Citation: Hong Yao, Liping Cui, Hang Liu, Xueyu Li, Lin Shen, Ruige Yang, Shangshang Qin, Yong Guo. Quinoline-based anti-MRSA agents: Current development, structure-activity relationships, and mechanisms[J]. Chinese Chemical Letters, ;2024, 35(1): 108511. doi: 10.1016/j.cclet.2023.108511 shu

Quinoline-based anti-MRSA agents: Current development, structure-activity relationships, and mechanisms

Hong Yao ^{a, 1} ,
Liping Cui ^{b, 1} ,
Hang Liu ^b ,
Xueyu Li ^b ,
Lin Shen ^b ,
Ruige Yang ^{b, *,} ,
Shangshang Qin ^{b, *,} ,
Yong Guo ^{b, c, *,}

a.
College of Veterinary Medicine, Henan Agricultural University, Zhengzhou 450046, China
b.
School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China
c.
Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, School of Pharmaceutical Science, Hengyang Medical School, University of South China, Hengyang 421001, China

yrggg@zzu.edu.cn

qinshangshang@126.com

guoyong_122@zzu.edu.cn

Received Date: 11 March 2023
Revised Date: 25 April 2023
Accepted Date: 26 April 2023
Available Online: 27 April 2023

Figures(20)

Methicillin-resistant Staphylococcus aureus (MRSA), the most common pathogen in hospital and community environments, can cause serious and even fatal infections. The antibiotics currently used for clinical treatment of MRSA have developed resistance, and there is an urgent need to develop new antimicrobials to treat infections caused by MRSA strains. Quinoline analogues play an important role in the development of antimicrobials. Herein, we discussed the current development of antibacterial activities of quinoline analogues, mainly for anti-MRSA activity, and their structure–activity relationships (SARs) from the perspective of using the quinoline nucleus to search for novel potential anti-MRSA candidates. Additionally, the mechanisms of some representative quinoline analogues against MRSA were clarified. Altogether, this review could provide further insights for the rational development of quinoline-based antibacterial drugs, especially against MRSA.
- Quinoline analogue,
- Methicillin-resistant Staphylococcus aureus,
- Antibacterial activity,
- Structure–activity relationship,
- Antibacterial mechanism
1. [1]
  A. Asadi, S. Razavi, M. Talebi, M. Gholami, Infection 47 (2019) 13–23. doi: 10.1007/s15010-018-1222-5
2. [2]
  L.N. Silva, K.R. Zimmer, A.J. Macedo, D.S. Trentin, Chem. Rev. 116 (2016) 9162–9236. doi: 10.1021/acs.chemrev.6b00184
3. [3]
  A.R. Brochado, A. Telzerow, J. Bobonis, et al., Nature 559 (2018) 259–263. doi: 10.1038/s41586-018-0278-9
4. [4]
  E.D. Brown, G.D. Wright, Nature 529 (2016) 336–343. doi: 10.1038/nature17042
5. [5]
  K. Bush, P. Courvalin, G. Dantas, et al., Nat. Rev. Microbiol. 9 (2011) 894–896. doi: 10.1038/nrmicro2693
6. [6]
  W. Cheng, T. Xu, L. Cui, et al., J. Med. Chem. 66 (2023) 962–975. doi: 10.1021/acs.jmedchem.2c01793
7. [7]
  N. Koyama, J. Inokoshi, H. Tomoda, Molecules 18 (2012) 204–224. doi: 10.3390/molecules18010204
