应用天然产物 ›› 2021, Vol. 11 ›› Issue (4): 365-377.DOI: 10.1007/s13659-021-00298-w
• REVIEWS • 下一篇
Jean-François Goossens1, Laurence Goossens1, Christian Bailly2
收稿日期:
2020-11-10
接受日期:
2021-01-16
出版日期:
2021-08-24
发布日期:
2021-07-30
通讯作者:
Christian Bailly
Jean-François Goossens1, Laurence Goossens1, Christian Bailly2
Received:
2020-11-10
Accepted:
2021-01-16
Online:
2021-08-24
Published:
2021-07-30
Contact:
Christian Bailly
摘要: Biflavonoids are divided in two classes: C-C type compounds represented by the dimeric compound amentoflavone and C-O-C-type compounds typified by hinokiflavone (HNK) with an ether linkage between the two connected apigenin units. This later sub-group of bisflavonyl ethers includes HNK, ochnaflavone, delicaflavone and a few other dimeric compounds, found in a variety of plants, notably Selaginella species. A comprehensive review of the anticancer properties and mechanism of action of HNK is provided, to highlight the anti-proliferative and anti-metastatic activities of HNK and derivatives, and HNK-containing plant extracts. The anticancer effects rely on the capacity of HNK to interfere with the ERK1-2/p38/NFκB signaling pathway and the regulation of the expression of the matrix metalloproteinases MMP-2 and MMP-9 (with a potential direct binding to MMP-9). In addition, HNK was found to function as a potent modulator of pre-mRNA splicing, inhibiting the SUMO-specific protease SENP1. As such, HNK represents a rare SENP1 inhibitor of natural origin and a scaffold to design synthetic compounds. Oral formulations of HNK have been elaborated to enhance its solubility, to facilitate the compound delivery and to enhance its anticancer efficacy. The review shed light on the anticancer potential of C-O-C-type biflavonoids and specifically on the pharmacological profile of HNK. This compound deserves further attention as a regulator of pre-mRNA splicing, useful to treat cancers (in particular hepatocellular carcinoma) and other human pathologies.
Jean-François Goossens, Laurence Goossens, Christian Bailly. Hinokiflavone and Related C-O-C-Type Biflavonoids as Anti-cancer Compounds: Properties and Mechanism of Action[J]. 应用天然产物, 2021, 11(4): 365-377.
Jean-François Goossens, Laurence Goossens, Christian Bailly. Hinokiflavone and Related C-O-C-Type Biflavonoids as Anti-cancer Compounds: Properties and Mechanism of Action[J]. Natural Products and Bioprospecting, 2021, 11(4): 365-377.
