Citation: Wei Sun, Anjing Liao, Li Lei, Xu Tang, Ya Wang, Jian Wu. Research progress on piperidine-containing compounds as agrochemicals[J]. Chinese Chemical Letters, ;2025, 36(1): 109855. doi: 10.1016/j.cclet.2024.109855 shu

Research progress on piperidine-containing compounds as agrochemicals

State Key Laboratory of Green Pesticide, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Guizhou University, Guiyang 550025, China

jwu6@gzu.edu.cn

Received Date: 9 January 2024
Revised Date: 26 March 2024
Accepted Date: 2 April 2024
Available Online: 3 April 2024

Figures(8)

Piperidine is a crucial pharmacophore and a special scaffold in the realm of drug discovery. Its flexibility increases the molecule's capability to bind to the receptor. The piperidine-containing compounds are distinguished by their remarkable activity, and are increasingly becoming a vital category of pesticides. In this review, the research progress of piperidines in the discovery of pesticides was updated according to their active characteristics. The structure-activity relationships (SARs), and mechanisms of action of piperidine-containing compounds were also discussed. This article is meant to enable readers to quickly understand piperidines, while providing ideas for creating piperidines with novel structures and unique mechanisms of action.
- Piperidine,
- Agrochemicals,
- Biological activity,
- Structure-activity relationships,
- Mechanism of action
1. [1]
  N.A. Frolov, A.N. Vereshchagin, Int. J. Mol. Sci. 24 (2023) 2937. doi: 10.3390/ijms24032937
2. [2]
  M.G.P. Buffat, Tetrahedron 60 (2004) 1701–1729. doi: 10.1016/j.tet.2003.11.043
3. [3]
  M. Lankelma, A.M. Olivares, B. de Bruin, Chem. Eur. J. 25 (2019) 5658–5663. doi: 10.1002/chem.201900587
4. [4]
  S.S. Sajadikhah, M.T. Maghsoodlou, N. Hazeri, S.M. Habibi-Khorassani, S.J. Shams-Najafi, Monatsh. Chem. 143 (2012) 939–945. doi: 10.1007/s00706-011-0671-7
5. [5]
  M.B. Smith, J. March, March’s Advanced Organic Chemistry, John Wiley Sons, Inc., New Jersey, 2007, pp. 872–892.
6. [6]
  A.M.M.M. Faisca, Synthetic Approaches to Nonaromatic Nitrogen Heterocycles, John Wiley Sons, Inc., Hoboken, 2021, pp. 171–249.
7. [7]
  H. Franquet-Griell, C. Gómez-Canela, F. Ventura, S. Lacorte, Environ. Pollut. 229 (2017) 505–515. doi: 10.1016/j.envpol.2017.06.011
8. [8]
  E. Vitaku, D.T. Smith, J.T. Njardarson, J. Med. Chem. 57 (2014) 10257–10274. doi: 10.1021/jm501100b
9. [9]
  H. Furukawa, Y. Miyamoto, Y. Hirata, et al., J. Med. Chem. 63 (2020) 10352–10379. doi: 10.1021/acs.jmedchem.0c00843
10. [10]
  J.I. Yun, H.J. Jung, C.S. Yun, et al., B. Korean Chem. Soc. 36 (2015) 1929–1932. doi: 10.1002/bkcs.10357
11. [11]
  L.F. Hennequin, E.S.E. Stokes, A.P. Thomas, et al., J. Med. Chem. 45 (2002) 1300–1312. doi: 10.1021/jm011022e
12. [12]
  A.E. Shchekotikhin, A.A. Shtil, Y.N. Luzikov, et al., Bioorgan. Med. Chem. 13 (2005) 2285–2291. doi: 10.1016/j.bmc.2004.12.044
