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Volumn 72, Issue 4-5, 2011, Pages 385-390

Ent-Rosane and abietane diterpenoids as cancer chemopreventive agents

Author keywords

Abietane; Chemopreventive agents; Crossopetalum uragoga; ent Rosane; Epstein Barr virus; Maytenus cuzcoina; Two stage carcinogenesis

Indexed keywords

6 DEHYDROXYCUZCOL; 6-DEHYDROXYCUZCOL; ABIETANE DERIVATIVE; ANTINEOPLASTIC AGENT; CARNOSOL; DITERPENE; EPSTEIN BARR VIRUS ANTIGEN; SALVADORIOL;

EID: 79952188341     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2011.01.017     Document Type: Article
Times cited : (20)

References (43)
  • 1
    • 77957038399 scopus 로고    scopus 로고
    • Potentially cancer chemopreventive and anti-inflammatory terpenoids from natural sources
    • Atta-ur-Rahman Elsevier Science Publishers Amsterdam
    • T. Akihisa, K. Yasukawa, and H. Tokuda Potentially cancer chemopreventive and anti-inflammatory terpenoids from natural sources Atta-ur-Rahman Studies in Natural Products Chemisty, Bioactive Natural Products (Part J) 2003 Elsevier Science Publishers Amsterdam 73 126
    • (2003) Studies in Natural Products Chemisty, Bioactive Natural Products (Part J) , pp. 73-126
    • Akihisa, T.1    Yasukawa, K.2    Tokuda, H.3
  • 2
    • 85010186597 scopus 로고
    • Syntheses of optically active (+)-bemadienolide from dehydroabietic acid
    • H. Akita, A. Anazawa, and T. Oishi Syntheses of optically active (+)-bemadienolide from dehydroabietic acid Chem. Pharm. Bull. 29 1981 1588 1593
    • (1981) Chem. Pharm. Bull. , vol.29 , pp. 1588-1593
    • Akita, H.1    Anazawa, A.2    Oishi, T.3
  • 3
    • 0343953010 scopus 로고    scopus 로고
    • Cytotoxic cardenolides and antibacterial terpenoids from Crossopetalum gaumeri
    • DOI 10.1016/S0031-9422(00)00144-8, PII S0031942200001448
    • A. Ankli, J. Heilman, M. Heinrich, and O. Sticher Cytotoxic cardenolides and antibacterial terpenoids from Crossopetalum gaumeri Phytochemisty 54 2000 531 537 (Pubitemid 30484560)
    • (2000) Phytochemistry , vol.54 , Issue.5 , pp. 531-537
    • Ankli, A.1    Heilmann, J.2    Heinrich, M.3    Sticher, O.4
  • 4
    • 15644364656 scopus 로고
    • The mechanism of carcinogenesis: A study of the significance of cocarcinogenic action and related phenomena
    • M.D.I. Berenblum The mechanism of carcinogenesis: a study of the significance of cocarcinogenic action and related phenomena Cancer J. Clin. 31 1981 241 253
    • (1981) Cancer J. Clin. , vol.31 , pp. 241-253
    • Berenblum, M.D.I.1
  • 7
    • 33847278423 scopus 로고    scopus 로고
    • Medicinal chemistry and pharmacology of genus Tripterygium (Celastraceae)
    • DOI 10.1016/j.phytochem.2006.11.029, PII S0031942206007370
    • A.M. Brinker, J. Ma, P.E. Lipsky, and I. Raskin Medicinal chemistry and pharmacology of genus Tripterygium (Celastraceae) Phytochemistry 68 2007 732 766 (Pubitemid 46330437)
    • (2007) Phytochemistry , vol.68 , Issue.6 , pp. 732-766
    • Brinker, A.M.1    Ma, J.2    Lipsky, P.E.3    Raskin, I.4
  • 8
    • 0033017613 scopus 로고    scopus 로고
    • Triterpene caffeoyl esters and diterpenes from Celastrus stephanotifolius
    • DOI 10.1016/S0031-9422(99)00079-5, PII S0031942299000795
    • B. Chen, H. Duan, and Y. Takaishi Triterpene caffeoyl esters and diterpenes from Celastrus stephanotifolius Phytochemistry 51 1999 683 687 (Pubitemid 29282504)
    • (1999) Phytochemistry , vol.51 , Issue.5 , pp. 683-687
    • Chen, B.1    Duan, H.2    Takaishi, Y.3
  • 9
    • 77956670232 scopus 로고    scopus 로고
    • Anti-proliferative and apoptosis-inducible activity of labdane and abietane diterpenoids from the pulp of Torreya nucifera in HeLa cells
