Biological Characterization of the Chemical Structures of Naturally Occurring Substances with Cytotoxicity

  • Published : 2006.12.30

Abstract

Screening for the cytotoxicity from plant origin is the first stage for anti-cancer drug development. A variety of terpenoids with exomethylene, epoxide, allyl, $\alpha,\beta-unsaturated$ carbonyl, acetylenes, and $\alpha-methylene-\gamma-lactone$ induces apoptosis and/or differentiation as well as cytotoxicity through the ROS signal transduction pathways. These are found among monoterpenes, sesquiterpenes, triterpenes, flavonoids, coumarins, diarylheptanoids, and even organosulfuric compounds. The most essential characteristics of natural cytotoxic substances is to possess the strong electrophilicity that is susceptible to nucleophilic biomolecules in the cell. Thiol-reductants and superoxide dismutase can block or delay apoptosis. Thus, ROS and the resulting cellular redox-potential changes can be parts of the signal transduction pathway during apoptosis. Disturbance of the balance of oxireduction by the pigment of natural quinones also caused the induction of the differentiation and apoptosis. Saponins with the cytotoxicity are restricted to their monodesmosides, rather than to bisdesmosides. Those saponins exhibited calcium ion-mediated apoptosis in addition to cytotoxicity whereas they showed also differentiation without extracellular calcium ion. The properties on cytotoxicity, apoptosis, and differentiation were assumed to depend on resultant oxidative stress to the cells. In this review, we describe a spectrum of cytotoxic compounds with various action mechanisms.

Keywords

References

  1. Andreasen, M.F., Landbo, A.K., Christensen, L.P., and Hansen, A.A, Antioxidant effects of phenolic rye cereale extracts, monoeric hydroxycinnamates, and ferulic dehydrodimers on human low-density lipoproteins. J. Agric. Food. Chem., 49, 4090-4096 (2001) https://doi.org/10.1021/jf0101758
  2. Ankli, A., Heimann, J., Heinrich, M., and Sticher, O., Cytotoxic cardenolides and antibacterial terpenoids from Crossopetalum gaumeri. Phytochemistry, 54, 531-537 (2000) https://doi.org/10.1016/S0031-9422(00)00144-8
  3. Ahn, K.S., Kim, J.H., Kwon, O.K., Park, S.H., Oh, S.R., and Lee, H.K., Triterpenes and oleanolic acid glycosides isolated from Tiarella polyphylla with apoptotic activities on HL-60 clone15 cells. The 31th Annual Meeting of the Korean Society of Pharmacognosy, 52-52 (2000)
  4. Azizan, A. and Blevins, R.D., Mutagenicity testing of six chemicals associated with the pungent properties of specific sp. revealed by the Ames Salmonella/microsomal assay. Arch. Environ. Contam. Toxicol., 28, 248-258 (1995)
  5. Bae, E.A., Han, M.J., Lee, K.T., Choi, J.W., Park, H.J., and Kim, D.H., Metabolism of 6'-xylosyltectoridin and tectoridin by human intestinal bacteria and their hypoglycemic and in vitro cytotoxic activities. Biol. Pharm. Bull., 22, 1314-1318 (1999) https://doi.org/10.1248/bpb.22.1314
  6. Bae, E.A., Han, M.J., Lee, K.T., Choi, J.W., Park, H.J., and Kim, D.H., Metabolism of 6'-xylosyltectoridin and tectoridin by human intestinal bacteria and their hypoglycemic and in vitro cytotoxic activities. Biol. Pharm. Bull., 22, 1314-1318 (1999) https://doi.org/10.1248/bpb.22.1314
  7. Bang, K.H., Mode of Action and Structure-Activity Relationship of Antifungal Trans-Cinnamaldehyde. Thesis for Doctor Degree. Chungnam University, 2000
