메뉴 건너뛰기




Volumn 84, Issue 1, 2013, Pages 22-31

Anti-inflammatory and cytotoxic cyathane diterpenoids from the medicinal fungus Cyathus africanus

Author keywords

Cyathane diterpenes; Cyathus africanus; Cytotoxicity; NO inhibition; Structure elucidation

Indexed keywords

11 O ACETYLCYATHATRIOL; 11,14,15 O,O TRIACETYLCYATHATRIOL; 11,15 O,O DIACETYLCYATHATRIOL; ANTIINFLAMMATORY AGENT; CYATHATRIOL; CYATHIN E; DITERPENOID; LIPOPOLYSACCHARIDE; NEOSARCODONIN O; NITRIC OXIDE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84873337715     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2012.10.001     Document Type: Article
Times cited : (54)

References (46)
  • 1
    • 33846688072 scopus 로고    scopus 로고
    • Therapeutic potential of mushrooms
    • M. Rai, G. Tidke, and S.P. Wasser Therapeutic potential of mushrooms Nat Prod Rad 4 2005 246 257
    • (2005) Nat Prod Rad , vol.4 , pp. 246-257
    • Rai, M.1    Tidke, G.2    Wasser, S.P.3
  • 3
    • 0034364829 scopus 로고    scopus 로고
    • Recent progress on the synthesis of cyathane type diterpenes
    • D.L. Wright, and C.R. Whitehead Recent progress on the synthesis of cyathane type diterpenes Org Prep Proced Int 32 2000 307 331
    • (2000) Org Prep Proced Int , vol.32 , pp. 307-331
    • Wright, D.L.1    Whitehead, C.R.2
  • 4
    • 41149084527 scopus 로고    scopus 로고
    • The structure, medicinal properties and biosynthesis of cyathane diterpenoids
    • W. Krzyczkowshi, E. Malinowska, and F. Herold The structure, medicinal properties and biosynthesis of cyathane diterpenoids Biotechnologia 1 2008 146 147
    • (2008) Biotechnologia , vol.1 , pp. 146-147
    • Krzyczkowshi, W.1    Malinowska, E.2    Herold, F.3
  • 5
    • 0002517056 scopus 로고
    • 3, members of a new group of diterpenoids
    • 3, members of a new group of diterpenoids Tetrahedron Lett 19 1972 1917 1920
    • (1972) Tetrahedron Lett , vol.19 , pp. 1917-1920
    • Ayer, W.A.1    Taube, H.2
  • 6
    • 79957460414 scopus 로고    scopus 로고
    • Cyathane diterpenes from Chinese mushroom Sarcodon scabrosus and their neurite outgrowth-promoting activity
    • X.W. Shi, L. Liu, J.M. Gao, and A.L. Zhang Cyathane diterpenes from Chinese mushroom Sarcodon scabrosus and their neurite outgrowth-promoting activity Eur J Med Chem 46 2011 3112 3117
    • (2011) Eur J Med Chem , vol.46 , pp. 3112-3117
    • Shi, X.W.1    Liu, L.2    Gao, J.M.3    Zhang, A.L.4
  • 7
    • 23744499310 scopus 로고    scopus 로고
    • A new bitter diterpenoid from Sarcodon scabrosus
    • B.J. Ma, and J.K. Liu A new bitter diterpenoid from Sarcodon scabrosus J Basic Microbiol 45 2005 328 330
    • (2005) J Basic Microbiol , vol.45 , pp. 328-330
    • Ma, B.J.1    Liu, J.K.2
  • 9
    • 11144260112 scopus 로고    scopus 로고
    • Isolation and characterization of new bitter diterpenoids from the basidiomycete Sarcodon scabrosus
    • B.J. Ma, H.J. Zhu, and J.K. Liu Isolation and characterization of new bitter diterpenoids from the basidiomycete Sarcodon scabrosus Helv Chim Acta 87 2004 2877 2881
    • (2004) Helv Chim Acta , vol.87 , pp. 2877-2881
    • Ma, B.J.1    Zhu, H.J.2    Liu, J.K.3
  • 10
    • 0036372245 scopus 로고    scopus 로고
    • Anti-inflammatory compounds from the bitter mushroom, Sarcodon scabrosus
    • M. Hirota, K. Morimura, and H. Shibata Anti-inflammatory compounds from the bitter mushroom, Sarcodon scabrosus Biosci Biotechnol Biochem 66 2002 179 184
    • (2002) Biosci Biotechnol Biochem , vol.66 , pp. 179-184