    • S.P. Chen, M. Dong, K. Kita, Q.W. Shi, B. Cong, W.Z. Guo, S. Sugaya, K. Sugita, and N. Suzuki Anti-proliferative and apoptosis-inducible activity of labdane and abietane diterpenoids from the pulp of Torreya nucifera in HeLa cells Mol. Med. Rep. 3 2010 673 678
    • (2010) Mol. Med. Rep. , vol.3 , pp. 673-678
    • Chen, S.P.1    Dong, M.2    Kita, K.3    Shi, Q.W.4    Cong, B.5    Guo, W.Z.6    Sugaya, S.7    Sugita, K.8    Suzuki, N.9
  • 10
    • 1642540576 scopus 로고    scopus 로고
    • SAR Studies of Dihydro-β-agarofuran Sesquiterpenes as Inhibitors of the Multidrug-Resistance Phenotype in a Leishmania tropica Line Overexpressing a P-Glycoprotein-Like Transporter
    • DOI 10.1021/jm0309699
    • F. Cortes-Selva, M. Campillo, C.P. Reyes, I.A. Jiménez, S. Castanys, I.L. Bazzocchi, L. Pardo, F. Gamarro, and A.G. Ravelo SAR studies of dihydro-β-agarofuran sesquiterpenes as inhibitors of the multidrug-resistance phenotype in a Leishmania tropica line overexpressing a P-glycoprotein-like transporter J. Med. Chem. 47 2004 576 587 (Pubitemid 38129716)
    • (2004) Journal of Medicinal Chemistry , vol.47 , Issue.3 , pp. 576-587
    • Cortes-Selva, F.1    Campillo, M.2    Reyes, C.P.3    Jimenez, I.A.4    Castanys, S.5    Bazzocchi, I.L.6    Pardo, L.7    Gamarro, F.8    Ravelo, A.G.9
  • 11
    • 56249084949 scopus 로고    scopus 로고
    • Mechanisms of cancer chemopreventive agents: A perspective
    • J. Francy-Guilford, and J.M. Pezzuto Mechanisms of cancer chemopreventive agents: a perspective Planta Med. 74 2008 1644 1650
    • (2008) Planta Med. , vol.74 , pp. 1644-1650
    • Francy-Guilford, J.1    Pezzuto, J.M.2
  • 14
    • 55049130518 scopus 로고    scopus 로고
    • Antioxidant effect rosemary (Rosmarinus officinalis L.) and oregano (Origanum vulgare L.) extracts on TBARS and colour of model raw pork batters
    • E. Hernández-Hernández, E. Ponce-Alquicira, M.E. Jaramillo-Flores, and I.G. Legarreta Antioxidant effect rosemary (Rosmarinus officinalis L.) and oregano (Origanum vulgare L.) extracts on TBARS and colour of model raw pork batters Meat Sci. 81 2009 410 417
    • (2009) Meat Sci. , vol.81 , pp. 410-417
    • Hernández-Hernández, E.1    Ponce-Alquicira, E.2    Jaramillo-Flores, M.E.3    Legarreta, I.G.4
  • 15
    • 0000147542 scopus 로고    scopus 로고
    • Recent advances in chemoprevention of cancer
    • DOI 10.1126/science.278.5340.1073
    • W.K. Hong, and M.B. Sporn Recent advances in chemoprevention of cancer Science 278 1997 1073 1077 (Pubitemid 27517878)
    • (1997) Science , vol.278 , Issue.5340 , pp. 1073-1077
    • Hong, W.K.1    Sporn, M.B.2
  • 16
    • 0019500737 scopus 로고
    • Combined effect of the extracts from Croton tiglium, Euphorbia lathyris or Euphorbia tirucalli and n-butyrate on Epstein-Barr virus expression in human lymphoblastoid P3HR-1 and Raji cells
    • DOI 10.1016/0304-3835(81)90066-5
    • Y. Ito, M. Kawanishi, T. Haranaya, and S. Takabayashi Combined effect of extracts from Croton tiglium, Euphorbia lathyris or Euphorbia tirucalli and n-butyrate on Epstein-Barr virus expression in human lymphoblastoid P3HR-1 and Raji cells Cancer Lett. 12 1981 175 180 (Pubitemid 11111737)
    • (1981) Cancer Letters , vol.12 , Issue.3 , pp. 175-180
    • Ito, Y.1    Kawanishi, M.2    Harayama, T.3    Takabayashi, S.4
  • 17
    • 77956411543 scopus 로고    scopus 로고
    • Disruption of androgen and estrogen receptor activity in prostate cancer by a novel dietary diterpene carnosol: Implications for chemoprevention
    • J.J. Johnson, D.N. Syed, Y. Suh, C.R. Heren, M. Saleem, I.A. Siddiqui, and H. Mukhtar Disruption of androgen and estrogen receptor activity in prostate cancer by a novel dietary diterpene carnosol: implications for chemoprevention Cancer Prev. Res. 3 2010 1112 1122