  8. Bang, K.H., Lee, D.W., Park, H.M., and Rhee, Y.H., Inhibition of Fungal Cell Wall Synthesizing enzymes by trans-cinnamaldehyde, Bioscience of Biotechnology and Biochemistry, 64, 1061-1063 (2000) https://doi.org/10.1271/bbb.64.1061
  9. Bergan, R.C., Waggle, D.H., Carter, S.K., Horak, I., and Slichenmyer, W.M., Tyrosine kinase inhibitors and signal transduction modulators: Rationale, current status as chemopreventive agents for prostate cancer. Urology, 57, 77-80 (2001) https://doi.org/10.1016/S0090-4295(00)00946-8
  10. Bloor. S., Cytotoxic saponins from newzealand from nyrsine species. J. Nat. Prod., 57, 1354-1360 (1994) https://doi.org/10.1021/np50112a004
  11. Chen, Y.J., Shiao, M.S., and Wang, S.Y., The Antioxidant Caffeic acid Phenethyl Ester Induces Apoptosis asociated with Selective Scavenging of Hydroperoxide in Human Leukemic HL-60 Cells. Anticancer Drugs, 12, 143-149 (2001) https://doi.org/10.1097/00001813-200102000-00008
  12. Choi, J.H., Seo, B.L., Park, H.J., Lee, J.Y, Lee, Y.S., Park, H.J., Kwon, S.H., and Lee, K.T., Exomethylene group of costunolide induces intracellular thiol depletion and is essential for apoptosis, The Spring Convention of The pharmaceutical society of Korea, PC1-10 (2001)
  13. Choi, J.S., Park, K.Y., Moon, S.H., Rhee, S.H., and Young, H.S., Antimutagenic effect of plant flavonoids in the salmonella assay system. Arch. Pharm. Res., 17, 71-75 (1994) https://doi.org/10.1007/BF02974226
  14. Choi, J.W., Huh, K., Kim, S.H., Lee, K.T., Park, H.J., and Han, Y.N., antinociceptive and anti-rheumatoidal effects of knlopanax pictus extract and its saponin components in experimental animals. J. Ethnopharmcol., 94, 199-204 (2002)
  15. Choi, J.W., Lee, K.T., Ka, H., Jung, W.T., Jung H.J., and Park, H.J., Constituents of the Essential Oil of the Cinnamomum cassia Stem Bark and the Biological Properties, Arch. Pharm. Res., 24, 418-423 (2001) https://doi.org/10.1007/BF02975187
  16. Choi, J.W., Huh, K., Kim, S.H., Lee, K.T., Kwon, S.H., and Park, H.J., Toxicology of Kalopanax pictus extract and hematological effect of the isolated anti-rheumatoidal kalopanaxsaponin a on the freunds complete adjuvant reagent-treated Rat. Arch. Pharm. Res., 24, 119-125 (2001) https://doi.org/10.1007/BF02976479
  17. Cui, B., Lee, Y.H., Chai, H., Tucker, J., and Fairchild, C., Cytotoxic Sesquiterpenoids from Columnifera. J. Nat. Prod., 62, 1545-1550 (1999) https://doi.org/10.1021/np990260y
  18. Delmas, F., Giorgio, C., Elias, R., Gasquet, M., Azas, N., Mshvildadze, V., Dekanosidze, G., Kemertelidze, E., and Tino-David, P., Antileishmanial activity of three saponins isolated from ${\alpha}$-hederin, ${\beta}$-hederin and hederacolchiside a compared to their action on mammalian cells culture vitro. Planta Med., 66, 343-347 (2000) https://doi.org/10.1055/s-2000-8541
  19. Delaey, E.M., Kamuhabwa, A.R., Vandenbogaerde, A.L., and de Witte, P.A., Photocytotoxicity of protohypericin after photoconversion to hypericin. Planta Med., 65, 719-722 (1999) https://doi.org/10.1055/s-1999-14050
  20. Fiorio, R. and Bronzetti, A., Effects of cinnamaldehyde on suvival and formatin HGPRT-mutants in V79 cells treated with methyl methanesulfonate, N-nitroso-N-metylurea, ethyl methanesulfonate and UV Light. Mutation Research, 324, 51-57 (1994) https://doi.org/10.1016/0165-7992(94)90067-1
  21. Fujita, T., Takeda, Y., Han, D.S., Minami, Y., Marunaka, T., Takeda, S., Yamada, Y., and Togo, T., Cytotoxic and antitumor activities of rabdosia diterpenoids. Planta Med., 54, 414-417 (1988) https://doi.org/10.1055/s-2006-962485