13. [13]
  E. Khazanov, Y. Barenholz, D. Gibson, Y. Najajreh, J. Med. Chem. 45 (2002) 5196–5204. doi: 10.1021/jm020817y
14. [14]
  G.L. Balaji, V. Vijayakumar, K. Rajesh, Arabian J. Chem. 9 (2016) S1101–S1104. doi: 10.1016/j.arabjc.2011.12.011
15. [15]
  M. Srinivasan, S. Perumal, S. Selvaraj, Chem. Pharm. Bull. 54 (2006) 795–801. doi: 10.1248/cpb.54.795
16. [16]
  H.I. El-Subbagh, S.M. Abu-Zaid, M.A. Mahran, F.A. Badria, A.M. Al-Obaid, J. Med. Chem. 43 (2000) 2915–2921. doi: 10.1021/jm000038m
17. [17]
  S. Liu, F. Wang, J. Yang, et al., Arch Pharm. 356 (2023) 2300416. doi: 10.1002/ardp.202300416
18. [18]
  X. Zhang, C. Zhang, L. Tang, et al., Chin. Chem. Lett. 31 (2020) 136–140. doi: 10.1016/j.cclet.2019.04.045
19. [19]
  P. Ji, A.S. Csinos, L.L. Hickman, U. Hargett, Plant. Dis. 98 (2014) 1551–1554. doi: 10.1094/PDIS-02-14-0172-RE
20. [20]
  J.B. Pasteris, A.M. Hanagan, R. Shapiro, Patent, WO2008013925A2, 2008.
21. [21]
  L. Huang, P. Zhao, J.J. Tan, Zhejiang Chem. Ind. 53 (2022) 19–25. doi: 10.1007/978-3-031-14595-7_3
22. [22]
  M. Muehlebach, A. Buchholz, W. Zambach, et al., Pest. Manag. Sci. 76 (2020) 3440–3450. doi: 10.1002/ps.5743
23. [23]
  F. Zhang, S. Bai, H. Wang, W. Liu, J. Wang, Sci. Rep. 9 (2019) 1625. doi: 10.1038/s41598-018-38221-y
24. [24]
  L. Lian, Y.R. Zheng, B. He, et al., Patent, CN105218449A, 2016.
25. [25]
  E.F.S. Authority, EFSA J. 14 (2016) e04504.
26. [26]
  L. Lian, H. Wang, F. Zhang, et al., J. Agr. Food Chem. 71 (2023) 8825–8833. doi: 10.1021/acs.jafc.3c01239
27. [27]
  V. Mahdavi, H. Gordan, A. Heidari, J. Food Compos Anal. 121 (2023) 105353. doi: 10.1016/j.jfca.2023.105353
28. [28]
  A. Mishra, J.K. Punia, C. Bladen, G.W. Zamponi, R.K. Goel, Channels 9 (2015) 317–323. doi: 10.1080/19336950.2015.1092836
29. [29]
  M.R. Siegel, H.D. Sisler, Nature 200 (1963) 675–676. doi: 10.1038/200675a0
30. [30]
  T. Kodama, T. Tsukaguchi, M. Yoshida, O. Kondoh, H. Sakamoto, Cancer. Lett. 351 (2014) 215–221. doi: 10.1016/j.canlet.2014.05.020
31. [31]
  S. Peters, D.R. Camidge, A.T. Shaw, et al., New. Engl. J. Med. 377 (2017) 829–838. doi: 10.1056/NEJMoa1704795
32. [32]
  L.J. Scott, Drugs 80 (2020) 741–746. doi: 10.1007/s40265-020-01301-3
33. [33]
  X.Q. Liu, Y.Q. Liu, X.S. Shao, et al., Chin. Chem. Lett. 27 (2016) 7–10. doi: 10.1016/j.cclet.2015.10.002
34. [34]
  Y.F. Fan, W.W. Zhang, X.S. Shao, et al., Chin. Chem. Lett. 26 (2015) 1–5. doi: 10.1016/j.cclet.2014.10.019
35. [35]
  H. Mei, K. Aradi, L. Kiss, J. Han, Chin. Chem. Lett. 34 (2023) 108657. doi: 10.1016/j.cclet.2023.108657
36. [36]
  G. Pemawat, A. Bhatnagar, R.K. Khangarot, Mini-Rev Org. Chem. 21 (2024) 346–369. doi: 10.2174/1570193x20666230213123453
37. [37]
  P. Goel, O. Alam, M.J. Naim, et al., Eur. J. Med. Chem. 157 (2018) 480–502. doi: 10.1016/j.ejmech.2018.08.017
38. [38]
