应用天然产物 ›› 2021, Vol. 11 ›› Issue (6): 611-628.DOI: 10.1007/s13659-021-00317-w
Oyere Tanyi Ebob1, Smith B. Babiaka1, Fidele Ntie-Kang1,2
收稿日期:
2021-07-30
出版日期:
2021-12-24
发布日期:
2021-12-10
通讯作者:
Fidele Ntie-Kang, Oyere Tanyi Ebob, Smith B. Babiaka
Oyere Tanyi Ebob1, Smith B. Babiaka1, Fidele Ntie-Kang1,2
Received:
2021-07-30
Online:
2021-12-24
Published:
2021-12-10
Contact:
Fidele Ntie-Kang, Oyere Tanyi Ebob, Smith B. Babiaka
摘要: For the past 2 years, the coronavirus responsible for the COVID-19 infection has become a world pandemic, ruining the lives and economies of several nations in the world. This has scaled up research on the virus and the resulting infection with the goal of developing new vaccines and therapies. Natural products are known to be a rich source of lead compounds for drug discovery, including against infectious diseases caused by microbes (viruses, bacteria and fungi). In this review article, we conducted a literature survey aimed at identifying natural products with inhibitory concentrations against the coronaviruses or their target proteins, which lie below 10 μM. This led to the identification of 42 compounds belonging to the alkaloid, flavonoid, terpenoid, phenolic, xanthone and saponin classes. The cut off concentration of 10 μM was to limit the study to the most potent chemical entities, which could be developed into therapies against the viral infection to make a contribution towards limiting the spread of the disease.
Oyere Tanyi Ebob, Smith B. Babiaka, Fidele Ntie-Kang. Natural Products as Potential Lead Compounds for Drug Discovery Against SARS-CoV-2[J]. 应用天然产物, 2021, 11(6): 611-628.
Oyere Tanyi Ebob, Smith B. Babiaka, Fidele Ntie-Kang. Natural Products as Potential Lead Compounds for Drug Discovery Against SARS-CoV-2[J]. Natural Products and Bioprospecting, 2021, 11(6): 611-628.
1. T. Elmer, K. Mepham, C. Stadtfeld, PLoS ONE 15, e0236337 (2020) 2. F.A. Bahkir, S.S. Grandee, Indian J. Ophthalmol. 68, 2378–2383 (2020) 3. R. Kirwan, D. McCullough, T. Butler, F. Perez de Heredia, I.G. Davies, C. Stewart, Geroscience. 42, 1547–1578 (2020) 4. M.F. Akkoç, S. Bülbüloğlu, M. Özdemir, Int. Wound J. 18, 367– 374 (2021) 5. WHO, Coronavirus disease (COVID-19) pandemic, situation reports? (2021). https://www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports. Accessed 12 May 2021 