메뉴 건너뛰기




Volumn 11, Issue 12, 2011, Pages 1056-1074

Natural products with antitumor activity from endophytic fungi

Author keywords

Antitumor activity; Fungal endophytes; Natural products; Secondary metabolites

Indexed keywords

ALIPHATIC COMPOUND; ALKALOID DERIVATIVE; AMIDE; ANTHRAQUINONE DERIVATIVE; ANTINEOPLASTIC AGENT; BENZOQUINONE DERIVATIVE; CHROMONE DERIVATIVE; DITERPENE; ESTER; FLAVONOID; INDOLE DERIVATIVE; ISOCOUMARIN DERIVATIVE; LACTONE; LIGNAN; NAPHTHOQUINONE; NATURAL PRODUCT; PEPTIDE; QUINOLINE DERIVATIVE; QUINONE DERIVATIVE; SESQUITERPENE DERIVATIVE; STEROID; TERPENOID; XANTHONE DERIVATIVE;

EID: 82955250122     PISSN: 13895575     EISSN: 18755607     Source Type: Journal    
DOI: 10.2174/138955711797247716     Document Type: Review
Times cited : (43)

References (111)
  • 1
    • 34247109045 scopus 로고    scopus 로고
    • Natural products as sources of newdrugs over the last 25 years
    • Newman, D.J.; Cragg, G.M. Natural products as sources of newdrugs over the last 25 years. J. Nat. Prod., 2007, 70, 461-477.
    • (2007) J. Nat. Prod. , vol.70 , pp. 461-477
    • Newman, D.J.1    Cragg, G.M.2
  • 2
    • 1442310075 scopus 로고    scopus 로고
    • Natural productsfrom endophytic microorganisms
    • Strobel, G.; Daisy, B.; Castillo, U.; Harper, J. Natural productsfrom endophytic microorganisms. J. Nat. Prod., 2004, 67, 257-268.
    • (2004) J. Nat. Prod. , vol.67 , pp. 257-268
    • Strobel, G.1    Daisy, B.2    Castillo, U.3    Harper, J.4
  • 3
    • 0348109344 scopus 로고    scopus 로고
    • Bioprospecting for microbial endophytes andtheir natural products
    • Strobel, G.; Daisy, B. Bioprospecting for microbial endophytes andtheir natural products. Microbiol. Mol. Biol. Rev., 2003, 67, 491-502.
    • (2003) Microbiol. Mol. Biol. Rev. , vol.67 , pp. 491-502
    • Strobel, G.1    Daisy, B.2
  • 4
    • 0027270462 scopus 로고
    • Taxol and taxane production byTaxomyces andreanae, an endophytic fungus of Pacific yew
    • Stierle, A.; Strobel, G.; Stierle, D. Taxol and taxane production byTaxomyces andreanae, an endophytic fungus of Pacific yew. Science, 1993, 260, 214-216.
    • (1993) Science , vol.260 , pp. 214-216
    • Stierle, A.1    Strobel, G.2    Stierle, D.3
  • 5
    • 0036305688 scopus 로고    scopus 로고
    • Decipinin A anddecipienolides A and B: New bioactive metabolites from thecoprophilous fungi Podospora decipiens
    • Che, Y.S.; Gloer, J.B.; Koster, B.; Malloch, D. Decipinin A anddecipienolides A and B: new bioactive metabolites from thecoprophilous fungi Podospora decipiens. J. Nat. Prod., 2002, 65, 916-919.
    • (2002) J. Nat. Prod. , vol.65 , pp. 916-919
    • Che, Y.S.1    Gloer, J.B.2    Koster, B.3    Malloch, D.4
  • 6
    • 0037188596 scopus 로고    scopus 로고
    • Isopestacin, anisobenzofuranone from Pestalotiopsis microspora, possessingantifungal and antioxidant activities
    • Strobel, G.; Ford, E.; Worapong, J.; Harper, J.K.; Arif, A.M.;Grant, D.M.; Fung, P.; Ming Wah Chau, R. Isopestacin, anisobenzofuranone from Pestalotiopsis microspora, possessingantifungal and antioxidant activities. Phytochemistry, 2002, 60, 179-183.
    • (2002) Phytochemistry , vol.60 , pp. 179-183
    • Strobel, G.1    Ford, E.2    Worapong, J.3    Harper, J.K.4    Arif, A.M.5    Grant, D.M.6    Fung, P.7    Ming Wah Chau, R.8
  • 9
    • 0028845809 scopus 로고
    • Subglutinols A and B: Immunosuppressive compounds from theendophytic fungus Fusarium subglutinans
    • Lee, J.C.; Lobkovsky, E.; Pliam, N.B.; Strobel, G.; Clardy, J. Subglutinols A and B: immunosuppressive compounds from theendophytic fungus Fusarium subglutinans. J. Org. Chem., 1995, 60, 7076-7077.
    • (1995) J. Org. Chem. , vol.60 , pp. 7076-7077
    • Lee, J.C.1    Lobkovsky, E.2    Pliam, N.B.3    Strobel, G.4    Clardy, J.5
  • 10
    • 40749116854 scopus 로고    scopus 로고
    • Alachalasins A-G, new cytochalasins from the fungi Stachybotryscharatum
    • Zhang, Y.G.; Tian, R.X.; Liu, S.; Chen, X.L.; Liu, X.Z.; Che, Y.S. Alachalasins A-G, new cytochalasins from the fungi Stachybotryscharatum. Bioorg. Med. Chem., 2008, 16, 2627-2634.
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 2627-2634
    • Zhang, Y.G.1    Tian, R.X.2    Liu, S.3    Chen, X.L.4    Liu, X.Z.5    Che, Y.S.6
  • 11
    • 75649124469 scopus 로고    scopus 로고
    • Unique metabolites of Pestalotiopsis fici suggest abiosynthetic hypothesis involving a Diels-Alder reaction and thenmechanistic diversification
    • Liu, L.; Niu, S.B.; Lu, X.H.; Chen, X.L.; Zhang, H.; Guo, L.D.;Che, Y.S. Unique metabolites of Pestalotiopsis fici suggest abiosynthetic hypothesis involving a Diels-Alder reaction and thenmechanistic diversification. Chem. Commu., 2010, 41, 460-462.
    • (2010) Chem. Commu. , vol.41 , pp. 460-462
    • Liu, L.1    Niu, S.B.2    Lu, X.H.3    Chen, X.L.4    Zhang, H.5    Guo, L.D.6    Che, Y.S.7
  • 12
    • 21144434815 scopus 로고    scopus 로고
    • Characterization of graphislactone A as the antioxidant and freeradical-scavenging substance from the culture of Cephalosporiumsp. IFB-E001, an endophytic fungus in Trachelospermumjasminoides
    • Song, Y.C.; Huang, W.Y.; Sun, C.; Wang, F.W.; Tan, R.X. Characterization of graphislactone A as the antioxidant and freeradical-scavenging substance from the culture of Cephalosporiumsp. IFB-E001, an endophytic fungus in Trachelospermumjasminoides. Biol. Pharm. Bull., 2005, 28, 506-509.
    • (2005) Biol. Pharm. Bull. , vol.28 , pp. 506-509
    • Song, Y.C.1    Huang, W.Y.2    Sun, C.3    Wang, F.W.4    Tan, R.X.5
  • 13
    • 34247222521 scopus 로고    scopus 로고
    • A potentialantioxidant resource: Endophytic fungi from medicinal plants
    • Huang, W.Y.; Cai, Y. Z.; Xing, J.; Corke, H.; Sun, M. A potentialantioxidant resource: endophytic fungi from medicinal plants. Econ. Bot., 2007, 61, 14-30.