  22. Habtemariam. S., Flavonoids as inhibitors or enhancers of the Cytotoxicity of tumor necrosis factor-${\alpha}$ in L-929 tumor cells. J. Nat. Prod., 60, 775-778 (1997) https://doi.org/10.1021/np960581z
  23. Han D.S., Saengyakhak, Dongmyungsa, Seoul, pp. 402-410, 1992
  24. Hayashi, T., Nakano, T., Kozuka, M., McPhail, d., Mcphail, a., and Lee, K.H., Antitumor agents. 190. absolute stereochemistry of the cytotoxic germacranolides, tomenphantins a and b, from elephantopus tomentosus. J. Nat. Prod., 62, 302-304 (1999) https://doi.org/10.1021/np980185b
  25. Herbert, J.M., Mafferand, J.P., Taoubi, K., Augereau, J.M., Fouraste, I., and Gleye, J., Verbascoside isolated from lantana camara, an inhibitor of protein kinase C. J. Nat. Prod., 54, 1595-1600 (1991) https://doi.org/10.1021/np50078a016
  26. Hikino, H., Tohkin, M., Kiso, Y., Namiki, T., Nishimura, S., and Takeyama, K., Antihepatotoxic actions of Allium sativum bulbs. Planta Med., 51, 163-168 (1986)
  27. Hou, R.S., Duh, C.Y., Wang, S.K., and Chang, T.T., Cytotoxic flavonoid, from the leaves of melicope triphyla. Phtychemistry, 35, 271-272 (1994)
  28. Hsu, M.J., Cheng, J.S., and Huang, H.C., Effect of sakosaponin, a triterpene saponin, on apoptosis in lymphocytes: association with C-myc, p53 and Bcl-2 Mrna. Br. J. Pharmacol., 131, 1285-1293 (2000) https://doi.org/10.1038/sj.bjp.0703559
  29. Hyun, J.W., Shin, J.E., Lim, K.W., Sung, M.S., Park, J.W., Yu, J.H., Kim., B.K., Park, W.H., Kang, S.S., and Park, J.K., Evomonoside: the Cytotoxic xardiac glycoside from lepidium apetalum. Planta Med., 61, 294-195 (1995) https://doi.org/10.1055/s-2006-958084
  30. Iszard, M.B., Liu, J., and Klaasen C.D., Effect of several metallothionein inducers on oxidative stree defense mechanisms in rats. Toxicology, 15, 25-33 (1995)
  31. Ka, H., Choi, J.H., Park, H.J., Han, H.N., and Lee, K.T., Induction of Apoptosis in HL-60 Cells by Cinnamaldehyde Isolated from the Stem Bark of Cinnamomum cassia through Depletion of Intracellular Glutathione. The spring convention of the pharmaceutical society of Korea, PC1-6, 2001
  32. Kang, T.H., Jeong, S.J., Ko, W.G., Kim, N.Y., Lee, B.H., Inagaki, M., Miyamoto, T., Higuchi, R., and Kim, Y.C., Cytotoxic lavadulyl flavanones from sophora flavescens. J. Nat. Prod., 63, 680-681 (2000) https://doi.org/10.1021/np990567x
  33. Kim, D.H., Yu, K.W., Bae, E.A., Park, H.J., and Choi, J.W., Metabolism of kaopanaxsaponin B and H by human intestinal bacteria and antidiabetic activity of their metabolites. Biol. Pharm. Bull., 21, 360-365 (1998) https://doi.org/10.1248/bpb.21.360
  34. Kim, J.I., Park, J.H., Park, H.J., Choi, S.K., and Lee, K.T., Induction of differentiation of the human histocytic lymphoma cell line U-937 by hypericin. Arch. Pharm. Res., 21, 41-45 (1998) https://doi.org/10.1007/BF03216751
  35. Kim, J.L., Kim H.J., Park, H.J., and Lee, K.T., Mechanism of costunolide-induced differentiation in U937. Bull. K. H. Pharm., 25, 71-74 (1997)
  36. Kim, Y.K., Park, S.J., Ha, J.H., Choi, J.W., Park, H.J., and Lee, K.T., In vitro antiinflammatory activity of kalopanaxsaponin A isolated from Kalopanax pictus in murine macrophage RAW 264.7 cells. Biol. Pharm. Bull., 25, 472-476 (2002) https://doi.org/10.1248/bpb.25.472
  37. Kim, S.H., Ahn, B.Z., and Ryu, S.Y., Antitumor effects of ursolic acid isolated from oldenlandia diffusa. Phtytherapy Res., 12, 553-556 (1998) https://doi.org/10.1002/(SICI)1099-1573(199812)12:8<553::AID-PTR359>3.0.CO;2-W