6. R. Lu, X. Zhao, J. Li, P. Niu, B. Yang, H. Wu, W. Wang, H. Song, B. Huang, N. Zhu, Y. Bi, X. Ma, F. Zhan, L. Wang, T. Hu, H. Zhou, Z. Hu, W. Zhou, L. Zhao, J. Chen, Y. Meng, J. Wang, Y. Lin, J. Yuan, Z. Xie, J. Ma, W.J. Liu, D. Wang, W. Xu, E.C. Holmes, G.F. Gao, G. Wu, W. Chen, W. Shi, W. Tan, Lancet 395, 565–574 (2020) 7. Z. Wu, J.M. McGoogan, JAMA 323, 1239–1242 (2020) 8. A. Wu, Y. Peng, B. Huang, X. Ding, X. Wang, P. Niu, J. Meng, Z. Zhu, Z. Zhang, J. Wang, J. Sheng, L. Quan, Z. Xia, W. Tan, G. Cheng, T. Jiang, Cell Host Microbe. 27, 325–328 (2020) 9. G. Lu, Q. Wang, G.F. Gao, Trends Microbiol. 23, 468–478 (2015) 10. C.A. Devaux, J.-M. Rolain, P. Colson, D. Raoult, Int. J. Antimicrob. Agents 55, 105938 (2020) 11. H. Lu, Biosci. Trends. 14, 69–71 (2020) 12. J. Stebbing, A. Phelan, I. Griffin, C. Tucker, O. Oechsle, D. Smith, P. Richardson, Lancet Infect. Dis. 20, 400–402 (2020) 13. J.S. Mani, J.B. Johnson, J.C. Steel, D.A. Broszczak, P.M. Neilsen, K.B. Walsh, M. Naiker, Virus Res. 284, 197989 (2020) 14. Y. Yang, S. Islam, J. Wan, Y. Li, X. Chen, Int. J. Biol. Sci. 16, 1708–1717 (2020) 15. S. Wan, Y. Xiang, W. Fang, Y. Zheng, B. Li, Y. Hu, C. Lang, D. Huang, Q. Sun, Y. Xiong, X. Huang, J. Lv, Y. Luo, L. Shen, H. Yang, G. Huang, R. Yang, J. Med. Virol. 95, 9 (2020) 16. D.J. Newman, G.M. Cragg, J. Nat. Prod. 83, 770–803 (2020) 17. I.E. Orhan, F.S.S. Deniz, Nat. Prod. Bioprospect. 10, 171–186 (2020) 18. R.R. Narkhede, A.V. Pise, R.S. Cheke, S.D. Shinde, Nat. Prod. Bioprospect. 10, 297–306 (2020) 19. A.F. Attah, A.A. Fagbemi, O. Olubiyi, H. Dada-Adegbola, A. Oluwadotun, A. Elujoba, C.P. Babalola, Front. Pharmacol. 12, 596855 (2021) 20. S. Ahmad, S. Zahiruddin, B. Parveen, P. Basist, A. Parveen, R. Parveen, M. Ahmad, Front. Pharmacol. 11, 578970 (2020) 21. B. Adhikari, B.P. Marasini, B. Rayamajhee, B.R. Bhattarai, G. Lamichhane, K. Khadayat, A. Adhikari, S. Khanal, N. Parajuli, Phytother. Res. 35, 1298–1312 (2021) 22. H.Y. Kim, H.S. Shin, H. Park, Y.C. Kim, Y.G. Yun, S. Park, H.J. Shin, K. Kim, J. Clin. Virol. 41, 122–128 (2008) 23. D.E. Kim, J.S. Min, M.S. Jang, J.Y. Lee, Y.S. Shin, J.H. Song, H.R. Kim, S. Kim, Y.H. Jin, S. Kwon, Biomolecules 9, 6920086 (2019) 24. Y.C. Tsai, C.L. Lee, H.R. Yen, Y.S. Chang, Y.P. Lin, S.H. Huang, C.W. Lin, Biomolecules 10, 8947 (2020) 25. J.Y. Park, H.J. Jeong, J.H. Kim, Y.M. Kim, S.J. Park, D. Kim, K.H. Park, W.S. Lee, Y.B. Ryu, Biol. Pharm. Bull. 35, 2036– 2042 (2012) 26. J.K. Cho, B.Y. Ryu, M.J. Curtis-Long, H.W. Ryu, H.J. Yuk, D.W. Kim, H.J. Kim, W.S. Lee, K.H. Park, Bioorg. Med. Chem. 20, 2595 (2012) 