  M. Abdelrahim, S. Konduri, R. Basha, P.A. Philip, C.H. Baker, Int. J. Oncol. 36 (2009) 5–18.
39. [39]
  B.T. Green, S.T. Lee, K.E. Panter, D.R. Brown, Food. Chem. Toxicol. 50 (2012) 2049–2055. doi: 10.1016/j.fct.2012.03.049
40. [40]
  C.X. Zhu, X.L. Jiang, D.Y. Sun, Fine. Spec. Chem. 16 (2002).
41. [41]
  K. Barrett-Bee, G. Dixon, Acta Biochim. Pol. 42 (1995) 465–479. doi: 10.18388/abp.1995_4900
42. [42]
  R.I. Baloch, E.I. Mercer, Phytochemistry. 26 (1987) 663–668. doi: 10.1016/S0031-9422(00)84762-7
43. [43]
  Q.F. Wu, Z.S. Hao, Z.J. Fan, Chin. J. Pestic. Sci. 21 (2019) 595–608.
44. [44]
  G. Qiao, S.P. Wei, Z.Q. Ji, Chin. J. Pestic. Sci. 14 (2012) 440–444.
45. [45]
  D.L. Xie, C.F. Ni, C.X. Zhu, K.H. Huang, D. Kong, Chin. J. Biol. Control. 6 (1990) 74–77.
46. [46]
  Y. Ren, D. Li, S. Jiang, et al., Phytopathology, 111 (2021) 2238–2249. doi: 10.1094/phyto-02-21-0073-r
47. [47]
  Y. Cohen, A.E. Rubin, M. Galperin, Phytoparasitica, 46 (2018) 689–704. doi: 10.1007/s12600-018-0702-6
48. [48]
  M. Kono, T. Matsumoto, T. Kawamura, et al., Bioorgan. Med. Chem. 21 (2013) 28–41. doi: 10.1016/j.bmc.2012.11.006
49. [49]
  X. Feng, K. Wang, L. Pan, et al., J. Agric. Food Chem. 66 (2018) 8489–8495. doi: 10.1021/acs.jafc.8b02056
50. [50]
  J. Miao, Y. Chi, D. Lin, B.M. Tyler, X. Liu, Phytopathology, 108 (2018) 1412–1419. doi: 10.1094/phyto-01-18-0010-r
51. [51]
  R.J. Bittner, A.L. Mila, Crop. Prot. 93 (2017) 9–18. doi: 10.1016/j.cropro.2016.10.019
52. [52]
  V.M. Olkkonen, S. Li, Prog. Lipid Res. 52 (2013) 529–538. doi: 10.1016/j.plipres.2013.06.004
53. [53]
  V.M. Olkkonen, M. Johansson, M. Suchanek, et al., Biochem. Soc. T. 34 (2006) 389–391. doi: 10.1042/BST0340389
54. [54]
  Y. Gao, X. Zhao, X. Sun, et al., J. Agric. Food Chem. 69 (2021) 3289–3297. doi: 10.1021/acs.jafc.0c04163
55. [55]
  Q. Peng, Z. Wang, P. Liu, et al., Int. J. Mol. Sci. 21 (2020) 1223. doi: 10.3390/ijms21041223
56. [56]
  B. Olenik, S. Hillebrand, P. asnaire, M. Weiss, U. Wachendorff-neumann, Patent, EP3057967A1, 2016.
57. [57]
