Citation: Zhu Xiang, Wu Qinglai, Li Junkai. Research Progress of Phenazine-1-carboxylic Acid and Its Analogue[J]. Chinese Journal of Organic Chemistry, ;2019, 39(10): 2744-2758. doi: 10.6023/cjoc201904023 shu

Research Progress of Phenazine-1-carboxylic Acid and Its Analogue

Zhu Xiang ^a ,
Wu Qinglai ^a,b,, ,
Li Junkai ^a,b,,

a.
School of Agriculture, Yangtze University, Jingzhou 434025
b.
Institute of Pesticides, Yangtze University, Jingzhou 434025

Corresponding author: Wu Qinglai, wql106@163.com Li Junkai, junkaili@sina.com.com
Received Date: 9 April 2019
Revised Date: 16 May 2019
Available Online: 3 October 2019
Fund Project: the National Natural Science Foundation of China 31672069the National Key R&D Program of China 2018YFD0200500Project supported by the National Key R&D Program of China (No. 2018YFD0200500), the National Natural Science Foundation of China (No. 31672069) and the Funds for Excellent Doctoral Dissertation Cultivation Program in Yangtze University

Figures(28)

Phenazine-1-carboxylic acid (PCA) as a natural product widely exists in microbial metabolites of Pseudomonads and Streptomycetes, which displays potent inhibitory activities against plant pathogens, and has medical antibacterial and antitumor effects, and so on. In this review, the biosynthesis and chemosynthesis of phenazine-1-carboxylic acid are summarized. At the same time, the diverse biological evaluations of its biosynthetic and chemosynthetic analogues are summarized, which could provide reference for the study of structural modifications and biological activities of these analogues.
- phenazine-1-carboxylic acid,
- analogues,
- research progress
1. [1]
  Abdelfattah, M. S.; Toume, K.; Ishibashi, M. J. Antibiot. 2011, 64, 271. doi: 10.1038/ja.2010.172
2. [2]
  Jasim, B.; Anisha, C.; Rohini, S.; Kurian, J. M.; Jyothis, M.; Radhakrishnan, E. K. World J. Microb. Biot. 2014, 30, 1649. doi: 10.1007/s11274-013-1582-z
3. [3]
  Kögl, F.; Postowsky, J. J. Justus Liebig's Ann. Chem. 1930, 480, 280. doi: 10.1002/jlac.19304800117
4. [4]
  Ou, J. G.; Lu, Y. H. Chem. Reag. 1982, 4, 41(in Chinese).
5. [5]
  Isono, K.; Suzuki, S.; Sawazaki, T.; Nakamura, G.; Kawasaki, M.; Yamashita, T.; Anzai, K.; Serizawa, Y.; Sekiyama, Y. J. Antibiot. 1955, 8, 19.
6. [6]
  Nelson, C. D.; Toohey, J. I. US 3367765, 1968.
7. [7]
  Abdelfattah, M. S.; Ishikawa, N.; Karmakar, U. K.; Yamaku, K.; Ishibashi, M. J. Antibiot. 2016, 69, 446. doi: 10.1038/ja.2015.129
8. [8]
  Thanabalasingam, D.; Kumar, N. S.; Jayasinghe, L.; Fujimoto, Y. Nat. Prod. Commun. 2015, 10, 1659.
9. [9]
  Wu, Q. L.; Xu, Z. H.; Li, J. K. Chin. J. Pestic. Sci. 2016, 18, 669(in Chinese).
10. [10]
  Hu, H. B.; Xu, Y. Q.; Feng, C.; Xue, H. Z.; Hur, B. K. J Microbiol. Biotechnol. 2005, 15, 86.
11. [11]
  Wang, C. H.; Zhu, X. D.; Xu, Y. Q.; Feng, Z. T. J. Shanghai Jiaotong Univ. 2000, 34, 1574(in Chinese). doi: 10.3321/j.issn:1006-2467.2000.11.030
12. [12]
  Xu, Y. Q.; Tang, W. N.; Zheng, Y. L.; Zhong, Z. X.; Xu, T. W. J. Shanghai Jiaotong Univ. 1999, 33, 210(in Chinese). doi: 10.3321/j.issn:1006-2467.1999.02.024
13. [13]
  Zheng, W. J.; Xu, S.; Zhou, M. G. Chin. J. Pestic. Sci. 2011, 13, 28(in Chinese). doi: 10.3969/j.issn.1008-7303.2011.01.05
14. [14]
  Jin, Y.; Hu, H. B.; Zhang, X. H.; Xu, Y. Q. Acta Agric. Shanghai 2005, 21, 106(in Chinese).