8. [8]
  H.F. Chambers, F.R. Deleo, Nat. Rev. Microbiol. 7 (2009) 629–641. doi: 10.1038/nrmicro2200
9. [9]
  H. Grundmann, M. Aires-de-Sousa, J. Boyce, E. Tiemersma, Lancet 368 (2006) 874–885. doi: 10.1016/S0140-6736(06)68853-3
10. [10]
  Z. Yi, X. Xu, X. Meng, et al., Chin. Chem. Lett. 34 (2023) 108238. doi: 10.1016/j.cclet.2023.108238
11. [11]
  T.Y. Zhang, C. Li, Y.S. Tian, et al., Chin. Chem. Lett. 28 (2017) 1737–1742. doi: 10.1016/j.cclet.2017.05.022
12. [12]
  R. Hope, D.M. Livermore, G. Brick, M. Lillie, R. Reynolds, J. Antimicrob. Chemother. 62 (2008) 65–74. doi: 10.1093/jac/dkn166
13. [13]
  P.D. Stapleton, P.W. Taylor, Sci. Prog. 85 (2002) 57–72. doi: 10.3184/003685002783238870
14. [14]
  Y. Guo, E. Hou, T. Wen, et al., J. Med. Chem. 64 (2021) 12903–12916. doi: 10.1021/acs.jmedchem.1c01073
15. [15]
  C. Liu, H. Shen, S. Wang, et al., Chin. Chem. Lett. 29 (2018) 1824–1828. doi: 10.1016/j.cclet.2018.10.025
16. [16]
  R. Yang, E. Hou, W. Cheng, et al., J. Med. Chem. 65 (2022) 16879–16892. doi: 10.1021/acs.jmedchem.2c01674
17. [17]
  Y. Bouzian, Y. Sert, K. Khalid, et al., J. Mol. Struct. 1246 (2021) 131217. doi: 10.1016/j.molstruc.2021.131217
18. [18]
  S.I. Eissa, A.M. Farrag, S.Y. Abbas, et al., Bioorg. Chem. 110 (2021) 104803. doi: 10.1016/j.bioorg.2021.104803
19. [19]
  L. Xu, X. Mu, M. Liu, et al., Chin. Chem. Lett. 34 (2023) 108063. doi: 10.1016/j.cclet.2022.108063
20. [20]
  B. Sureshkumar, Y.S. Mary, C.Y. Panicker, et al., Arab. J. Chem. 13 (2020) 632–648. doi: 10.1016/j.arabjc.2017.07.006
21. [21]
  H. Kumar, V. Devaraji, R. Joshi, et al., RSC Adv. 5 (2015) 65496–65513. doi: 10.1039/C5RA08778C
22. [22]
  A.M. Ghanim, A.S. Girgis, B.M. Kariuki, et al., Bioorg. Chem. 119 (2022) 105557. doi: 10.1016/j.bioorg.2021.105557
23. [23]
  K. Douadi, S. Chafaa, T. Douadi, M. Al-Noaimi, I. Kaabi, J. Mol. Struct. 1217 (2020) 128305. doi: 10.1016/j.molstruc.2020.128305
24. [24]
  K.B. Patel, P. Kumari, J. Mol. Struct. 1268 (2022) 133634. doi: 10.1016/j.molstruc.2022.133634
25. [25]
  R.D. Overacker, S. Banerjee, G.F. Neuhaus, et al., Bioorg. Med. Chem. 27 (2019) 3595–3604. doi: 10.1016/j.bmc.2019.06.044
26. [26]
  T.G. Shruthi, S. Eswaran, P. Shivarudraiah, et al., Bioorg. Med. Chem. Lett. 29 (2019) 97–102. doi: 10.1016/j.bmcl.2018.11.002
27. [27]
  J. Mo, H. Yang, T. Chen, et al., Bioorg. Chem. 93 (2019) 103310. doi: 10.1016/j.bioorg.2019.103310
28. [28]
  V.G. Ugale, H.M. Patel, S.J. Surana, Arab. J. Chem. 10 (2017) S1980–S2003. doi: 10.1016/j.arabjc.2013.07.026
29. [29]
  A.A. Boteva, O.P. Krasnykh, Chem. Heterocycl. Compd. 45 (2009) 757–785. doi: 10.1007/s10593-009-0360-1
30. [30]
  S.B.S. Kumar, H. Gupta, Med. Chem. 9 (2009) 1648–1654.
31. [31]
  T.L. Lauderdale, Y.R. Shiau, J.F. Lai, H.C. Chen, C.H. King, Antimicrob. Agents Chemother. 54 (2010) 1338–1342. doi: 10.1128/AAC.01197-09
32. [32]
  C.R. Li, Y. Li, G.Q. Li, et al., J. Antimicrob. Chemother. 65 (2010) 2411–2415. doi: 10.1093/jac/dkq341