  C. Lamberth, S. Trah, L. Quaranta, et al., Patent, WO2014154530A1, 2014.
58. [58]
  F. Cederbaum., Patent, WO2014118142A1, 2014.
59. [59]
  T. Tsuchiya, S. Hoffmann, P. Cristau, et al., Patent, WO2012025557A1, 2012.
60. [60]
  D. Lin, Z. Xue, J. Miao, Z. Huang, X. Liu, J. Agric. Food Chem. 68 (2020) 13651–13660. doi: 10.1021/acs.jafc.0c05531
61. [61]
  J. Miao, M. Cai, X. Dong, et al., Front. Microbiol. 7 (2016) 615.
62. [62]
  L.J. Andreassi II, S. Gutteridge, O.S. Pember, A.J. Sweigard, Patent, WO2013009971A1, 2013.
63. [63]
  Z. Wang, Q. Ke, K. Tao, et al., J. Agric. Food Chem. 70 (2022) 14140–14147. doi: 10.1021/acs.jafc.2c06707
64. [64]
  J. Miao, X. Liu, G. Li, X. Du, X. Liu, Pest. Manag. Sci. 76 (2020) 2434–2440. doi: 10.1002/ps.5784
65. [65]
  J. Miao, C. Li, X. Liu, et al., J. Agric. Food Chem. 69 (2021) 3827–3835. doi: 10.1021/acs.jafc.0c05119
66. [66]
  C. Li, X. Liu, Z. Liu, et al., J. Agric. Food Chem. 70 (2022) 4881–4888. doi: 10.1021/acs.jafc.1c08199
67. [67]
  J. Miao, X. Dong, D. Lin, et al., Pest. Manag. Sci. 72 (2015) 1572–1577.
68. [68]
  Z. Wang, X. Lv, R. Wang, et al., Pest. Manag. Sci. 79 (2022) 381–390.
69. [69]
  T. Qu, T.L. Grey, A.S. Csinos, P. Ji, Plant. Dis. 100 (2016) 1931–1936. doi: 10.1094/PDIS-03-16-0370-RE
70. [70]
  J.L. Li, L.M. Zhou, M.Q. Gao, et al., Pestic. Biochem. Phys. 169 (2020) 104673. doi: 10.1016/j.pestbp.2020.104673
71. [71]
  J.L. Li, J.F. Yang, L.M. Zhou, et al., J. Agric. Food Chem. 71 (2023) 9519–9527. doi: 10.1021/acs.jafc.3c00990
72. [72]
  Q. Wu, B. Zhao, Z. Fan, et al., J. Agric. Food Chem. 67 (2019) 1360–1370. doi: 10.1021/acs.jafc.8b06054
73. [73]
  L.F. Yun, Y.J. Zhu, Z.J. Fan, et al., Chin. J. Struct. Chem. 34 (2015) 659–666.
74. [74]
  S. Sulzer-Mosse, F. Cederbaum, C. Lamberth, et al., Bioorgan. Med. Chem. 23 (2015) 2129–2138. doi: 10.1016/j.bmc.2015.03.007
75. [75]
  W.S. Choi, J. Korean. Soc. Appl. Bio. Chem. 53 (2010) 206–214.
76. [76]
  S.W. Nam, J. Korean. Soc. Appl. Bio. Chem. 54 (2011) 395–402. doi: 10.3839/jksabc.2011.062
77. [77]
  S.W. Nam, G.R. Lee, T.J. Kim, B.J. Chung, W.S. Choi, Korean J. Pestic. Sci. 16 (2012) 1–10. doi: 10.7585/kjps.2012.16.1.001
78. [78]
  W.S. Choi, S.W. Nam, I.D. Kim, et al., J. Chem-Ny. 2015 (2015) 1–6.