15. [15]
  Xu, Y. Q. Fine Spec. Chem. 2004, 12, 8(in Chinese).
16. [16]
  Guttenberger, N.; Blankenfeldt, W.; Breinbauer, R. Bioorg. Med. Chem. 2017, 25, 6149. doi: 10.1016/j.bmc.2017.01.002
17. [17]
  Mavrodi, D. V.; Blankenfeldt, W.; Thomashow, L. S. Annu. Rev. Phytopathol. 2006, 44, 417. doi: 10.1146/annurev.phyto.44.013106.145710
18. [18]
  Price-Whelan, A.; Dietrich, L. E.; Newman, D. K. Nat. Chem. Biol. 2006, 2, 71. doi: 10.1038/nchembio764
19. [19]
  Zhang, F. H.; Xu, Y. Q.; Zhang, X. H. Agrochem. Res. Appl. 2006, 10, 4(in Chinese).
20. [20]
  Chin-A-Woeng, T. F.; Bloemberg, G. V.; Lugtenberg, B. J. New Phytol. 2003, 157, 503. doi: 10.1046/j.1469-8137.2003.00686.x
21. [21]
  Laursen, J. B.; Nielsen, J. Chem. Rev. 2004, 104, 1663. doi: 10.1021/cr020473j
22. [22]
  Ingledew, W. M.; Campbell, J. J. R. Can. J. Microbiol. 1969, 15, 535. doi: 10.1139/m69-092
23. [23]
  Calhoun, D. H.; Carson, M.; Jensen, R. A. Microbiology 1972, 72, 581.
24. [24]
  Turner, J. M.; Messenger, A. J. Adv. Microb. Physiol. 1986, 27, 211. doi: 10.1016/S0065-2911(08)60306-9
25. [25]
  Pierson, L. S.; Pierson, E. A. Appl. Microbiol. Biotechnol. 2010, 86, 1659. doi: 10.1007/s00253-010-2509-3
26. [26]
  Blankenfeldt, W.; Parsons, J. F. Curr. Opin. Struct. Biol. 2014, 29, 26. doi: 10.1016/j.sbi.2014.08.013
27. [27]
  Ahuja, E. G.; Janning, P.; Mentel, M.; Graebsch, A.; Breinbauer, R.; Hiller, W.; Costisella, B.; Thomashow, L. S.; Mavrodi, D. V.; Blankenfeldt, W. J. Am. Chem. Soc. 2008, 130, 17053. doi: 10.1021/ja806325k
28. [28]
  Chen, M.; Cao, H.; Peng, H.; Hu, H.; Wang, W.; Zhang, X. PloS One 2014, 9, e98537. doi: 10.1371/journal.pone.0098537
29. [29]
  Mavrodi, D. V.; Bonsall, R. F.; Delaney, S. M.; Soule, M. J.; Phillips, G.; Thomashow, L. S. J. Bacteriol. 2001, 183, 6454. doi: 10.1128/JB.183.21.6454-6465.2001
30. [30]
  Girard, G.; van Rij, E. T.; Lugtenberg, B. J.; Bloemberg, G. V. Microbiology 2006, 152, 43. doi: 10.1099/mic.0.28284-0
31. [31]
  Clemo, G. R.; Mcilwain, H. J. Chem. Soc. 1934, 1991. doi: 10.1039/jr9340001991
32. [32]
  Spicer, J. A.; Gamage, S. A.; Rewcastle, G. W.; Finlay, G. J.; Bridewell, D. J.; Baguley, B. C.; Denny, W. A. J. Med. Chem. 2000, 43, 1350. doi: 10.1021/jm990423f
33. [33]
  Zhu, H. J.; Zhu, X. L.; He, G. K.; Song, G. L.; Huang, R. J.; Shi, L. CN 103304496, 2013.