33. [33]
  J.M. Remy, C.A. Tow-Keogh, T.S. McConnell, J.M. Dalton, J.A. Devito, J. Antimicrob. Chemother. 67 (2012) 2814–2820. doi: 10.1093/jac/dks307
34. [34]
  B. Li, J. Yao, J. Wei, et al., J. Global. Antimicrob. Resist. 12 (2018) 77–78. doi: 10.1016/j.jgar.2017.12.004
35. [35]
  Y.Q. Hu, S. Zhang, Z. Xu, et al., Eur. J. Med. Chem. 141 (2017) 335–345. doi: 10.1016/j.ejmech.2017.09.050
36. [36]
  G.F. Zhang, S. Zhang, B. Pan, X. Liu, L.S. Feng, Eur. J. Med. Chem. 143 (2018) 710–723. doi: 10.1016/j.ejmech.2017.11.082
37. [37]
  Y. Hu, A.R. Coates, J. Antimicrob. Chemother. 68 (2013) 374–384. doi: 10.1093/jac/dks384
38. [38]
  Y. Hu, A. Shamaei-Tousi, Y. Liu, A. Coates, PLoS One 5 (2010) e11818. doi: 10.1371/journal.pone.0011818
39. [39]
  L.Z. Gao, Y.S. Xie, T. Li, W.L. Huang, G.Q. Hu, Chin. Chem. Lett. 26 (2015) 149–151. doi: 10.1016/j.cclet.2014.09.017
40. [40]
  L. Zhang, D. Addla, J. Ponmani, et al., Eur. J. Med. Chem. 111 (2016) 160–182. doi: 10.1016/j.ejmech.2016.01.052
41. [41]
  X. Huang, Y. Bao, S. Zhu, et al., Bioorg. Med. Chem. Lett. 25 (2015) 3928–3932. doi: 10.1016/j.bmcl.2015.07.044
42. [42]
  T. Zhang, W. Shen, M. Liu, et al., Eur. J. Med. Chem. 104 (2015) 73–85. doi: 10.1016/j.ejmech.2015.09.030
43. [43]
  H.J. Yun, Y.H. Min, J.A. Lim, et al., Antimicrob. Agents. Chemother. 46 (2002) 3071–3074. doi: 10.1128/AAC.46.9.3071-3074.2002
44. [44]
  S.F. Cui, Y. Ren, S.L. Zhang, et al., Bioorg. Med. Chem. Lett. 23 (2013) 3267–3272. doi: 10.1016/j.bmcl.2013.03.118
45. [45]
  S.F. Cui, D. Addla, C.H. Zhou, J. Med. Chem. 59 (2016) 4488–4510. doi: 10.1021/acs.jmedchem.5b01678
46. [46]
  M. Norouzbahari, S. Salarinejad, M. Güran, et al., Daru, J. Pharm. Sci. 28 (2020) 661–672. doi: 10.1007/s40199-020-00373-6
47. [47]
  D.T. Chu, Patent, US4687770, 1987.
48. [48]
  D.T. Chu, Patent, US4689325, 1987.
49. [49]
  J.A. Wiles, Q. Wang, E. Lucien, et al., Bioorg. Med. Chem. Lett. 16 (2006) 1272–1276. doi: 10.1016/j.bmcl.2005.11.065
50. [50]
  J.A. Wiles, Y. Song, Q. Wang, et al., Bioorg. Med. Chem. Lett. 16 (2006) 1277–1281. doi: 10.1016/j.bmcl.2005.11.064
51. [51]
  J.A. Wiles, A. Hashimoto, J.A. Thanassi, et al., J. Med. Chem. 49 (2006) 39–42. doi: 10.1021/jm051066d
52. [52]
  Q.L. Wang, E. Lucien, A. Hashimoto, et al., J. Med. Chem. 50 (2007) 199–210. doi: 10.1021/jm060844e
53. [53]
  H.Y. Kim, J.A. Wiles, Q. Wang, et al., J. Med. Chem. 54 (2011) 3268–3282. doi: 10.1021/jm101604v
54. [54]
  F. O'donnell, T.J. Smyth, V.N. Ramachandran, W.F. Smyth, Int. J. Antimicrob. Agents. 35 (2010) 30–38. doi: 10.1016/j.ijantimicag.2009.06.031
55. [55]
  Y. Abouelhassan, A.T. Garrison, G.M. Burch, et al., Bioorg. Med. Chem. Lett. 24 (2014) 5076–5080. doi: 10.1016/j.bmcl.2014.09.009
56. [56]
  A. Basak, Y. Abouelhassan, V.M. Norwood, et al., Chemistry 22 (2016) 9181–9189. doi: 10.1002/chem.201600926
57. [57]
  D.J. Musk Jr, P.J. Hergenrother, Curr. Med. Chem. 13 (2006) 2163–2177. doi: 10.2174/092986706777935212
58. [58]