79. [79]
  C. Ding, Y. Pan, X. Yin, C. Tan, X. Wang, Chin. J. Org. Chem. 39 (2019) 2062. doi: 10.6023/cjoc201901009
80. [80]
  C. Ding, Y. Pan, C. Tan, Chin. J. Org. Chem. 40 (2020) 528. doi: 10.6023/cjoc201907034
81. [81]
  C. Ding, Y. Pan, X. Yin, C. Tan, Chin. J. Org. Chem. 39 (2019) 2099. doi: 10.6023/cjoc201812027
82. [82]
  Q. Bian, R.Q. Zhao, X.J. Peng, et al., J. Agric. Food Chem. 69 (2021) 3848–3858. doi: 10.1021/acs.jafc.0c07581
83. [83]
  P. Qi, N. Wang, T. Zhang, et al., Int. J. Mol. Sci. 24 (2023) 2897. doi: 10.3390/ijms24032897
84. [84]
  J.F. Tang, H.W. Chi, J.T. Wu, J. Han, Y. Liu, Patent, CN110551124A, 2019.
85. [85]
  S. Ghosh, J.R. Greenwood, G.C. Harriman, S.M. Leit De Moradei, Patent, WO 2017091617A1, 2017.
86. [86]
  X. Zhang, P. Lei, T. Sun, et al., Molecules. 22 (2017) 2085. doi: 10.3390/molecules22122085
87. [87]
  Y. Ling, X. Zhang, X. Yang, et al., Chin. J. Org. Chem. 39 (2019) 2965. doi: 10.6023/cjoc201903031
88. [88]
  H.W. Liu, Q.T. Ji, G.G. Ren, et al., J. Agric. Food Chem. 68 (2020) 12558–12568. doi: 10.1021/acs.jafc.0c02528
89. [89]
  T. Pitterna, M. Muehlebach, H.J. Schaetzer, Patent, WO2011067131A1, 2011.
90. [90]
  T. Pitterna, M. Muehlebach, H.J. Schaetzer, Patent, US8703165B2, 2014.
91. [91]
  T. Pitterna, M. Muehlebach, H.J. Schaetzer, Patent, US8541343B2, 2013.
92. [92]
  L.F. Mao, S.H. Jia, W. Li, et al., Patent, CN105017252A, 2015.
93. [93]
  C. Ding, Y. Pan, X. Yin, C. Tan, G. Zhang, Chin. J. Org. Chem. 39 (2019) 836. doi: 10.6023/cjoc201809009
94. [94]
  R. Tyagi, A.R. Maddirala, M. Elfawal, et al., ACS Infect. Dis. 4 (2018) 1130–1145. doi: 10.1021/acsinfecdis.8b00090
95. [95]
  Y.J. Zhu, X.F. Guo, Z.J. Fan, et al., RSC Adv. 6 (2016) 112704–112711. doi: 10.1039/C6RA24342H
96. [96]
  J.Y. Wang, B.L. Xu, S.Y. Si, H. Li, G.H. Song, Mol. Divers. 18 (2014) 887–893. doi: 10.1007/s11030-014-9531-9
97. [97]
  D.I. Knueppel, M.C. Yap, M.T. Sullenberger, et al., Patent, WO2015175719A1, 2015.
98. [98]
  I.A. Arif, A. Ahamed, R.S. Kumar, A. Idhayadhulla, A. Manilal, Saudi J. Biol. Sci. 26 (2019) 673–680. doi: 10.1016/j.sjbs.2017.12.007
99. [99]
  H. Qu, M. Lv, X. Yu, X. Lian, H. Xu, Sci. Rep. 5 (2015) 13077. doi: 10.1038/srep13077
100. [100]
  A.H. Tantawy, S.M. Farag, L. Hegazy, H. Jiang, M.Q. Wang, Bioorg. Chem. 94 (2020) 103464. doi: 10.1016/j.bioorg.2019.103464
101. [101]
  H. Qu, M. Lv, H. Xu, Mini-Rev. Med. Chem. 15 (2015) 145–156. doi: 10.2174/1389557515666150101100509
102. [102]
  M. Lv, S. Li, H. Wen, Y. Wang, J. Du, H. Xu, Pest Manag. Sci. 79 (2023) 3459–3470. doi: 10.1002/ps.7521
103. [103]
  I. Hamamoto, J. Takahashi, M. Yano, D. Hanai, T. Iwasa, Patent, WO2005095380A1, 2005.
104. [104]
  I. Hamamoto, J. Takahashi, M. Yano, et al., Patent, WO2007040280A1, 2007.
105. [105]
  I. Hamamoto, K. Koizumi, M. Kawaguchi, et al., Patent, WO2011105506A1, 2011.
106. [106]
  T.W. Wu, H.J. Ma, H.K. Tian, J.P. Ni, Z. Yun, Chin. J. Org. Chem. 30 (2010) 713–718.
