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Volumn 57, Issue 16, 2009, Pages 7288-7292

Study on the anthraquinones separated from the cultivation of Trichoderma harzianum strain Th-R16 and their biological activity

Author keywords

Anthraquinones; Structure activity relation; Trichoderma

Indexed keywords

ANTHRAQUINONE DERIVATIVE;

EID: 70349194917     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf901405c     Document Type: Article
Times cited : (50)

References (33)
  • 1
    • 0036562197 scopus 로고    scopus 로고
    • Trichosetin, a novel tetramic acid antibiotic produced in dual culture of Trichoderma harzianum and Catharanthus roseus Callus
    • Marfori, E. C.; Kajiyama, S.; Fukusaki, E.; Kobayashi, A. Trichosetin, a novel tetramic acid antibiotic produced in dual culture of Trichoderma harzianum and Catharanthus roseus Callus. Z. Naturforsch. C 2002, 57, 465-1410
    • (2002) Z. Naturforsch. C , vol.57 , pp. 465-1410
    • Marfori, E.C.1    Kajiyama, S.2    Fukusaki, E.3    Kobayashi, A.4
  • 2
    • 34548013767 scopus 로고    scopus 로고
    • Trichoderma harzianum: A biocontrol agent against Bipolaris oryzae
    • Abdel-Fattah, G. M.; Shabana, Y. M.; Ismail, A. E.; Rashad, Y. M. Trichoderma harzianum: A biocontrol agent against Bipolaris oryzae. Mycopathologia 2001, 164, 81-89.
    • (2001) Mycopathologia , vol.164 , pp. 81-89
    • Abdel-Fattah, G.M.1    Shabana, Y.M.2    Ismail, A.E.3    Rashad, Y.M.4
  • 3
    • 0027489188 scopus 로고
    • Antifungal metabolites from Trichoderma harzianum
    • Ghisalberti, E. L.; Rowland, C. Y. Antifungal metabolites from Trichoderma harzianum. J. Nat. Prod. 1993, 56, 1799-1804.
    • (1993) J. Nat. Prod. , vol.56 , pp. 1799-1804
    • Ghisalberti, E.L.1    Rowland, C.Y.2
  • 4
    • 36849085370 scopus 로고    scopus 로고
    • Secondary metabolites from species of the biocontrol agent Trichoderma
    • DOI 10.1007/s11101-006-9032-2, Perspectives on Natural Biopesticides
    • Reino, J. L.; Guerrero, R. F.; Hernández-Galán, R.; Collado, I. G. Secondary metabolites from species of the biocontrol agent Trichoderma. Phytochem. Rev. 2008, 7, 89-123. (Pubitemid 350233978)
    • (2008) Phytochemistry Reviews , vol.7 , Issue.1 , pp. 89-123
    • Reino, J.L.1    Guerrero, R.F.2    Hernandez-Galan, R.3    Collado, I.G.4
  • 5
    • 0034727718 scopus 로고    scopus 로고
    • Anti-platelet stilbenes from aerial parts of Rheum palaestinum
    • Aburjai, T. A. Anti-platelet stilbenes from aerial parts of Rheum palaestinum. Phytochemistry 2000, 55, 407-410.
    • (2000) Phytochemistry , vol.55 , pp. 407-410
    • Aburjai, T.A.1
  • 7
    • 33847666876 scopus 로고    scopus 로고
    • Efficient isolation of anthraquinone-derivatives from Trichoderma harzianumETS 323
    • Liu, S. Y.; Lo, C. T.; Chen, C.; Liu, M. Y.; Chen, J. H.; Peng, K. C. Efficient isolation of anthraquinone-derivatives from Trichoderma harzianumETS 323. J. Biochem. Biophys. Methods 2007, 70, 391-395.
    • (2007) J. Biochem. Biophys. Methods , vol.70 , pp. 391-395
    • Liu, S.Y.1    Lo, C.T.2    Chen, C.3    Liu, M.Y.4    Chen, J.H.5    Peng, K.C.6
  • 8
    • 0023219642 scopus 로고
    • Laxative potency and acute toxicity of some anthraquinone derivatives, senna extracts and fractions of senna extracts
    • Hietala, P.; Marvola, M.; Parviainen, T.; Lainonen, H. Laxative potency and acute toxicity of some anthraquinone derivatives, senna extracts and fractions of senna extracts. Pharmacol Toxicol 1987, 61, 153-156. (Pubitemid 17122973)
    • (1987) Pharmacology and Toxicology , vol.61 , Issue.2 , pp. 153-156