27. H.W. Ryu, Y.J. Park, S.U. Lee, S. Lee, H.J. Yuk, K.H. Seo, Y.U. Kim, B.Y. Hwang, S.Y. Oh, J. Nat. Prod. 80, 2659–2665 (2017) 28. H. Parhiz, A. Roohbakhsh, F. Soltani, R. Rezaee, M. Iranshahi, Phytother. Res. 29, 323–331 (2014) 29. M.S. Yu, J. Lee, J.M. Lee, Y. Kim, Y.W. Chin, J.G. Jee, Y.S. Keum, Y.J. Jeong, Med. Chem. Lett. 22, 4049–4054 (2012) 30. J.Y. Park, H.J. Yuk, H.W. Ryu, S.H. Lim, K.S. Kim, K.H. Park, Y.B. Ryu, W.S. Lee, J. Enzym. Inhib. Med. Chem. 32, 504–512 (2017) 31. J.Y. Park, J.A. Ko, D.W. Kim, Y.M. Kim, H.J. Kwon, H.J. Jeong, C.Y. Kim, K.H. Park, W.S. Lee, Y.B. Ryu, J. Enzym. Inhib. Med. Chem. 31, 23–30 (2016) 32. J. Du, Z.D. He, R.W. Jiang, W.C. Ye, H.X. Xu, P.P.H. But, Phytochemistry 62, 1235–1238 (2003) 33. Y. Pei, Y.F. Xiang, J.N. Chen, C.H. Luc, J. Hao, Q. Du, CQu. Chi-C Lai, S. Li, H.Q. Ju, Z. Ren, Q.Y. Liu, S. Xiong, C.W. Qian, F.L. Zeng, P.Z. Zhang, C.R. Yang, Y.J. Zhang, J. Xu, K. Kitazato, Y.F. Wang, Antivir. Res. 89, 98–108 (2011) 34. L. Yi, Z. Li, K. Yuan, X. Qu, J. Chen, G. Wang, H. Zhang, H. Luo, L. Zhu, P. Jiang, L. Chen, Y. Shen, M. Luo, G. Zuo, J. Hu, D. Duan, Y. Nie, X. Shi, W. Wang, Y. Han, T. Li, Y. Liu, M. Ding, H. Deng, X. Xu, J. Virol. 78, 11334–11339 (2004) 35. C.Y. Wu, J.T. Jan, S.H. Ma, C.J. Kuo, H.F. Juan, Y.S. Cheng, H.H. Hsu, H.C. Huang, D. Wu, A. Brik, F.S. Liang, R.S. Liu, J.M. Fang, S.T. Chen, P.H. Liang, C.H. Wong, Proc. Natl. Acad. Sci. USA 101, 10012–10017 (2004) 36. J.Y. Park, J.H. Kim, Y.M. Kim, H.J. Jeong, D.W. Kim, K.H. Park, H.J. Kwon, S.J. Park, W.S. Lee, Y.B. Ryu, Bioorg. Med. Chem. 20, 5928–5935 (2012) 37. J.L. Yang, T.K.Q. Ha, B. Dhodary, E. Pyo, N.H. Nguyen, H. Cho, E. Kim, W.K. Oh, J. Med. Chem. 58, 1268–1280 (2015) 38. Y.B. Ryu, S.J. Park, Y.M. Kim, J.Y. Lee, W.D. Seo, J.S. Chang, K.H. Park, M.C. Rho, W.S. Lee, Bioorg. Med. Chem. Lett. 20, 1873–1876 (2010) 39. B.Q.J. Wang, Med. Plant. Res. 4, 2813 (2010) 40. H. Najaran, H.H. Bafrani, H.H. Rashtbari, F. Izadpanah, M.R. Rajabi, H.H. Kashani, A. Mohammadi, Orient. Pharm. Exp. Med. 19, 157–165 (2019) 41. L. Peng, S. Kang, Z. Yin, R. Jla, X. Song, Z. Li, Y. Zou, X. Liang, L. Li, C. He, G. Ye, L. Yin, F. Shi, L. Ch, B. Jing, Int. J. Clin. Exp. Pathol. 8, 5217–5223 (2015) 42. Y.C. Shen, L.T. Wang, A.T. Khalil, L.C. Chiang, P.W. Cheng, Chem. Pharm. Bull. 53, 244–247 (2005) 43. J.T. Wang, J.G. Peng, J.Q. Zhang, Z.X. Wang, Y. Zhang, X.R. Zhou, J. Miao, L. Tang, Bioorg. Med. Chem. Lett. 29, 126709 (2019) 44. Y. Ma, L. Liang, Y.B. Zhang, B.F. Wag, Y.G. Bai, M.J. Xie, Z.W. Wang, J. Mol. Endocrinol. 