    • (2007) Econ. Bot. , vol.61 , pp. 14-30
    • Huang, W.Y.1    Cai, Y.Z.2    Xing, J.3    Corke, H.4    Sun, M.5
  • 14
    • 0035787076 scopus 로고    scopus 로고
    • Discovery of a smallmolecule insulin receptor activator
    • Salituro, G.M.; Pelaez, F.; Zhang, B.B. Discovery of a smallmolecule insulin receptor activator. Recent Prog. Horm. Res., 2001, 56, 107-126.
    • (2001) Recent Prog. Horm. Res. , vol.56 , pp. 107-126
    • Salituro, G.M.1    Pelaez, F.2    Zhang, B.B.3
  • 15
    • 43749109407 scopus 로고    scopus 로고
    • Cytotoxic activities of trichothecenes isolated froman endophytic fungus belonging to Order Hypocreales
    • Chinworrungsee, M.; Wiyakrutta, S.; Sriubolmas, N.; Chuailua, P.;Suksamrarn, A. Cytotoxic activities of trichothecenes isolated froman endophytic fungus belonging to Order Hypocreales. Arch. Pharm. Res., 2008, 31, 611-616.
    • (2008) Arch. Pharm. Res. , vol.31 , pp. 611-616
    • Chinworrungsee, M.1    Wiyakrutta, S.2    Sriubolmas, N.3    Chuailua, P.4    Suksamrarn, A.5
  • 18
    • 77952837839 scopus 로고    scopus 로고
    • A review: Recent advances and future prospects of taxol-producing endophyticfungi
    • Zhou, X.W.; Zhu, H.F.; Liu, L.; Lin, J.; Tang, K.X. A review:recent advances and future prospects of taxol-producing endophyticfungi. Appl. Microbiol. Biotechnol., 2010, 86, 1707-1717.
    • (2010) Appl. Microbiol. Biotechnol. , vol.86 , pp. 1707-1717
    • Zhou, X.W.1    Zhu, H.F.2    Liu, L.3    Lin, J.4    Tang, K.X.5
  • 19
    • 1642546962 scopus 로고    scopus 로고
    • Periconicins, two newfusicoccane diterpenes produced by an endophytic fungus Periconia sp. with antibacterial activity
    • Kim, S.; Shin, D.; Lee, T.; Oh, K. Periconicins, two newfusicoccane diterpenes produced by an endophytic fungus Periconia sp. with antibacterial activity. J. Nat. Prod., 2004, 67, 448-450.
    • (2004) J. Nat. Prod. , vol.67 , pp. 448-450
    • Kim, S.1    Shin, D.2    Lee, T.3    Oh, K.4
  • 21
    • 34548398960 scopus 로고    scopus 로고
    • Cytotoxicsecondary metabolites from fermentation broth of Brucea javanicaendophytic fungus1.2.11
    • Kumala, S.; Utji, R.; Sudarmono, P.; Kardono, L.B.S. Cytotoxicsecondary metabolites from fermentation broth of Brucea javanicaendophytic fungus1.2.11. Res. J. Microbiol., 2007, 2, 625-631.
    • (2007) Res. J. Microbiol. , vol.2 , pp. 625-631
    • Kumala, S.1    Utji, R.2    Sudarmono, P.3    Kardono, L.B.S.4
  • 23
    • 0002130755 scopus 로고
    • Thecytochalasins, a new class of biologically active mould metabolites
    • Aldridge, D.C.; Armstrong, J.J.; Speake, R.N.; Turner, W.B. Thecytochalasins, a new class of biologically active mould metabolites. Chem. Commun, 1967, 1, 26-27.
    • (1967) Chem. Commun , vol.1 , pp. 26-27
    • Aldridge, D.C.1    Armstrong, J.J.2    Speake, R.N.3    Turner, W.B.4
  • 25
    • 0034518542 scopus 로고    scopus 로고
    • Three newcytochalasins produced by an endophytic fungus in the genusRhinocladiella
    • Wagenaar, M.M.; Corwin, J.; Strobel, G.; Clardy, J. Three newcytochalasins produced by an endophytic fungus in the genusRhinocladiella. J. Nat. Prod., 2000, 63, 1692-1695.
    • (2000) J. Nat. Prod. , vol.63 , pp. 1692-1695
    • Wagenaar, M.M.1    Corwin, J.2    Strobel, G.3    Clardy, J.4
  • 26
    • 0019320646 scopus 로고
    • Cytochalasins block actin filamentelongation by binding to high affinity sites associated with F-acti
    • Flanagan, M.D.; Lin, S. Cytochalasins block actin filamentelongation by binding to high affinity sites associated with F-acti.J. Biol. Chem., 1980, 255, 835-838.
    • (1980) J. Biol. Chem. , vol.255 , pp. 835-838
    • Flanagan, M.D.1    Lin, S.2
  • 28
    • 67649314113 scopus 로고    scopus 로고
    • Cytotoxic cytochalasin metabolites of endophytic Endothia gyrosa
    • Xu, S.; Ge, H.M.; Song, Y.C.; Shen, Y.; Ding, H.; Tan, R.X. Cytotoxic cytochalasin metabolites of endophytic Endothia gyrosa. Chem. Biodivers., 2009, 6, 739-745.
    • (2009) Chem. Biodivers. , vol.6 , pp. 739-745
    • Xu, S.1    Ge, H.M.2    Song, Y.C.3    Shen, Y.4    Ding, H.5    Tan, R.X.6
  • 29
    • 77952922417 scopus 로고    scopus 로고
    • Bioactive alkaloids from the plant endophytic fungus Aspergillusterreus
    • Ge, H.M.; Peng, H.; Guo, Z.K.; Cui, J.T.; Song, Y.C.; Tan, R.X. Bioactive alkaloids from the plant endophytic fungus Aspergillusterreus. Planta Med., 2010, 76, 822-824.
    • (2010) Planta Med. , vol.76 , pp. 822-824
    • Ge, H.M.1    Peng, H.2    Guo, Z.K.3    Cui, J.T.4    Song, Y.C.5    Tan, R.X.6
  • 30
    • 33745011559 scopus 로고    scopus 로고
    • A new cytotoxic compound from Penicillium auratiogriseum, symbiotic or epiphytic fungi of sponge Mycale plumose
    • Xin, Z.H.; Zhu, W.M.; Gu, Q.Q.; Fang, Y.C.; Duan, L.; Cui, C.B. A new cytotoxic compound from Penicillium auratiogriseum, symbiotic or epiphytic fungi of sponge Mycale plumose. ChineseChem. Lett., 2005, 16, 1227-1229.
    • (2005) ChineseChem. Lett. , vol.16 , pp. 1227-1229
    • Xin, Z.H.1    Zhu, W.M.2    Gu, Q.Q.3    Fang, Y.C.4    Duan, L.5    Cui, C.B.6
  • 32
    • 0019941269 scopus 로고
    • Chaetoglobosins, cytotoxic 10-(indol-3-yl)-(13) cytochalasans from Chaetomium spp. I. Production, isolationand some cytological effects of chaetoglobosins
    • Sekita, S.; Yoshihira, K.; Natori, S.; Udagawa, S.; Sakabe, F.;Kurata, H.; Umeda, M. Chaetoglobosins, cytotoxic 10-(indol-3-yl)-(13) cytochalasans from Chaetomium spp. I. Production, isolationand some cytological effects of chaetoglobosins A-J. Chem. Pharm. Bull., 1982, 30, 1609-1617.