107. [107]
  Y. Endo, G. Uenaka, Y. Shirai, Patent, WO2008026658A1, 2008.
108. [108]
  L.P. Molleyres, J. Cassayre, F. Cederbaum, P. Maienfisch, Patent, WO2005061500A1, 2005.
109. [109]
  T. Pitterna, J. Cassayre, L.P. Molleyres, P. Maienfisch, Patent, WO2007085945A1, 2007.
110. [110]
  J. Cassayre, P. Maienfisch, F. Cederbaum, L.P. Molleyres, Patent, US8338443B2, 2012.
111. [111]
  Y.J. Cassayre, T. Pitterna, C. Corsi, P. Maienfisch, Patent, WO2011003684, 2011.
112. [112]
  T. Yuyama, S. Shirakura, K. Ishizuka, Zeitschrift für Naturforschung C. 46 (1991) 887–892. doi: 10.1515/znc-1991-9-1027
113. [113]
  J.M. Leah, J.C. Caseley, C.R. Riches, B. Valverde, Pest Manag. Sci. 43 (1995) 347–354. doi: 10.1002/ps.2780430415
114. [114]
  T. Müller, H. Helmke, M.C. Sullenberger, et al., Patent, WO2018178012A1, 2018.
115. [115]
  A.D. Satterfield, J.F. Bereznak, M.J. Campbell, Patent, WO2016003997A1, 2016.
116. [116]
  N.R. Smith, M. Muehlebach, J.H. Schaetzer, Patent, WO2013079672A1, 2013.
117. [117]
  T. Fan, C. Chen, T. Fan, F. Liu, Q. Peng, J. Hazard Mater. 297 (2015) 340–346. doi: 10.1016/j.jhazmat.2015.05.034
118. [118]
  A. Zajac, R. Kukawka, A. Pawlowska-Zygarowicz, O. Stolarska, M. Smiglak, Green. Chem. 20 (2018) 4764–4789. doi: 10.1039/c8gc01424h
119. [119]
  J. Pernak, M. Niemczak, K. Materna, et al., RSC Adv. 6 (2016) 7330–7338. doi: 10.1039/C5RA23997D
120. [120]
  M.S.B. Brandao, Encycl. Surf. Colloid Sci. (2015) 336–351.
121. [121]
  M. Wojcieszak, A. Syguda, A. Lewandowska, et al., J. Agric. Food Chem. 71 (2023) 4550–4560. doi: 10.1021/acs.jafc.3c00356
122. [122]
  W. Rademacher, Annu. Rev. Plant Physiol. Plant Mol. Biol. 51 (2000) 501–531. doi: 10.1146/annurev.arplant.51.1.501
123. [123]
  Z.J. Fang, Y.J. Zhu, S. Zhou, et al., Patent, CN108558857A, 2018.