  38. Kim, Y.K. and Ryu, S.Y., Cytotoxic components from stem bark of magnolia obovafa. Planta Med., 65, 291-292 (1999) https://doi.org/10.1055/s-2006-960784
  39. Kim, Y.K., Yoon, S.K., and Ryu, S.Y., Cytotoxic triterpenes from stem bark of physocarpus intermedius. Planta Med., 66, 485-486 (2000) https://doi.org/10.1055/s-2000-8585
  40. Ko, H.H., Yen, M.H., Wu, R.R., Won, S.J., and Lin, C.N., Cytototoxic isoprenylated flavans of Broussonetia kazinoki. J. Nat. Prod., 62, 164-166 (1999) https://doi.org/10.1021/np980281c
  41. Kumi-Diaka, J. and Butler, A., Caspase-3 protease activation during the process of genistein-induced apoptosis in TM4 testicular cells. Biol. Cell, 92, 115-124 (2000) https://doi.org/10.1016/S0248-4900(00)89019-X
  42. Kuo, Y.H., Lin, C.H., Hwang, S.Y., Shen, Y.C., Lee, Y.L., and Li, S.Y., A Novel cytotoxic c-methylated biflavone from the stem bark of Cephalotaxus wilsoniana. Chem. Pharm. Bull., 48, 440-441 (2000) https://doi.org/10.1248/cpb.48.440
  43. Kwon, B.M., Lee, S.H., Choi, S.U., Park, S.H., Lee, C.O., Cho, Y.K., Sung, N.D., and Bok, S.H., Synthesis and in vitro cytotoxicity of cinnamaldehyde to human solid tumor cells. Arch. Pharm. Res., 21, 147-153 (1998) https://doi.org/10.1007/BF02974019
  44. Lee, C.W., Hong, D.H., Han, S.B., Park, S.Y., Kim, H.K., and Kwon, B.M., Inhibition of Human Tumor Cell Growth by 2'-hydroxy-and 2'-bezoyloxycinnamaldehyde, Planta Med., 65, 263-266 (1999) https://doi.org/10.1055/s-2006-960772
  45. Lawson, L.D., Wang, Z.J., and Hughes, B.G., ${\gamma}$-Glutamyl-S-alkylcysteines in garlic and other allium spp.: Precursors of age-dependent trans-1-propenylthiosulfinates. J. Nat. Prod., 54, 436-444 (1991) https://doi.org/10.1021/np50074a014
  46. Lee H.J., Lee, K.T., Park, H.J., Chi, S.G., and Park, J.H., Costunolide induces mitochodrial cytochrome c release through ROS generation. The spring convention of the pharmeceutical society of Korea, PC1-4 (2001)
  47. Lee, H.K., Oh. S.R., and Lim. J.I., Agastaquinone, a new cytotoxic diterpenoid quinone from Agastache rugosa. J. Nat. Prod. 58, 1718-1721 (1995) https://doi.org/10.1021/np50125a011
  48. Lee, J.W., Lee, B., and Kim, N.D., Synthesis of 2-(allylthio)pyrazines as a novel cancer chemopreventive agent. Arch. Pharm. Res., 24, 16-20 (2001) https://doi.org/10.1007/BF02976487
  49. Lee, K.T., Choi, J.H., Kim, D.H., Son, K.H., Kim, W.B., Kwon, S.H., and Park, H.J., Constituents and the antitumor principle of Allium victorialis var. platyphyllum. Arch. Pharm. Res., 24, 44-50 (2001) https://doi.org/10.1007/BF02976492
  50. Lee, K.T., Kim, J.I., Rho, Y.S., Chang, S.G., Jung, J.C., Park, J.H., and Miyamoto, K., Hypericin induces both differentiation and apoptosis in human promyelocytic leukemia HL-60 cells. Biol. Pharm. Bull., 22, 1271-1274 (1999) https://doi.org/10.1248/bpb.22.1271
  51. Lee, K.T., Koo, S.J., Jeong, S.H., Kwon, S.H., and Park, H.J., Structures of three new terpenoids, spiciformisins a and b, and monocyclosqualene, isolated from the herbs of Ligularia fischeri var. spiciformis and cytotoxicity, The Spring Convention of Korea, PD2-19 (2001)
  52. Lee, K.T., Sohn, I.C., Kim, Y.K., Choi, J.H., Choi, J.W., Park, H.J., and Miyamoto, K., Tectorigenin, an isoflavone of pueraria thunbergiana, induces differentiation and apoptosis on human promyelocytic leukemia cells. Biol. Pharm. Bull., 24, 1117-1121 (2001) https://doi.org/10.1248/bpb.24.1117
