Citation: Ping Sun, Yuanqin Huang, Shunhong Chen, Xining Ma, Zhaokai Yang, Jian Wu. Indole derivatives as agrochemicals: An overview[J]. Chinese Chemical Letters, ;2024, 35(7): 109005. doi: 10.1016/j.cclet.2023.109005 shu

Indole derivatives as agrochemicals: An overview

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

yangzhaokai@cau.edu.cn

jwu6@gzu.edu.cn

Received Date: 4 July 2023
Revised Date: 20 August 2023
Accepted Date: 27 August 2023
Available Online: 29 August 2023

Figures(2)

Indole is a biologically active compound formed by the fusion of benzene and pyrrole, and it is widely found in natural products and drugs. Due to the unique structure and properties of indole, its derivatives often exhibit distinctive physiological activities, which has led to widespread attention in the field of pesticide development. Analyzing the design strategies and structure-activity relationships (SARs) of compounds is a crucial step in developing novel pesticides. This review mainly summarizes indole compounds with plant growth regulating, antiviral, fungicidal, herbicidal, and insecticidal activities, with the aim of providing new insights into the discovery and mechanism of action of novel indole-based pesticides.
- Indole compounds,
- Agrochemicals,
- Biological activity,
- Structure–activity relationship,
- Mechanism of action
1. [1]
  B. Zdrazil, R. Guha, J. Med. Chem. 61 (2018) 4688–4703. doi: 10.1021/acs.jmedchem.7b00954
2. [2]
  T. Chen, H. Xiong, J.F. Yang, et al., J. Agric. Food Chem. 68 (2020) 9839–9877. doi: 10.1021/acs.jafc.0c03369
3. [3]
  F.R. De Sá Alves, E.J. Barreiro, C.A. Fraga, Mini Rev. Med. Chem. 9 (2009) 782–793. doi: 10.2174/138955709788452649
4. [4]
  B.E. Evans, K.E. Rittle, M.G. Bock, et al., J. Med. Chem. 31 (1988) 2235–2246. doi: 10.1021/jm00120a002
5. [5]
  M.E. Welsch, S.A. Snyder, B.R. Stockwell, Curr. Opin. Chem. Biol. 14 (2010) 347–361. doi: 10.1016/j.cbpa.2010.02.018
6. [6]
  N.K. Kaushik, N. Kaushik, P. Attri, Molecules 18 (2013) 6620–6662. doi: 10.3390/molecules18066620
7. [7]
  R.E. Dolle, K.H. Nelson, J. Comb. Chem. 1 (1999) 235–282. doi: 10.1021/cc9900192
8. [8]
  R.G. Franzén, J. Comb. Chem. 2 (2000) 195–214. doi: 10.1021/cc000002f
9. [9]
  R.E. Dolle, J. Comb. Chem. 3 (2001) 477–517. doi: 10.1021/cc010049g
10. [10]
  T.N. Akhaja, J.P. Raval, Chin. Chem. Lett. 23 (2012) 785–788. doi: 10.1016/j.cclet.2012.05.004
11. [11]
  Z.N. Xu, Y.Q. Wang, Y.C. Zheng, et al., Org. Chem. Front. 7 (2020) 3709–3714. doi: 10.1039/D0QO01120G
12. [12]
  S.Y. Zhou, G.L. Huang, G.Y. Chen, Bioorg. Med. Chem. Lett. 41 (2021) 128009. doi: 10.1016/j.bmcl.2021.128009
13. [13]
  A. Hilgeroth, K. Yasrebi, S. Suzen, et al., Med. Chem. 15 (2019) 833–839. doi: 10.2174/1573406415666190208170126
