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Volumn 65, Issue 1, 2009, Pages 60-65

New asperxanthone and asperbiphenyl from the marine fungus Aspergillus sp.

Author keywords

Aspergillus sp.; Biphenyl; Difuranxanthone; Marine fungus; TMV

Indexed keywords

ANTIVIRUS AGENT; ASPERBIPHENYL; ASPERXANTHONE; BENZOPYRAN DERIVATIVE; FATTY ACID; XANTHONE DERIVATIVE;

EID: 58549118428     PISSN: 1526498X     EISSN: 15264998     Source Type: Journal    
DOI: 10.1002/ps.1645     Document Type: Article
Times cited : (30)

References (14)
  • 1
    • 0028817726 scopus 로고
    • Halicylindrosides, antifungal and cytotoxic cerebrosides from the marine sponge Halichondria cylindrata
    • Li HY, Matsunaga S and Fusetani N, Halicylindrosides, antifungal and cytotoxic cerebrosides from the marine sponge Halichondria cylindrata. Tetrahedron 51:2273-2279 (1995).
    • (1995) Tetrahedron , vol.51 , pp. 2273-2279
    • Li, H.Y.1    Matsunaga, S.2    Fusetani, N.3
  • 2
    • 0027177356 scopus 로고
    • Agelasphins, novel α- galactosylceramides from the marine sponge Agelas mauritianus
    • Natori T, Koezuka Y and Higa T, Agelasphins, novel α- galactosylceramides from the marine sponge Agelas mauritianus. Tetrahedron Lett 34:5591-5595 (1993).
    • (1993) Tetrahedron Lett , vol.34 , pp. 5591-5595
    • Natori, T.1    Koezuka, Y.2    Higa, T.3
  • 3
    • 0028204397 scopus 로고
    • Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus
    • Natori T, Morita M, Akimoto K and Koezuka Y, Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus. Tetrahedron 50:2771-2778 (1994).
    • (1994) Tetrahedron , vol.50 , pp. 2771-2778
    • Natori, T.1    Morita, M.2    Akimoto, K.3    Koezuka, Y.4
  • 4
    • 0035906056 scopus 로고    scopus 로고
    • Seki M, Kayo A and Mori K, Synthesis of (2S, 3R, 11S, 12R, 2‴R, 11‴S, 12‴R)-plakoside A, a prenylated and immunosuppressive marine galactosphingolipid with cyclopropane-containing alkyl chains. Tetrahedron Lett 42:2357-2361 (2001).
    • Seki M, Kayo A and Mori K, Synthesis of (2S, 3R, 11S, 12R, 2‴R, 11‴S, 12‴R)-plakoside A, a prenylated and immunosuppressive marine galactosphingolipid with cyclopropane-containing alkyl chains. Tetrahedron Lett 42:2357-2361 (2001).
  • 5
    • 0018220145 scopus 로고
    • Aplidiasphingosine, an antimicrobial and antitumor terpenoid from an Aplidium sp. (marine Tunicate)
    • Carter GT and Rinehart KL, Aplidiasphingosine, an antimicrobial and antitumor terpenoid from an Aplidium sp. (marine Tunicate). J Am Chem Soc 100:7441-7442 (1978).
    • (1978) J Am Chem Soc , vol.100 , pp. 7441-7442
    • Carter, G.T.1    Rinehart, K.L.2
  • 6
    • 1342311386 scopus 로고    scopus 로고
    • Marine-derived fungi: A chemically and biologically diverse group of microorganisms
    • Bugni TS and Ireland CM, Marine-derived fungi: a chemically and biologically diverse group of microorganisms. Nat Prod Rep 21:143-163 (2004).
    • (2004) Nat Prod Rep , vol.21 , pp. 143-163
    • Bugni, T.S.1    Ireland, C.M.2
  • 7
    • 26044469153 scopus 로고    scopus 로고
    • A new cerebroside, Asperiamide A, from the marine fungus Aspergillus sp
    • Ouyang MA, Liu R and Kuo YH, A new cerebroside, Asperiamide A, from the marine fungus Aspergillus sp. J Asian Nat Prod Res 7:761-765 (2005).
    • (2005) J Asian Nat Prod Res , vol.7 , pp. 761-765
    • Ouyang, M.A.1    Liu, R.2    Kuo, Y.H.3
  • 8
    • 29244462819 scopus 로고    scopus 로고
    • A new adenosyl-alkaloid from Ostrea rivularis
    • Ouyang MA, A new adenosyl-alkaloid from Ostrea rivularis. Nat Prod Res 20:79-83 (2006).
    • (2006) Nat Prod Res , vol.20 , pp. 79-83
    • Ouyang, M.A.1
  • 10
    • 39649115273 scopus 로고    scopus 로고
    • Growth characteristics and antibiotic action of marine fungi Penicilliun sp. W02A
    • Chen BE, Ouyang MA and Wang LN, Growth characteristics and antibiotic action of marine fungi Penicilliun sp. W02A. Amino Acids and Biotic Resources 2:5-7 (2005).
    • (2005) Amino Acids and Biotic Resources , vol.2 , pp. 5-7
    • Chen, B.E.1    Ouyang, M.A.2    Wang, L.N.3
  • 12
    • 33947610187 scopus 로고    scopus 로고
    • Anti-Tobacco Mosaic Virus (TMV) triterpenoid saponins from the leaves of IIex oblonga
    • Wu ZJ, Ouyang MA, Wang CZ, Zhang ZK and Shen JG, Anti-Tobacco Mosaic Virus (TMV) triterpenoid saponins from the leaves of IIex oblonga. J Agric Food Chem 55:1712-1717 (2007).
    • (2007) J Agric Food Chem , vol.55 , pp. 1712-1717
    • Wu, Z.J.1    Ouyang, M.A.2    Wang, C.Z.3    Zhang, Z.K.4    Shen, J.G.5
  • 13
    • 0006256643 scopus 로고
    • Metabolites of bird's nest fungi. Part 5. The isolation of 1-hydroxy-6-methyl-8-hydroxymethylxanthone, a new xanthone, from Cyathusintermedius. Synthesis via photoenolisation
    • Ayer WA and Taylor DR, Metabolites of bird's nest fungi. Part 5. The isolation of 1-hydroxy-6-methyl-8-hydroxymethylxanthone, a new xanthone, from Cyathusintermedius. Synthesis via photoenolisation. Can J Chem 54:1703-1706 (1976).
    • (1976) Can J Chem , vol.54 , pp. 1703-1706
    • Ayer, W.A.1    Taylor, D.R.2
  • 14
    • 0003178418 scopus 로고
    • Evidence for the probable final steps in aflatoxin biosynthesis
    • Chatterjee M and Townsend CA, Evidence for the probable final steps in aflatoxin biosynthesis. J Org Chem 59:4424-4429 (1994).
    • (1994) J Org Chem , vol.59 , pp. 4424-4429
    • Chatterjee, M.1    Townsend, C.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.