메뉴 건너뛰기




Volumn 98, Issue , 2014, Pages 77-83

Diphenyl ethers from Aspergillus sp. and their anti-Aβ42 aggregation activities

Author keywords

Aspergillus sp.; Diphenyl ethers

Indexed keywords

9 ACETYLDIORCINOL B; AMYLOID BETA PROTEIN[1-42]; DIORCINOL B; DIPHENYL ETHER DERIVATIVE; EPIGALLOCATECHIN GALLATE; OXISTERIGMATOCYSTIN A; OXISTERIGMATOCYSTIN C; OXISTERIGMATOCYSTIN D; STERIGMATOCYSTIN; THIOFLAVINE; UNCLASSIFIED DRUG; VIOLACEOL I; VIOLACEOL II; 9-ACETYLDIORCINOL B; AMYLOID BETA PROTEIN; AMYLOID BETA-PROTEIN (1-42); PEPTIDE FRAGMENT; PROTEIN AGGREGATE;

EID: 84905391012     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2014.07.007     Document Type: Article
Times cited : (39)

References (30)
  • 1
    • 84876942803 scopus 로고    scopus 로고
    • Bioactive indole alkaloids and phenyl ether derivatives from a marine-derived Aspergillus sp. Fungus
    • M. Chen, C.L. Shao, X.M. Fu, R.F. Xu, J.J. Zheng, and D.L. Zhao et al. Bioactive indole alkaloids and phenyl ether derivatives from a marine-derived Aspergillus sp. fungus J Nat Prod 76 2013 547 553
    • (2013) J Nat Prod , vol.76 , pp. 547-553
    • Chen, M.1    Shao, C.L.2    Fu, X.M.3    Xu, R.F.4    Zheng, J.J.5    Zhao, D.L.6
  • 2
  • 3
    • 0344348915 scopus 로고    scopus 로고
    • Tenellic acids A-D: New bioactive diphenyl ether derivatives from the aquatic fungus Dendrospora tenella
    • DOI 10.1021/np980496m
    • H. Oh, T.O. Kwon, J.B. Gloer, L. Marvanova, and C.A. Shearer Tenellic acids A-D: new bioactive diphenyl ether derivatives from the aquatic fungus Dendrospora tenella J Nat Prod 62 1999 580 583 (Pubitemid 29200738)
    • (1999) Journal of Natural Products , vol.62 , Issue.4 , pp. 580-583
    • Oh, H.1    Kwon, T.O.2    Gloer, J.B.3    Marvanova, L.4    Shearer, C.A.5
  • 4
    • 0025006288 scopus 로고
    • A new brominated diphenyl ether from a philippine Dysidea species
    • J. Salvfi, and D.J. Faulkner A new brominated diphenyl ether from a Philippine Dyszdea species J Nat Prod 53 1990 757 760 (Pubitemid 20311289)
    • (1990) Journal of Natural Products (Lloydia) , vol.53 , Issue.3 , pp. 757-760
    • Salva, J.1    Faulkner, D.J.2
  • 5
    • 0028838743 scopus 로고
    • Enzyme inhibitors: New and known polybromena ted phenols and diphenyl ethers from four Indo-Pacific Dyszdea sponges
    • X. Fu, F.J. Schmitz, M. Govindan, S.A. Abbas, K.M. Hanson, and P.A. Horton et al. Enzyme inhibitors: new and known polybromena ted phenols and diphenyl ethers from four Indo-Pacific Dyszdea sponges J Nat Prod 58 1995 1384 1391
    • (1995) J Nat Prod , vol.58 , pp. 1384-1391
    • Fu, X.1    Schmitz, F.J.2    Govindan, M.3    Abbas, S.A.4    Hanson, K.M.5    Horton, P.A.6
  • 7
    • 0029955960 scopus 로고    scopus 로고
    • 13C NMR data for some brominated diphenyl ethers
    • DOI 10.1021/np960542n
    • 13C NMR data for some brominated diphenyl ethers J Nat Prod 59 1996 1102 1103 (Pubitemid 26408670)
    • (1996) Journal of Natural Products , vol.59 , Issue.11 , pp. 1102-1103
    • Fu, X.1    Schmitz, F.J.2
  • 8
    • 0026644046 scopus 로고
    • New bioactive metabolites from a freshwater isolate of the fungus Kirschsteiniothelia sp
    • G.K. Poch, J.B. Gloer, and C.A. Shearer New bioactive metabolites from a freshwater isolate of the fungus Kirschsteiniothelia sp. J Nat Prod 55 1992 1093 1099
    • (1992) J Nat Prod , vol.55 , pp. 1093-1099