1. V.S. Gontijo, M.H. Dos Santos, C. Viegas Jr., Mini Rev. Med. Chem. 17, 834-862 (2017) 2. T. Kariyone, T. Sawada, Yakugaku Zasshi (J. Pharm. Soc. Japan) 78, 1020-1022 (1958) 3. T. Kariyone, Y. Fukui, Yakugaku Zasshi (J. Pharm. Soc. Japan) 80, 746-749 (1958) 4. Y. Fukui, N. Kawano, J. Am. Chem. Soc. 81, 6331 (1959) 5. Y.M. Lin, F.C. Chen, K.H. Lee, Planta Med. 55, 166-168 (1989) 6. J.A. López-Sáez, M.J. Pérez-Alonso, A.V. Negueruela, Z. Naturforsch. 49c, 267-270 (1994) 7. Y. Yuan, B. Wang, L. Chen, H. Luo, D. Fisher, I.A. Sutherland, Y. Wei, J. Chrom. A 1194, 192-198 (2008) 8. O. Kunert, R.C. Swamy, M. Kaiser, A. Presser, S. Buzzi, A.V.N.A. Rao, W. Schühlu, Phytochem. Lett. 1, 171-174 (2008) 9. A.N.B. Singab, I.M. Ayoub, M. El-Shazly, M. Korinek, T.Y. Wu, Y.B. Cheng, F.R. Chang, Y.C. Wu, Indus. Crops Prod. 92, 308-335 (2016) 10. S. Lee, N.J. Park, S.K. Bong, J. Jegal, S.A. Park, S.N. Kim, M.H. Yang, J. Ethnopharmacol. 214, 160-167 (2018) 11. B. Zhuang, Z.M. Bi, Z.Y. Wang, L. Duan, C.J. Lai, E.H. Liu, J. Pharm. Biomed. Anal. 154, 207-215 (2018) 12. K. Nakazawa, Tetrahedron Lett. 8, 5223-5225 (1967) 13. K. Nakazawa, Chem. Pharm. Bull. 16, 2503-2511 (1968) 14. M. Rahman, M. Riaz, U.R. Desai, Chem. Biodiv. 4, 2495-2527 (2007) 15. G. Sagrera, A. Bertucci, A. Vazquez, G. Seoane, Bioorg. Med. Chem. 19, 3060-3073 (2011) 16. Y.M. Lin, H. Anderson, M.T. Flavin, Y.H. Pai, E. Mata-Greenwood, T. Pengsuparp, J.M. Pezzuto, R.F. Schinazi, S.H. Hughes, F.C. Chen, J. Nat. Prod. 60, 884-888 (1997) 17. J. Lee, M. Kim, S.E. Jeong, H.Y. Park, C.O. Jeon, W. Park, J. Hazard. Mater. 384, 121312 (2020) 18. N.A. Konan, N. Lincopan, I.E. Díaz, J.J. de Fátima, M.M. Tiba, J.G. Amarante Mendes, E.M. Bacchi, B. Spira, Exp. Toxicol. Pathol. 64, 435-440 (2012) 19. S. Yu, H. Yan, L. Zhang, M. Shan, P. Chen, A. Ding, S.F. Li, Molecules 22, 299 (2017) 20. M.T. Islam, S.M.N.K. Zihad, M.S. Rahman, N. Sifat, M.R. Khan, S.J. Uddin, R. Rouf, IUBMB Life 71, 1192-1200 (2019) 21. G. Wang, S. Yao, X.X. Zhang, H. Song, Int. J. Anal. Chem. 2015, 849769 (2015) 22. M.S. Abdel-Kader, A.T. Abulhamd, A.M. Hamad, A.H. Alanazi, R. Ali, S.I. Alqasoumi, Saudi Pharm. J. 26, 496-503 (2018) 23. P. Fong, H.H. Tong, K.H. Ng, C.K. Lao, C.I. Chong, C.M. Chao, J. Ethnopharmacol. 175, 470-480 (2015) 24. H.P. Kim, H. Park, K.H. Son, H.W. Chang, S.S. Kang, Arch. Pharm. Res. 31, 265-273 (2008) 25. S.Y. Shim, S.G. Lee, M. Lee, Molecules 23, 926 (2018) 26. A. Thapa, E.R. Woo, E.Y. Chi, M.G. Sharoar, H.G. Jin, S.Y. Shin, I.S. Park, Biochemistry 50, 2445-2455 (2011) 27. A. Thapa, E.Y. Chi, Adv. Exp. Med. Biol. 863, 55-77 (2015) 28. N. Zhao, C. Sun, M. Zheng, S. Liu, R. Shi, Life Sci. 239, 117043 (2019) 29. L. Sun, A.K. Sharma, B.H. Han, L.M. Mirica, ACS Chem. Neurosci. 11, 2741-2752 (2020) 30. M.S. Uddin, M.T. Kabir, D. Tewari, B. Mathew, L. Aleya, Sci. Total Environ. 