59, 191–204 (2017) 45. R. Dimitrovic, H. Jakovac, G. Blagojevic, Toxicology 280, 33–43 (2011) 46. S. Song, M. Quin, Y. Chu, D. Chen, A. Su, Z. Wu, Antimicrob. Agents Chemother. 58, 5068–5078 (2014) 47. K. Zou, Z. Li, Y. Zhang, H. Zhang, B. Li, W. Zhu, J. Shi, Q. Jia, Y. Li, Acta Pharmacol. Sin. 38, 157–166 (2017) 48. W. Liu, X. Zhang, P. Lin, X. Shen, T. Lan, W. Li, Q. Ijang, X. Xie, H. Huang, Eur J Pharmacol. 638, 150–155 (2010) 49. S. Suryavanshi, Y.A. Kulkarni, Front. Pharmacol. 8, 798 (2017) 50. A. Warowicka, R. Nawrot, A. Goździcka-Józefiak, Arch. Virol. 165, 1935–1945 (2020) 51. N. Bhagya, K.R. Chandrashekar, Phytochemistry 125, 5–13 (2016) 52. Y. Zhang, D. Qi, Y. Gao, C. Liang, Y. Zhang, Z. Ma, Y. Liu, H. Peng, Y. Zhang, H. Qin, X. Song, X. Sun, Y. Li, Z. Liu, J. Ethnopharmacol. 260, 112995 (2020) 53. Y. Sakurai, A.A. Kolokoltsov, C.C. Chen, M.W. Tidwell, W.E. Bauta, N. Klugbauer, C. Grimm, C.W. Schott, M. Biel, R.A. Davey, Science 347, 995–998 (2015) 54. M. Baba, M. Okamoto, N. Kashiwaba, M. Ono, Antivir. Chem. Chemother. 12, 307–312 (2001) 55. X. Liu, Y. Wang, M. Zhang, G. Li, Y. Cen, Zhong Yao Cai 2004(27), 107–110 (2004) 56. Z. Wan, Y. Lu, Q. Liao, Y. Wu, X. Chen, PLoS ONE 7, e39225 (2012) 57. C.L. Lee, C.M. Wang, H.C. Hu, H.R. Yen, Y.C. Song, S.J. Yu, C.J. Chen, W.C. Li, Y.C. Wu, Phytochemistry 162, 39–46 (2019) 58. B.C. Liau, T.T. Jong, M.R. Lee, S.S. Chen, J. Pharm. Biomed. Anal. 43, 346–351 (2007) 59. W. Lin, W. Huang, S. Ning, X. Wang, Q. Ye, D. Wei, PLoS ONE 13, 0199788 (2018) 60. H. Chen, J. Shao, H. Zhang, M. Jiang, L. Huang, Z. Zhang, D. Yang, M. He, M. Ronaghi, X. Luo, B. Sun, W. Wu, C. Liu, Front. Plant. Sci. 9, 324 (2018) 61. W. Gu, Y. Zhang, X.J. Hao, F.M. Yang, Q.Y. Sun, S.L. MorrisNatschke, K.H. Lee, Y.H. Wang, C.L. Long, J. Nat. Prod. 77, 2590–2604 (2014) 62. M. Tripathi, M.B. Pandey, R.N. Jha, V.B. Pandey, P.N. Tripathi, J.P. Singh, Fitoterapia 75, 507–510 (2001) 63. R. Tschesche, I. Khokhar, H. Wilhelm, G. Eckhardt, Phytochemistry 15, 541–542 (1976) 64. P. Panseeta, K. Lomchoey, S. Prabpai, P. Kongsaeree, A. Suksamrarn, S. Ruchirawat, S. Suksamrarn, Phytochemistry 72, 909–915 (2011) 65. G.M. Keserü, M. Nógrádi, Nat. Prod. Chem. 17, 357–394 (1995) 66. T. Akihisa, Y. Taguchi, K. Yasukawa, H. Tokuda, H. Akazawa, T. Suzuki, Y. Kimura, Chem. Pharm. Bull. 54, 735–739 (2006) 67. T. Nagano, Y. Oyama, N. Kajita, L. Chikahisa, M. Nakata, E. Okazaki, T. Masuda, Jpn. J. Pharmacol. 