    • Hirota, M.1    Morimura, K.2    Shibata, H.3
  • 11
    • 0032242793 scopus 로고    scopus 로고
    • New antibacterial diterpenoids from the Sarcodon scabrosus fungus, Biosci, Biotechnol
    • H. Shibata, A. Irie, and Y. Morita New antibacterial diterpenoids from the Sarcodon scabrosus fungus, Biosci, Biotechnol Biosci Biotechnol Biochem 62 1998 2450 2452
    • (1998) Biosci Biotechnol Biochem , vol.62 , pp. 2450-2452
    • Shibata, H.1    Irie, A.2    Morita, Y.3
  • 12
    • 0032563997 scopus 로고    scopus 로고
    • Scabronines B, C, D, e and F, novel diterpenoids showing stimulating activity of nerve growth factor-synthesis, from the mushroom Sarcodon scabrosus
    • T. Kita, Y. Takaya, and Y. Oshima Scabronines B, C, D, E and F, novel diterpenoids showing stimulating activity of nerve growth factor-synthesis, from the mushroom Sarcodon scabrosus Tetrahedron 54 1998 11,877 11,886
    • (1998) Tetrahedron , vol.54 , pp. 11
    • Kita, T.1    Takaya, Y.2    Oshima, Y.3
  • 13
    • 0032552150 scopus 로고    scopus 로고
    • Scabronine A, a novel diterpenoid having potent inductive activity of the nerve growth factor synthesis, isolated from the mushroom Sarcodon scabrosus
    • T. Ohta, T. Kita, N. Kobayashi, Y. Obara, N. Nakahata, and Y. Ohizumi Scabronine A, a novel diterpenoid having potent inductive activity of the nerve growth factor synthesis, isolated from the mushroom Sarcodon scabrosus Tetrahedron Lett 39 1998 6229 6232
    • (1998) Tetrahedron Lett , vol.39 , pp. 6229-6232
    • Ohta, T.1    Kita, T.2    Kobayashi, N.3    Obara, Y.4    Nakahata, N.5    Ohizumi, Y.6
  • 14
    • 0001722822 scopus 로고
    • Isolation and characterization of new bitter diterpenoids from the fungus Sarcodon scabrosus
    • H. Shibata, T. Tokunaga, D. Karadawa, A. Hirota, M. Nakayama, and H. Nozaki Isolation and characterization of new bitter diterpenoids from the fungus Sarcodon scabrosus Agric Biol Chem 53 1989 3373 3375
    • (1989) Agric Biol Chem , vol.53 , pp. 3373-3375
    • Shibata, H.1    Tokunaga, T.2    Karadawa, D.3    Hirota, A.4    Nakayama, M.5    Nozaki, H.6
  • 15
    • 14944371452 scopus 로고    scopus 로고
    • Glaucopines A and B, new cyathane diterpenes from the fruiting bodies of Sarcodon glaucopus
    • M. Curini, F. Maltese, M.C. Marcotullio, L. Menghini, R. Pagiotti, and O. Rosati Glaucopines A and B, new cyathane diterpenes from the fruiting bodies of Sarcodon glaucopus Planta Med 71 2005 194 196
    • (2005) Planta Med , vol.71 , pp. 194-196
    • Curini, M.1    Maltese, F.2    Marcotullio, M.C.3    Menghini, L.4    Pagiotti, R.5    Rosati, O.6
  • 17
    • 33947095604 scopus 로고    scopus 로고
    • Cyathane diterpenes from Sarcodon cyrneus and evaluation of their activities of neuritegenesis and nerve growth factor production
    • M.C. Marcotullio, R. Pagiotti, F. Maltese, G.N. Oball-Mond Mwankie, T. Hoshino, and Y. Obara Cyathane diterpenes from Sarcodon cyrneus and evaluation of their activities of neuritegenesis and nerve growth factor production Bioorg Med Chem 15 2007 2878 2882
    • (2007) Bioorg Med Chem , vol.15 , pp. 2878-2882
    • Marcotullio, M.C.1    Pagiotti, R.2    Maltese, F.3    Oball-Mond Mwankie, G.N.4    Hoshino, T.5    Obara, Y.6
  • 18
    • 33747020061 scopus 로고    scopus 로고
    • Neurite outgrowth activity of cyathane diterpenes from Sarcodon cyrneus, cyrneines A and B