124. [124]
  S. Bai, S. Liu, Y. Zhu, K. Zhao, Q. Wu, Synlett 29 (2018) 1921–1925. doi: 10.1055/s-0037-1609910
125. [125]
  S. Yun, B. Yang, J.D. Anair, et al. Nat. Neurosci. 26 (2023) 1417–1428. doi: 10.1038/s41593-023-01390-9
126. [126]
  J. Carlier, R. Giorgetti, M.R. Varì, et al. Eur. Rev. Med. Pharmacol. Sci. 23 (2019) 3–15.
127. [127]
  W. Xiong, L. Qi, D. Si, et al., Nanoscale 13 (2021) 13473–13486. doi: 10.1039/d1nr02880d
1. [1]
  Ping Sun , Yuanqin Huang , Shunhong Chen , Xining Ma , Zhaokai Yang , Jian Wu . Indole derivatives as agrochemicals: An overview. Chinese Chemical Letters, 2024, 35(7): 109005-. doi: 10.1016/j.cclet.2023.109005
2. [2]
  Ali Dai , Zhiguo Zheng , Liusheng Duan , Jian Wu , Weiming Tan . Small molecule chemical scaffolds in plant growth regulators for the development of agrochemicals. Chinese Chemical Letters, 2025, 36(4): 110462-. doi: 10.1016/j.cclet.2024.110462
3. [3]
  Tao Yu , Vadim A. Soloshonok , Zhekai Xiao , Hong Liu , Jiang Wang . Probing the dynamic thermodynamic resolution and biological activity of Cu(Ⅱ) and Pd(Ⅱ) complexes with Schiff base ligand derived from proline. Chinese Chemical Letters, 2024, 35(4): 108901-. doi: 10.1016/j.cclet.2023.108901
4. [4]
  Anjing Liao , Wei Sun , Yaming Liu , Han Yan , Zhi Xia , Jian Wu . Pyrrole and pyrrolidine analogs: The promising scaffold in discovery of pesticides. Chinese Chemical Letters, 2025, 36(3): 110094-. doi: 10.1016/j.cclet.2024.110094
5. [5]
  Xiaofang Luo , Ye Wu , Xiaokun Zhang , Min Tang , Feiye Ju , Zuodong Qin , Gregory J Duns , Wei-Dong Zhang , Jiang-Jiang Qin , Xin Luan . Peptide-based strategies for overcoming multidrug-resistance in cancer therapy. Chinese Chemical Letters, 2025, 36(1): 109724-. doi: 10.1016/j.cclet.2024.109724
6. [6]
  Jian Song , Shenghui Wang , Qiuge Liu , Xiao Wang , Shuo Yuan , Hongmin Liu , Saiyang Zhang . N-Benzyl arylamide derivatives as novel and potent tubulin polymerization inhibitors against gastric cancers: Design, structure–activity relationships and biological evaluations. Chinese Chemical Letters, 2025, 36(2): 109678-. doi: 10.1016/j.cclet.2024.109678
7. [7]
  Jia JI , Zhaoyang GUO , Wenni LEI , Jiawei ZHENG , Haorong QIN , Jiahong YAN , Yinling HOU , Xiaoyan XIN , Wenmin WANG . Two dinuclear Gd(Ⅲ)-based complexes constructed by a multidentate diacylhydrazone ligand: Crystal structure, magnetocaloric effect, and biological activity. Chinese Journal of Inorganic Chemistry, 2025, 41(4): 761-772. doi: 10.11862/CJIC.20240344
8. [8]
  Hongling Liu , Yue Xia , Guang Xu , Yafei Yang , Chunhua Qu . Bitter Cold Medicine, Good for Healing. University Chemistry, 2025, 40(3): 328-332. doi: 10.12461/PKU.DXHX202405039
9. [9]
  Yao HUANG , Yingshu WU , Zhichun BAO , Yue HUANG , Shangfeng TANG , Ruixue LIU , Yancheng LIU , Hong LIANG . Copper complexes of anthrahydrazone bearing pyridyl side chain: Synthesis, crystal structure, anticancer activity, and DNA binding. Chinese Journal of Inorganic Chemistry, 2025, 41(1): 213-224. doi: 10.11862/CJIC.20240359
10. [10]