34. [34]
  Zhu, H. J.; Zhan, Q. Y.; Zhu, X. L.; He, G. K.; Song, G. L.; Liu, R.; Liu, Q. CN 104045601, 2014 (in Chinese).
35. [35]
  Vivian, D. L.; Hartwell, J. L.; Watermans, H. C. J. Org. Chem. 1954, 19, 1641. doi: 10.1021/jo01375a013
36. [36]
  Rewcastle, G. W.; Denny, W. A.; Baguley, B. C. J. Med. Chem. 1987, 30, 843. doi: 10.1021/jm00388a017
37. [37]
  Wolfe, J. P.; Buchwald, S. L. J. Org. Chem. 1997, 62, 1264. doi: 10.1021/jo961915s
38. [38]
  Raju, B. C.; Prasad, K. V.; Saidachary, G.; Sridhar, B. Org. Lett. 2014, 16, 420. doi: 10.1021/ol4033122
39. [39]
  Laha, J. K.; Tummalapalli, K. S.; Gupta, A. Org. Lett. 2014, 16, 4392. doi: 10.1021/ol501766m
40. [40]
  Leisinger, T.; Margraff, R. Microbiol. Rev. 1979, 43, 422.
41. [41]
  Budzikiewicz, H. FEMS Microbiol. Lett. 1993, 104, 209. doi: 10.1111/j.1574-6968.1993.tb05868.x
42. [42]
  Brisbane, P. G.; Janik, L. J.; Tate, M. E.; Warren, R. F. Antimicrob. Agents Chemother. 1987, 31, 1967. doi: 10.1128/AAC.31.12.1967
43. [43]
  Jayatilake, G. S.; Thornton, M. P.; Leonard, A. C.; Grimwade, J. E.; Baker, B. J. J. Nat. Prod. 1996, 59, 293. doi: 10.1021/np960095b
44. [44]
  Zhou, L.; Jiang, H. X.; Jin, K. M.; Sun, S.; Zhang, W.; Zhang, X. H.; He, Y. W. Acta Microbiol. Sin. 2015, 55, 401(in Chinese).
45. [45]
  Gong, X. J.; Feng, Z. T.; Zhang, H. Y.; Shen, L. J.; Wang, X. X.; Zhang, J. W. CN 103343150, 2013.
46. [46]
  Sakamoto, S.; Watanabe, T.; Kohda, Y.; Iijima, M.; Sawa, R.; Okada, M.; Kawada, M. J. Antibiot. 2017, 70, 1146. doi: 10.1038/ja.2017.129
47. [47]
  Dasgupta, D.; Kumar, A.; Mukhopadhyay, B.; Sengupta, T. K. Appl. Microbiol. Biotechnol. 2015, 99, 8653. doi: 10.1007/s00253-015-6707-x
48. [48]
  Parsons, J. F.; Calabrese, K.; Eisenstein, E.; Ladner, J. E. Acta Crystallogr., Sect. D:Biol. Crystallogr. 2004, 60, 2110. doi: 10.1107/S0907444904022474
49. [49]
  Messenger, A. J.; Turner, J. M. FEMS Microbiol. Lett. 1983, 18, 65. doi: 10.1111/j.1574-6968.1983.tb00450.x
50. [50]
  Umezawa, H.; Hayano, S.; Maeda, K.; Ogata, Y.; Okami, Y. Jpn. Med. J. 1950, 3, 111. doi: 10.7883/yoken1948.3.111
51. [51]
  Kidani, Y. Chem. Pharm. Bull. 1959, 7, 74. doi: 10.1248/cpb.7.74
52. [52]
  Chatterjee, S.; Vijayakumar, E. K. S.; Franco, C. M. M.; Maurya, R.; Blumbach, J.; Ganguli, B. N. J. Antibiot. 1995, 48, 1353. doi: 10.7164/antibiotics.48.1353
53. [53]
  Krastel, P.; Zeeck, A.; Gebhardt, K.; Fiedler, H. P.; Rheinheimer, J. ChemInform 2003, 34, 794.