75, 363–370 (1997) 68. H.B. Lee, H.K. Lee, J.R. Kim, Y.J. Ahn, J. Korean Soc. Appl. Biol. Chem. 52, 367–370 (2009) 69. W. Hu, M.H. Wang, Biotechnol. Bioprocess Eng. 16, 120–126 (2011) 70. Y.C. Lai, C.K. Chai, W.W. Lin, S.S. Lee, Phytochemistry 73, 84–94 (2012) 71. W.S. Lee, J.R. Kim, K.R. Im, K.H. Cho, D.E. Sok, T.S. Jeong, Planta Med. 71, 295–299 (2005) 72. N.H. Tung, H.J. Kwon, J.H. Kim, J.C. Ra, Y. Ding, J.A. Kim, Y.H. Kim, Bioorg. Med. Chem. Lett. 20, 1000–1003 (2010) 73. N. Adhikari, S. Baidya, A. Saha, T. Jha, Structural insight into the viral 3C-like protease inhibitors: comparative SAR/QSAR approaches, in Viral proteases and their inhibitors. ed. by S. Gupta (Academic Press, Cambridge, 2017), pp. 317–409 74. B.A.C. Rattis, S.G. Ramos, M.R.N. Celes, Front. Pharmacol. 12, 675287 (2021) 75. T. He, B.N. Vaidya, Z.D. Perry, P. Parajuli, N. Joshee, Eur. J. Med. Plants. 14, 1–15 (2016) 76. A. Navratilova, K. Schneiderova, D. Vesela, Z. Hanakova, A. Fontana, S. Dall’Acqua, J. Cvacka, G. Innocenti, J. Novotna, M. Urbanova, J. Pelletier, A. Cízek, H. Zemlickova, K. Smejkal, Phytochemistry 89, 104–113 (2013) 77. C.H. Chiang, C.Y. Yeh, J.G. Chung, I.T. Chiang, F.T. Hsu, Anticancer Res. 39, 3641–3649 (2019) 78. B.H. Chen, Y.C. Li, Y.H. Zhao, M.H. Fu, Med. Res. 18, 357– 359 (2007) 79. H.K. An, K.S. Kim, J.W. Lee, M.H. Park, H.I. Moon, S.J. Park, J.S. Baik, C.H. Kim, Y.C. Lee, PLoS ONE 9, 114607 (2014) 80. T. Asai, N. Hara, S. Kobayashi, Y. Fujimoto, Phytochemistry 69, 1234–1241 (2008) 81. Y.S. Kil, S.T. Pham, E.K. Seo, M. Jafari, Arch. Pharm. Res. 40, 655–675 (2017) 82. Y. Kimura, K. Baba, Int. J. Cancer. 106, 429–437 (2003) 83. Y.B. Ryu, H.J. Jeong, J.H. Kim, Y.M. Kim, J.Y. Park, D. Kim, T.T.H. Naguyen, S.J. Park, J.S. Chang, K.H. Park, M.C. Rho, W.S. Lee, Bioorg. Med. Chem. 18, 7940–7947 (2010) 84. N. Zhao, C. Sun, M. Zheng, S. Liu, R. Shi, Life Sci. 239, 117043 (2019) 85. S.C. Ma, P.P. But, V.E. Ooi, Y.H. He, S.H. Lee, S.F. Lee, R.C. Lin, Biol. Pharm. Bull. 24, 311–312 (2001) 86. W.P. Lee, K.L. Lan, S.X. Liao, Y.H. Huang, M.C. Hou, K.H. Lan, AJCM 46, 835–852 (2018) 87. D. Fritz, C.R. Venturi, S. Cargnin, J. Schripsema, P.M. Roehe, J.A. Montanha, G.L. von Poser, J. Ethnopharmacol. 113, 517– 520 (2007) 88. Y.M. Lin, M.T. Flavin, R. Schure, F.C. Chen, R. Sidwell, D.L. Barnard, J. Huffman, E.R. Kern, Planta Med. 65, 120–125 (1999) 89. S. Bhargava, T. Patel, R. Gaikwad, U.K. Patil, S. Gayen, Nat. Prod. Res. 33, 851–857 (2019) 90. A.G. Perkin, J.J. Hummel, J. Chem. Soc. Trans. 