14. [14]
  Y. Liu, Y. Cui, L.Y. Lu, et al., Arch. Pharm. 353 (2020) e2000120.
15. [15]
  Q.Q. Tan, Y.Z. Li, T.T. Li, et al., Microporous Mesoporous Mater. 325 (2021) 111342. doi: 10.1016/j.micromeso.2021.111342
16. [16]
  M. Budovská, R. Michalková, J. Mojžiš, Tetrahedron 143 (2023) 133573. doi: 10.1016/j.tet.2023.133573
17. [17]
  H.Y. Sun, K.P. Sun, J.Y. Sun, Molecules 28 (2023) 2204. doi: 10.3390/molecules28052204
18. [18]
  C.L. Wei, L. Zhao, Z.R. Sun, et al., Pestic. Biochem. Physiol. 166 (2020) 104568. doi: 10.1016/j.pestbp.2020.104568
19. [19]
  Y.B. Sun, H. Wu, W.N. Zhou, et al., Pestic. Biochem. Physiol. 183 (2022) 105077. doi: 10.1016/j.pestbp.2022.105077
20. [20]
  G.Y. Yang, J.M. Dai, Q.L. Mi, et al., Phytochemistry 198 (2022) 113137. doi: 10.1016/j.phytochem.2022.113137
21. [21]
  Y.N. Zhu, M.X. Liu, B.B. Cai, et al., Chem. Nat. Compd. 58 (2022) 712–716. doi: 10.1007/s10600-022-03774-y
22. [22]
  X.H. Gao, X.L. Pan, P.Y. Wang, et al., Org. Chem. Front. 9 (2022) 5790–5797. doi: 10.1039/D2QO01091G
23. [23]
  H. Guo, Eur. J. Med. Chem. 164 (2019) 678–688. doi: 10.1016/j.ejmech.2018.12.017
24. [24]
  H. Wu, M.L. Qin, K. Fan, et al., J. Asian Nat. Prod. Res. 25 (2022) 429–437.
25. [25]
  Y.H. Zhang, L. Li, Y.Q. Li, et al., J. Nat. Prod. 85 (2022) 1880–1885. doi: 10.1021/acs.jnatprod.2c00322
26. [26]
  X.J. Zhao, L.Z. Zhao, Y. Zhao, et al., Viruses 13 (2021) 1433. doi: 10.3390/v13081433
27. [27]
  S. Jin, H.K. Do, C. Hwang, et al., Int. J. Environ. Sci. 30 (2021) 369–378. doi: 10.5322/JESI.2021.30.5.369
28. [28]
  P.D. Miranda de Menezes Neves, B.M. Coelho Ferreira, S. Mohrbacher, et al., Lancet Infect. Dis. 20 (2020) 1215-1215. doi: 10.1016/S1473-3099(20)30323-6
29. [29]
  Y.H. Xie, Y. Song, Z.W. Cong, Chem. Biodivers. 19 (2022) e202200731. doi: 10.1002/cbdv.202200731
30. [30]
  L.J. Funkhouser-Jones, R. Xu, G. Wilke, et al., Cell Rep. 42 (2023) 112680. doi: 10.1016/j.celrep.2023.112680
31. [31]
  D.R. Duca, B.R. Glick, Appl. Microbiol. Biotechnol. 104 (2020) 8607–8619. doi: 10.1007/s00253-020-10869-5
32. [32]
  K.I. Hayashi, K. Arai, Y. Aoi, et al., Nat. Commun. 12 (2021) 6752. doi: 10.1038/s41467-021-27020-1
33. [33]
  M.H. Ma, E. Batsaikhan, C.M. Wu, et al., J. Chin. Chem. Soc. 70 (2023) 1200–1207. doi: 10.1002/jccs.202300023
34. [34]
  Q. Yin, J. Zhang, S. Wang, Hortic. Res. 8 (2021) 229. doi: 10.1038/s41438-021-00658-0
35. [35]
  S.K. Jaiswal, M. Mohammed, F.Y.I. Ibny, et al., Front. Sustain. Food Syst. 4 (2021) 619676. doi: 10.3389/fsufs.2020.619676
36. [36]
  K.G. Thanuja, B. Annadurai, S. Thankappan, et al., Arch. Microbiol. 202 (2020) 2739–2749. doi: 10.1007/s00203-020-01983-z
37. [37]