  53. Lee, K.T., Sohn I.C., Kong, E.A., Kim, D.H., Choi, S.K., Choi, J.W., and Park, H.J., Antioxidative and cytoprotective effects of isoflavones isolated from Pueraria thunbergiana flowers. Yakhak Hoeji, 43, 736-742 (1999)
  54. Lee, K.T., Sohn, I.C., Kim, D.H., Choi, J.W., Kwon, S.H., and Park, H.J., Hypoglycemic and hypolipidemic effects of tectorigenin and kaikasaponin in the streptozotocin-induced diabetic rat and their antioxidant activity in vitro, Arch. Pharm. Res., 23, 461-466 (2000) https://doi.org/10.1007/BF02976573
  55. Lee, K.T., Sohn, I.C., Park, H.J., Kim, D.W., Jung, G.O., and Park, K.Y., Essential moiety for antimutagenic and cytotoxic activity of hederagenin monodesmosides isolated from the stem bark of Kalopanax pictus, Planta Med., 66, 329-332 (2000) https://doi.org/10.1055/s-2000-8539
  56. Lee, M.W., Kim, J.H., Jeong, D.W., Ahn, K.H., Toh, S.H., and Surh, Y.J., Inhibition of cyclooxigenase-2 expression by diarylheptanoids from the bark of Alnus hirsuta var sibirica. Biol. Pharm. Bull., 23, 517-518 (2000) https://doi.org/10.1248/bpb.23.517
  57. Lee, M.W., Kim, N.Y., Park. M.S., Ahn, K.H., Toh, S.H., Hahn, D.R., Kim, Y.C., and Chung, H.T., Diarylahepatnoids with in vitro inducible nitric oxide activity from Alnus hirsuta. Planta Med., 66, 551-553 (2000) https://doi.org/10.1055/s-2000-8606
  58. Lee, S.K., Luyengy, L., Gerhauser, C., Mar, W., Lee, K., Mehta, R.G., Kinghorn, D., and Pezzuto J.M., Inhibitory effect of muneone, an isoflavonoid, on 12-O-tetradecanoylphorbol 13-acetate-induced ornithine decarboxylase Activity. Cancer Letters, 136, 59-65 (1999) https://doi.org/10.1016/S0304-3835(98)00309-7
  59. Lee, S.K., Song, L., Mata-Greenwood, E., Kelloff, G.J., Steele V., and Pezzuto, J.M., Modulation of in vitro biomarkers of the carcinogenic process by chemopreventive agents. Anticancer res., 19, 35-44 (1999)
  60. Lee S.Y., Chemistry of Organic Natural Products, Younglimsa, Seoul, 1995, pp. 97-98
  61. Lim, Y.J., Kim, J.S., Im, K.S., Jung, J.H., Lee, C.O., Hong, J., and Kim, D.K., New cytotoxic polyacetylenes from the marine sponge petrosia. J. Nat. Prod., 62, 1215-1217 (1999) https://doi.org/10.1021/np9900371
  62. Lim, Y.J., Park, H.S., Im, K.S., Hong, J.K., Lee, M.Y., Kim, D.K., and Jung, J.H., Additional cytotoxic polyacetylenes from the marinesponge petrosia species. J. Nat. Prod., 64, 46-53 (2001) https://doi.org/10.1021/np000252d
  63. Lin, L.C., Kuo, Y.C., and Chou, C.J., Cytotoxic biflavonoids from selaginella delicatula. J. Nat. Prod., 63, 627-630 (2000) https://doi.org/10.1021/np990538m
  64. Lin, Y.H., Chen, F.C., and Lee, K.H., Hinokiflavone, A Cytotoxic principle from Rhus succedanea and the cytotoxicity of the related biflavonoids. Planta Med., 55, 166-168 (1989) https://doi.org/10.1055/s-2006-961914
  65. Matsuura, H., Ushiroguchi, T., Itakura, Y., and Fuwa, T., Further studies on steroidal glycosides from bulbs, roots and leaves of Allium sativum. Chem. Pharm. Bull., 37, 2741-2743 (1989) https://doi.org/10.1248/cpb.37.2741
  66. McKee, T., Bokesch, H., McCormick, J., Rashid, M., Spielvogel, D., Gustafson, K., Alavanja, M., Cardellina, J., and Boyd, M., Isolation and charaterization of new anti-HIV and cytototoxic leads from plants, marine and microbial organisms. J. Nat. Prod., 60, 431-438 (1997) https://doi.org/10.1021/np970031g