    • M.C. Marcotullio, R. Pagiott, F. Maltese, Y. Obara, T. Hoshino, and N. Nakahata Neurite outgrowth activity of cyathane diterpenes from Sarcodon cyrneus, cyrneines A and B Planta Med 72 2006 819 823
    • (2006) Planta Med , vol.72 , pp. 819-823
    • Marcotullio, M.C.1    Pagiott, R.2    Maltese, F.3    Obara, Y.4    Hoshino, T.5    Nakahata, N.6
  • 19
    • 0000671455 scopus 로고
    • Metabolites of bird's nest fungi. Part 8. Some minor metabolites of Cyathus helenae and some correlations among the cyathins
    • W.A. Ayer, L.M. Browne, J.R. Mercer, D.R. Taylor, and D.E. Ward Metabolites of bird's nest fungi. Part 8. Some minor metabolites of Cyathus helenae and some correlations among the cyathins Can J Chem 56 1978 717 721
    • (1978) Can J Chem , vol.56 , pp. 717-721
    • Ayer, W.A.1    Browne, L.M.2    Mercer, J.R.3    Taylor, D.R.4    Ward, D.E.5
  • 21
    • 0015738827 scopus 로고
    • Metabolites of Cyathus helenae. A new class of diterpenoids
    • W.A. Ayer, and H. Taube Metabolites of Cyathus helenae. A new class of diterpenoids Can J Chem 51 1973 3842 3854
    • (1973) Can J Chem , vol.51 , pp. 3842-3854
    • Ayer, W.A.1    Taube, H.2
  • 22
    • 0018086917 scopus 로고
    • Metabolites of bird's nest fungi. Part 9. Diterpenoid metabolites of Cyathus africanus Brodie
    • W.A. Ayer, T. Yoshida, and D.M.J. van Schie Metabolites of bird's nest fungi. Part 9. Diterpenoid metabolites of Cyathus africanus Brodie Can J Chem 56 1978 2113 2120
    • (1978) Can J Chem , vol.56 , pp. 2113-2120
    • Ayer, W.A.1    Yoshida, T.2    Van Schie, D.M.J.3
  • 23
    • 0018606553 scopus 로고
    • Metabolites of bird's nest fungi. Part 11. Diterpenoid metabolites of Cyathus earlei
    • W.A. Ayer, and S.P. Lee Metabolites of bird's nest fungi. Part 11. Diterpenoid metabolites of Cyathus earlei Can J Chem 57 1979 3332 3337
    • (1979) Can J Chem , vol.57 , pp. 3332-3337
    • Ayer, W.A.1    Lee, S.P.2
  • 24
    • 37049099112 scopus 로고
    • Striatin A, B, and C, novel diterpenoid antibiotics from Cyathus striatus, X-ray crystal structure of striatin A
    • H.J. Hecht Striatin A, B, and C, novel diterpenoid antibiotics from Cyathus striatus, X-ray crystal structure of striatin A J Chem Soc Chem Commun 15 1978 665 666
    • (1978) J Chem Soc Chem Commun , vol.15 , pp. 665-666
    • Hecht, H.J.1
  • 25
    • 56149092745 scopus 로고    scopus 로고
    • Two cyathane-type diterpenoids from the liquid culture of Strobilurus tenacellus
    • Y. Shiono, F. Hiramatsu, T. Murayama, T. Koseki, and T. Funakoshi Two cyathane-type diterpenoids from the liquid culture of Strobilurus tenacellus Chem Biodivers 5 2008 1811 1816
    • (2008) Chem Biodivers , vol.5 , pp. 1811-1816
    • Shiono, Y.1    Hiramatsu, F.2    Murayama, T.3    Koseki, T.4    Funakoshi, T.5
  • 26
    • 16044366456 scopus 로고    scopus 로고
    • Erinacines E, F, and G, stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum
    • H. Kawagishi, A. Simada, S. Hosokawa, H. Mori, H. Sakamoto, and Y. Ishiguro Erinacines E, F, and G, stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum Tetrahedron Lett 37 1996 7399 7402
    • (1996) Tetrahedron Lett , vol.37 , pp. 7399-7402
    • Kawagishi, H.1    Simada, A.2    Hosokawa, S.3    Mori, H.4    Sakamoto, H.5    Ishiguro, Y.6
  • 28
    • 0028293541 scopus 로고
    • Erinacines A, B and C, strong stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum
    • H. Kawagishi, A. Shimada, R. Shirai, K. Okamoto, F. Ojima, and H. Sakamoto Erinacines A, B and C, strong stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum Tetrahedron Lett 35 1994 1569 1572