  X. Sun, N. Wang, P. Li, et al., Plant Cell Environ. 43 (2020) 358–373. doi: 10.1111/pce.13667
38. [38]
  G. Gomes, K. Scortecci, Plant Biol. 23 (2021) 894–904. doi: 10.1111/plb.13303
39. [39]
  M.R.A. de Figueiredo, L.C. Strader, Trends Biochem. Sci. 47 (2022) 865–874. doi: 10.1016/j.tibs.2022.06.004
40. [40]
  B. Kloosterman, R.G.F. Visser, C.W.B. Bachem, Plant Physiol. Biochem. 44 (2006) 766–775. doi: 10.1016/j.plaphy.2006.10.026
41. [41]
  S. Piya, S.K. Shrestha, B. Binder, et al., Front. Plant Sci. 5 (2014) 744.
42. [42]
  S. Damodaran, L.C. Strader, Front. Plant Sci. 10 (2019) 851. doi: 10.3389/fpls.2019.00851
43. [43]
  H.Q. Dong, M.C. Guo, Y. Liang, et al., Mater. Sci. Eng. 89 (2018) 175–181. doi: 10.1016/j.msec.2018.04.004
44. [44]
  S. Aihebaier, T. Muhammad, A. Wei, et al., ACS Omega 4 (2019) 16789–16793. doi: 10.1021/acsomega.9b01550
45. [45]
  L. Fattorini, A. Veloccia, F. Della Rovere, et al., BMC Plant Biol. 17 (2017) 121. doi: 10.1186/s12870-017-1071-x
46. [46]
  R.M. Napier, Auxin receptors and perception, in: E. Zažímalová, J. Petrášek, E. Benková (Eds. ), Auxin and Its Role in Plant Development, Springer Vienna, Vienna, 2014, pp. 101–116.
47. [47]
  S. Marumo, H. Hattori, H. Abe, et al., Nature 219 (1968) 959–960.
48. [48]
  C.P.A. Jayasinghege, J.A. Ozga, K.D. Waduthanthri, et al., J. Exp. Bot. 68 (2017) 4137–4151. doi: 10.1093/jxb/erx217
49. [49]
  K. Dziurka, M. Dziurka, M. Warchoł, et al., In Vitro Cell. Dev. Biol. Plant 55 (2019) 221–229.
50. [50]
  X. Cao, H.L. Yang, C.Q. Shang, et al., Int. J. Mol. Sci. 20 (2019) 6343. doi: 10.3390/ijms20246343
51. [51]
  M.M. Pérez-Alonso, P. Ortiz-García, J. Moya-Cuevas, et al., J. Exp. Bot. 72 (2020) 459–475.
52. [52]
  Z.Y. Han, H. Ghanizadeh, H.T. Zhang, et al., J. Fungi 8 (2022) 1166. doi: 10.3390/jof8111166
53. [53]
  D. Szymaniak, T. Kleiber, M. Wojcieszak, et al., ChemistrySelect 6 (2021) 5614–5621. doi: 10.1002/slct.202101084
54. [54]
  P. Staswick, M. Rowe, E.P. Spalding, et al., Front. Plant Sci. 8 (2017) 736. doi: 10.3389/fpls.2017.00736
55. [55]
  S. Park, K. Back, J. Pineal Res. 53 (2012) 385–389. doi: 10.1111/j.1600-079X.2012.01008.x
56. [56]
  M. Zhang, C.X. Gao, L. Xu, et al., Cells 11 (2022) 3250. doi: 10.3390/cells11203250
57. [57]
  H.Y. Lee, K. Lee, K. Back, Biomolecules 9 (2019) 712. doi: 10.3390/biom9110712
58. [58]
  H.B. Zhao, T. Su, L.Q. Huo, et al., J. Pineal Res. 59 (2015) 255–266. doi: 10.1111/jpi.12258
59. [59]
  C. de Meester, Mutat. Res. 339 (1995) 139–153. doi: 10.1016/0165-1110(95)90008-X
60. [60]
  J.C. Callaway, J. Psychoact. Drugs 37 (2005) 151–155. doi: 10.1080/02791072.2005.10399796
61. [61]
  Z.Z. Wang, D.D. Xie, X.H. Gan, et al., Bioorg. Med. Chem. Lett. 27 (2017) 4096–4100. doi: 10.1016/j.bmcl.2017.07.038