    • (1982) A-J. Chem. Pharm. Bull. , vol.30 , pp. 1609-1617
    • Sekita, S.1    Yoshihira, K.2    Natori, S.3    Udagawa, S.4    Sakabe, F.5    Kurata, H.6    Umeda, M.7
  • 33
    • 33644915823 scopus 로고    scopus 로고
    • Chaetoglobosin U, a cytochalasan alkaloid fromendophytic chaetomium globosum IFB-E019
    • Ding, G.; Song, Y.C.; Chen, J.R.; Xu, C.; Ge, H.M.; Wang, X.T.;Tan, R.S.; Chaetoglobosin U, a cytochalasan alkaloid fromendophytic chaetomium globosum IFB-E019. J. Nat. Prod., 2006, 69, 302-304.
    • (2006) J. Nat. Prod. , vol.69 , pp. 302-304
    • Ding, G.1    Song, Y.C.2    Chen, J.R.3    Xu, C.4    Ge, H.M.5    Wang, X.T.6    Tan, R.S.7
  • 34
    • 57749096909 scopus 로고    scopus 로고
    • Chaetoglobosinas produzidas por Chaetomium globosum, fungo endofítico associado a Viguiera robusta Gardn.(Asteraceae)
    • Momesso, L. S; Kawano, C. Y; Ribeiro, P. H; Nomizo, A.; Goldman, G. H; Chaetoglobosinas produzidas por Chaetomium globosum, fungo endofítico associado a Viguiera robusta Gardn.(Asteraceae). Quim. Nova, 2008, 31, 1680-1685.
    • (2008) Quim. Nova , vol.31 , pp. 1680-1685
    • Momesso, L.S.1    Kawano, C.Y.2    Ribeiro, P.H.3    Nomizo, A.4    Goldman, G.H.5
  • 35
    • 0019961398 scopus 로고
    • Chaetoglobosins, cytotoxic 10-(Indol-3-yl)-(13) cytochalasans from Chaetomium spp. II. production, isolationand some cytological effects of chaetoglobosins A, B and D
    • Sekita, S.; Yoshihira, K.; Natori, S.; Udagawa, S.; Sakabe, F.;Kurata, H.; Umeda, M. Chaetoglobosins, cytotoxic 10-(Indol-3-yl)-(13) cytochalasans from Chaetomium spp. II. production, isolationand some cytological effects of chaetoglobosins A, B and D. Chem. Pharm. Bull., 1982, 30, 1618-1628.
    • (1982) Chem. Pharm. Bull. , vol.30 , pp. 1618-1628
    • Sekita, S.1    Yoshihira, K.2    Natori, S.3    Udagawa, S.4    Sakabe, F.5    Kurata, H.6    Umeda, M.7
  • 36
    • 0036290931 scopus 로고    scopus 로고
    • Isolation and determination of the anticancersubstance of chaetoglobosin A producing by endophyticfungus in Maytenus hookeri
    • Zhang, L.Q.; Wang, H.K.; Shao, H.; Shen, Y.M.; Zeng, S.R.; Xu, C.D.; Xuan, Q.; Wei, R.C. Isolation and determination of the anticancersubstance of chaetoglobosin A producing by endophyticfungus in Maytenus hookeri. Chin. Pharm. J., 2002, 37, 172-175.
    • (2002) Chin. Pharm. J. , vol.37 , pp. 172-175
    • Zhang, L.Q.1    Wang, H.K.2    Shao, H.3    Shen, Y.M.4    Zeng, S.R.5    Xu, C.D.6    Xuan, Q.7    Wei, R.C.8
  • 38
    • 0033864419 scopus 로고    scopus 로고
    • TAN-1813, a novel ras-farnesyl transferase inhibitor produced by Phomasp. taxonomy, fermentation, isolation and biological activities invitro and in vivo
    • Ishii, T.; Hayashi, K.; Hida, T.; Yamamoto, Y.; Nozaki, Y. TAN-1813, a novel ras-farnesyl transferase inhibitor produced by Phomasp. taxonomy, fermentation, isolation and biological activities invitro and in vivo. J. Antibiot., 2000, 53, 765-778.
    • (2000) J. Antibiot. , vol.53 , pp. 765-778
    • Ishii, T.1    Hayashi, K.2    Hida, T.3    Yamamoto, Y.4    Nozaki, Y.5
  • 40
    • 33746563455 scopus 로고    scopus 로고
    • Neoplaether, a new cytotoxic and antifungalendophyte metabolite from Neoplaconema napellum IFB-E016
    • Wang, F.W.; Ye, Y.H.; Chen, J.R.; Wang, X.T.; Zhu, H.L.; Song, Y.C.; Tan, R.X. Neoplaether, a new cytotoxic and antifungalendophyte metabolite from Neoplaconema napellum IFB-E016. FEMS. Microbiol. Lett., 2006, 261, 218-223.
    • (2006) FEMS. Microbiol. Lett. , vol.261 , pp. 218-223
    • Wang, F.W.1    Ye, Y.H.2    Chen, J.R.3    Wang, X.T.4    Zhu, H.L.5    Song, Y.C.6    Tan, R.X.7
  • 41
    • 38849205749 scopus 로고    scopus 로고
    • Penicillenols from Penicillium sp. GQ-7, an endophytic fungusassociated with Aegiceras corniculatum
    • Lin, Z.J.; Lu, Z.Y.; Zhu, T.J.; Fang, Y.C.; Gu, Q.Q.; Zhu, W.M. Penicillenols from Penicillium sp. GQ-7, an endophytic fungusassociated with Aegiceras corniculatum. Chem. Pharm. Bull., 2008, 56, 217-221.
    • (2008) Chem. Pharm. Bull. , vol.56 , pp. 217-221
    • Lin, Z.J.1    Lu, Z.Y.2    Zhu, T.J.3    Fang, Y.C.4    Gu, Q.Q.5    Zhu, W.M.6
  • 42
    • 55549118879 scopus 로고    scopus 로고
    • Pyrrospirones A and B, apoptosisinducers in HL-60 cells, from an endophytic fungus, Neonectriaramulariae Wollenw KS-246
    • Shiono, Y.; Shimanuki, K.; Hiramatsu, F.; Koseki, T.; Tetsuya, M.;Fujisawa, N.; Kimura, K. Pyrrospirones A and B, apoptosisinducers in HL-60 cells, from an endophytic fungus, Neonectriaramulariae Wollenw KS-246. Bioorg. Med. Chem. Lett., 2008, 18, 6050-6053.
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 6050-6053
    • Shiono, Y.1    Shimanuki, K.2    Hiramatsu, F.3    Koseki, T.4    Tetsuya, M.5    Fujisawa, N.6    Kimura, K.7
  • 43
    • 33745021906 scopus 로고    scopus 로고
    • Bioreactor studies on theendophytic fungus Entrophospora infrequens for the production ofan anticancer alkaloid camptothecin
    • Amna, T.; Puri, S.C.; Verma, V.; Sharma, J.P.; Khajuria, R.K.;Musarrat, J.; Spiteller, M.; Qazi, G.N. Bioreactor studies on theendophytic fungus Entrophospora infrequens for the production ofan anticancer alkaloid camptothecin. Can. J. Microbiol., 2006, 52, 189-196.
    • (2006) Can. J. Microbiol. , vol.52 , pp. 189-196
    • Amna, T.1    Puri, S.C.2    Verma, V.3    Sharma, J.P.4    Khajuria, R.K.5    Musarrat, J.6    Spiteller, M.7    Qazi, G.N.8
  • 44
    • 0023924786 scopus 로고
    • Identification of mammalian DNAtopoisomerase I as an intracellular target of the anticancer drugCamptothecin
    • Hsiang, Y.H.; Liu, L.F. Identification of mammalian DNAtopoisomerase I as an intracellular target of the anticancer drugCamptothecin. Cancer Res., 1988, 48, 1722-1726.