700, 134836 (2020) 31. N. Sirimangkalakitti, L.D. Juliawaty, E.H. Hakim, I. Waliana, N. Saito, K. Koyama, K. Kinoshita, Bioorg. Med. Chem. Lett. 29, 1994-1997 (2019) 32. Y.M. Lin, E.Z. Zembower, M.T. Flavin, R.M.S. Schure, H.M. Anderson, B.E. Korba, F.C. Chen, Bioorg. Med. Chem. Lett. 7, 2325-2328 (1997) 33. K.C. Chinsembu, Rev. Brasil Farmaco. 29, 504-528 (2019) 34. K. Miki, T. Nagai, T. Nakamura, M. Tuji, K. Koyama, K. Kinoshita, K. Furuhata, H. Yamada, K. Takahoshi, Heterocycles 75, 879-885 (2008) 35. Y.M. Lin, M.T. Flavin, R. Schure, F.C. Chen, R. Sidwell, D.L. Barnard, J.H. Huffman, E.R. Kearn, Planta Med. 65, 120-125 (1999) 36. P. Coulerie, C. Eydoux, E. Hnawia, L. Stuhl, A. Maciuk, N. Lebouvier, B. Canard, B. Figadère, J.C. Guillemot, M. Nour, Planta Med. 78, 672-677 (2012) 37. P. Coulerie, M. Nour, A. Maciuk, C. Eydoux, J.C. Guillemot, N. Lebouvier, E. Hnawia, K. Leblanc, G. Lewin, B. Canard, B. Figadère, Planta Med. 79, 1313-1318 (2013) 38. J.S. Yang, C.W. Lin, Y.S. Hsieh, H.L. Cheng, K.H. Lue, S.F. Yang, K.H. Lu, Food Chem. Toxicol. 59, 801-807 (2013) 39. C.H. Hsin, B.C. Wu, C.Y. Chuang, S.F. Yang, Y.H. Hsieh, H.Y. Ho, H.P. Lin, M.K. Chen, C.W. Lin, Altern. Med. 13, 234 (2013) 40. G.G. Zhang, Y. Jing, H.M. Zhang, E.L. Ma, J. Guan, F.N. Xue, H.X. Liu, X.Y. Sun, Planta Med. 78, 390-392 (2012) 41. I.S. Lee, A. Nishikawa, F. Furukawa, K. Kasahara, S.U. Kim, Cancer Lett. 144, 93-99 (1999) 42. S.H. Ahn, Y.J. Mun, S.W. Lee, S. Kwak, M.K. Choi, S.K. Baik, Y.M. Kim, W.H. Woo, J. Med. Food. 9, 138-144 (2006) 43. S.F. Yang, S.C. Chu, S.J. Liu, Y.C. Chen, Y.Z. Chang, Y.S. Hsieh, J. Ethnopharmacol. 110, 483-489 (2007) 44. Y.J. Jung, E.H. Lee, C.G. Lee, K.J. Rhee, W.S. Jung, Y. Choi, C.H. Pan, K. Kang, J. Ethnopharmacol. 202, 78-84 (2007) 45. C.G. Lee, E.H. Lee, C.H. Pan, K. Kang, K.J. Rhee, Data Brief. 13, 162-165 (2017) 46. H. Huang, J. Hao, K. Pang, Y. Lv, D. Wan, C. Wu, Y. Ma, X. Yang, W.K. Zhang, J. Cell. Mol. Med. 24, 11922-11935 (2020) 47. Y. Cao, N.H. Tan, J.J. Chen, G.Z. Zeng, Y.B. Ma, Y.P. Wu, H. Yan, J. Yang, L.F. Lu, Q. Wang, Fitoterapia 81, 253-258 (2010) 48. J.Z. Wang, J. Li, P. Zhao, W.T. Ma, X.H. Feng, K.L. Chen, Evid. Based Complement. Alternat. Med. 2015, 865714 (2015) 49. L.F. Liu, H.H. Sun, J.B. Tan, Q. Huang, F. Cheng, K.P. Xu, Z.X. Zou, G.S. Tan, Nat. Prod. Res. 34, 1-7 (2019) 50. D. Li, C. Sun, J. Yang, X. Ma, Y. Jiang, S. Qiu, G. Wang, Molecules 24, 2507 (2019) 51. Y. Sui, S. Li, P. Shi, Y. Wu, Y. Li, W. Chen, L. Huang, H. Yao, X. Lin, J. Ethnopharmacol. 190, 261-271 (2016) 52. Y.M. Lin, F.C. Chen, K.H. Lee, Planta Med. 55, 166-168 (1899) 53. J. Zhou, R. Zhao, T. Ye, S. Yang, Y. Li, F. Yang, G. Wang, Y. Xie, Q. Li, J. Gastroenterol. Hepatol. 