62. [62]
  Y.M. Ma, X.A. Liang, Y. Kong, et al., J. Agric. Food Chem. 64 (2016) 6659–6671. doi: 10.1021/acs.jafc.6b01772
63. [63]
  B.E.M. El-Gendy, M.E. Rateb, Bioorg. Med. Chem. Lett. 25 (2015) 3125–3128. doi: 10.1016/j.bmcl.2015.06.010
64. [64]
  X.P. Zhang, W.B. Huang, X. Lu, et al., J. Agric. Food Chem. 69 (2021) 7458–7466. doi: 10.1021/acs.jafc.1c00897
65. [65]
  J.L. Xie, W.T. Xu, H.J. Song, et al., J. Agric. Food Chem. 68 (2020) 5555–5571. doi: 10.1021/acs.jafc.0c00875
66. [66]
  H.Q. Wang, H.J. Song, J. Agric. Food Chem. 68 (2020) 2631–2638. doi: 10.1021/acs.jafc.9b07694
67. [67]
  X. Lv, M.T. Yuan, Y.H. Pei, et al., J. Agric. Food Chem. 69 (2021) 4992–5002. doi: 10.1021/acs.jafc.1c00941
68. [68]
  C.L. Wei, J. Zhang, J. Shi, et al., J. Agric. Food Chem. 67 (2019) 13882–13891. doi: 10.1021/acs.jafc.9b05357
69. [69]
  C.L. Wei, X. Yang, S.J. Shi, et al., J. Agric. Food Chem. 71 (2023) 267–275. doi: 10.1021/acs.jafc.2c06881
70. [70]
  K.B. Oh, W. Mar, S. Kim, et al., Bioorg. Med. Chem. Lett. 15 (2005) 4927–4931. doi: 10.1016/j.bmcl.2005.08.021
71. [71]
  X.F. Ji, Z.W. Wang, J. Dong, et al., J. Agric. Food Chem. 64 (2016) 9143–9151. doi: 10.1021/acs.jafc.6b04020
72. [72]
  J.C. Guo, Y.A. Hao, X.F. Ji, et al., J. Agric. Food Chem. 67 (2019) 10018–10031. doi: 10.1021/acs.jafc.9b04093
73. [73]
  T.A. Wang, L. Li, Y.A. Zhou, et al., J. Agric. Food Chem. 69 (2021) 10093–10103. doi: 10.1021/acs.jafc.1c04098
74. [74]
  A.D. Lu, T.A. Wang, H. Hui, et al., J. Agric. Food Chem. 67 (2019) 2148–2156. doi: 10.1021/acs.jafc.8b06859
75. [75]
  L.J. Yu, A.L. Dai, W. Zhang, et al., J. Agric. Food Chem. 70 (2022) 10693–10707. doi: 10.1021/acs.jafc.2c02301
76. [76]
  L.W. Chen, Y.X. Liu, H.J. Song, et al., Mol. Divers. 21 (2017) 61–68. doi: 10.1007/s11030-016-9697-4
77. [77]
  Q.M. Wang, Q. Wang, Y. Qu, et al., Patent, CN111269237A, 2020.
78. [78]
  L.W. Chen, Y.K. Hao, H.J. Song, et al., J. Agric. Food Chem. 68 (2020) 10618–10625. doi: 10.1021/acs.jafc.0c04488
79. [79]
  Q. Wang, H. Song, Q. Wang, Chin. Chem. Lett. 33 (2022) 859–862. doi: 10.1016/j.cclet.2021.08.005
80. [80]
  Q.M. Wang, H.J. Song, L.W. Chen, C.L. Li, G.Q. Yu, Patent, CN107353292A, 2017.
81. [81]
  Q.M. Wang, Q. Wang, Y. Qu, Patent, CN111264542A, 2020.
82. [82]
  F.Z. Xu, Y.Y. Wang, F. He, et al., Green Chem. Lett. Rev. 15 (2022) 139–152. doi: 10.1080/17518253.2021.2023660
83. [83]
  H. Gadegoni, S. Manda, Chin. Chem. Lett. 24 (2013) 127–130. doi: 10.1016/j.cclet.2013.01.001
84. [84]
  Z.J. Zhang, Y. Zeng, Z.Y. Jiang, et al., Pest Manag. Sci. 74 (2018) 1736–1746. doi: 10.1002/ps.4873
85. [85]
  J.M. Xi, Z.J. Zhang, Q. Zhu, G.H. Zhong, Int. J. Mol. Sci. 19 (2018) 4044. doi: 10.3390/ijms19124044