    • Hietala, P.1    Marvola, M.2    Parviainen, T.3    Lainonen, H.4
  • 9
    • 0023721257 scopus 로고
    • Biochemical study of Chinese rhubarb. XXII. Inhibitory effect of anthraquinone derivatives on Na+-K+ATPase of the rabbit renal medulla and their diuretic action
    • Zhou, X. M.; Chen, Q. H. Biochemical study of Chinese rhubarb. XXII. Inhibitory effect of anthraquinone derivatives on Na+-K+ATPase of the rabbit renal medulla and their diuretic action. Yao Xue Xue Bao 1988, 23, 17-20.
    • (1988) Yao Xue Xue Bao , vol.23 , pp. 17-20
    • Zhou, X.M.1    Chen, Q.H.2
  • 10
    • 0035939373 scopus 로고    scopus 로고
    • Phytoestrogens from the roots of Polygonum cuspidatum (Polygonaceae): Structure-requirement of hydroxyanthraquinones for estrogenic activity
    • DOI 10.1016/S0960-894X(01)00318-3, PII S0960894X01003183
    • Matsuda, H.; Shimoda, H.; Morikawa, T.; Yoshikawa, M. Phytoestrogens from the roots of Polygonum cuspidatum (Polygonaceae): Structure-requirement of hydroxyanthraquinones for estrogenic activity. Bioorg. Med. Chem. Lett. 2001, 11, 1839-1842. (Pubitemid 32675300)
    • (2001) Bioorganic and Medicinal Chemistry Letters , vol.11 , Issue.14 , pp. 1839-1842
    • Matsuda, H.1    Shimoda, H.2    Morikawa, T.3    Yoshikawa, M.4
  • 11
    • 40849133966 scopus 로고    scopus 로고
    • The necrotroph Botrytis cinerea induces a non-host type II resistance mechanism in Firms pinaster suspension-cultured cells
    • Azevedo, H.; Lino-Neto, T.; Tavares, R. M. The necrotroph Botrytis cinerea induces a non-host type II resistance mechanism in Firms pinaster suspension-cultured cells. Plant Cell Physiol 2008, 49, 386-395.
    • (2008) Plant Cell Physiol , vol.49 , pp. 386-395
    • Azevedo, H.1    Lino-Neto, T.2    Tavares, R.M.3
  • 12
    • 0043062850 scopus 로고    scopus 로고
    • Cynodontin: A fungal metabolite with antifungal properties
    • Chrysayi-Tokousbalides, M.; Kastanias, M. A. Cynodontin: A fungal metabolite with antifungal properties. J. Agric. Food Chem. 2003, 51, 4920-4923.
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 4920-4923
    • Chrysayi-Tokousbalides, M.1    Kastanias, M.A.2
  • 13
    • 0034284560 scopus 로고    scopus 로고
    • Antifungal activity of anthraquinone derivatives from Rheum emodi
    • Agarwal, S. K.; Singh, S. S.; Verma, S.; Kumar, S. Antifungal activity of anthraquinone derivatives from Rheum emodi. J. Ethnopharmacol. 2000, 72, 43-46.
    • (2000) J. Ethnopharmacol. , vol.72 , pp. 43-46
    • Agarwal, S.K.1    Singh, S.S.2    Verma, S.3    Kumar, S.4
  • 14
    • 0035046141 scopus 로고    scopus 로고
    • In vitro antiviral activity of the anthraquinone chrysophanic acid against poliovirus
    • DOI 10.1016/S0166-3542(01)00125-5, PII S0166354201001255
    • Semple, S. J.; Pyke, S. M.; Reynolds, G. D.; Flower, R. L. In vitro antiviral activity of the anthraquinone chrysophanic acid against poliovirus. Antiviral Res. 2001, 49, 169-178. (Pubitemid 32322470)
    • (2001) Antiviral Research , vol.49 , Issue.3 , pp. 169-178
    • Semple, S.J.1    Pyke, S.M.2    Reynolds, G.D.3    Flower, R.L.P.4
  • 15
    • 0031915292 scopus 로고    scopus 로고
    • Screening of Australian medicinal plants for antiviral activity
    • DOI 10.1016/S0378-8741(97)00152-9, PII S0378874197001529
    • Semple, S. J.; Reynolds, G. D.; O'Leary, M. C.; Flower, R. L. Screening of Australian medicinal plants for antiviral activity. J. Ethnopharmacol. 1998, 60, 163-172. (Pubitemid 28143727)
    • (1998) Journal of Ethnopharmacology , vol.60 , Issue.2 , pp. 163-172
    • Semple, S.J.1    Reynolds, G.D.2    O'Leary, M.C.3    Flower, R.L.P.4