34, 1571-1580 (2019) 54. S. Yang, Y. Zhang, Y. Luo, B. Xu, Y. Yao, Y. Deng, F. Yang, T. Ye, G. Wang, Z. Cheng, Y. Zheng, Y. Xie, Biomed. Pharmacother. 103, 101-110 (2018) 55. W. Mu, X. Cheng, X. Zhang, Y. Liu, Q. Lv, G. Liu, J. Zhang, X. Li, J. Cell. Mol. Med. 24, 8151-8165 (2020) 56. W. Huang, C. Liu, F. Liu, Z. Liu, G. Lai, J. Yi, Cell. Biochem. Funct. 38, 249-256 (2020) 57. K.C. Lee, W.T. Chen, Y.C. Liu, S.S. Lin, F.T. Hsu, Vivo. 32, 1097-1103 (2018) 58. J.H. Lee, Arch. Pharm. Res. 34, 1209-1217 (2011) 59. C. Guruvayoorappan, G. Kuttan, J. Exp. Ther. Oncol. 6, 285- 295 (2007) 60. S. Napoli, C. Scuderi, G. Gattuso, V.D. Bella, S. Candido, M.S. Basile, M. Libra, L. Falzone, Cells 9, 1151 (2020) 61. G. Gonzalez-Avila, B. Sommer, A.A. García-Hernández, C. Ramos, Adv. Exp. Med. Biol. 1245, 97-131 (2020) 62. H. Huang, Sensors (Basel). 18, 3249 (2018) 63. G.B. Kumar, B.G. Nair, J.J.P. Perry, D.B.C. Martin, Medchemcomm. 10, 2024-2037 (2019) 64. K. Umezawa, Y. Lin, Biochim. Biophys. Acta Proteins Proteom. 1868, 140412 (2020) 65. S.O. Yoon, S. Shin, H.J. Lee, H.K. Chun, A.S. Chung, Mol. Cancer Ther. 5, 2666-2675 (2006) 66. N. Lian, J. Tong, W. Li, J. Wu, Y. Li, Biomed. Pharmacother. 102, 510-516 (2018) 67. W.H. Hu, G.K. Chan, R. Duan, H.Y. Wang, X.P. Kong, T.T. Dong, K.W. Tsim, Cancers (Basel) 11, 1828 (2019) 68. C. Guruvayoorappan, G. Kuttan, Immunopharmacol. Immunotoxicol. 30, 711-727 (2008) 69. Y.J. Lee, J.G. Chung, Y.T. Chien, S.S. Lin, F.T. Hsu, Anticancer Res. 39, 3669-3675 (2019) 70. F.T. Hsu, I.T. Chiang, Y.C. Kuo, T.C. Hsia, C.C. Lin, Y.C. Liu, J.G. Chung, Am. J. Chin. Med. 47, 913-931 (2019) 71. S.J. Suh, U.H. Jin, S.H. Kim, H.W. Chang, J.K. Son, S.H. Lee, K.H. Son, C.H. Kim, J. Cell. Biochem. 99, 1298-1307 (2006) 72. C.M. Lin, Y.L. Lin, S.Y. Ho, P.R. Chen, Y.H. Tsai, C.H. Chung, C.H. Hwang, N.M. Tsai, S.C. Tzou, C.Y. Ke, J. Chang, Y.L. Chan, Y.S. Wang, K.H. Chi, K.W. Liao, Oncotarget 8, 60046-60059 (2016) 73. U. Lewandowska, K. Szewczyk, K. Owczarek, Z. Hrabec, A. Podsędek, D. Sosnowska, E. Hrabec, Nutr. Cancer 65, 1219-1231 (2013) 74. J. Cao, Q. Lu, N. Liu, Y.X. Zhang, J. Wang, M. Zhang, H.B. Wang, W.C. Sun, Int. Immunopharmacol. 49, 109-117 (2017) 75. S. Kalva, E.R. Azhagiya Singam, V. Rajapandian, L.M. Saleena, V. Subramanian, J. Mol. Graph. Model. 