86. [86]
  Y.X. Liu, H.J. Song, Y.Q. Huang, et al., J. Agric. Food Chem. 62 (2014) 9987–9999. doi: 10.1021/jf503794g
87. [87]
  Z.J. Zhang, Z.Y. Jiang, Q. Zhu, G.H. Zhong, J. Agric. Food Chem. 66 (2018) 9598–9607. doi: 10.1021/acs.jafc.8b02124
88. [88]
  X.Y. Zhao, A.C. Liao, F. Zhang, et al., J. Heterocycl. Chem. 57 (2020) 761–767. doi: 10.1002/jhet.3817
89. [89]
  G.P. Ouyang, Z.C. Wang, W.N. Hu, Y.Y. Qi, W. Li, Patent, CN111285860A, 2020.
90. [90]
  B. Liu, R. Li, Y.A. Li, et al., J. Agric. Food Chem. 67 (2019) 1795–1806. doi: 10.1021/acs.jafc.8b06175
91. [91]
  Z.Y. Yu, H. Jiang, L. Wang, et al., Front. Chem. 8 (2020) 717. doi: 10.3389/fchem.2020.00717
92. [92]
  Y. Gao, D.C. Huang, C. Liu, et al., Bioorg. Med. Chem. 35 (2021) 116073. doi: 10.1016/j.bmc.2021.116073
93. [93]
  K.L. Keel, J.J. Tepe, Org. Lett. 23 (2021) 5368–5372. doi: 10.1021/acs.orglett.1c01681
94. [94]
  J. Zeng, Z.J. Zhang, Q. Zhu, Z.Y. Jiang, G.H. Zhong, Molecules 25 (2020) 1189. doi: 10.3390/molecules25051189
95. [95]
  L.W. Chen, J.L. Xie, H.J. Song, et al., J. Agric. Food Chem. 64 (2016) 6508–6516. doi: 10.1021/acs.jafc.6b02683
96. [96]
  B. Jia, Y.M. Ma, B. Liu, et al., Front. Chem. 7 (2019) 837. doi: 10.3389/fchem.2019.00837
97. [97]
  Y. Wang, S. Guo, L. Yu, et al., Chin. Chem. Lett. 35 (2024) 108207. doi: 10.1016/j.cclet.2023.108207
98. [98]
  M. Zhang, L. Chen, J.K. Hong, Y.T. Shen, L.Q. Yang, Patent, CN113735871A, 2021.
99. [99]
  L.Q. Yang, L. Chen, M. Zhang, M. Xia, T. Zhao, Patent, CN112898311A, 2021.
100. [100]
  H.D. Li, S. Wu, X. Yang, et al., J. Agric. Food Chem. 70 (2022) 12341–12354. doi: 10.1021/acs.jafc.2c04213
101. [101]
  R.R. King, L.A. Calhoun, Phytochemistry 70 (2009) 833–841. doi: 10.1016/j.phytochem.2009.04.013
102. [102]
  H.B. Zhang, Q.P. Wang, X. Ning, H. Hang, et al., J. Agric. Food Chem. 63 (2015) 3734–3741. doi: 10.1021/jf506153t
103. [103]
  H. Li, J. Xiao, Y.Q. Gao, et al., J. Agric. Food Chem. 62 (2014) 3734–3741. doi: 10.1021/jf500390h
104. [104]
  J.M. de Souza, B.R. Fazolo, J.W. Ferreira Lacerda, et al., Photochem. Photobiol. 96 (2020) 1233–1242. doi: 10.1111/php.13295
105. [105]
  M.C. da Silva Mendes, B.R. Fazolo, J.M. de Souza, et al., Photochem. Photobiol. Sci. 18 (2019) 1350–1358. doi: 10.1039/c8pp00506k
106. [106]
  W. Chotpatiwetchkul, N. Chotsaeng, C. Laosinwattana, P. Charoenying, ACS Omega 7 (2022) 29002–29012. doi: 10.1021/acsomega.2c02704
107. [107]
  J.B. Liu, Y.B. Shi, W. Wen, et al. Patent, CN113354645, 2021.
108. [108]
  J.B. Liu, Y.B. Shi, Z.C. Tian, et al., J. Agric. Food Chem. 70 (2022) 5197–5206. doi: 10.1021/acs.jafc.1c08297
109. [109]
  J.H. Lee, Y.G. Kim, M. Kim, et al., Environ. Microbiol. 19 (2017) 1776–1790. doi: 10.1111/1462-2920.13649