  • 16
    • 0033910817 scopus 로고    scopus 로고
    • 1,4-Anthraquinone: An anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro
    • Perchellet, E. M.; Magill, M. J.; Huang, X.; Dalke, D. M.; Hua, D. H.; Perchellet, J. P. 1,4-Anthraquinone: An anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro. Anticancer Drugs 2000, 11, 339-352.
    • (2000) Anticancer Drugs , vol.11 , pp. 339-352
    • Perchellet, E.M.1    Magill, M.J.2    Huang, X.3    Dalke, D.M.4    Hua, D.H.5    Perchellet, J.P.6
  • 18
    • 33847655040 scopus 로고    scopus 로고
    • Screening strains of Trichoderma spp for plant growth enhancement in Taiwan
    • Lo, C. T.; Lin, C. Y. Screening strains of Trichoderma spp for plant growth enhancement in Taiwan. Plant Pathol Bull 2002, 11, 215-220.
    • (2002) Plant Pathol Bull , vol.11 , pp. 215-220
    • Lo, C.T.1    Lin, C.Y.2
  • 19
    • 70349205260 scopus 로고    scopus 로고
    • Control of monosporascus root rot of melon using Trichoderma spp. in Taiwan
    • Lo, C. T.; Huang, J. H. Control of monosporascus root rot of melon using Trichoderma spp. in Taiwan. Phytopathology 2002, 92, S48.
    • (2002) Phytopathology , vol.92
    • Lo, C.T.1    Huang, J.H.2
  • 20
    • 0036431503 scopus 로고    scopus 로고
    • Antimicrobial activity of methyl cis-7-oxo deisopropyldehydroabietate on Botrytis cinerea and Lophodermium seditiosum: Ultrastructural observations by transmission electron microscopy
    • DOI 10.1046/j.1365-2672.2002.01744.x
    • Feio, S. S.; Franca, S.; Silva, A. M.; Gigante, B.; Roseiro, J. C.; Marcelo Curto, M. J. Antimicrobial activity of methyl cis-7-oxo deisopropyldehydroabietate on Botrytis cinerea and Lophodermium seditiosum: Ultrastructural observations by transmission electron microscopy. J. Appl Microbiol 2002, 93, 765-771. (Pubitemid 35340877)
    • (2002) Journal of Applied Microbiology , vol.93 , Issue.5 , pp. 765-771
    • Feio, S.S.1    Franca, S.2    Silva, A.M.3    Gigante, B.4    Roseiro, J.C.5    Marcelo Curto, M.J.6
  • 21
    • 0032804197 scopus 로고    scopus 로고
    • Evaluation of reference dilution test methods for antimicrobial susceptibility testing of Pseudomonas aeruginosa strains isolated from patients with cystic fibrosis
    • Saiman, L.; Burns, J. L.; Whittier, S.; Krzewinski, J.; Marshall, S. A.; Jones, R. N. Evaluation of reference dilution test methods for antimicrobial susceptibility testing of Pseudomonas aeruginosa strains isolated from patients with cystic fibrosis. J. Clin. Microbiol. 1999, 37, 2987-2991.
    • (1999) J. Clin. Microbiol. , vol.37 , pp. 2987-2991
    • Saiman, L.1    Burns, J.L.2    Whittier, S.3    Krzewinski, J.4    Marshall, S.A.5    Jones, R.N.6
  • 22
    • 33749571004 scopus 로고    scopus 로고
    • Novel anthraquinone derivatives produced by Phoma sorghina, an endophyte found in association with the medicinal plant Tithonia diversifolia (Asteraceae)
    • Borges, W. S.; Pupo, M. T. Novel anthraquinone derivatives produced by Phoma sorghina, an endophyte found in association with the medicinal plant Tithonia diversifolia (Asteraceae). J. Braz. Chem. Soc. 2006, 17, 929-934.
    • (2006) J. Braz. Chem. Soc. , vol.17 , pp. 929-934
    • Borges, W.S.1    Pupo, M.T.2
  • 23
    • 0004571904 scopus 로고
    • Anthraquinones in Digitalis species
    • Imre, S.; Sar, S.; Thomson, R. H. Anthraquinones in Digitalis species. Phytochemistry 1976, 15, 317-320.
    • (1976) Phytochemistry , vol.15 , pp. 317-320
    • Imre, S.1    Sar, S.2    Thomson, R.H.3
  • 25
    • 0028268756 scopus 로고