49, 25-37 (2014) 76. Q. Gao, Y. Wang, J. Hou, Q. Yao, J. Zhang, J. Comput. Aided Mol. Des. 31, 625-641 (2017) 77. J. Hou, Q. Zou, Y. Wang, Q. Gao, W. Yao, Q. Yao, J. Zhang, J. Biomol. Struct. Dyn. 37, 3135-3149 (2019) 78. C.G. Wang, W.N. Yao, B. Zhang, J. Hua, D. Liang, H.S. Wang, Bioorg. Med. Chem. Lett. 28, 2413-2417 (2018) 79. J. Mercado-Camargo, L. Cervantes-Ceballos, R. Vivas-Reyes, A. Pedretti, M.L. Serrano-García, H. Gómez-Estrada, ACS Omega 5, 14741-14749 (2020) 80. P. Chymkowitch, P.A. Nguéa, J.M. Enserink, BioEssays 37, 1095-1105 (2015) 81. Y. Jia, L.A. Claessens, A.C.O. Vertegaal, H. Ovaa, ACS Chem. Biol. 14, 2389-2395 (2019) 82. S. Chen, D. Dong, W. Xin, H. Zhou, Curr. Issues Mol. Biol. 35, 17-34 (2020) 83. Z. Wang, Y. Liu, J. Zhang, S. Ullah, N. Kang, Y. Zhao, H. Zhou, Eur. J. Med. Chem. 204, 112553 (2020) 84. Y.S. Kim, S.G. Keyser, J.S. Schneekloth Jr., Bioorg. Med. Chem. Lett. 24, 1094-1097 (2014) 85. M. Lorente, A. García-Casas, N. Salvador, A. Martínez-López, E. Gabicagogeascoa, G. Velasco, L. López-Palomar, S. CastilloLluva, J. Cell. Sci. 132, 234120 (2019) 86. P. Zhou, X. Chen, M. Li, J. Tan, Y. Zhang, W. Yuan, J. Zhou, G. Wang, Biochem. Biophys. Res. Commun. 513, 1063-1069 (2019) 87. A. Rabellino, K.K. Khanna, Crit. Rev. Biochem. Mol. Biol. 55, 54-70 (2020) 88. M.L. Tomasi, K. Ramani, Transl. Gastroenterol. Hepatol. 3, 20 (2018) 89. A. Pawellek, U. Ryder, T. Tammsalu, L.J. King, H. Kreinin, T. Ly, R.T. Hay, R.C. Hartley, A.I. Lamond, Elife 6, 27402 (2017) 90. J. Liu, X. Tao, J. Zhang, P. Wang, M. Sha, Y. Ma, X. Geng, L. Feng, Y. Shen, Y. Yu, S. Wang, S. Fang, Y. Shen, Oncotarget 7, 22206-22218 (2016) 91. W. Zhang, H. Sun, X. Shi, H. Wang, C. Cui, F. Xiao, C. Wu, X. Guo, L. Wang, Tumour Biol. 37, 7741-7748 (2016) 92. D. Arango, K. Morohashi, A. Yilmaz, K. Kuramochi, A. Parihar, B. Brahimaj, E. Grotewold, A.I. Doseff, Proc. Natl. Acad. Sci. USA 110, 2153-2162 (2013) 93. M. Chiba, H. Ariga, H. Maita, Chem. Biol. Drug Des. 87, 275-282 (2016) 94. M. Kurata, N. Fujiwara, K.I. Fujita, Y. Yamanaka, S. Seno, H. Kobayashi, Y. Miyamae, N. Takahashi, Y. Shibuya, S. Masuda, iScience 22, 336-352 (2019) 95. K. O'Brien, A.J. Matlin, A.M. Lowell, M.J. Moore, J. Biol. Chem. 283, 33147-33154 (2008) 96. K.I. Fujita, T. Ishizuka, M. Mitsukawa, M. Kurata, S. Masuda, Int. J. Mol. Sci. 21, 2026 (2020) 97. E.J. Vanzyl, K.R.C. Rick, A.B. Blackmore, E.M. MacFarlane, B.C. McKay, PLoS ONE 13, e0191178 (2018) 98. M. Sivaramakrishnan, K.D. McCarthy, S. Campagne, S. Huber, S. Meier, A. Augustin, T. Heckel, H. Meistermann, M.N. Hug, P. Birrer, A. Moursy, S. Khawaja, R. Schmucki, N. Berntenis, N. Giroud, S. Golling, M. Tzouros, B. Banfai, G. Duran-Pacheco, J. Lamerz, Y. Hsiu Liu, T. Luebbers, H. Ratni, M. Ebeling, A. Cléry, S. Paushkin, A.R. Krainer, F.H. Allain, F. Metzger, Nat. Commun. 8, 1476 (2017) 99. J. Tsalikis, M. Abdel-Nour, A. Farahvash, M.T. Sorbara, S. Poon, D.J. Philpott, S.E. Girardin, Mol. Cell. Biol. 39, e00489-e518 (2019) 100. S.A. Boswell, A. Snavely, H.M. Landry, L.S. Churchman, J.M. Gray, M. Springer, Nat. Chem. Biol. 13, 501-507 (2017) 101. J. Yongmei, L. Xiaofei, L. Xinmin, L. Qinmei, W. Gang, Y. Jiaqiang, Chinese Patent CN108553476A (publication date:2018-09-21). 