110. [110]
  S.K. Rajasekharan, J.H. Lee, V. Ravichandran, J. Lee, Sci. Rep. 7 (2017) 6803. doi: 10.1038/s41598-017-07074-2
111. [111]
  S.K. Rajasekharan, J.H. Lee, V. Ravichandran, et al., Sci. Rep. 9 (2019) 2010. doi: 10.1038/s41598-019-38561-3
112. [112]
  S.K. Rajasekharan, S. Kim, J.C. Kim, J. Lee, Pestic. Biochem. Physiol. 163 (2020) 76–83. doi: 10.1016/j.pestbp.2019.10.012
113. [113]
  Â. C. Costa, S.C. Cavalcanti, A.S. Santana, et al., Ecotoxicology 28 (2019) 973–982. doi: 10.1007/s10646-019-02095-1
114. [114]
  J. Zhang, R.J. Song, S. Wu, et al., J. Agric. Food Chem. 70 (2022) 5349–5356. doi: 10.1021/acs.jafc.2c00838
115. [115]
  J. Cassayre, L.P. Molleyres, P. Maienfisch, F. Cederbaum, Patent, US8309567, 2012.
116. [116]
  J. Cassayre, L.P. Molleyres, P. Maienfisch, F. Cederbaum, Patent, US8299058, 2012.
1. [1]
  Wei Sun , Anjing Liao , Li Lei , Xu Tang , Ya Wang , Jian Wu . Research progress on piperidine-containing compounds as agrochemicals. Chinese Chemical Letters, 2025, 36(1): 109855-. doi: 10.1016/j.cclet.2024.109855
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]
  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
7. [7]
  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
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]
  Hualei Xu , Manman Han , Haiqiang Liu , Liang Qin , Lulu Chen , Hao Hu , Ran Wu , Chenyu Yang , Hua Guo , Jinrong Li , Jinxiang Fu , Qichen Hao , Yijun Zhou , Jinchao Feng , Xiaodong Wang . 4-Nitrocatechol as a novel matrix for low-molecular-weight compounds in situ detection and imaging in biological tissues by MALDI-MSI. Chinese Chemical Letters, 2024, 35(6): 109095-. doi: 10.1016/j.cclet.2023.109095
12. [12]
  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
13. [13]
  Teng Wang , Jiachun Cao , Juan Li , Didi Li , Zhimin Ao . A novel photocatalytic mechanism of volatile organic compounds degradation on BaTiO₃ under visible light: Photo-electrons transfer from photocatalyst to pollutant. Chinese Chemical Letters, 2025, 36(3): 110078-. doi: 10.1016/j.cclet.2024.110078
14. [14]
  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
15. [15]
  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
16. [16]
  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
17. [17]
  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
18. [18]
  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
19. [19]
  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
20. [20]
  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

Get Citation

PDF

XML

Metrics

PDF Downloads(2)
Abstract views(286)
HTML views(5)

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