  Guangyao Wang , Zhitong Xu , Ye Qi , Yueguang Fang , Guiling Ning , Junwei Ye . Electrospun nanofibrous membranes with antimicrobial activity for air filtration. Chinese Chemical Letters, 2024, 35(10): 109503-. doi: 10.1016/j.cclet.2024.109503
11. [11]
  Hai-Ling Wang , Zhong-Hong Zhu , Hua-Hong Zou . Structure and assembly mechanism of high-nuclear lanthanide-oxo clusters. Chinese Journal of Structural Chemistry, 2024, 43(9): 100372-100372. doi: 10.1016/j.cjsc.2024.100372
12. [12]
  Ting Wang , Xin Yu , Yaqiang Xie . Unlocking stability: Preserving activity of biomimetic catalysts with covalent organic framework cladding. Chinese Chemical Letters, 2024, 35(6): 109320-. doi: 10.1016/j.cclet.2023.109320
13. [13]
  Fangping Yang , Jin Shi , Yuansong Wei , Qing Gao , Jingrui Shen , Lichen Yin , Haoyu Tang . Mixed-charge glycopolypeptides as antibacterial coatings with long-term activity. Chinese Chemical Letters, 2025, 36(2): 109746-. doi: 10.1016/j.cclet.2024.109746
14. [14]
  Chong Liu , Ling Li , Jiahui Gao , Yanwei Li , Nazhen Zhang , Jing Zang , Cong Liu , Zhaopei Guo , Yanhui Li , Huayu Tian . The study of antibacterial activity of cationic poly(β-amino ester) regulating by amphiphilic balance. Chinese Chemical Letters, 2025, 36(2): 110118-. doi: 10.1016/j.cclet.2024.110118
15. [15]
  Di ZHANG , Tianxiang XIE , Xu HE , Wanyu WEI , Qi FAN , Jie QIAO , Gang JIN , Ningbo LI . Construction and antitumor activity of pH/GSH dual-responsive magnetic nanodrug. Chinese Journal of Inorganic Chemistry, 2025, 41(4): 786-796. doi: 10.11862/CJIC.20240329
16. [16]
  Xiangyuan Zhao , Jinjin Wang , Jinzhao Kang , Xiaomei Wang , Hong Yu , Cheng-Feng Du . Ni nanoparticles anchoring on vacuum treated Mo2TiC2Tx MXene for enhanced hydrogen evolution activity. Chinese Journal of Structural Chemistry, 2023, 42(10): 100159-100159. doi: 10.1016/j.cjsc.2023.100159
17. [17]
  Xinyi Hu , Riguang Zhang , Zhao Jiang . Depositing the PtNi nanoparticles on niobium oxide to enhance the activity and CO-tolerance for alkaline methanol electrooxidation. Chinese Journal of Structural Chemistry, 2023, 42(11): 100157-100157. doi: 10.1016/j.cjsc.2023.100157
18. [18]
  Anqiu LIU , Long LIN , Dezhi ZHANG , Junyu LEI , Kefeng WANG , Wei ZHANG , Junpeng ZHUANG , Haijun HAO . Synthesis, structures, and catalytic activity of aluminum and zinc complexes chelated by 2-((2,6-dimethylphenyl)amino)ethanolate. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 791-798. doi: 10.11862/CJIC.20230424
19. [19]
  Bin Dong , Ning Yu , Qiu-Yue Wang , Jing-Ke Ren , Xin-Yu Zhang , Zhi-Jie Zhang , Ruo-Yao Fan , Da-Peng Liu , Yong-Ming Chai . Double active sites promoting hydrogen evolution activity and stability of CoRuOH/Co₂P by rapid hydrolysis. Chinese Chemical Letters, 2024, 35(7): 109221-. doi: 10.1016/j.cclet.2023.109221
20. [20]
  Jia Chen , Yun Liu , Zerong Long , Yan Li , Hongdeng Qiu . Colorimetric detection of α-glucosidase activity using Ni-CeO₂ nanorods and its application to potential natural inhibitor screening. Chinese Chemical Letters, 2024, 35(9): 109463-. doi: 10.1016/j.cclet.2023.109463

Get Citation

PDF

XML

Metrics

PDF Downloads(1)
Abstract views(367)
HTML views(13)

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142