    • (2010) Cancer Prev. Res. , vol.3 , pp. 1112-1122
    • Johnson, J.J.1    Syed, D.N.2    Suh, Y.3    Heren, C.R.4    Saleem, M.5    Siddiqui, I.A.6    Mukhtar, H.7
  • 19
    • 77949655882 scopus 로고    scopus 로고
    • Microtropiosides A-F: Ent-labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae)
    • Y. Koyama, K. Matsunami, H. Otsuka, T. Shinzato, and Y. Takeda Microtropiosides A-F: ent-labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae) Phytochemistry 71 2010 675 681
    • (2010) Phytochemistry , vol.71 , pp. 675-681
    • Koyama, Y.1    Matsunami, K.2    Otsuka, H.3    Shinzato, T.4    Takeda, Y.5
  • 20
    • 33644929517 scopus 로고    scopus 로고
    • Ent-Rosane and labdane diterpenoids from Sagittaria sagittifolia and their antibacterial activity against three oral pathogens
    • X.T. Liu, Q. Pan, I.D. Shi, I.D. Williams, H.H.Y. Sun, Q. Zhang, J.Y. Liang, N.Y. Ip, and Z.D. Min ent-Rosane and labdane diterpenoids from Sagittaria sagittifolia and their antibacterial activity against three oral pathogens J. Nat. Prod. 69 2006 255 260
    • (2006) J. Nat. Prod. , vol.69 , pp. 255-260
    • Liu, X.T.1    Pan, Q.2    Shi, I.D.3    Williams, I.D.4    Sun, H.H.Y.5    Zhang, Q.6    Liang, J.Y.7    Ip, N.Y.8    Min, Z.D.9
  • 22
    • 77953205368 scopus 로고    scopus 로고
    • Cancer chemoprevention by natural products: How far have we come?
    • R.G. Mehta, G. Murillo, R. Naithani, and X. Peng Cancer chemoprevention by natural products: how far have we come? Pharm. Res. 27 2010 950 961
    • (2010) Pharm. Res. , vol.27 , pp. 950-961
    • Mehta, R.G.1    Murillo, G.2    Naithani, R.3    Peng, X.4
  • 23
    • 0342600980 scopus 로고
    • New diterpenoids extractives of Maytenus dispermus
    • J.D. Martin New diterpenoids extractives of Maytenus dispermus Tetrahedron 29 1973 2553 2559
    • (1973) Tetrahedron , vol.29 , pp. 2553-2559
    • Martin, J.D.1
  • 24
    • 0024341197 scopus 로고
    • Chemoprevention of experimental carcinogenesis in animals
    • DOI 10.1016/0091-7435(89)90031-5
    • R.C. Moon, and R.G. Mehta Chemoprevention of experimental carcinogenesis in animals Prev. Med. 18 1989 576 591 (Pubitemid 20009353)
    • (1989) Preventive Medicine , vol.18 , Issue.5 , pp. 576-591
    • Moon, R.C.1    Mehta, R.G.2
  • 25
    • 0030019570 scopus 로고    scopus 로고
    • Anti-tumor promotion with food phytochemical: A strategy for cancer chemoprevention
    • A. Murakami, H. Ohigashi, and K. Koshimizu Anti-tumor promotion with food phytochemical: a strategy for cancer chemoprevention Biosci. Biotechnol. Biochem. 60 1996 1 8
    • (1996) Biosci. Biotechnol. Biochem. , vol.60 , pp. 1-8
    • Murakami, A.1    Ohigashi, H.2    Koshimizu, K.3
  • 27
    • 77950234271 scopus 로고    scopus 로고
    • Celastrol suppresses angiogenesis-mediated tumor growth through inhibition of AKT/mammalian target of rapamycin pathway
    • X. Pang, Z. Yi, J. Zhang, B. Lu, B. Sung, W. Qu, B.B. Aggarwal, and M. Liu Celastrol suppresses angiogenesis-mediated tumor growth through inhibition of AKT/mammalian target of rapamycin pathway Cancer Res. 70 2010 1951 1959
    • (2010) Cancer Res. , vol.70 , pp. 1951-1959
    • Pang, X.1    Yi, Z.2    Zhang, J.3    Lu, B.4    Sung, B.5    Qu, W.6    Aggarwal, B.B.7    Liu, M.8
  • 28
    • 79952194963 scopus 로고    scopus 로고
    • PCMODEL from Serena Sotware, P.O. Box 3076, Bloomington, IN 47402-3076, version 9.0 with MMX force field
    • PCMODEL from Serena Sotware, P.O. Box 3076, Bloomington, IN 47402-3076, version 9.0 with MMX force field.