    • (1994) Tetrahedron Lett , vol.35 , pp. 1569-1572
    • Kawagishi, H.1    Shimada, A.2    Shirai, R.3    Okamoto, K.4    Ojima, F.5    Sakamoto, H.6
  • 29
    • 33746272717 scopus 로고    scopus 로고
    • Erinacines J and K from the mycelia of Hericium erinaceum
    • H. Kawagishi, A. Masui, S. Tokuyamab, and T. Nakamura Erinacines J and K from the mycelia of Hericium erinaceum Tetrahedron 62 2006 8463 8466
    • (2006) Tetrahedron , vol.62 , pp. 8463-8466
    • Kawagishi, H.1    Masui, A.2    Tokuyamab, S.3    Nakamura, T.4
  • 31
    • 0034622057 scopus 로고    scopus 로고
    • Isolation of erinacine P, a new parental metabolite of cyathane-xylosides, from Hericium erinaceum and its biomimetic conversion into erinacines A and B
    • H. Kenmoku, T. Sassa, and N. Kato Isolation of erinacine P, a new parental metabolite of cyathane-xylosides, from Hericium erinaceum and its biomimetic conversion into erinacines A and B Tetrahedron Lett 41 2000 4389 4393
    • (2000) Tetrahedron Lett , vol.41 , pp. 4389-4393
    • Kenmoku, H.1    Sassa, T.2    Kato, N.3
  • 32
    • 0036490819 scopus 로고    scopus 로고
    • Erinacine Q, a new erinacine from Hericium erinaceum, and its biosynthetic route to erinacine C in the basidiomycete
    • H. Kenmoku, T. Shimai, T. Toyomasu, N. Kato, and T. Sassa Erinacine Q, a new erinacine from Hericium erinaceum, and its biosynthetic route to erinacine C in the basidiomycete Biosci Biotechnol Biochem 66 2002 571 575
    • (2002) Biosci Biotechnol Biochem , vol.66 , pp. 571-575
    • Kenmoku, H.1    Shimai, T.2    Toyomasu, T.3    Kato, N.4    Sassa, T.5
  • 33
    • 0035888067 scopus 로고    scopus 로고
    • Isolation of (-)-cyatha-3,12-diene, a common biosynthetic intermediate of cyathane diterpenoids, from an erinacine-producing basidiomycete, Hericium erinaceum
    • H. Kenmoku, N. Kato, M. Shimada, M. Omoto, A. Mori, and W. Mituhashi Isolation of (-)-cyatha-3,12-diene, a common biosynthetic intermediate of cyathane diterpenoids, from an erinacine-producing basidiomycete, Hericium erinaceum Tetrahedron Lett 42 2001 7439-7422
    • (2001) Tetrahedron Lett , vol.42 , pp. 7439-7422
    • Kenmoku, H.1    Kato, N.2    Shimada, M.3    Omoto, M.4    Mori, A.5    Mituhashi, W.6
  • 34
    • 0032898427 scopus 로고    scopus 로고
    • Stimulation of neurotrophic factor secretion from 1321N1 human astrocytoma cells by novel diterpenoids, scabronines A and G
    • Y. Obara, N. Nakahata, T. Kita, Y. Takaya, H. Kobayashi, and S. Hosoi Stimulation of neurotrophic factor secretion from 1321N1 human astrocytoma cells by novel diterpenoids, scabronines A and G Eur J Pharmacol 370 1999 79 84
    • (1999) Eur J Pharmacol , vol.370 , pp. 79-84
    • Obara, Y.1    Nakahata, N.2    Kita, T.3    Takaya, Y.4    Kobayashi, H.5    Hosoi, S.6
  • 36
    • 49649087995 scopus 로고    scopus 로고
    • Two new megastigmane glycosides, physanosides A and B, from Physalis alkekengi L. var. franchetii, and their effect on NO release in macrophages
    • L. Qiu, F. Zhao, H.W. Liu, L.X. Chen, J.H. Jiang, and H.X. Liu Two new megastigmane glycosides, physanosides A and B, from Physalis alkekengi L. var. franchetii, and their effect on NO release in macrophages Chem Biodivers 5 2008 758 763
    • (2008) Chem Biodivers , vol.5 , pp. 758-763
    • Qiu, L.1    Zhao, F.2    Liu, H.W.3    Chen, L.X.4    Jiang, J.H.5    Liu, H.X.6
  • 37
    • 0023130372 scopus 로고