  67. Moon, K.S., Components and utilization of medicinal plants. Ilweolseogak, Pyongyang, pp. 419, 1991
  68. Mori, A., Nishino, C., Enoki, N., and Tawata, S., Cytotoxicity of pant flavonoids against heLa cells. Phytochemistry, 27, 1017-1020 (1988) https://doi.org/10.1016/0031-9422(88)80264-4
  69. Mimaki, Y., Kuroda, M., Asano, T., and Sashida, Y., Triterpene saponins and lignans from the roots of Pulsatilla chinensis and their cytotoxic aactivity against HL-60 Cells. J. Nat. Prod., 62, 1279-1283 (1999) https://doi.org/10.1021/np9901837
  70. Min, B.S., Kim, Y.H., Lee, S.M., Jung, H.J., Lee, J.S., Na, M.K., Lee, J.O., Lee, J.P., and Bae, K.H., Cytotoxic triterpenes from craetaegus pinnaifida, Arch. Pharm. Res., 23, 155-158 (2000) https://doi.org/10.1007/BF02975505
  71. Neto, C., Vaisberg, A., Zhou, B.N., Kingston D., and Hammond G., Cytotoxic triterpene acids from the peruvian medidinal plant Polylepis racemosa. Planta Med., 66, 483-484 (2000) https://doi.org/10.1055/s-2000-8583
  72. Nishimura, H., Wijaya, C.H., and Mizutani, J., Volatile flavor components and antithrombotic agents: Vinyldithiins from llium victorialis. J. Agric. Food. Chem., 36, 563-566 (1988) https://doi.org/10.1021/jf00081a039
  73. Noda. Y., Kaiya, T., and Kohda, K., Enhanced cytotoxicity of some triterpenes toward leukemia L1210 cells cultured in low pH media: possibility of a new mode of cell killing. Chem. Pharm. Bull., 45, 1665-1670 (1997) https://doi.org/10.1248/cpb.45.1665
  74. Noda, Y., Kawazoe, Y., and Hakura, A., Cytotoxicity of naphthaquinones toward cultured resting murine leukemia L1210 cells in the presence of glutathione, diethyl maleate, or iodoacetamide. Biol. Pharm. Bull., 20, 1250-1256 (1997) https://doi.org/10.1248/bpb.20.1250
  75. Nelson, D.L. and Michael, M.C., Lehninger Principles of Biochemistry 3rd Edition, Worth, New York, pp. 389-489, 1993
  76. Nelson, D.L. and Michael, M.C., Lehninger principles of biochemistry 3rd edition, Ed.; Ryan M., Press: Worth, NY, pp. 389-489, 1993
  77. Park, H.J., Lee, M.S., Lee, K.T., Sohn, I.C., and Han, Y.N., Studies on constituents with cytotoxic activity from the stem bark of syringa velutina. Chem. Pharm. Bull., 47, 1029-1031 (1999) https://doi.org/10.1248/cpb.47.1029
  78. Park, H.J., Kim, D.H., Choi, J.W., Park, J.H., and Han, Y.N., A Potent anti-diabetic agent from Kalopanax pictus, Arch. Pharm Res., 21, 24-29 (1998) https://doi.org/10.1007/BF03216748
  79. Park, H.J., Kwon, S.H., Han, Y.N., Choi, J.W., Miyamoto, K., Lee, S.H., and Lee, K.T., Apoptosis-inducing costunolide and a novel acyclic monoterpene from the stem bark of Maguolia sieboldii. Arch. Pharm. Res., 24, 342-348 (2001) https://doi.org/10.1007/BF02975104
  80. Park, H.J., Kwon, S.H., Lee, J.H., Lee, K.H., Miyamoto, K., and Lee K.T., Kalopanaxsaponin A is a basic saponin structure for the antitumor activity of hederagenin monodesmosides. Planta Med., 67, 118-121 (2001) https://doi.org/10.1055/s-2001-11516
  81. Park, H.J., Kwon, S.H., Yoo, K.O., Sohn I.C., Lee, K.T., and Lee, H.K., Sesquiterpenes from the leaves of Ligularia fischeri var. spiciformis. Planta Med., 66, 783-784 (2000) https://doi.org/10.1055/s-2000-9602
  82. Park, H.J., Kwon, S.H., Han, Y.N., Choi, J.W., Miyamoto, K., Lee, S.H., and Lee, K.T., Apoptosis-inducing costunolide and a novel acyclic monoterpene from the stem bark of Magnolia sieboldii, Arch. Pharm. Res., 24, 342-348 (2001) https://doi.org/10.1007/BF02975104