    • An improved procedure for the oxidative transformation of hydroanthracenones and hydronaphthacenones to hydroxyanthraquinones and hydroxynapht hacenediones
    • Hauser, F. M.; Takeuchi, C.; Yin, H.; Corlett, S. A. An improved procedure for the oxidative transformation of hydroanthracenones and hydronaphthacenones to hydroxyanthraquinones and hydroxynapht hacenediones. J. Org. Chem. 1994, 59, 258-259.
    • (1994) J. Org. Chem. , vol.59 , pp. 258-259
    • Hauser, F.M.1    Takeuchi, C.2    Yin, H.3    Corlett, S.A.4
  • 26
    • 0013870997 scopus 로고
    • Anthraquinone pigments from Phomafoveata foister
    • Bick, I. R. C.; Rhee, C. Anthraquinone pigments from Phomafoveata foister. Biochem. J. 1966, 95, 112.
    • (1966) Biochem. J. , vol.95 , pp. 112
    • Bick, I.R.C.1    Rhee, C.2
  • 27
    • 0001574114 scopus 로고    scopus 로고
    • Extraction and identification of an antioxidative component from jue ming zi (Cassia tora 1.)
    • Yen, G. C.; Chen, H. W.; Duh, P. D. Extraction and identification of an antioxidative component from jue ming zi (Cassia tora 1.). J. Agric. Food Chem. 1998, 46, 820-824.
    • (1998) J. Agric. Food Chem. , vol.46 , pp. 820-824
    • Yen, G.C.1    Chen, H.W.2    Duh, P.D.3
  • 28
    • 0001173296 scopus 로고
    • Studies in anthracycline synthesis: Simple diels-alder routes to pachybasin, ω-hydroxypachybasin, aloe-emodin, and fallacinol
    • Benfaremo, N.; Cava, M. P. Studies in anthracycline synthesis: Simple diels-alder routes to pachybasin, ω-hydroxypachybasin, aloe-emodin, and fallacinol. J. Org. Chem. 1985, 50, 139-141.
    • (1985) J. Org. Chem. , vol.50 , pp. 139-141
    • Benfaremo, N.1    Cava, M.P.2
  • 29
    • 33745887817 scopus 로고    scopus 로고
    • Major secondary metabolites produced by two commercial Trichoderma strains active against different phytopathogens
    • DOI 10.1111/j.1472-765X.2006.01939.x
    • Vinale, F.; Marra, R.; Scala, F.; Ghisalberti, E. L.; Lorito, M.; Sivasithamparam, K. Major secondary metabolites produced by two commercial Trichoderma strains active against different phytopathogens. Lett. Appl. Microbiol. 2006, 43, 143-148. (Pubitemid 44050627)
    • (2006) Letters in Applied Microbiology , vol.43 , Issue.2 , pp. 143-148
    • Vinale, F.1    Marra, R.2    Scala, F.3    Ghisalberti, E.L.4    Lorito, M.5    Sivasithamparam, K.6
  • 30
    • 35148870158 scopus 로고    scopus 로고
    • Synthesis and antifungal properties of alpha-methoxy and alpha-hydroxyl substituted 4-thiatetradecanoic acids
    • Carballeira, N. M.; O'Neill, R.; Parang, K. Synthesis and antifungal properties of alpha-methoxy and alpha-hydroxyl substituted 4-thiatetradecanoic acids. Chem. Phys. Lipids 2007, 150, 82-88.
    • (2007) Chem. Phys. Lipids , vol.150 , pp. 82-88
    • Carballeira, N.M.1    O'Neill, R.2    Parang, K.3
  • 31
    • 51649120622 scopus 로고    scopus 로고
    • Methoxylation enhances stilbene bioactivity in Caenorhabditis elegans
    • Wilson, M. A.; Rimando, A. M.; Wolkow, C. A. Methoxylation enhances stilbene bioactivity in Caenorhabditis elegans. BMC Pharmacol. 2008, 5, 15.
    • (2008) BMC Pharmacol. , vol.5 , pp. 15
    • Wilson, M.A.1    Rimando, A.M.2    Wolkow, C.A.3
  • 33
    • 34447627650 scopus 로고    scopus 로고
    • Production of reactive oxygen species on photolysis of dilute aqueous quinone solutions
    • Garg, S.; Rose, A. L.; Waite, T. D. Production of reactive oxygen species on photolysis of dilute aqueous quinone solutions. Photochem. Photobiol. 2001, 83, 904-913.
    • (2001) Photochem. Photobiol. , vol.83 , pp. 904-913
    • Garg, S.1    Rose, A.L.2    Waite, T.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.