69, 1287–1294 (1896) 91. K.C. Ong, H.E. Khoo, Gen. Pharmacol. 29, 121–126 (1997) 92. Q. Zhao, X.Y. Chen, C. Martin, Sci. Bull. 61, 1391–1398 (2016) 93. D.A.V. Anand, R. Arulmoli, S. Parasuraman, Pharmacogn. Rev. 10, 84–89 (2016) 94. M. Endale, S.C. Park, S. Kim, S.H. Kim, Y. Yang, J.Y. Cho, M.H. Rhee, Immunobiology 218, 1452–1467 (2013) 95. K.M. Lee, M.K. Hwang, D.E. Lee, K.W. Lee, H.J. Lee, J. Agric. Food Chem. 58, 5815–5820 (2010) 96. H.P. Kim, I. Mani, L. Iversen, V.A. Ziboh, Prostaglandins Leukot. Essent. Fat. Acids. 58, 17–24 (1998) 97. J. Mlcek, T. Jurikova, S. Skrovankova, J. Sochor, Molecules 21, 623 (2016) 98. G. Bureau, F. Longpre, M.G. Martinoli, J. Neurosci. Res. 86, 403–410 (2008) 99. W. Krol, Z. Czuba, S. Scheller, J. Gabrys, S. Grabiec, J. Shani, Biochem. Int. 21, 593–597 (1990) 100. R.L. Edwards, T. Lyon, S.E. Litwin, A. Rabovsky, J.D. Symons, T. Jalili, J. Nutr. 137, 2405–2411 (2007) 101. F. Javadi, S. Eghtesadi, A. Ahmadzadeh, N. Aryaeian, M. Zabihiyeganeh, A.R. Foroushani, S. Jazayeri, Int. J. Prev. Med. 5, 293– 301 (2014) 102. A. Garg, S. Garg, L.J. Zaneveld, A.K. Singla, Phytother. Res. 15, 655–669 (2001) 103. C.W. Lin, F.J. Tsai, C.H. Tsai, C.C. Lai, L. Wan, T.Y. Ho, C.C. Hsieh, P.D.L. Chao, Antivir. Res. 68, 36–42 (2005) 104. W. Ngwa, R. Kumar, D. Thompson, W. Lyerly, R. Moore, T.E. Reid, H. Lowe, N. Toyang, Molecules 25, 25112707 (2020) 105. K.H. Son, S.J. Kwon, H.W. Chang, H.P. Kim, S.S. Kang, Fitoterapia 72, 456–458 (2001) 106. S.Y. Kim, J.H. Kim, S.K. Kim, M.J. Oh, M.Y.J. Jung, Am. Oil Chem. Soc. 71, 633–640 (1994) 107. Y.S. Kim, K.H. Park, Kor. J. Pharmacogn. 25, 388–394 (1994) 108. J. Sun, S. Liu, C. Zhang, L. Yu, J. Bi, F. Zhu, Q. Yang, PLoS ONE 7, 32021 (2012) 109. D. Lee, K.P. Bhat, H.H. Fong, N.R. Farnsworth, J.M. Pezzuto, A.D. Kinghorn, J. Nat. Prod. 64, 1286–1293 (2001) 110. V. Kumar, S. Chauhan, J. Med. Plant. Res. 2, 271–278 (2008) 111. P. Mena, E.M.S. Salcedo, M. Tassoti, J.J. Martínez, F. Hernández, D.D. Rio, Food Res. Int. 89, 1116–1122 (2016) 112. E.M.S. Salcedo, A. Amorós, F. Hernández, J.J. Martínez, J. Food Nutr. Res. 5, 253–261 (2017) 113. N. Desideri, C. Conti, P. Mastromarino, F. Mastropaolo, Antivir. Chem. Chemother. 11, 373–381 (2000) 114. M. Maryam, K.K. Te, F.C. Wong, T.T. Chai, G.K.K. Low, S.C. Gan, H.Y. Chee, J. Integr. Agric. 