102. L. Dan, L. Xiaofei, L. Xinmin, W. Gang, X. Wen, Y. Jiaqiang, Chinese Patent CN108299366A (publication date:2018-07-20). 103. K. Xu, C. Yang, Y. Xu, D. Li, S. Bao, Z. Zou, F. Kang, G. Tan, S.M. Li, X. Yu, Org. Biomol. Chem. 18, 28-31 (2020) 104. I.M. Ayoub, M. Korinek, T.L. Hwang, B.H. Chen, F.R. Chang, M. El-Shazly, A.N.B. Singab, J. Nat. Prod. 81, 243-253 (2018) 105. M.J. Son, T.C. Moon, E.K. Lee, K.H. Son, H.P. Kim, S.S. Kang, J.K. Son, S.H. Lee, H.W. Chang, Arch. Pharm. Res. 29, 282-286 (2006) 106. T.C. Moon, H.S. Hwang, Z. Quan, K.H. Son, C.H. Kim, H.P. Kim, S.S. Kang, J.K. Son, H.W. Chang, Biol. Pharm. Bull. 29, 2359-2361 (2006) 107. S.J. Lee, J.H. Choi, K.H. Son, H.W. Chang, S.S. Kang, H.P. Kim, Life Sci. 57, 551-558 (1995) 108. Y. Sui, H. Yao, S. Li, L. Jin, P. Shi, Z. Li, G. Wang, S. Lin, Y. Wu, Y. Li, L. Huang, Q. Liu, X. Lin, J. Mol. Med. (Berl). 95, 311-322 (2017) 109. W. Yao, Z. Lin, G. Wang, S. Li, B. Chen, Y. Sui, J. Huang, Q. Liu, P. Shi, X. Lin, Q. Liu, H. Yao, Phytomedicine 62, 152973 (2019) 110. W. Yao, Z. Lin, P. Shi, B. Chen, G. Wang, J. Huang, Y. Sui, Q. Liu, S. Li, X. Lin, Q. Liu, H. Yao, Biochem. Pharmacol. 171, 113680 (2020) 111. W.K. Sim, J.H. Park, K.Y. Kim, I.S. Chung, Sci. Rep. 10, 11070 (2020) 112. H. Wan, L. Ge, J. Li, K. Zhang, W. Wu, S. Peng, X. Zou, H. Zhou, B. Zhou, X. Zeng, Phytomedicine 57, 282-291 (2019) 113. A. Al Groshi, H.A. Jasim, A.R. Evans, F.M.D. Ismail, N.M. Dempster, L. Nahar, S.D. Sarker, Phytother. Res. 33, 2075-2082 (2019) 114. E. Al-Sayed, H.A. Gad, M. El-Shazly, M.M. Abdel-Daim, S.A. Nasser, Drug Dev. Res. 79, 22-28 (2018) 115. Y. Chen, X. Feng, L. Li, X. Zhang, K. Song, X. Diao, Y. Sun, L. Zhang, J. Pharm. Biomed. Anal. 169, 19-29 (2019) 116. R. Yin, K. Xiong, S. Wen, Y. Wang, F. Xu, Biomed. Chromatogr. 31, 3821 (2017) 117. Y. Chen, X. Feng, L. Li, K. Song, L. Zhang, Drug Deliv. 27, 565-574 (2020) 118. B. Chen, X. Wang, D. Lin, D. Xu, S. Li, J. Huang, S. Weng, Z. Lin, Y. Zheng, H. Yao, X. Lin, Int. J. Nanomedicine. 14, 6691-6706 (2019) 119. B. Chen, X. Wang, Y. Zhang, K. Huang, H. Liu, D. Xu, S. Li, Q. Liu, J. Huang, H. Yao, X. Lin, Drug Deliv. 27, 309-322 (2020) 120. H. Miura, N. Kawano, A.C. Waiss Jr., Chem Pharm Bull. (Tokyo) 14, 1408-1413 (1966) 121. H. Miura, Yakugaku Zasshi (J. Pharm. Soc. Japan 87, 871-874 (1967) 122. J. Lee, Y. Choi, E.R. Woo, D.G. Lee, J. Microbiol. Biotechnol. 19, 204-207 (2009) 123. J. Lee, Y. Choi, E.R. Woo, D.G. Lee, Biochem. Biophys. Res. Commun. 