  • 29
  • 31
    • 34948839413 scopus 로고    scopus 로고
    • Biological evaluation, structure-activity relationships, and three-dimensional quantitative structure-activity relationship studies of dihydro-β-agarofuran sesquiterpenes as modulators of P-glycoprotein- dependent multidrug resistance
    • DOI 10.1021/jm070290v
    • C.P. Reyes, F. Muñoz-Martínez, I.R. Torrecillas, C.R. Mendoza, F. Gamarro, I.L. Bazzocchi, M.J. Núñez, L. Pardo, S. Castanys, M. Campillo, and I.A. Jiménez Biological evaluation, structure-activity relationships, and three-dimensional quantitative structure-activity relationship studies of dihydro-β-agarofuran sesquiterpenes as modulators of P-glycoprotein-dependent multidrug resistance J. Med. Chem. 50 2007 4808 4817 (Pubitemid 47525466)
    • (2007) Journal of Medicinal Chemistry , vol.50 , Issue.20 , pp. 4808-4817
    • Reyes, C.P.1    Munoz-Martinez, F.2    Torrecillas, I.R.3    Mendoza, C.R.4    Gamarro, F.5    Bazzocchi, I.L.6    Nunez, M.J.7    Pardo, L.8    Castanys, S.9    Campillo, M.10    Jimenez, I.A.11
  • 32
    • 39149137869 scopus 로고    scopus 로고
    • Plant-derived compounds in clinical trials
    • A. Saklani, and S.K. Kutty Plant-derived compounds in clinical trials Drug Discov. Today 13 2008 161 171
    • (2008) Drug Discov. Today , vol.13 , pp. 161-171
    • Saklani, A.1    Kutty, S.K.2
  • 33
    • 0942277395 scopus 로고    scopus 로고
    • The assignment of absolute configuration by NMR
    • J.M. Seco, E. Quiñoa, and R. Riguera The assignment of absolute configuration by NMR Chem. Rev. 104 2004 17 117
    • (2004) Chem. Rev. , vol.104 , pp. 17-117
    • Seco, J.M.1    Quiñoa, E.2    Riguera, R.3
  • 34
    • 0029885105 scopus 로고    scopus 로고
    • Inhibition by rosemary and carnosol of 7, 12-dimethylbenz[a]anthracene (DMBA)-induced rat mammary tumorigenesis and in vivo DMBA-DNA adduct formation
    • K. Singletary, C. MacDonal, and M. Walling Inhibition by rosemary and carnosol of 7, 12-dimethylbenz[a]anthracene (DMBA)-induced rat mammary tumorigenesis and in vivo DMBA-DNA adduct formation Cancer Lett. 104 1996 43 48
    • (1996) Cancer Lett. , vol.104 , pp. 43-48
    • Singletary, K.1    MacDonal, C.2    Walling, M.3
  • 35
    • 3242816064 scopus 로고    scopus 로고
    • Kaurane and abietane diterpenoids from Tripterygium doianum (Celastraceae)
    • DOI 10.1016/j.phytochem.2004.04.032, PII S0031942204001980
    • N. Tanaka, N. Ooba, H. Duan, Y. Takaishi, Y. Nakanishi, K. Bastow, and K.L. Lee Kaurane and abietane diterpenoids from Tripterygium doianum (Celastraceae) Phytochemisty 65 2004 2071 2076 (Pubitemid 38981657)
    • (2004) Phytochemistry , vol.65 , Issue.14 , pp. 2071-2076
    • Tanaka, N.1    Ooba, N.2    Duan, H.3    Takaishi, Y.4    Nakanishi, Y.5    Bastow, K.6    Lee, K.-H.7
  • 36
    • 53849094775 scopus 로고    scopus 로고
    • Cancer chemopreventive activity of "rosin" constituents of Pinus spez. and their derivates in two-stage mouse skin carcinogenesis test