  83. Park, H.J., Nam, J.H., Jung, H.J., Ko, C.D., Lee, K.T., and Jung, W.T., Structure of codonoposide isolated from codonopsis lanceolata roots and the cytotoxicity of prosapogenins. J. Agric. Food Chem., 50, 4190-4193 (2002) https://doi.org/10.1021/jf011647l
  84. Park, H.J., Park, H.S., Jung, W.T., Choi, J.W., and Lee, K.T., Toxicological Aspects of Eugenol Isolated from the Essential Oil of Eugenia caryophyllata. The Spring Convention of Korea, PD2-42 (2001)
  85. Park, H.J., Park, J.H., Moon, J.O., Lee, K.T., Jung, W.T., Oh, S.R., and Lee, H.K., Isoflavone glycosides from the flowers of Pueraria thunbergiana. Phytochemistry, 51, 147-151 (1999) https://doi.org/10.1016/S0031-9422(98)00729-8
  86. Park, K.Y., Jung, K.O., Choi, J.W., Lee, K.T., and Park, H.J., Kaikasaponin III, a potent antimutagenic saponin, isolated from the flower of Pueraria thunbergiana. Arch. Pharm. Res., 25, 320-324 (2002) https://doi.org/10.1007/BF02976633
  87. Park, S.H., Oh, S.R., Jung, K.Y., Lee, I.S., Ahn, K.S., Kim, J.G., and Lee, J.J., Anticomplement activities of oleanolic acid monodesmosides and bisdesmosides isolated from Tiarella polyphylla. Arch. Pharm. Res., 22, 428-431 (1999) https://doi.org/10.1007/BF02979071
  88. Rao, M.M. and Kingston, D.G.I., Plant anticancer agents. XII. isolation and structure elucidation of new cytotoxic quinines from tabebuia cassinoides. J. Nat. Prod., 45, 600-604 (1992) https://doi.org/10.1021/np50023a014
  89. Ridoux, O., Di, G.C., Delmas, F., Elias, R., Mshvildadze V., Dekanosidze, G., Kemertelidze, E., and Balansard, G., In vitro Antileishmanial activity of three saponins isolated from ivy, ${\alpha}$-hederin, ${\beta}$-hederin and hederacolehiside A (1), in association with pentamidine and amphotericin B. Phytotherapy Res., 15, 298-301 (2001) https://doi.org/10.1002/ptr.723
  90. Ryu, S.Y., Lee, C.O., and Choi. S.U., In vitro cytotoxicity of tanshinones from salvia miltiorrhiza. Planta Med., 63, 339-342 (1997) https://doi.org/10.1055/s-2006-957696
  91. Ryu, S.Y., Lee, S.H., Choi, S.U., Lee, C.O., No, Z., and Ahn, J.W., antitumor activity of trichosanthes kirilowii, Arch. Pharm. Res., 17, 348-353 (1994) https://doi.org/10.1007/BF02974175
  92. Ryu, S.Y., Choi, S.U., Lee, S.H., Lee, C.O., No, Z., and Ahn, J.W., Cytotoxicity of cucurbitacins in vitro. Arch. Pharm. Res., 18, 60-61 (1995) https://doi.org/10.1007/BF02976511
  93. Sano, K., Sanada, S., Ida, Y., and Shoji, J., Studies on the constituents of the stem bark of Kalopanax pictus. Chem. Pharm. Bull., 39, 865-870 (1991) https://doi.org/10.1248/cpb.39.865
  94. Seo, E.K., Silva, G.L., Chai, H.B., Farnswoth, N.R., Cordell, G.A., Pezzuto, J., and Kinghorn, A., Cytotoxic prenylated flavanones from Monotes engleri. Phytochemistry, 45, 509-515 (1997) https://doi.org/10.1016/S0031-9422(96)00871-0
  95. Singer, B., The chemical effects of nucleic acid alkylation and their relation to mutagenesis and carcinogenesis. Prog. Nucleic Acid Res. Mol. Biol., 15, 219-284 (1975) https://doi.org/10.1016/S0079-6603(08)60121-X
  96. Shao, C.J., Kasai, R., Xu, J.D., and Tanaka, O., Saponins from Roots of kalopanax septemlobus (Yhunb.) koidz., ciqiu: structures of kalopanaxsaponins la, lb and lc. Chem. Pharm. Bull., 37, 311-314 (1989) https://doi.org/10.1248/cpb.37.311
  97. Shin, K.H., Kim, Y.P., Lim, S.S., Lee, S., Ryu, N., Yamada, M., and Ohuchi, K., Inhibition of prostaglandin $E_{2}$ production by the soflavones tectorigenin and tectoridin isolated from the rhizome Belamcanda chinensis. Planta Med., 65, 776-777 (1999) https://doi.org/10.1055/s-2006-960868