379, 676-680 (2009) 124. C. Shivanika, D.S. Kuma, V. Ragunathan, P. Tiwari, A. Sumitha, B.P. Devi, J. Biomol. Struct. Dyn. (2020). https://doi.org/10.1080/07391102.2020.1815584 125. V.K. Singh, D. Arora, M.I. Ansari, P.K. Sharma, Phytother. Res. 33, 3064-3089 (2019) 126. K.M. Chauhan, Y. Chen, Y. Chen, A.T. Liu, X.X. Sun, M.S. Dai, J. Cell. Biochem. 122, 189-197 (2021) 127. K. Liu, J. Zhang, H. Wang, J. Clin. Lab. Anal. 32, e22611 (2018) 128. D.M. Bouchard, M.J. Matunis, J. Gastrointest. Oncol. 10, 821-830 (2019) 129. Y. Tao, R. Li, C. Shen, J. Li, Q. Zhang, Z. Ma, F. Wang, Z. Wang, Aging (Albany NY) 12, 1563-1576 (2020) 130. Y. Chen, D. Wen, Z. Huang, M. Huang, Y. Luo, B. Liu, H. Lu, Y. Wu, Y. Peng, J. Zhang, Bioorg. Med. Chem. Lett. 22, 6867-6870 (2012) 131. Y. Zhao, Z. Wang, J. Zhang, H. Zhou, Eur. J. Med. Chem. 122, 178-184 (2016) 132. U. Lindenmann, M. Brand, F. Gall, D. Frasson, L. Hunziker, I. Kroslakova, M. Sievers, R. Riedl, ChemMedChem 15, 675-679 (2020) 133. J. Wu, H. Lei, J. Zhang, X. Chen, C. Tang, W. Wang, H. Xu, W. Xiao, W. Gu, Y. Wu, Oncotarget. 7, 58995-59005 (2016) 134. W. Huang, T. He, C. Chai, Y. Yang, Y. Zheng, P. Zhou, X. Qiao, B. Zhang, Z. Liu, J. Wang, C. Shi, L. Lei, K. Gao, H. Li, S. Zhong, L. Yao, M.E. Huang, M. Lei, PLoS ONE 7, e37693 (2012) 135. N.D. Ambaye, Acta. Crystallogr. F Struct. Biol. Commun. 75, 332-339 (2019) |
[1] | Haoqi Dong, Xinni Yang, Peiying Wang, Weiya Huang, Liang Zhang, Song Song, Jiangxin Liu. Identification and verification of methylenetetrahydrofolate dehydrogenase 1-like protein as the binding target of natural product pseudolaric acid A[J]. 应用天然产物, 2025, 15(3): 21-21. |
[2] | Hesham R. El-Seedi, Mohamed S. Refaey, Nizar Elias, Mohamed F. El-Mallah, Faisal M. K. Albaqami, Ismail Dergaa, Ming Du, Mohamed F. Salem, Haroon Elrasheid Tahir, Maria Dagliaa, Nermeen Yosri, Hongcheng Zhang, Awg H. El-Seedi, Zhiming Guo, Shaden A. M. Khalifa. Marine natural products as a source of novel anticancer drugs: an updated review (2019-2023)[J]. 应用天然产物, 2025, 15(2): 13-13. |
[3] | Xiaoxia Gu, Xiaotian Zhang, Xueke Zhang, Xinyu Wang, Weiguang Sun, Yonghui Zhang, Zhengxi Hu. Unveiling the mechanism of action of a novel natural dual inhibitor of SARS-CoV-2 Mpro and PLpro with molecular dynamics simulations[J]. 应用天然产物, 2025, 15(1): 3-3. |
[4] | María I. Osella, Mario O. Salazar, Carlos M. Solís, Ricardo L. E. Furlan. New semisynthetic α-glucosidase inhibitor from a doubly-chemically engineered extract[J]. 应用天然产物, 2025, 15(1): 4-4. |
[5] | Ahmed H. Elbanna, Xinhui Kou, Dilip V. Prajapati, Surasree Rakshit, Rebecca A. Butcher. Discovery of a parallel family of euglenatide analogs in Euglena gracilis[J]. 应用天然产物, 2025, 15(1): 10-10. |