19, 1085–1096 (2020) 115. D.J. McGarvey, R. Croteau, Plant Cell 7, 1015–1026 (1995) 116. K.W. Wahle, I. Brown, D. Rotondo, S.D. Heys, Adv. Exp. Med. Biol. 698, 36–51 (2010) 117. N. Kumar, S. Gupta, T.C. Yadav, V. Pruthi, P.K. Varadwaj, N. Goel, J. Biomol. Struct. Dyn. 37, 2355–2369 (2019) 118. A. Bhattacharya, P. Sood, V. Citovsky, Mol. Plant Pathol. 11, 705– 719 (2010) 119. R. Chirinos, I.B. Pallardel, A. Huamán, C. Arbizu, R. Pedreschi, D. Campos, Food Chem. 113, 1243–1251 (2009) 120. Y.J. Zhang, T. Abe, T. Tanaka, C.R. Yang, I. Kouno, J. Nat. Prod. 64, 1527–1532 (2001) 121. T. Zhao, Q. Sun, M. Marques, M. Witcher, Oxid. Med. Cell Longev. 2015, 950890 (2015) 122. W. Li, X. Zhang, R. Chen, Y. Li, J. Miao, G. Liu, Y. Lan, Y. Chen, Y. Cao, J. Ethnopharmacol. 254, 112740 (2019) 123. B.J. Taiwo, T.D. Popoola, F.R. van Heerden, A.A. Fatokun, BMC Complement. Med. Ther. 20, 287 (2020) 124. N. Sharma, P. Kumar, R. Giri, J. Biomol. Struct. Dyn. 24, 1–13 (2020) 125. S.J. Lee, H.K. Lee, M.K. Jung, W. Mar, Biol. Pharm. Bull. 29, 2131–2134 (2006) 126. S.J. Yeo, Y.J. Yun, M.A. Lyu, S.Y. Woo, E.R. Woo, S.J. Kim, H.J. Lee, H.K. Park, Y.H. Kook, Arch. Virol. 147, 229–242 (2002) 127. S.G. Sparg, M.E. Light, J. van Staden, J Ethnopharmacol. 94, 219–243 (2004) 128. M.J. Just, M.C. Recio, R.M. Giner, M.J. Cuéllar, S. Máñez, A.R. Bilia, J.L. Ríos, Planta Med. 64, 404–407 (1998) 129. E. Bombardelli, P. Morazzoni, A. Griffini, Fitoterapia 67, 483–511 (1996) 130. R. Chauhan, K. Ruby, J. Dwivedi, Int. J. Drug Dev. Res. 4, 50–68 (2012) 131. C.R. Sirtori, Pharmacol. Res. 44, 183–193 (2001) 132. R.W. Frick, Angiology 51, 197–205 (2000) 133. G. Bazzoni, E. Dejana, A.D. Maschio, Haematologica 76, 491–499 (1991) 134. W. Xin, L. Zhang, F. Sun, N. Jiang, H. Fan, T. Wang, Z. Li, J. He, F. Fu, Phytomedicine 18, 272–277 (2011) 135. M. Montopoli, G. Froldi, M.C. Comelli, M. Prosdocimi, L. Caparrotta, Planta Med. 73, 285–288 (2007) 136. V. Prakash, Asian J. Pharm. Clin. Res. 10, 68–76 (2017) 137. A.G. Guimarães, J.S. Quintans, L.J. Quintans, Phytother. Res. 27, 1–15 (2013) 138. A.C. Guimarães, L.M. Meireles, M.F. Lemos, M.C.C. Guimarães, D.C. Endringer, M. Fronza, R. Scherer, Molecules 24, 2471 (2019) 139. A. Astani, J. Reichling, P. Schnitzler, Phytother. Res. 24, 673–679 (2010) 140. L. Zhou, Z. Zuo, M.S.S. Chow, J. Clin. Pharmacol. 45, 1345 (2005) 141. S. Gao, L. Li, L. Li, J. Ni, R. Guo, J. Mao, G. Fan, J. Mol. Cell. Cardiol. 137, 59–70 (2019) 142. S. Nakamura, T. Moriura, S. Park, K. Fujimoto, T. Matsumoto, T. Ohta, H. Matsuda, H. Yoshikawa, J. Nat. Prod. 75, 1425–1430 (2012) 143. H.R.W. Dharmaratne, W.M.N.M. Wijesinghe, V. Thevanasem, J. Ethnopharmacol. 