    • (1988) Cancer Res. , vol.48 , pp. 1722-1726
    • Hsiang, Y.H.1    Liu, L.F.2
  • 45
    • 0024316466 scopus 로고
    • DNA topoisomerases as anticancer drug targets
    • Liu, L.F. DNA topoisomerases as anticancer drug targets. Adv. Pharmacol., Annu. Rev. Biochem., 1989, 58:351-375
    • (1989) Adv. Pharmacol., Annu. Rev. Biochem. , vol.58 , pp. 351-375
    • Liu, L.F.1
  • 46
    • 7144248725 scopus 로고
    • Plant antitumor agents. I. The isolation and structure ofcamptothecin, a novel alkaloidal leukemia and tumor inhibitor fromCamptotheca acuminata
    • Wall, M.E.; Wani, M.C.; Cook, C.E.; Palmer, K.H.; McPhail, A.T.;Sim, G.A. Plant antitumor agents. I. The isolation and structure ofcamptothecin, a novel alkaloidal leukemia and tumor inhibitor fromCamptotheca acuminata. J. Am. Chem. Soc., 1966, 88, 3888-3890.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 3888-3890
    • Wall, M.E.1    Wani, M.C.2    Cook, C.E.3    Palmer, K.H.4    McPhail, A.T.5    Sim, G.A.6
  • 47
    • 30544436426 scopus 로고    scopus 로고
    • Anendophytic fungus from Nothapodytes foetida that producescamptothecin
    • Puri, S.C.; Verma, V.; Amna, T.; Qazi, G.N.; Spiteller, M. Anendophytic fungus from Nothapodytes foetida that producescamptothecin. J. Nat. Prod., 2005, 68, 1717-1719.
    • (2005) J. Nat. Prod. , vol.68 , pp. 1717-1719
    • Puri, S.C.1    Verma, V.2    Amna, T.3    Qazi, G.N.4    Spiteller, M.5
  • 48
    • 7444240423 scopus 로고    scopus 로고
    • Aspergillus fumigatus CY018, an endophytic fungus inCynodon dactylon as a versatile producer of new and bioactivemetabolites
    • Liu, J.Y.; Song, Y.C.; Zhang, Z.; Wang, L.; Guo, Z.J.; Zou, W.X.;Tan, R.X. Aspergillus fumigatus CY018, an endophytic fungus inCynodon dactylon as a versatile producer of new and bioactivemetabolites. J. biotechnol., 2004, 114, 279-287.
    • (2004) J. biotechnol. , vol.114 , pp. 279-287
    • Liu, J.Y.1    Song, Y.C.2    Zhang, Z.3    Wang, L.4    Guo, Z.J.5    Zou, W.X.6    Tan, R.X.7
  • 49
    • 50249163750 scopus 로고    scopus 로고
    • Bioactivemetabolites from Penicillium sp., an endophytic fungus esiding inHopea hainanensis
    • Wang, F.W.; Hou, Z.M.; Wang, C.R.; Li, P.; Shi, D.H. Bioactivemetabolites from Penicillium sp., an endophytic fungus esiding inHopea hainanensis. World J. Microbiol. Biotechnol., 2008, 24, 2143-2147.
    • (2008) World J. Microbiol. Biotechnol. , vol.24 , pp. 2143-2147
    • Wang, F.W.1    Hou, Z.M.2    Wang, C.R.3    Li, P.4    Shi, D.H.5
  • 51
    • 56749155595 scopus 로고    scopus 로고
    • Chaetoglobins A and B, two unusualalkaloids from endophytic Chaetomium globosum culture
    • Ge, H. M.; Zhang, W. Y.; Ding, G.; Saparpakorn, P.; Song, Y. C.;Hannongbua, S.; Tan, R. X. Chaetoglobins A and B, two unusualalkaloids from endophytic Chaetomium globosum culture. Chem. Commun., 2008, 45, 5978-5980.
    • (2008) Chem. Commun. , vol.45 , pp. 5978-5980
    • Ge, H.M.1    Zhang, W.Y.2    Ding, G.3    Saparpakorn, P.4    Song, Y.C.5    Hannongbua, S.6    Tan, R.X.7
  • 52
    • 0029895763 scopus 로고    scopus 로고
    • Torreyanic acid: A selectively cytotoxic quinone dimer from the endophytic fungusPestalotiopsis microspora
    • Lee, J.C.; Strobel, G.A.; Lobkovsky, E.; Clardy, J. Torreyanic acid:a selectively cytotoxic quinone dimer from the endophytic fungusPestalotiopsis microspora. J. Org. Chem., 1996, 61, 3232-3233.
    • (1996) J. Org. Chem. , vol.61 , pp. 3232-3233
    • Lee, J.C.1    Strobel, G.A.2    Lobkovsky, E.3    Clardy, J.4
  • 53
    • 3042664030 scopus 로고    scopus 로고
    • Newsecondary metabolites from the marine endophytic fungusApiospora montagnei
    • Klemke, C.; Kehraus, S.; Wright, A. D; Knig, G.M. Newsecondary metabolites from the marine endophytic fungusApiospora montagnei. J. Nat. Prod., 2004, 67, 1058-1063.
    • (2004) J. Nat. Prod. , vol.67 , pp. 1058-1063
    • Klemke, C.1    Kehraus, S.2    Wright, A.D.3    Knig, G.M.4
  • 54
    • 40549084959 scopus 로고    scopus 로고
    • Sesquiterpene quinonesand related metabolites from Phyllosticta spinarum, a fungal strainendophytic in Platycladus orientalis of the Sonoran Desert
    • Wijeratne, E.M.; Paranagama, P.A.; Marron, M.T.; Gunatilaka, M.K.; Arnold, A.E.; Gunatilaka, A. A.L. Sesquiterpene quinonesand related metabolites from Phyllosticta spinarum, a fungal strainendophytic in Platycladus orientalis of the Sonoran Desert. J. Nat. Prod., 2008, 71, 218-222.
    • (2008) J. Nat. Prod. , vol.71 , pp. 218-222
    • Wijeratne, E.M.1    Paranagama, P.A.2    Marron, M.T.3    Gunatilaka, M.K.4    Arnold, A.E.5    Gunatilaka, A.A.L.6
  • 55
    • 0014898699 scopus 로고
    • Bikaverin, an antibioticfrom Gibberella fujikuroi, effective against Leishmaniabrasiliensis
    • Balan, J.; Fuska, J.; Kuhr, I.; Kuhrova, V. Bikaverin, an antibioticfrom Gibberella fujikuroi, effective against Leishmaniabrasiliensis. Folia Microbiol., 1970, 15, 479-484.
    • (1970) Folia Microbiol. , vol.15 , pp. 479-484
    • Balan, J.1    Fuska, J.2    Kuhr, I.3    Kuhrova, V.4
  • 56
    • 33947356980 scopus 로고    scopus 로고
    • Search for cell motility and angiogenesis inhibitors withpotential anticancer activity: Beauvericin and other constituents oftwo endophytic strains of Fusarium oxysporum
    • Zhan, J.X.; Burns, A.M.; Liu, M.X.; Faeth, S.H.; Leslie Gunatilaka, A.A. Search for cell motility and angiogenesis inhibitors withpotential anticancer activity: beauvericin and other constituents oftwo endophytic strains of Fusarium oxysporum. J. Nat. Prod., 2007, 70, 227-232.