  U. Römling, C. Balsalobre, J. Intern. Med. 272 (2012) 541–561. doi: 10.1111/joim.12004
59. [59]
  A.T. Garrison, Y. Abouelhassan, H. Yang, et al., MedChemComm 8 (2017) 720–724. doi: 10.1039/C6MD00381H
60. [60]
  Y. Abouelhassan, A.T. Garrison, F. Bai, et al., ChemMedChem 10 (2015) 1157–1162. doi: 10.1002/cmdc.201500179
61. [61]
  J.P.H. Fan, M.T. Hamann, J.F. Hu, Chem. Rev. 108 (2008) 264–287. doi: 10.1021/cr078199m
62. [62]
  T.K. Wood, S.H. Hong, Q. Ma, Trends. Biotechnol. 29 (2011) 87–94. doi: 10.1016/j.tibtech.2010.11.001
63. [63]
  J.H. Lee, J. Lee, FEMS Microbiol. Rev. 34 (2010) 426–444. doi: 10.1111/j.1574-6976.2009.00204.x
64. [64]
  C. Challa, J. Ravindran, M.M. Konai, et al., ACS Omega 2 (2017) 5187–5195. doi: 10.1021/acsomega.7b00840
65. [65]
  N. Sun, R.L. Du, Y.Y. Zheng, et al., Eur. J. Med. Chem. 135 (2017) 1–11. doi: 10.1016/j.ejmech.2017.04.018
66. [66]
  H. Yang, H.W. Wang, T.W. Zhu, et al., Eur. J. Med. Chem. 127 (2017) 166–173. doi: 10.1016/j.ejmech.2016.12.054
67. [67]
  L.M. Oppegard, B.L. Hamann, K.R. Streck, et al., Antimicrob. Agents. Chemother. 53 (2009) 2110–2119. doi: 10.1128/AAC.01440-08
68. [68]
  X.W. Wu, Z.P. Wu, L.X. Wang, et al., Eur. J. Med. Chem. 46 (2011) 4625–4633. doi: 10.1016/j.ejmech.2011.07.042
69. [69]
  L.K. An, Z.C. Li, X.W. Wu, X.Y. Zou, L.Q. Gu, Afr. J. Pharm. Pharmacol. 7 (2013) 1020–1025. doi: 10.5897/AJPP12.544
70. [70]
  Y. Cheng, L.K. An, N. Wu, et al., Bioorg. Med. Chem. 16 (2008) 4617–4625. doi: 10.1016/j.bmc.2008.02.036
71. [71]
  M. Yanato, Y. Takeuchi, M.R. Chang, K. Hashigaki, et al., Chem. Pharm. Bull. 38 (1990) 3048–3052. doi: 10.1248/cpb.38.3048
72. [72]
  A. Paulo, A. Duarte, E.T. Gomes, J. Ethnopharmacol. 44 (1994) 127–130. doi: 10.1016/0378-8741(94)90079-5
73. [73]
  L.G. Mardenborough, X.Y. Zhu, P. Fan, et al., Bioorg. Med. Chem. 13 (2005) 3955–3963. doi: 10.1016/j.bmc.2005.04.008
74. [74]
  X.Y. Zhu, L.G. Mardenborough, S. Li, et al., Bioorg. Med. Chem. 15 (2007) 686–695. doi: 10.1016/j.bmc.2006.10.062
75. [75]
  S. Shiota, M. Shimizu, T. Mizushima, H. Ito, et al., Biol. Pharm. Bull. 22 (1999) 1388–1390. doi: 10.1248/bpb.22.1388
76. [76]
  M. Zhao, T. Kamada, A. Takeuchi, et al., Bioorg. Med. Chem. Lett. 25 (2015) 5551–5554. doi: 10.1016/j.bmcl.2015.10.058
77. [77]
  M. Shiria, A. Nejatinejhad-Arani, Z. Faghihi, S.A. Shintre, N.A. Koorbanally, Org. Chem. Res. 2 (2016) 113–119.
78. [78]
  M.O. Puskullu, I. Celik, M. Erol, et al., Bioorg. Chem. 101 (2020) 104014. doi: 10.1016/j.bioorg.2020.104014
79. [79]
  M. Guo, C.J. Zheng, M.X. Song, et al., Bioorg. Med. Chem. Lett. 23 (2013) 4358–4361. doi: 10.1016/j.bmcl.2013.05.082
80. [80]
  X. Bai, Y. Chen, Z. Liu, et al., Chem. Biodivers. 16 (2019) e1900056. doi: 10.1002/cbdv.201900056
81. [81]
  H.R. Piao, Med. Chem. 4 (2014) 441–448.
82. [82]
  W. Cieslik, R. Musiol, J.E. Nycz, et al., Bioorg. Med. Chem. 20 (2012) 6960–6968. doi: 10.1016/j.bmc.2012.10.027
83. [83]
