid derivatives: synthesis and biological activity. Pest Manag Sci 79:274–283. https://doi.org/10.1002/ps.7197
Tang XM, Zhan WL, Chen S, Zhou R, Hu D, Sun N, Fei Q, Wu WN, Xue W (2022) Synthesis, bioactivity and preliminary mechanism of action of novel trifluoromethyl pyrimidine derivatives. Arab J Chem 15:104110. https://doi.org/10.1016/j.arabjc.2022.104110
Chen Y, Li P, Su SJ, Chen M, He J, Liu LW, He M, Wang H, Xue W (2019) Synthesis and antibacterial and antiviral activities of myricetin derivatives containing a 1,2,4-triazole Schiff base. RSC Adv 9:23045–23052. https://doi.org/10.1039/c9ra05139b
Rostamizadch S, Zekri N, Tahershamsi L (2015) Nanosilica-supported dual acidic ionic liquid as a heterogeneous and reusable catalyst for the synthesis of flavanones under solvent-free conditions. Chem Heterocycl Compd 51:526–530. https://doi.org/10.1007/s10593-015-1728-z
Wan ZH, Hu DY, Li P, Xie DD, Gan XH (2015) Antiviral bioactivity of novel 4-thioquinazoline derivatives containing chalcone moiety. Molecules 20:11861–11874. https://doi.org/10.3390/molecules200711861