메뉴 건너뛰기




Volumn 6, Issue 5, 2008, Pages 391-394

One new ten-membered lactone from Phomopsis sp. B27, an endophytic fungus of Annona squamosa L

Author keywords

Chemical constituents; Phomopsis sp. B27; Spectroscopic analyses

Indexed keywords

1 METHOXY 8 HYDROXY 9,10 ANTHRAQUINONE; ALTILOXIN A; CYTOSPORONE C; DANTRON; LACTONE DERIVATIVE; NATURAL PRODUCT; PHOMOLIDE C; UNCLASSIFIED DRUG;

EID: 54449088219     PISSN: 20956975     EISSN: 18755364     Source Type: Journal    
DOI: 10.3724/SP.J.1009.2008.00391     Document Type: Article
Times cited : (12)

References (18)
  • 1
    • 0032442691 scopus 로고    scopus 로고
    • Fungal endophytes: A continuum of interactions with host plants [J]
    • Saikkonen K, Faeth SH, Helander M, et al. Fungal endophytes: a continuum of interactions with host plants [J]. Ann Rev Ecol Syst, 1998, 29: 319-343.
    • (1998) Ann Rev Ecol Syst , vol.29 , pp. 319-343
    • Saikkonen, K.1    Faeth, S.H.2    Helander, M.3
  • 2
    • 0348109344 scopus 로고    scopus 로고
    • Bioprospecting for microbial endophytes and their natural products [J]
    • Strobel G, Daisy B. Bioprospecting for microbial endophytes and their natural products [J]. Microbiol Mol Biol Rev, 2003, 67(4): 491-502.
    • (2003) Microbiol Mol Biol Rev , vol.67 , Issue.4 , pp. 491-502
    • Strobel, G.1    Daisy, B.2
  • 3
    • 85193609574 scopus 로고    scopus 로고
    • Tan RX, Zou WX. Endophytes, a rich source of functional metabolites [J]. Nat Prod Rep, 2001, 18(4): 448-459.
    • Tan RX, Zou WX. Endophytes, a rich source of functional metabolites [J]. Nat Prod Rep, 2001, 18(4): 448-459.
  • 4
    • 0031417176 scopus 로고    scopus 로고
    • Bioprotective alkaloids of grass-fungal endophyte symbiosis [J]
    • Bush LP, Wilkinson HH, Schardl CL. Bioprotective alkaloids of grass-fungal endophyte symbiosis [J]. Plant Physiol, 1997, 114: 1-7.
    • (1997) Plant Physiol , vol.114 , pp. 1-7
    • Bush, L.P.1    Wilkinson, H.H.2    Schardl, C.L.3
  • 5
    • 0037959544 scopus 로고    scopus 로고
    • A new macrolide antibiotic with antitumor activity produced by Streptomyces sp. CS a commensal microbe of Maytenus hookeri [J]
    • Lu CH, Shen YM. A new macrolide antibiotic with antitumor activity produced by Streptomyces sp. CS a commensal microbe of Maytenus hookeri [J]. J Antibiot, 2003, 56(4): 415-418.
    • (2003) J Antibiot , vol.56 , Issue.4 , pp. 415-418
    • Lu, C.H.1    Shen, Y.M.2
  • 6
    • 0347572305 scopus 로고    scopus 로고
    • Structural, optical, and electrical characterization of hot wall epitaxy grown 1-methoxy-8-hydroxy-9, 10-anthraquinone films [J]
    • Mahajan A, Bedi RK. Structural, optical, and electrical characterization of hot wall epitaxy grown 1-methoxy-8-hydroxy-9, 10-anthraquinone films [J]. J Appl Phys, 2001, 89(12): 7866-7870.
    • (2001) J Appl Phys , vol.89 , Issue.12 , pp. 7866-7870
    • Mahajan, A.1    Bedi, R.K.2
  • 7
    • 84986793649 scopus 로고
    • Carbon-13 nuclear magnetic resonance studies of anthraquinones. Part II. Hydroxymethoxyanthraquinones, acetoxymethoxyanthraquinones and naturally occurring anthraquinone analogs [J]
    • Berger Y, Castonguay A, Brassard P. Carbon-13 nuclear magnetic resonance studies of anthraquinones. Part II. Hydroxymethoxyanthraquinones, acetoxymethoxyanthraquinones and naturally occurring anthraquinone analogs [J]. Org Magn Resonance, 1980, 14(2): 103-108.
    • (1980) Org Magn Resonance , vol.14 , Issue.2 , pp. 103-108
    • Berger, Y.1    Castonguay, A.2    Brassard, P.3
  • 8
    • 84986849882 scopus 로고
    • The carbon-13 nuclear magnetic resonance spectra of anthraquinone, eight polyhydroxyanthraquinones, and eight polymethoxyanthraquinones [J]
    • Berger Y, Castonguay A. The carbon-13 nuclear magnetic resonance spectra of anthraquinone, eight polyhydroxyanthraquinones, and eight polymethoxyanthraquinones [J]. Org Magn Resonance, 1978, 11(8): 375-377.
    • (1978) Org Magn Resonance , vol.11 , Issue.8 , pp. 375-377
    • Berger, Y.1    Castonguay, A.2
  • 9
    • 0034649733 scopus 로고    scopus 로고
    • The Cytosporones, new octaketide antibiotics isolated from an endophytic fungus [J]