  98. Soonthornchareonnon, N., Suwanborirux, K., Bavovada, R., Patarapanich, C., and Cassady, J., New cytotoxic 1-azaanthraquinones and 3-aminonaphthoquinone from the stem bark of goniothalamus mareanii, J. Nat. Prod., 62, 1390-1394 (1999) https://doi.org/10.1021/np990197c
  99. Syu, W.J., Shen, C.C., Don, M.J., Ou, J.C., Lee, G.H., and Sun, C.M., Cytotoxicity of curcumonoids and some novel compounds from Curcuma zedoaria. J. Nat. Prod., 61, 1531-1534 (1998) https://doi.org/10.1021/np980269k
  100. Van lerzel, M.L., Ploemen, J.P., Lo Bello, M., Federici, G., and Van Bla, P.J., Interactions of ${\alpha},{\beta}$-unsaturated aldehyde and ketones with human gluthathione S-transferase Pl-1. Chem. Biol. Interact., 108, 67-78 (1997) https://doi.org/10.1016/S0009-2797(97)00096-3
  101. Wei, H., Bowen, R., Cai, Q., Barnes, S., and Wang, Y., Antioxidant and antipromotional effects of the soybean isoflavone genistein. Proc. Soc. Exp. Biol Med., 208, 124-1128 (1995)
  102. Xiao, K., Yi, Y.H., Wang, Z.Z., Tang, H.F., Li, Y.Q., and Lin, H.W.A., Cytotoxic triterpene saponin from the root bark of aralia dasyphylla. J. Nat. Prod., 62, 1030-1032 (1999) https://doi.org/10.1021/np9805185
  103. Xiong, Q., Tezuka, Y., Kaneko, T., Li, H., Tran, L.Q., Hase, K., Namba, T, and Kadota, S., Inhibition of nitric oxide by phenylethanoid in activated macrophages. Eur. J. Pharm., 400, 137-144 (2000) https://doi.org/10.1016/S0014-2999(00)00354-X
  104. Yang, J., Nakagawa, H., Tsuta, K., and Tsubura, A., Influence of perinatal genistein exposure on the development of MNU-induced mammary carcinoma female sprague-dawley rats. Cancer Letters, 149, 171-179 (2000) https://doi.org/10.1016/S0304-3835(99)00357-2
  105. Young, H.S., Kim M.S., Chung, H.Y., Choi, J.S., and Kim B.W., Separation of active chemical components components against sarcoma 180 from stem bark of Catalpa ovata. J. Korean Cancer Assoc., 24, 167-172 (1992)
  106. Yoon, Y.S., Kim, Y.O., Joen, W.K., Park, H.J., and Sung, H.J., Tanshinoe IIA, an Ingredient of salvia miltiorrhiza induced apoptosis in HL60 human premyelocytic leukemia cell line. J. Ethnopharmcol., 121-127 (1999)
  107. Yoon, Y., Kim, Y.O., Lim, N.Y., Jeon, W.K., and Sung, H.J., Shikonin, An Ingredient of lithospermum erythrorhizon induced apoptosis in HL60 human premyelocytic leukemia cell line. Planta Med., 65, 532-535 (1999) https://doi.org/10.1055/s-1999-14010
  108. Yoshikawa, M., Shimada, H., Morikawa, T., Yoshizumi, S., Natsumura, N., Murakami, T., Matsuda, H., Hori, K., and Yamahara, J., Meicinal foodstuffs. VII. On the Saponin constituents with glucose and alcohol absorption-inhibitory activity from a food garnish 'Tonuri', the fruit of Japanese Kochia scoparia (L.) schard.: Structures of scoparianosides A, B, and C. Chem. Pharm. Bull., 45, 1300-1305 (1997) https://doi.org/10.1248/cpb.45.1300
  109. Yusuf, A.H., Apoptosis and the dilemma of cancer chemotherapy. Blood, 89, 1845-1853 (1997)
  110. Zahir, A., Jossang, A., and Bodo, B., DNA Topoisomerase I inhibitors: Cytotoxic flavones from Lethedon tannaensis. J. Nat. Prod., 59, 701-703 (1996) https://doi.org/10.1021/np960336f
  111. Zhang, D., Haruna, M., McPhail, A., and Lee, K.H., Cytotoxic ermacranolides of Elephantopus Carolinianus and the structure and stereochemistry of isodeoxyelephantopin. Phytochemistry, 25, 899-904 (1986) https://doi.org/10.1016/0031-9422(86)80023-1