    • (2007) J. Nat. Prod. , vol.70 , pp. 227-232
    • Zhan, J.X.1    Burns, A.M.2    Liu, M.X.3    Faeth, S.H.4    Leslie Gunatilaka, A.A.5
  • 57
    • 27844439394 scopus 로고    scopus 로고
    • Bioactive deoxypreussomerins and dimeric naphthoquinones fromDiospyros ehretioides fruits: Deoxypreussomerins may not be plantmetabolites but may be from fungal epiphytes or endophytes
    • Prajoubklang, A.; Sirithunyalug, B.; Charoenchai, P.; Suvannakad, R.; Sriubolmas, N.; Piyamongkol, S.; Kongsaeree, P.; Kittakoop, P. Bioactive deoxypreussomerins and dimeric naphthoquinones fromDiospyros ehretioides fruits: deoxypreussomerins may not be plantmetabolites but may be from fungal epiphytes or endophytes. Chem. Biodivers., 2005, 2, 1358-1367.
    • (2005) Chem. Biodivers. , vol.2 , pp. 1358-1367
    • Prajoubklang, A.1    Sirithunyalug, B.2    Charoenchai, P.3    Suvannakad, R.4    Sriubolmas, N.5    Piyamongkol, S.6    Kongsaeree, P.7    Kittakoop, P.8
  • 58
    • 0034649727 scopus 로고    scopus 로고
    • Cytoskyrins A andB, new bioactive santhraquinones isolated from an endophyticfungus
    • Brady, S.F.; Singh, M.P.; Janso, J. E.; Clardy, J. Cytoskyrins A andB, new bioactive santhraquinones isolated from an endophyticfungus. Org. Lett., 2000, 2, 4047-4049.
    • (2000) Org. Lett. , vol.2 , pp. 4047-4049
    • Brady, S.F.1    Singh, M.P.2    Janso, J.E.3    Clardy, J.4
  • 59
    • 34848833882 scopus 로고    scopus 로고
    • Cytoskyrins and cytosporonesproduced by Cytospora sp. CR200: Taxonomy, fermentation andbiological activities
    • Singh, M.P.; Janso, J.E.; Brady, S.F. Cytoskyrins and cytosporonesproduced by Cytospora sp. CR200: taxonomy, fermentation andbiological activities. Mar. Drugs, 2007, 5, 71-84.
    • (2007) Mar. Drugs , vol.5 , pp. 71-84
    • Singh, M.P.1    Janso, J.E.2    Brady, S.F.3
  • 60
    • 76449101999 scopus 로고    scopus 로고
    • SZ-685C, a marineanthraquinone, is a potent inducer of apoptosis with anticanceractivity by suppression of the Akt/FOXO pathway
    • Xie, G.E.; Zhu, X.; Li, Q.; Gu, M.H.; He, Z.J.; Wu, J.H.; Li, J.; Lin, Y.C.; Li, M.F.; She, Z.G.; Yuan, J. SZ-685C, a marineanthraquinone, is a potent inducer of apoptosis with anticanceractivity by suppression of the Akt/FOXO pathway. Brit. J. Pharmacol., 2010, 159, 689-697.
    • (2010) Brit. J. Pharmacol. , vol.159 , pp. 689-697
    • Xie, G.E.1    Zhu, X.2    Li, Q.3    Gu, M.H.4    He, Z.J.5    Wu, J.H.6    Li, J.7    Lin, Y.C.8    Li, M.F.9    She, Z.G.10    Yuan, J.11
  • 63
    • 29144444658 scopus 로고    scopus 로고
    • New andcytotoxic anthraquinones from Pleospora sp. IFB-E006, anendophytic fungus in Imperata cylindrical
    • Ge, H.M.; Song, Y.C.; Shan, C.Y.; Ye, Y.H.; Tan, R.X. New andcytotoxic anthraquinones from Pleospora sp. IFB-E006, anendophytic fungus in Imperata cylindrical. Planta Med., 2005, 71, 1063-1065.
    • (2005) Planta Med. , vol.71 , pp. 1063-1065
    • Ge, H.M.1    Song, Y.C.2    Shan, C.Y.3    Ye, Y.H.4    Tan, R.X.5
  • 64
    • 42749093846 scopus 로고    scopus 로고
    • Bioactive metabolites fromthe endophytic fungus Ampelomyces sp. isolated from themedicinal plant Urospermum picroides
    • Aly, A.H.; Edrada-Ebel, R.A.; Wray, V.; Müller, W.E. G; Kozytska, S.; Hentschel, U.; Proksch, P.; Ebel, R. Bioactive metabolites fromthe endophytic fungus Ampelomyces sp. isolated from themedicinal plant Urospermum picroides. Phytochemistry, 2008, 69, 1716-1725.
    • (2008) Phytochemistry , vol.69 , pp. 1716-1725
    • Aly, A.H.1    Edrada-Ebel, R.A.2    Wray, V.3    Müller, W.E.G.4    Kozytska, S.5    Hentschel, U.6    Proksch, P.7    Ebel, R.8
  • 65
    • 70350501142 scopus 로고    scopus 로고
    • Lightindependentmetabolomics of endophytic Thielavia subthermophilaprovides insight into microbial hypericin biosynthesis
    • Kusari, S.; Zühlke, S.; Kouth, J.; Cellárová E.; Spiteller, M. Lightindependentmetabolomics of endophytic Thielavia subthermophilaprovides insight into microbial hypericin biosynthesis. J. Nat. Prod., 2009, 72, 1825-1835.
    • (2009) J. Nat. Prod. , vol.72 , pp. 1825-1835
    • Kusari, S.1    Zühlke, S.2    Kouth, J.3    Cellárová, E.4    Spiteller, M.5
  • 67
    • 73949132159 scopus 로고    scopus 로고
    • Structureelucidation and NMR assignments for two xanthone derivativesfrom a mangrove endophytic fungus (No. ZH19)
    • Huang, Z.J.; Yang, R.Y.; Yin, X.H.; She, Z.Q.; Lin, Y.C.; Structureelucidation and NMR assignments for two xanthone derivativesfrom a mangrove endophytic fungus (No. ZH19). Magn. Reson. Chem., 2010, 48, 80-82.
    • (2010) Magn. Reson. Chem. , vol.48 , pp. 80-82
    • Huang, Z.J.1    Yang, R.Y.2    Yin, X.H.3    She, Z.Q.4    Lin, Y.C.5
  • 68
    • 0034861657 scopus 로고    scopus 로고
    • Dicerandrols, new antibiotic andcytotoxic dimers produced by the fungi Phomopsis longicollaisolated from an endangered mint
    • Wagenaar, M.; Clardy, J.; Dicerandrols, new antibiotic andcytotoxic dimers produced by the fungi Phomopsis longicollaisolated from an endangered mint. J. Nat. Prod., 2001, 64, 1006-1009.
    • (2001) J. Nat. Prod. , vol.64 , pp. 1006-1009
    • Wagenaar, M.1    Clardy, J.2
  • 71
    • 33750090717 scopus 로고    scopus 로고
    • A new dihydroxanthenone from a plantassociatedstrain of the fungi Chaetomium globosum demonstratesanticancer activity
    • Kithsiri Wijeratne, E.M.; Turbyville, T.J.; Fritz, A.; Whitesell, L.;Gunatilaka, A. A. L. A new dihydroxanthenone from a plantassociatedstrain of the fungi Chaetomium globosum demonstratesanticancer activity. Bioorgan. Med. Chem., 2006, 14, 7917-7923.
    • (2006) Bioorgan. Med. Chem. , vol.14 , pp. 7917-7923
    • Kithsiri Wijeratne, E.M.1    Turbyville, T.J.2    Fritz, A.3    Whitesell, L.4    Gunatilaka, A.A.L.5
  • 72
    • 33846447789 scopus 로고    scopus 로고
    • Absolute configurations ofglobosuxanthone A and secondary metabolites from Microdiplodiasp.-a novel solid-state CD/TDDFT approach
    • Hussain, H.; Krohn, K.; Floerke, U.; Schulz, B.; Draeger, S.;Pescitelli, G.; Antus, S.; Kurtán, T. Absolute configurations ofglobosuxanthone A and secondary metabolites from Microdiplodiasp.-a novel solid-state CD/TDDFT approach. Eur. J. Org. Chem., 2007, 2, 292-295.