    • R. Tanaka, H. Tokuda, and Y. Ezaki Cancer chemopreventive activity of "rosin" constituents of Pinus spez. and their derivates in two-stage mouse skin carcinogenesis test Phytomedicine 15 2008 985 992
    • (2008) Phytomedicine , vol.15 , pp. 985-992
    • Tanaka, R.1    Tokuda, H.2    Ezaki, Y.3
  • 37
    • 0023032498 scopus 로고
    • Inhibitory effects of ursolic and oleanolic acid on skin tumor promotion by 12-O-tetradecanoylphorbol-13-acetate
    • DOI 10.1016/0304-3835(86)90067-4
    • H. Tokuda, H. Ohigashi, K. Koshimizu, and K. Ito Inhibitory effects of ursolic and oleanolic acid on skin tumor promotion by 12-O- tetradecanoylphorphol-13-acetate Cancer Lett. 33 1986 279 285 (Pubitemid 17208491)
    • (1986) Cancer Letters , vol.33 , Issue.3 , pp. 279-285
    • Tokuda, H.1    Ohigashi, H.2    Koshimizu, K.3    Ito, Y.4
  • 39
    • 33644813216 scopus 로고    scopus 로고
    • Novel skeleton terpenes from Celastrus hypoleucus with anti-tumor activities
    • K.W. Wang, J.S. Mao, Y.P. Tai, and Y.J. Pan Novel skeleton terpenes from Celastrus hypoleucus with anti-tumor activities Bioorg. Med. Chem. Lett. 16 2006 2274 2277
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 2274-2277
    • Wang, K.W.1    Mao, J.S.2    Tai, Y.P.3    Pan, Y.J.4
  • 41
    • 77957109492 scopus 로고
    • Two new diterpene lactones from Tripterygium, hypolide and tripterolide
    • D.G. Wu, X.C. Sun, and F. Li Two new diterpene lactones from Tripterygium, hypolide and tripterolide Yunnan Zhiwu Yanjiu 1 1979 29 36
    • (1979) Yunnan Zhiwu Yanjiu , vol.1 , pp. 29-36
    • Wu, D.G.1    Sun, X.C.2    Li, F.3
  • 42
    • 0031127528 scopus 로고    scopus 로고
    • 4 antagonistic 19(4 → 3)-abeo- abietanes from Tripterygium wilfordii
    • DOI 10.1016/S0031-9422(96)00782-0, PII S0031942296007820
    • J. Xu, T. Ikekawa, M. Ohkawa, I. Yokota, N. Hara, and Y. Fujimoto Triptinins A and B, two leukotriene D4 antagonistic 19(4→3)-abeo-abietanes from Triterygium wilfordii Phytochemistry 44 1997 1511 1514 (Pubitemid 27142301)
    • (1997) Phytochemistry , vol.44 , Issue.8 , pp. 1511-1514
    • Xu, J.1    Ikekawa, T.2    Ohkawa, M.3    Yokota, I.4    Hara, N.5    Fujimoto, Y.6
  • 43
    • 33845622034 scopus 로고    scopus 로고
    • Asymmetric synthesis of abietane diterpenoids via B-alkyl Suzuki-Miyaura coupling. Formal total asymmetric synthesis of 12-deoxyroyleanone and cryptoquinone
    • DOI 10.1016/j.tet.2006.11.072, PII S0040402006018904
    • A. Yajima, A. Yamaguchi, F. Saitou, T. Nukada, and G. Yabuta Asymmetric synthesis of abietane diterpenoids via B-alkyl Suzuki-Miyaura coupling. Formal total asymmetric synthesis of 12-deoxyroyleanone and cryptoquinone Tetrahedron 63 2007 1080 1084 (Pubitemid 44958913)
    • (2007) Tetrahedron , vol.63 , Issue.5 , pp. 1080-1084
    • Yajima, A.1    Yamaguchi, A.2    Saitou, F.3    Nukada, T.4    Yabuta, G.5


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