  Z. Fang, L. Ban, Y. Li, et al., J. Pharmacol. Sci. 137 (2018) 283–289. doi: 10.1016/j.jphs.2018.07.005
84. [84]
  P. Teng, C. Li, Z. Peng, et al., Bioorg. Med. Chem. 26 (2018) 3573–3579. doi: 10.1016/j.bmc.2018.05.031
85. [85]
  N. Manhas, P. Singh, N.A. Koorbanally, Polycycl. Aromat. Compd. 42 (2022) 5183–5195. doi: 10.1080/10406638.2021.1926293
86. [86]
  D.B. Farag, N.A. Farag, A. Esmat, et al., MedChemComm 6 (2015) 283–299. doi: 10.1039/C4MD00392F
87. [87]
  M. Dinakaran, S. Palaniappan, Y. Perumal, et al., Med. Chem. 4 (2008) 482–491. doi: 10.2174/157340608785700225
88. [88]
  J. Strigacova, D. Hudecová, L'. Varečka, A. Lásiková, D. Végh, Folia Microbiol. 45 (2000) 305–309. doi: 10.1007/BF02817551
89. [89]
  X. Wang, X. Xie, Y. Cai, et al., Molecules 21 (2016) 340. doi: 10.3390/molecules21030340
90. [90]
  F. Sevgi, A.D. Bedük, World. Appl. Sci. J. 19 (2012) 192–197.
91. [91]
  D. Paul, R.G. Reddy, S.P. Rajendran, J. Chil. Chem. Soc. 63 (2018) 3974–3982. doi: 10.4067/s0717-97072018000203974
92. [92]
  P.A. Enquist, A. Gylfe, U. Hägglund, et al., Bioorg. Med. Chem. Lett. 22 (2012) 3550–3553. doi: 10.1016/j.bmcl.2012.03.096
93. [93]
  X. Zhang, Y. Li, W. Wang, et al., Int. J. Antimicrob. Agents 53 (2019) 442–448. doi: 10.1016/j.ijantimicag.2018.11.016
94. [94]
  H.G. Fu, Z.W. Li, X.X. Hu, et al., Molecules 24 (2019) 548. doi: 10.3390/molecules24030548
95. [95]
  N. Dolan, D.P. Gavin, A. Eshwika, et al., Bioorg. Med. Chem. Lett. 26 (2016) 630–635. doi: 10.1016/j.bmcl.2015.11.058
96. [96]
  J. Lutkenhaus, S. Pichoff, S. Du, Cytoskeleton 69 (2012) 778–790. doi: 10.1002/cm.21054
97. [97]
  G.M. Nepomuceno, K.M. Chan, V. Huynh, et al., ACS Med Chem. Lett. 6 (2015) 308–312. doi: 10.1021/ml500497s
98. [98]
  X Yang, Z. Lyu, A. Miguel, et al., Science 355 (2017) 744–747. doi: 10.1126/science.aak9995
1. [1]
  Jinjie Lu , Qikai Liu , Yuting Zhang , Yi Zhou , Yanbo Zhou . Antibacterial performance of cationic quaternary phosphonium-modified chitosan polymer in water. Chinese Chemical Letters, 2024, 35(9): 109406-. doi: 10.1016/j.cclet.2023.109406
2. [2]
  Xingyu Chen , Sihui Zhuang , Weiyao Yan , Zhengli Zeng , Jianguo Feng , Hongen Cao , Lei Yu . Synthesis, antibacterial evaluation, and safety assessment of Se@PLA as a potent bactericide against Xanthomonas oryzae pv. oryzae. Chinese Chemical Letters, 2024, 35(10): 109635-. doi: 10.1016/j.cclet.2024.109635
3. [3]
  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
4. [4]
  Chao LIU , Jiang WU , Zhaolei JIN . Synthesis, crystal structures, and antibacterial activities of two zinc(Ⅱ) complexes bearing 5-phenyl-1H-pyrazole group. Chinese Journal of Inorganic Chemistry, 2024, 40(10): 1986-1994. doi: 10.11862/CJIC.20240153
5. [5]
  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
6. [6]
  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
7. [7]
  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
8. [8]
  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
9. [9]