    • (2007) Eur. J. Org. Chem. , vol.2 , pp. 292-295
    • Hussain, H.1    Krohn, K.2    Floerke, U.3    Schulz, B.4    Draeger, S.5    Pescitelli, G.6    Antus, S.7    Kurtán, T.8
  • 73
    • 65649114056 scopus 로고    scopus 로고
    • Chromones from the endophyticfungus Pestalotiopsis sp. isolated from the Chinese mangrove plantRhizophora mucronata
    • Xu, J.; Kjer, J.; Sendker, J.; Wray, V.; Guan, H.S.; Edrada, R.A.;Lin, W.H.; J. Wu, Proksch, P. Chromones from the endophyticfungus Pestalotiopsis sp. isolated from the Chinese mangrove plantRhizophora mucronata. J. Nat. Prod., 2009, 72, 662-665.
    • (2009) J. Nat. Prod. , vol.72 , pp. 662-665
    • Xu, J.1    Kjer, J.2    Sendker, J.3    Wray, V.4    Guan, H.S.5    Edrada, R.A.6    Lin, W.H.7    Wu, J.8    Proksch, P.9
  • 74
    • 39749132763 scopus 로고    scopus 로고
    • A new isocoumarin from mangrove endophytic fungus(No. dz17) on the South China Sea coast
    • Huang, Z.J.; Shao, C.L.; Chen, Y.G.; She, Z.G. Lin, Y.C.; Zhou, S.N. A new isocoumarin from mangrove endophytic fungus(No. dz17) on the South China Sea coast. Chem. Nat. Compd., 2007, 43, 655-658.
    • (2007) Chem. Nat. Compd. , vol.43 , pp. 655-658
    • Huang, Z.J.1    Shao, C.L.2    Chen, Y.G.3    She, Z.G.4    Lin, Y.C.5    Zhou, S.N.6
  • 75
    • 18744373344 scopus 로고    scopus 로고
    • Podophyllotoxin derivatives. current synthetic approachesfor new anticancer agents
    • You, Y. Podophyllotoxin derivatives. current synthetic approachesfor new anticancer agents. Curr. Pharm. Des., 2005, 11, 1695-717.
    • (2005) Curr. Pharm. Des. , vol.11 , pp. 1695-1717
    • You, Y.1
  • 76
    • 33748774962 scopus 로고    scopus 로고
    • Endophyte fungalisolates from Podophyllum peltatum produce podophyllotoxin
    • Eyberger, A.L.; Dondapati, R.; Porter, J.R. Endophyte fungalisolates from Podophyllum peltatum produce podophyllotoxin. J. Nat. Prod., 2006, 69, 1121-1124.
    • (2006) J. Nat. Prod. , vol.69 , pp. 1121-1124
    • Eyberger, A.L.1    Dondapati, R.2    Porter, J.R.3
  • 77
    • 0036212896 scopus 로고    scopus 로고
    • Deoxypodophyllotoxin;the cytotoxic and antiangiogenic component from Pulsatillakoreana
    • Kim, Y.; Kim, S.B.; You, Y.J.; Ahn, B.Z. Deoxypodophyllotoxin;the cytotoxic and antiangiogenic component from Pulsatillakoreana. Planta med., 2002, 68, 271-274.
    • (2002) Planta med. , vol.68 , pp. 271-274
    • Kim, Y.1    Kim, S.B.2    You, Y.J.3    Ahn, B.Z.4
  • 78
    • 68849116722 scopus 로고    scopus 로고
    • Aspergillus fumigatusFresenius, an endophytic fungus from Juniperus communis L. Horstmann as a novel source of the anticancer pro-drugdeoxypodophyllotoxin
    • Kusari, S.; Lamshöft, M.; Spiteller, M. Aspergillus fumigatusFresenius, an endophytic fungus from Juniperus communis L. Horstmann as a novel source of the anticancer pro-drugdeoxypodophyllotoxin. J. Appl. Microbiol., 2009, 107, 1019-1030.
    • (2009) J. Appl. Microbiol. , vol.107 , pp. 1019-1030
    • Kusari, S.1    Lamshöft, M.2    Spiteller, M.3
  • 79
    • 0033597902 scopus 로고    scopus 로고
    • Sequoiatones A and B: Novelantitumor metabolites isolated from a redwood endophyte
    • Stierle, A.A.; Stierle, D.B.; Bugni, T. Sequoiatones A and B: novelantitumor metabolites isolated from a redwood endophyte. J. Org. Chem., 1999, 64, 5479-5484.
    • (1999) J. Org. Chem. , vol.64 , pp. 5479-5484
    • Stierle, A.A.1    Stierle, D.B.2    Bugni, T.3
  • 80
    • 0037602128 scopus 로고    scopus 로고
    • Sequoiamonascins A-D:Novel anticancer metabolites isolated from a redwood endophyte
    • Stierle, D.B.; Stierle, A.A.; Bugni, T. Sequoiamonascins A-D:Novel anticancer metabolites isolated from a redwood endophyte.J. Org. Chem., 2003, 68, 4966-4969.
    • (2003) J. Org. Chem. , vol.68 , pp. 4966-4969
    • Stierle, D.B.1    Stierle, A.A.2    Bugni, T.3
  • 81
    • 0028875394 scopus 로고
    • Structure, chemistry, and biology ofactinoplanic acids: Potent inhibitors of ras farnesyl-proteintransferase
    • Singh, S.B.; Liesch, J.M.; Lingham, R.B.; Silverman, K.C.;Sigmund, J.M.; Goetz, M.A. Structure, chemistry, and biology ofactinoplanic acids: Potent inhibitors of ras farnesyl-proteintransferase. J. Org. Chem., 1995, 60, 7896-7901.
    • (1995) J. Org. Chem. , vol.60 , pp. 7896-7901
    • Singh, S.B.1    Liesch, J.M.2    Lingham, R.B.3    Silverman, K.C.4    Sigmund, J.M.5    Goetz, M.A.6
  • 82
    • 0037031540 scopus 로고    scopus 로고
    • Brefeldin A, a cytotoxin produced byPaecilomyces sp. and Aspergillus clavatus isolated from Taxusmairei and Torreya grandis
    • Wang, J.F.; Huang, Y.J.; Fang, M.J.; Zhang, Y.J.; Zheng, Z.H.;Zhao, Y.F.; Su, W.J. Brefeldin A, a cytotoxin produced byPaecilomyces sp. and Aspergillus clavatus isolated from Taxusmairei and Torreya grandis. FEMS Immunol. Med. Microbiol., 2002, 34, 51-57.
    • (2002) FEMS Immunol. Med. Microbiol. , vol.34 , pp. 51-57
    • Wang, J.F.1    Huang, Y.J.2    Fang, M.J.3    Zhang, Y.J.4    Zheng, Z.H.5    Zhao, Y.F.6    Su, W.J.7
  • 83
    • 0032768258 scopus 로고    scopus 로고
    • Induction of terminal differentiation and apoptosisin human coloniccarcinoma cells by brefeldin A, adrugaffecting gangliosidebiosynthesis
    • Nojiri, H.; Manyaa, H.; Isonoa, H.; Yamana, H.; Nojima, S. Induction of terminal differentiation and apoptosisin human coloniccarcinoma cells by brefeldin A, adrugaffecting gangliosidebiosynthesis. FEBS Lett. 1999, 453, 140-144.