54. [54]
  Pusecker, K.; Laatsch, H.; Helmke, E.; Weyland, H. J. Antibiot. 1997, 50, 479. doi: 10.7164/antibiotics.50.479
55. [55]
  Gilpin, M. L.; Fulston, M.; Payne, D.; Cramp, R.; Hood, I. J. Antibiot. 1995, 48, 1081. doi: 10.7164/antibiotics.48.1081
56. [56]
  Gao, X.; Lu, Y.; Xing, Y.; Ma, Y.; Lu, J.; Bao, W.; Wang, Y.; Xi, T. Microbiol. Res. 2012, 167, 616. doi: 10.1016/j.micres.2012.02.008
57. [57]
  Choi, E. J.; Kwon, H. C.; Ham, J.; Yang, H. O. J. Antibiot. 2009, 62, 621. doi: 10.1038/ja.2009.92
58. [58]
  Smitka, T. A.; Bunge, R. H.; Wilton, J. H.; Hokanson, G. C.; French, J. C.; Cun-Heng, H. E.; Clardy, J. J. Antibiot. 1986, 39, 800. doi: 10.7164/antibiotics.39.800
59. [59]
  Hosoya, Y.; Adachi, H.; Nakamura, H.; Nishimura, Y.; Naganawa, H.; Okami, Y.; Takeuchi, T. Tetrahedron Lett. 1996, 37, 9227. doi: 10.1016/S0040-4039(96)02190-9
60. [60]
  Sakthivel, N.; Kumar, R. US 7365194, 2005.
61. [61]
  Tamaoki, T.; Kasai, M.; Shirahata, K.; Tomita, F. J. Antibiot. 1982, 35, 979. doi: 10.7164/antibiotics.35.979
62. [62]
  Abdel-Mageed, W. M.; Milne, B. F.; Wagner, M.; Schumacher, M.; Sandor, P.; Pathom-aree, W.; Goodfellow, M.; Bull, A. T.; Horikoshi, K.; Ebel. R.; Diederich, M.; Fiedler, H.; Jaspars, M. Org. Biomol. Chem. 2010, 8, 2352. doi: 10.1039/c001445a
63. [63]
  Wagner, M.; Abdel-Mageed, W. M.; Ebel, R.; Bull, A. T.; Goodfellow, M.; Fiedler, H. P.; Jaspars, M. J. Nat. Prod. 2014, 77, 416. doi: 10.1021/np400952d
64. [64]
  Abdelfattah, M. S.; Kazufumi, T.; Ishibashi, M. J. Nat. Prod. 2010, 73, 1999. doi: 10.1021/np100400t
65. [65]
  Abdelfattah, M. S.; Toume, K.; Ishibashi, M. Chem. Pharm. Bull. 2011, 59, 508. doi: 10.1248/cpb.59.508
66. [66]
  Liang, Y.; Chen, L.; Ye, X.; Anjum, K.; Lian, X. Y.; Zhang, Z. Nat. Prod. Res. 2017, 31, 411. doi: 10.1080/14786419.2016.1169419
67. [67]
  Gamage, S. A.; Rewcastle, G. W.; Baguley, B. C.; Charlton, P. A.; Denny, W. A. Bioorg. Med. Chem. 2006, 14, 1160. doi: 10.1016/j.bmc.2005.09.032
68. [68]
  Wang, S.; Miller, W.; Milton, J.; Vicker, N.; Stewart, A.; Charlton, P.; Mistry, P.; Hardick, D.; Denny, W. A. Bioorg. Med. Chem. Lett. 2002, 12, 415. doi: 10.1016/S0960-894X(01)00770-3
69. [69]
  De Logu, A.; Palchykovska, L. H.; Kostina, V. H.; Sanna, A.; Meleddu, R.; Chisu, L.; Alexeeva, I. V.; Shved, A. D. Int. J. Antimicrob. Agents 2009, 33, 223. doi: 10.1016/j.ijantimicag.2008.09.016
70. [70]
  Hovorun, D. M.; Deriabin, O. M.; Rybalko, S. L.; Samijlenko, S. P.; Starosyla, D. B.; Platonov, M. O.; Palchykovska, L. G. Biopolym. Cell 2012, 28, 477. doi: 10.7124/bc.00013A
71. [71]
  Gupta, A.; Jaiswal, A.; Prachnad, S. Int. J. Pharm. Life Sci. 2014, 5, 3230.