    • Brady SF, Wagenaar MM, Singh MP, et al. The Cytosporones, new octaketide antibiotics isolated from an endophytic fungus [J]. Org Lett, 2000, 2(25): 4043-4046.
    • (2000) Org Lett , vol.2 , Issue.25 , pp. 4043-4046
    • Brady, S.F.1    Wagenaar, M.M.2    Singh, M.P.3
  • 10
    • 0021234614 scopus 로고
    • Structures of altiloxins A and B, phytotoxins from Phoma asparagi Sacc [J]
    • Ichihara A, Sawamura S, Sakamura S. Structures of altiloxins A and B, phytotoxins from Phoma asparagi Sacc [J]. Tetrahedron Lett, 1984, 25(30): 3209-3212.
    • (1984) Tetrahedron Lett , vol.25 , Issue.30 , pp. 3209-3212
    • Ichihara, A.1    Sawamura, S.2    Sakamura, S.3
  • 11
    • 0027241159 scopus 로고
    • A Microwell cytotoxicity assay using artemia salina (Brine Shrimp) [J]
    • Solis PN, Wright CW, Anderson MM, et al. A Microwell cytotoxicity assay using artemia salina (Brine Shrimp) [J]. Planta Med, 1993, 59(3): 250-252.
    • (1993) Planta Med , vol.59 , Issue.3 , pp. 250-252
    • Solis, P.N.1    Wright, C.W.2    Anderson, M.M.3
  • 12
    • 0025825006 scopus 로고
    • Antibiotic disk diffusion testing revisited. Single strain regression analysis. Review article [J]
    • Kronvall G, Ringertz S. Antibiotic disk diffusion testing revisited. Single strain regression analysis. Review article [J]. APMIS, 1991, 99(4): 295-306.
    • (1991) APMIS , vol.99 , Issue.4 , pp. 295-306
    • Kronvall, G.1    Ringertz, S.2
  • 13
    • 0037454743 scopus 로고    scopus 로고
    • Absolute structure, biosynthesis, and anti-microtubule activity of phomopsidin, isolated from a marine-derived fungus Phomopsis sp. [J]
    • Kobayashi H, Meguro S, Yoshimoto T, et al. Absolute structure, biosynthesis, and anti-microtubule activity of phomopsidin, isolated from a marine-derived fungus Phomopsis sp. [J]. Tetrahedron, 2003, 59: 455-459.
    • (2003) Tetrahedron , vol.59 , pp. 455-459
    • Kobayashi, H.1    Meguro, S.2    Yoshimoto, T.3
  • 14
    • 0034868952 scopus 로고    scopus 로고
    • Phomoxanthones A and B, novel xanthone dimmers from the endophytic fungus Phomopsis species [J]
    • Isaka M, Jaturapat A, Rukseree K, et al. Phomoxanthones A and B, novel xanthone dimmers from the endophytic fungus Phomopsis species [J]. J Nat Prod, 2001, 64(8): 1015-1018.
    • (2001) J Nat Prod , vol.64 , Issue.8 , pp. 1015-1018
    • Isaka, M.1    Jaturapat, A.2    Rukseree, K.3
  • 15
    • 27644436008 scopus 로고    scopus 로고
    • X-ray structure determination, absolute configuration and biological activity of phomoxanthone A [J]
    • Elsaesser B, Krohn K, Floerke U, et al. X-ray structure determination, absolute configuration and biological activity of phomoxanthone A [J]. Eur J Org Chem, 2005, 21: 4563-4570.
    • (2005) Eur J Org Chem , vol.21 , pp. 4563-4570
    • Elsaesser, B.1    Krohn, K.2    Floerke, U.3
  • 16
    • 0028129379 scopus 로고
    • Isolation and characterization of phomodiol, a new antifungal from Phomopsis [J]
    • Horn WS, Schwartz RE, Simmonds MSJ, et al. Isolation and characterization of phomodiol, a new antifungal from Phomopsis [J]. Tetrahedron Lett, 1994, 35: 6037-6040.
    • (1994) Tetrahedron Lett , vol.35 , pp. 6037-6040
    • Horn, W.S.1    Schwartz, R.E.2    Simmonds, M.S.J.3
  • 17
    • 49649114350 scopus 로고    scopus 로고
    • Three new antimicrobial metabolites of Phomopsis sp.[J]
    • Du XP, Lu CH, Li YY, et al. Three new antimicrobial metabolites of Phomopsis sp.[J]. J Antibiot, 2008, 61(4): 250-253.
    • (2008) J Antibiot , vol.61 , Issue.4 , pp. 250-253
    • Du, X.P.1    Lu, C.H.2    Li, Y.Y.3
  • 18
    • 0017123102 scopus 로고
    • Toxicity and plant growth regulator effects of cytochalasin H isolated from Phomopsis sp. [J]
    • Wells JM, Cutler HG, Cole RJ. Toxicity and plant growth regulator effects of cytochalasin H isolated from Phomopsis sp. [J]. Can J Microbiol, 1976, 22(8): 1137-1143.
    • (1976) Can J Microbiol , vol.22 , Issue.8 , pp. 1137-1143
    • Wells, J.M.1    Cutler, H.G.2    Cole, R.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.