    • (1999) FEBS Lett , vol.453 , pp. 140-144
    • Nojiri, H.1    Manyaa, H.2    Isonoa, H.3    Yamana, H.4    Nojima, S.5
  • 84
    • 35549004397 scopus 로고    scopus 로고
    • Structural and biologicalproperties of vermistatin and two new vermistatin derivativesisolated from the marine-mangrove endophytic fungus Guignardiasp. No. 4382
    • Xia, X.K.; Huang, H.R.; She, Z.G.; Cai, J.W.; Lan, L.; Zhang, J.Y.;Fu, L.W.; Vrijmoed, L.L.P.; Lin, Y.C. Structural and biologicalproperties of vermistatin and two new vermistatin derivativesisolated from the marine-mangrove endophytic fungus Guignardiasp. No. 4382. Helv. Chim. Acta, 2007, 90, 1925-1931.
    • (2007) Helv. Chim. Acta , vol.90 , pp. 1925-1931
    • Xia, X.K.1    Huang, H.R.2    She, Z.G.3    Cai, J.W.4    Lan, L.5    Zhang, J.Y.6    Fu, L.W.7    Vrijmoed, L.L.P.8    Lin, Y.C.9
  • 86
    • 28444436309 scopus 로고    scopus 로고
    • Four 6H-Dibenzo [b, d]-pyran-6-one derivatives produced by theendophyte Cephalosporium acremonium IFB-E007
    • Zhang, H.W.; Huang, W.Y.; Song, Y.C.; Chen, J.R.; Tan, R.X.;Four 6H-Dibenzo [b, d]-pyran-6-one derivatives produced by theendophyte Cephalosporium acremonium IFB-E007. Helv. Chim. Acta, 2005, 88, 2861-2864.
    • (2005) Helv. Chim. Acta , vol.88 , pp. 2861-2864
    • Zhang, H.W.1    Huang, W.Y.2    Song, Y.C.3    Chen, J.R.4    Tan, R.X.5
  • 87
    • 53849103252 scopus 로고    scopus 로고
    • Isolation, structure elucidation, andmutagenicity of four alternariol derivatives produced by themangrove endophytic fungus No. 2240
    • Tan, N.; Tao, Y.W.; Pan, J.H.; Wang, S.Y.; Xu, F.; She, Z.G.; Lin, Y.C.; Gareth Jones, E.B. Isolation, structure elucidation, andmutagenicity of four alternariol derivatives produced by themangrove endophytic fungus No. 2240. Chem. Nat. Compd., 2008, 44, 296-300.
    • (2008) Chem. Nat. Compd. , vol.44 , pp. 296-300
    • Tan, N.1    Tao, Y.W.2    Pan, J.H.3    Wang, S.Y.4    Xu, F.5    She, Z.G.6    Lin, Y.C.7    Gareth Jones, E.B.8
  • 89
    • 72249119460 scopus 로고    scopus 로고
    • Chemistry and cytotoxic activities ofpolyketides produced by the mangrove endophytic fungusPhomopsis sp. ZSU-H76
    • Huang, Z.J.; Guo, Z.Y.; Yang, R.Y.; Yin, X.H.; Li, X.Y.; Luo, W.Q.; She, Z.G.; Lin, Y.C. Chemistry and cytotoxic activities ofpolyketides produced by the mangrove endophytic fungusPhomopsis sp. ZSU-H76. Chem. Nat. Compd., 2009, 45, 625-628.
    • (2009) Chem. Nat. Compd. , vol.45 , pp. 625-628
    • Huang, Z.J.1    Guo, Z.Y.2    Yang, R.Y.3    Yin, X.H.4    Li, X.Y.5    Luo, W.Q.6    She, Z.G.7    Lin, Y.C.8
  • 90
    • 20444442814 scopus 로고    scopus 로고
    • Globosumones A-C, cytotoxic orsellinic acid esters from theSonoran Desert endophytic fungus Chaetomium globosum1
    • Bashyal, B.P.; Wijeratne, E.M.; Faeth, S.H.; Gunatilaka, A.L.L. Globosumones A-C, cytotoxic orsellinic acid esters from theSonoran Desert endophytic fungus Chaetomium globosum1. J. Nat. Prod., 2005, 68, 724-728.
    • (2005) J. Nat. Prod. , vol.68 , pp. 724-728
    • Bashyal, B.P.1    Wijeratne, E.M.2    Faeth, S.H.3    Gunatilaka, A.L.L.4
  • 91
    • 0015603328 scopus 로고
    • Anew antibiotic leucinostatin derived from Penicillium lilacinum
    • Arai, T.; Mikami, Y.; Fukushima, K.; Utsumi, T.; Yazawa, K. Anew antibiotic leucinostatin derived from Penicillium lilacinum. J. Antibiot., 1973, 26, 157-161.
    • (1973) J. Antibiot. , vol.26 , pp. 157-161
    • Arai, T.1    Mikami, Y.2    Fukushima, K.3    Utsumi, T.4    Yazawa, K.5
  • 92
    • 0021059178 scopus 로고
    • Studieson peptide antibiotics, leucinostatins. II. The structures ofleucinostatins A and B
    • Fukushima, K. Arai, T.; Mori, Y.; Tsuboi, M.; Suzuki, M. Studieson peptide antibiotics, leucinostatins. II. The structures ofleucinostatins A and B. J. Antibiot., 1983, 36, 1613-1630.
    • (1983) J. Antibiot. , vol.36 , pp. 1613-1630
    • Fukushima, K.1    Arai, T.2    Mori, Y.3    Tsuboi, M.4    Suzuki, M.5
  • 93
    • 0030751039 scopus 로고    scopus 로고
    • Acremonium sp.-aleucinostatin A producing endophyte of European yew (Taxusbaccata)
    • Strobel, G.A.; Torczynski, R.; Bollon, A. Acremonium sp.-aleucinostatin A producing endophyte of European yew (Taxusbaccata). Plant Sci., 1997, 128, 97-108.
    • (1997) Plant Sci. , vol.128 , pp. 97-108
    • Strobel, G.A.1    Torczynski, R.2    Bollon, A.3
  • 94
    • 34249945556 scopus 로고    scopus 로고
    • Antiplasmodial and antiviral cyclohexadepsipeptides from theendophytic fungus Pullularia sp. BCC 8613
    • Isaka, M.; Berkaew, P.; Intereya, K.; Komwijit, S.; Sathitkunanon, T. Antiplasmodial and antiviral cyclohexadepsipeptides from theendophytic fungus Pullularia sp. BCC 8613. Tetrahedron, 2007, 63, 6855-6860.
    • (2007) Tetrahedron , vol.63 , pp. 6855-6860
    • Isaka, M.1    Berkaew, P.2    Intereya, K.3    Komwijit, S.4    Sathitkunanon, T.5
  • 95
    • 0000890985 scopus 로고
    • The structureof beauvericin, a new depsipeptide antibiotic toxic to Artemiasalina
    • Hamill, R.L.; Higgens, C.E.; Boaz, H.E.; Gorman, M. The structureof beauvericin, a new depsipeptide antibiotic toxic to Artemiasalina. Tetrahedron Lett., 1969, 10, 4255-4258.
    • (1969) Tetrahedron Lett. , vol.10 , pp. 4255-4258
    • Hamill, R.L.1    Higgens, C.E.2    Boaz, H.E.3    Gorman, M.4
  • 96
    • 33947356980 scopus 로고    scopus 로고
    • Search for cell motility and angiogenesis inhibitors withpotential anticancer activity: Beauvericin and other constituents oftwo endophytic strains of Fusarium oxysporum
    • Zhan, J.X., Burns, A.M., Liu, M.X., Faeth, S.H., Leslie Gunatilaka, A.A. Search for cell motility and angiogenesis inhibitors withpotential anticancer activity: beauvericin and other constituents oftwo endophytic strains of Fusarium oxysporum. J. Nat. Prod. 2007, 70, 227-232.