  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
10. [10]
  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
11. [11]
  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
12. [12]
  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
13. [13]
  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
14. [14]
  Guo-Ping Yin , Ya-Juan Li , Li Zhang , Ling-Gao Zeng , Xue-Mei Liu , Chang-Hua Hu . Citrinsorbicillin A, a novel homotrimeric sorbicillinoid isolated by LC-MS-guided with cytotoxic activity from the fungus Trichoderma citrinoviride HT-9. Chinese Chemical Letters, 2024, 35(8): 109035-. doi: 10.1016/j.cclet.2023.109035
15. [15]
  Simin Wei , Yaqing Yang , Junjie Li , Jialin Wang , Jinlu Tang , Ningning Wang , Zhaohui Li . The Mn/Yb/Er triple-doped CeO₂ nanozyme with enhanced oxidase-like activity for highly sensitive ratiometric detection of nitrite. Chinese Chemical Letters, 2024, 35(6): 109114-. doi: 10.1016/j.cclet.2023.109114
16. [16]
  Maitri Bhattacharjee , Rekha Boruah Smriti , R. N. Dutta Purkayastha , Waldemar Maniukiewicz , Shubhamoy Chowdhury , Debasish Maiti , Tamanna Akhtar . Synthesis, structural characterization, bio-activity, and density functional theory calculation on Cu(Ⅱ) complexes with hydrazone-based Schiff base ligands. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1409-1422. doi: 10.11862/CJIC.20240007
17. [17]
  Yiyue Ding , Qiuxiang Zhang , Lei Zhang , Qilu Yao , Gang Feng , Zhang-Hui Lu . Exceptional activity of amino-modified rGO-immobilized PdAu nanoclusters for visible light-promoted dehydrogenation of formic acid. Chinese Chemical Letters, 2024, 35(7): 109593-. doi: 10.1016/j.cclet.2024.109593
18. [18]
  Qi Tan , Run-Zhu Fan , Wencong Yang , Ge Zou , Tao Chen , Jianying Wu , Bo Wang , Sheng Yin , Zhigang She . (+)/(−)-Mycosphatide A, a pair of highly oxidized polyketides with lipid-lowering activity from the mangrove endophytic fungus Mycosphaerella sp. SYSU-DZG01. Chinese Chemical Letters, 2024, 35(9): 109390-. doi: 10.1016/j.cclet.2023.109390
19. [19]
  Ruiying Liu , Li Zhao , Baishan Liu , Jiayuan Yu , Yujie Wang , Wanqiang Yu , Di Xin , Chaoqiong Fang , Xuchuan Jiang , Riming Hu , Hong Liu , Weijia Zhou . Modulating pollutant adsorption and peroxymonosulfate activation sites on Co3O4@N,O doped-carbon shell for boosting catalytic degradation activity. Chinese Journal of Structural Chemistry, 2024, 43(8): 100332-100332. doi: 10.1016/j.cjsc.2023.100332
20. [20]
  Maosen Xu , Pengfei Zhu , Qinghong Cai , Meichun Bu , Chenghua Zhang , Hong Wu , Youzhou He , Min Fu , Siqi Li , Xingyan Liu . In-situ fabrication of TiO₂/NH₂−MIL-125(Ti) via MOF-driven strategy to promote efficient interfacial effects for enhancing photocatalytic NO removal activity. Chinese Chemical Letters, 2024, 35(10): 109524-. doi: 10.1016/j.cclet.2024.109524

Get Citation

PDF

XML

Metrics

PDF Downloads(3)
Abstract views(249)
HTML views(17)

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