    • Evaluation of a tetrazolium-based semiautomated colorimetric assay: Assessment of chemosensitivity testing
    • J. Carmichael, W.G. DeGraff, A.F. Gazdar, J.D. Minna, and J.B. Mitchell Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing Cancer Res 47 1987 936 942
    • (1987) Cancer Res , vol.47 , pp. 936-942
    • Carmichael, J.1    Degraff, W.G.2    Gazdar, A.F.3    Minna, J.D.4    Mitchell, J.B.5
  • 38
    • 0000012791 scopus 로고
    • Some applications of the conformational dissymmetry rule
    • J.H. Brewster Some applications of the conformational dissymmetry rule Tetrahedron 13 1961 106 122
    • (1961) Tetrahedron , vol.13 , pp. 106-122
    • Brewster, J.H.1
  • 39
    • 0033597416 scopus 로고    scopus 로고
    • 4] as an auxiliary chromophore in chiroptical studies on steroidal alcohols
    • 4] as an auxiliary chromophore in chiroptical studies on steroidal alcohols Tetrahedron Asymmetry 10 1999 1507 1520
    • (1999) Tetrahedron Asymmetry , vol.10 , pp. 1507-1520
    • Frelek, J.1    Szczepek, W.J.2
  • 42
    • 84856010659 scopus 로고    scopus 로고
    • New sesquiterpenoids from the dried flower buds of Tussilago farfara and their inhibition on NO production in LPS-induced RAW264.7 cells
    • W. Li, X. Huang, and X.W. Yang New sesquiterpenoids from the dried flower buds of Tussilago farfara and their inhibition on NO production in LPS-induced RAW264.7 cells Fitoterapia 83 2012 318 322
    • (2012) Fitoterapia , vol.83 , pp. 318-322
    • Li, W.1    Huang, X.2    Yang, X.W.3
  • 43
    • 84865516969 scopus 로고    scopus 로고
    • Lathyrane diterpenes from Euphorbia prolifera and their inhibitory activities on LPS-induced NO production
    • J. Xu, D.Q. Jin, H. Song, Y.Q. Guo, and Y.S. He Lathyrane diterpenes from Euphorbia prolifera and their inhibitory activities on LPS-induced NO production Fitoterapia 83 2012 1205 1209
    • (2012) Fitoterapia , vol.83 , pp. 1205-1209
    • Xu, J.1    Jin, D.Q.2    Song, H.3    Guo, Y.Q.4    He, Y.S.5
  • 44
    • 80051879653 scopus 로고    scopus 로고
    • Four new cryptoporic acid derivatives from the fruiting bodies of Cryptoporus sinensis, and their inhibitory effects on nitric oxide production
    • W. Wu, F. Zhao, R. Ding, L. Bao, H. Gao, and J.C. Lu Four new cryptoporic acid derivatives from the fruiting bodies of Cryptoporus sinensis, and their inhibitory effects on nitric oxide production Chem Biodivers 8 2011 1529 1538
    • (2011) Chem Biodivers , vol.8 , pp. 1529-1538
    • Wu, W.1    Zhao, F.2    Ding, R.3    Bao, L.4    Gao, H.5    Lu, J.C.6
  • 45
    • 79951681787 scopus 로고    scopus 로고
    • Sesquiterpenes from Vladimiria souliei and their inhibitory effects on NO production
    • J. Xu, D.Q. Jin, D.D. Shi, Y.G. Ma, B. Yang, and P. Zhao Sesquiterpenes from Vladimiria souliei and their inhibitory effects on NO production Fitoterapia 82 2011 508 511
    • (2011) Fitoterapia , vol.82 , pp. 508-511
    • Xu, J.1    Jin, D.Q.2    Shi, D.D.3    Ma, Y.G.4    Yang, B.5    Zhao, P.6
  • 46
    • 14744275164 scopus 로고    scopus 로고
    • Screening of Indonesian medicinal plants for inhibitor activity on nitric oxide production of RAW264.7 cells and antioxidant activity
    • E.M. Choi, and J.K. Hwang Screening of Indonesian medicinal plants for inhibitor activity on nitric oxide production of RAW264.7 cells and antioxidant activity Fitoterapia 76 2005 194 203
    • (2005) Fitoterapia , vol.76 , pp. 194-203
    • Choi, E.M.1    Hwang, J.K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.