    • (2007) J. Nat. Prod , vol.70 , pp. 227-232
    • Zhan, J.X.1    Burns, A.M.2    Liu, M.X.3    Faeth, S.H.4    Leslie Gunatilaka, A.A.5
  • 98
    • 42949089125 scopus 로고    scopus 로고
    • The isolation, structure determination and cytotoxicity of the new fungalmetabolite, trichodermamide
    • Davis, R.A.; Longden, J.; Avery, V.M.; Healy, P.C. The isolation, structure determination and cytotoxicity of the new fungalmetabolite, trichodermamide C. Bioorg. Med. chem. lett., 2008, 18, 2836-2839.
    • (2008) C. Bioorg. Med. chem. lett. , vol.18 , pp. 2836-2839
    • Davis, R.A.1    Longden, J.2    Avery, V.M.3    Healy, P.C.4
  • 99
    • 2342559790 scopus 로고    scopus 로고
    • A newcytotoxic sterol produced by an endophytic fungus fromCastaniopsis fissa at the South China Sea coast
    • Li, H.J.; Lin, Y.C.; Vrijmoed, L.L.P.; Jones, E.B.G. A newcytotoxic sterol produced by an endophytic fungus fromCastaniopsis fissa at the South China Sea coast. Chinese Chem. Lett., 2004, 15, 419-422.
    • (2004) Chinese Chem. Lett. , vol.15 , pp. 419-422
    • Li, H.J.1    Lin, Y.C.2    Vrijmoed, L.L.P.3    Jones, E.B.G.4
  • 100
    • 0001679909 scopus 로고
    • Minor and trace sterols in marine invertebrates. 26. Isolation andstructure elucidation of nine new 5α, 8α-epidioxy sterols from fourmarine organisms
    • Gunatilaka, A.A.L.; Goplchand, Y.; Schmitz, L.; Djerassi, C. Minor and trace sterols in marine invertebrates. 26. Isolation andstructure elucidation of nine new 5α, 8α-epidioxy sterols from fourmarine organisms. J. Org. Chem., 1981, 46, 3860-3866.
    • (1981) J. Org. Chem. , vol.46 , pp. 3860-3866
    • Gunatilaka, A.A.L.1    Goplchand, Y.2    Schmitz, L.3    Djerassi, C.4
  • 101
    • 22944434570 scopus 로고    scopus 로고
    • Anti-Helicobacter pylori substances from endophytic fungal cultures
    • Li, Y.; Song, Y.C.; Liu, J.Y.; Ma, Y.M.; Tan, R.X.; Anti-Helicobacter pylori substances from endophytic fungal cultures. World J. Microb. Biot., 2005, 21, 553-558.
    • (2005) World J. Microb. Biot. , vol.21 , pp. 553-558
    • Li, Y.1    Song, Y.C.2    Liu, J.Y.3    Ma, Y.M.4    Tan, R.X.5
  • 104
    • 67650482875 scopus 로고    scopus 로고
    • Study onsecondary metabolites from endophytic fungus S26 ofCephalotaxus hainanensis
    • Chen, P.; Dai, H.f.; Wu, J.; Dai, W.J.; Mei, W.L. Study onsecondary metabolites from endophytic fungus S26 ofCephalotaxus hainanensis. Chin. Pharm. J., 2009, 44, 825-827.
    • (2009) Chin. Pharm. J. , vol.44 , pp. 825-827
    • Chen, P.1    Dai, H.F.2    Wu, J.3    Dai, W.J.4    Mei, W.L.5
  • 106
    • 0342468769 scopus 로고    scopus 로고
    • Biologicallyactive metabolites from fungi. Part 16: New preussomerins J, K andL from an endophytic fungus: Structure elucidation, crystalstructure analysis and determination of absolute configuration byCD calculations
    • Krohn, K.; Florke, U.; John, M.; Root, N.; Steingrover, K.; Aust, H.; Draeger, S.; Schulz, B.; Antus, S.; Simonyi, M. Biologicallyactive metabolites from fungi. Part 16: New preussomerins J, K andL from an endophytic fungus: structure elucidation, crystalstructure analysis and determination of absolute configuration byCD calculations. Tetrahedron, 2001, 57, 4343-4348.
    • (2001) Tetrahedron , vol.57 , pp. 4343-4348
    • Krohn, K.1    Florke, U.2    John, M.3    Root, N.4    Steingrover, K.5    Aust, H.6    Draeger, S.7    Schulz, B.8    Antus, S.9    Simonyi, M.10
  • 107
    • 33744741354 scopus 로고    scopus 로고
    • Spiro-Mamakone A: A unique relative of the spirobisnaphthalene class of compounds
    • van der Sar, S.A.; Blunt, J.W.; Munro, M.H.G. spiro-Mamakone A:a unique relative of the spirobisnaphthalene class of compounds. Org. Lett., 2006, 8, 2059-2061.
    • (2006) Org. Lett. , vol.8 , pp. 2059-2061
    • van der Sar, S.A.1    Blunt, J.W.2    Munro, M.H.G.3
  • 108
    • 70349510596 scopus 로고    scopus 로고
    • Spirobisnaphthalene analogues from the endophytic fungusPreussia sp
    • Chen, X.M.; Shi, Q.Y.; Lin, G.; Guo, S.X.; Yang, J.S. Spirobisnaphthalene analogues from the endophytic fungusPreussia sp. J. Nat. Prod., 2009, 72, 1712-1715.
    • (2009) J. Nat. Prod. , vol.72 , pp. 1712-1715
    • Chen, X.M.1    Shi, Q.Y.2    Lin, G.3    Guo, S.X.4    Yang, J.S.5
  • 109
    • 77956680997 scopus 로고    scopus 로고
    • Spirobisnaphthalenes from fungi and their biological activities
    • Zhou, L.; Zhao, J.; Shan, T.; Cai, X.; Peng, Y. Spirobisnaphthalenes from fungi and their biological activities. Mini-Rew. Med. Chem., 2010, 10, 977-989.
    • (2010) Mini-Rew. Med. Chem. , vol.10 , pp. 977-989
    • Zhou, L.1    Zhao, J.2    Shan, T.3    Cai, X.4    Peng, Y.5
  • 110
    • 67649467491 scopus 로고    scopus 로고
    • Chloropestolide A, an antitumor metabolite with anunprecedented spiroketal skeleton from Pestalotiopsis fici
    • Liu, L.; Li, Y.; Liu, S.; Zheng, Z.; Chen, X.; Zhang, H.; Guo, L.;Che, Y. Chloropestolide A, an antitumor metabolite with anunprecedented spiroketal skeleton from Pestalotiopsis fici. Org. Lett., 2009, 11, 2836-2839.
    • (2009) Org. Lett. , vol.11 , pp. 2836-2839
    • Liu, L.1    Li, Y.2    Liu, S.3    Zheng, Z.4    Chen, X.5    Zhang, H.6    Guo, L.7    Che, Y.8
  • 111
    • 75649124469 scopus 로고    scopus 로고
    • Unique metabolites of Pestalotiopsis fici suggest abiosynthetic hypothesis involving a Diels-Alder reaction and thenmechanistic diversification
    • Liu, L.; Niu, S.B.; Lu, X.H.; Chen, X.L.; Zhang, H.; Guo, L.D.;Che, Y.S. Unique metabolites of Pestalotiopsis fici suggest abiosynthetic hypothesis involving a Diels-Alder reaction and thenmechanistic diversification. Chem. Commun., 2010, 46, 460-462.
    • (2010) Chem. Commun. , vol.46 , pp. 460-462
    • Liu, L.1    Niu, S.B.2    Lu, X.H.3    Chen, X.L.4    Zhang, H.5    Guo, L.D.6    Che, Y.S.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.