    • Poch, G.K.1    Gloer, J.B.2    Shearer, C.A.3
  • 9
    • 33746563455 scopus 로고    scopus 로고
    • Neoplaether, a new cytotoxic and antifungal endophyte metabolite from Neoplaconema napellum IFB-E016
    • DOI 10.1111/j.1574-6968.2006.00358.x
    • F.W. Wang, Y.H. Ye, J.R. Chen, X.T. Wang, H.L. Zhu, and Y.C. Song et al. Neoplaether, a new cytotoxic and antifungal endophyte metabolite from Neoplaconema napellum IFB-E016 FEMS Microbiol Lett 261 2006 218 223 (Pubitemid 44134155)
    • (2006) FEMS Microbiology Letters , vol.261 , Issue.2 , 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
  • 10
    • 84870166408 scopus 로고    scopus 로고
    • Meroterpenoid and diphenyl ether derivatives from Penicillium sp. MA-37, a fungus isolated from marine mangrove rhizospheric soil
    • Y. Zhang, X.M. Li, Z. Shang, C.S. Li, N.Y. Ji, and B.G. Wang Meroterpenoid and diphenyl ether derivatives from Penicillium sp. MA-37, a fungus isolated from marine mangrove rhizospheric soil J Nat Prod 75 2012 1888 1895
    • (2012) J Nat Prod , vol.75 , pp. 1888-1895
    • Zhang, Y.1    Li, X.M.2    Shang, Z.3    Li, C.S.4    Ji, N.Y.5    Wang, B.G.6
  • 11
    • 78649239440 scopus 로고    scopus 로고
    • Induced production of halogenated diphenyl ethers from the marine derived fungus Penicillium chrysogenum
    • G. Yang, K. Yun, V.N. Nenkep, H.D. Choi, J.S. Kang, and B.W. Son Induced production of halogenated diphenyl ethers from the marine derived fungus Penicillium chrysogenum Chem Biodivers 7 2010 2766 2770
    • (2010) Chem Biodivers , vol.7 , pp. 2766-2770
    • Yang, G.1    Yun, K.2    Nenkep, V.N.3    Choi, H.D.4    Kang, J.S.5    Son, B.W.6
  • 13
  • 14
    • 34548029961 scopus 로고    scopus 로고
    • Highly brominated mono- and bis-phenols from the marine red alga Symphyocladia latiuscula with radical-scavenging activity
    • X.J. Duan, X.M. Li, and B.G. Wang Highly brominated mono- and bis-phenols from the marine red alga Symphyocladia latiuscula with radical-scavenging activity J Nat Prod 70 2007 1210 1213
    • (2007) J Nat Prod , vol.70 , pp. 1210-1213
    • Duan, X.J.1    Li, X.M.2    Wang, B.G.3
  • 15
    • 84865475521 scopus 로고    scopus 로고
    • Violaceols function as actin inhibitors inducing cell shape elongation in fibroblast cells
    • Y. Asami, J.H. Jang, H. Oh, J.H. Sohn, W.K. Jong, and O.M. Dong et al. Violaceols function as actin inhibitors inducing cell shape elongation in fibroblast cells Biosci Biotechnol Biochem 76 2012 1431 1437
    • (2012) Biosci Biotechnol Biochem , vol.76 , pp. 1431-1437
    • Asami, Y.1    Jang, J.H.2    Oh, H.3    Sohn, J.H.4    Jong, W.K.5    Dong, O.M.6
  • 17
    • 0005928393 scopus 로고
    • Herbicidal diphenyl ethers: Stereochemical studies using enantiomers of a novel diphenyl ether phthalide
    • P. Camilleri, A. Gray, K. Weaver, J.R. Bowyer, and D.J. Williams Herbicidal diphenyl ethers: stereochemical studies using enantiomers of a novel diphenyl ether phthalide J Agric Food Chem 37 1989 519 523
    • (1989) J Agric Food Chem , vol.37 , pp. 519-523
    • Camilleri, P.1    Gray, A.2    Weaver, K.3    Bowyer, J.R.4    Williams, D.J.5
  • 18
    • 84905398281 scopus 로고    scopus 로고
    • A new diphenyl ether from an endolichenic fungal strain, Aspergillus sp
    • Y.F. Huang, X.X. Li, G.D. Chen, Gao Hao, L.D. Guo, and X.S. Yao A new diphenyl ether from an endolichenic fungal strain, Aspergillus sp. Mycosystema 31 2012 769 774