[6] | Song-Yu Hou, Bing-Chao Yan, Han-Dong Sun, Pema-Tenzin Puno. Recent advances in the application of [2+2] cycloaddition in the chemical synthesis of cyclobutane-containing natural products[J]. 应用天然产物, 2024, 14(5): 37-37. |
[7] | Felaine Anne Sumang, Alan Ward, Jeff Errington, Yousef Dashti. Hibiscus acid and hydroxycitric acid dimethyl esters from Hibiscus flowers induce production of dithiolopyrrolone antibiotics by Streptomyces Strain MBN2-2[J]. 应用天然产物, 2024, 14(5): 40-40. |
[8] | Chunsong Hu. Marine natural products and human immunity: novel biomedical resources for anti-infection of SARS-CoV-2 and related cardiovascular disease[J]. 应用天然产物, 2024, 14(2): 2-2. |
[9] | Shohreh Ariaeenejad, Javad Gharechahi, Mehdi Foroozandeh Shahraki, Fereshteh Fallah Atanaki, Jian-Lin Han, Xue-Zhi Ding, Falk Hildebrand, Mohammad Bahram, Kaveh Kavousi, Ghasem Hosseini Salekdeh. Precision enzyme discovery through targeted mining of metagenomic data[J]. 应用天然产物, 2024, 14(1): 7-7. |
[10] | Daniel W. Armstrong, Alain Berthod. Occurrence of D-amino acids in natural products[J]. 应用天然产物, 2023, 13(6): 47-47. |
[11] | Soumitra Sahana, Anupam Gautam, Rajveer Singh, Shivani Chandel. A recent update on development, synthesis methods, properties and application of natural products derived carbon dots[J]. 应用天然产物, 2023, 13(6): 51-51. |
[12] | Xinxin Li, Runlu Shi, Lingchen Yan, Weiwei Chu, Ruishuang Sun, Binkai Zheng, Shuai Wang, Hui Tan, Xusheng Wang, Ying Gao. Natural product rhynchophylline prevents stress-induced hair graying by preserving melanocyte stem cells via the β2 adrenergic pathway suppression[J]. 应用天然产物, 2023, 13(6): 54-54. |
[13] | Dalila Carbone, Carmela Gallo, Genoveffa Nuzzo, Giusi Barra, Mario Dell'Isola, Mario Affuso, Olimpia Follero, Federica Albiani, Clementina Sansone, Emiliano Manzo, Giuliana d'Ippolito, Angelo Fontana. Marine natural product lepadin A as a novel inducer of immunogenic cell death via CD91-dependent pathway[J]. 应用天然产物, 2023, 13(5): 34-34. |
[14] | Phanankosi Moyo, Luke Invernizzi, Sephora M. Mianda, Wiehan Rudolph, Warren A. Andayi, Mingxun Wang, Neil R. Crouch, Vinesh J. Maharaj. Leveraging off higher plant phylogenetic insights for antiplasmodial drug discovery[J]. 应用天然产物, 2023, 13(5): 35-35. |
[15] | Phanankosi Moyo, Luke Invernizzi, Sephora M. Mianda, Wiehan Rudolph, Andrew W. Andayi, Mingxun Wang, Neil R. Crouch, Vinesh J. Maharaj. Prioritised identification of structural classes of natural products from higher plants in the expedition of antimalarial drug discovery[J]. 应用天然产物, 2023, 13(5): 37-37. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||