66, 339–342 (1999) 144. K.S. Masters, S. Bräse, Chem. Rev. 112, 3717–3776 (2012) 145. L.M.M. Vieira, A. Kijjoa, Curr. Med. Chem. 12, 2413–2446 (2005) 146. A. Shagufta, I. Ahmad, Eur. J. Med. Chem. 116, 267–280 (2016) 147. S. Jindarat, J. Med. Assoc. Thail. 97, S196–S201 (2014) 148. M. Riscoe, J.X. Kelly, R. Winter, Curr. Med. Chem. 12, 2539–2549 (2005) 149. K.A. Shirey, Q.M. Nhu, K.C. Yim, Z.J. Roberts, J.R. Teijaro, D.L. Farber, J.C. Blanco, S.N. Vogel, J. Leukoc. Biol. 89, 351–357 (2011) 150. M. Iinuma, H. Tosa, T. Tanaka, F. Asai, Y. Kobayashi, R. Shimano, K.I. Miyauchi, J. Pharm. Pharmacol. 48, 861–865 (1996) 151. R.R. Chilpa, M.J. Estrada, E.E. Muniz, J. Chem. Ecol. 23, 1901– 1911 (1997) 152. M.J. Gonzalez, M.S.J. Nascimento, H.M. Cidade, M.M.M. Pinto, A. Kijjoa, C. Anantachoke, A.M.S. Silva, W. Herz, Planta Med. 65, 368–371 (1999) 153. C. Ito, M. Itoigawa, Y. Mishina, V.C. Filho, T. Mukainaka, H. Tokuda, H. Nishino, H. Furukawa, J. Nat. Prod. 65, 267–272 (2002) 154. H.R. Dharmaratne, G.T. Tan, G.P. Marasinghe, J.M. Pezzuto, Planta Med. 68, 86–87 (2002) 155. D.E. Gordon, J. Hiatt, M. Bouhaddou, V.V. Rezelj, S. Ulferts, H. Braberg, A.S. Jureka, K. Obernier, J.Z. Guo, J. Batra, R.M. Kaake, A.R. Weckstein, T.W. Owens, M. Gupta, S. Pourmal, E.W. Titus, M. Cakir, M. Soucheray, M. McGregor, Z. Cakir et al., Science 370, eabe9403 (2020) 156. S.T. Ngo, N.Q.A. Pham, L.T. Le, D.H. Pham, V.V. Vu, J. Chem. Inf. Model. 60, 5771–5780 (2020) 157. C.A. Geng, Y.B. Ma, X.M. Zhang, S.Y. Yao, J. Agric. Food Chem. 60, 8197–8202 (2012) 158. C. Li, Z. Li, Y. Zou, O. Wicht, F.J.M. van Kuppeveld, P.J.M. Rottier, B.J. Bosch, PLoS ONE 8, 69997 (2013) 159. S. Tamaru, K. Ohmachi, Y. Miyata, T. Tanaka, T. Kubayasi, Y. Nagata, K. Tanaka, J. Agric. Food Chem. 61, 5817–5823 (2013) 160. N.T.P. Thao, T.M. Hung, M.K. Lee, J.C. Kim, B.S. Min, K.H. Bae, Chem. Pharm. Bull. 58, 121–124 (2010) 161. J.S. Ma, A.R. Brach, Q.R. Liu, Edinb. J. Bot. 56, 33 (1999) 162. D.H. Kim, E.K. Shin, Y.H. Kim, B.W. Lee, J.G. Jun, J.H.Y. Park, J.K. Kim, Eur. J. Clin. Investig. 39, 819 (2009) 163. J.Y. Byun, M.J. Kim, D.Y. Eum, C.H. Yoon, W.D. Seo, K.H. Park, J.W. Hyun, Y.S. Lee, J.S. Lee, M.Y. Yoon, S.J. Lee, Mol. Pharm. 76, 734 (2009) 164. B. Hui, Y. Wu, H. Wang, X. Tian, Zhongguo Taolixue Tongbao 19, 656 (2003) 165. D. Liu, X. Memg, D. Wu, Z. Qiu, H.A. Luo, Front. Pharmacol. 10, 9 (2019) |
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