72. [72]
  Udumula, V.; Endres, J. L.; Harper, C. N.; Jaramillo, L.; Zhong, H. A.; Bayles, K. W.; Conda-Sheridan, M. Eur. J. Med. Chem. 2017, 125, 710. doi: 10.1016/j.ejmech.2016.09.079
73. [73]
  Krishnaiah, M.; de Almeida, N. R.; Udumula, V.; Song, Z.; Chhonker, Y. S.; Abdelmoaty, M. M.; do Nascimento, V. A.; Murry, D. J.; Conda-Sheridan, M. Eur. J. Med. Chem. 2018, 143, 936. doi: 10.1016/j.ejmech.2017.11.026
74. [74]
  Wang, M. Z.; Xu, H.; Yu, S. J.; Feng, Q.; Wang, S. H.; Li, Z. M. J. Agric. Food Chem. 2010, 58, 3651. doi: 10.1021/jf904408c
75. [75]
  Ye, L.; Zhang, H.; Xu, H.; Zou, Q.; Cheng, C.; Dong, D.; Xu, Y.; Li, R. Bioorg. Med. Chem. Lett. 2010, 20, 7369. doi: 10.1016/j.bmcl.2010.10.050
76. [76]
  Puopolo, G.; Masi, M.; Raio, A.; Andolfi, A.; Zoina, A.; Cimmino, A.; Evidente, A. Nat. Prod. Res. 2013, 27, 956. doi: 10.1080/14786419.2012.696257
77. [77]
  Li, B.; Lv, L.; Sun, Q.; Zhu, D. Q.; Li, Z. N.; Wang, G. CN 105418518, 2016.
78. [78]
  Zhang, S.; Chen, H. X.; Du, X. B.; Zhang, Q.; Xu, Y. Q. Acta Agric. Shanghai 2015, 31, 1(in Chinese).
79. [79]
  Niu, J.; Chen, J.; Xu, Z.; Zhu, X.; Wu, Q.; Li, J. Bioorg. Med. Chem. Lett. 2016, 26, 5384. doi: 10.1016/j.bmcl.2016.10.044
80. [80]
  Xiong, Z.; Niu, J.; Liu, H.; Xu, Z.; Li, J.; Wu, Q. Bioorg. Med. Chem. Lett. 2017, 27, 2010. doi: 10.1016/j.bmcl.2017.03.011
81. [81]
  Liu, H.; Yu, L. H.; Xiong, Z. P.; Zhang, M.; Li, J. K.; Xu, Z. H.; Wu, Q. L. Chin. J. Pest. Sci. 2017, 19, 290(in Chinese).
82. [82]
  Qin, C.; Yu, D. Y.; Zhou, X. D.; Zhang, M.; Wu, Q. L.; Li, J. K. J. Asian Nat. Prod. Res. 2018.
83. [83]
  Zhu, X.; Zhang, M.; Yu, L.; Xu, Z.; Yang, D.; Du, X.; Wu, Q.; Li, J. Nat. Prod. Res. 2018, 1.
84. [84]
  Lu, X.; Zhu, X.; Zhang, M.; Wu, Q.; Zhou, X.; Li, J. Nat. Prod. Res. 2018, 1.
85. [85]
  Zhu, X.; Yu, L.; Zhang, M.; Xu, Z.; Yao, Z.; Wu, Q.; Du, X.; Li, J. Chem. Cent. J. 2018, 12, 111. doi: 10.1186/s13065-018-0478-2
86. [86]
  Han, F.; Yan, R.; Zhang, M.; Xiang, Z.; Wu, Q.; Li, J. Nat. Prod. Res. 2019, 1.
87. [87]
  Niu, J.; Nie, D.; Yu, D.; Wu, Q.; Yu, L.; Yao, Z.; Du, X.; Li, J. Pestic. Biochem. Physiol. 2017, 143, 8. doi: 10.1016/j.pestbp.2017.10.004
88. [88]
  Yu, L.; Huang, D.; Zhu, X.; Zhang, M.; Yao, Z.; Wu, Q.; Xu, Z.; Li, J. Molecules 2018, 23, 2139. doi: 10.3390/molecules23092139
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