    • (2012) Mycosystema , vol.31 , pp. 769-774
    • Huang, Y.F.1    Li, X.X.2    Chen, G.D.3    Hao, G.4    Guo, L.D.5    Yao, X.S.6
  • 20
    • 79951925240 scopus 로고    scopus 로고
    • Sterigmatocystins from the deep-sea-derived fungus Aspergillus versicolor
    • S.X. Cai, T.J. Zhu, L. Du, B.Y. Zhao, D.H. Li, and Q.Q. Gu Sterigmatocystins from the deep-sea-derived fungus Aspergillus versicolor J Antibiot 64 2011 193 196
    • (2011) J Antibiot , vol.64 , pp. 193-196
    • Cai, S.X.1    Zhu, T.J.2    Du, L.3    Zhao, B.Y.4    Li, D.H.5    Gu, Q.Q.6
  • 21
    • 34548103596 scopus 로고    scopus 로고
    • Three xanthones from a marine-derived mangrove endophytic fungus
    • DOI 10.1007/s10600-007-0062-9
    • F. Zhu, and Y.C. Lin Three Xanthones from a marine-derived mangrove endophytic fungus Chem Nat Compd 43 2007 132 135 (Pubitemid 47290449)
    • (2007) Chemistry of Natural Compounds , vol.43 , Issue.2 , pp. 132-135
    • Zhu, F.1    Lin, Y.2
  • 22
    • 84885013881 scopus 로고    scopus 로고
    • Diorcinols B-E, new prenylated diphenyl ethers from the marine-derived fungus Aspergillus versicolor ZLN-60
    • H.Q. Gao, L.N. Zhou, S.X. Cai, G.J. Zhang, T.J. Zhu, and Q.Q. Gu et al. Diorcinols B-E, new prenylated diphenyl ethers from the marine-derived fungus Aspergillus versicolor ZLN-60 J Antibiot 66 2013 539 542
    • (2013) J Antibiot , vol.66 , pp. 539-542
    • Gao, H.Q.1    Zhou, L.N.2    Cai, S.X.3    Zhang, G.J.4    Zhu, T.J.5    Gu, Q.Q.6
  • 23
    • 1542786291 scopus 로고    scopus 로고
    • Phenyl ethers from cultured lichen mycobionts of Graphis scripta var. Serpentina and G. Rikuzensis
    • Y. Takenaka, T. Tanahashi, N. Nagakura, and N. Hamada Phenyl ethers from cultured lichen mycobionts of Graphis scriptavar. Serpentine and G. rikuzensis Chem Pharm Bull 51 2003 794 797 (Pubitemid 41694781)
    • (2003) Chemical and Pharmaceutical Bulletin , vol.51 , Issue.7 , pp. 794-797
    • Takenaka, Y.1    Tanahashi, T.2    Nagakura, N.3    Hamada, N.4
  • 24
    • 74549213772 scopus 로고    scopus 로고
    • Sterigmatocystin: Occurrence in foodstuffs and analytical methods - An overview
    • A. Veršilovskis, and S.S. De Sterigmatocystin: occurrence in foodstuffs and analytical methods - an overview Mol Nutr Food Res 54 2010 136 147
    • (2010) Mol Nutr Food Res , vol.54 , pp. 136-147
    • Veršilovskis, A.1    De, S.S.2
  • 27
    • 84885004271 scopus 로고    scopus 로고
    • Nodulisporisteriods A and B, the first 3, 4-seco-4-methyl-progesteroids from Nodulisporium sp
    • Q.C. Zheng, G.D. Chen, M.Z. Kong, G.Q. Li, J.Y. Cui, and X.X. Li et al. Nodulisporisteriods A and B, the first 3, 4-seco-4-methyl-progesteroids from Nodulisporium sp. Steroids 78 2013 896 901
    • (2013) Steroids , vol.78 , pp. 896-901
    • Zheng, Q.C.1    Chen, G.D.2    Kong, M.Z.3    Li, G.Q.4    Cui, J.Y.5    Li, X.X.6
  • 28
    • 0019156550 scopus 로고
    • 5,6-Dimethoxysterigmatocystin and related metabolites from Aspergillus multicolor
    • T. Hamasaki, T. Nakagomi, Y. Hatsuda, K. Fukuyama, and Y. Katsube 5,6-Dimethoxysterigmatocystin and related metabolites from Aspergillus multicolor Agric Biol Chem 44 1980 1149 1155 (Pubitemid 12096821)
    • (1980) Agricultural and Biological Chemistry , vol.44 , Issue.5 , pp. 1149-1155
    • Hamasaki, T.1    Nakagomi, T.2    Hatsuda, Y.3
  • 30
    • 54249143535 scopus 로고    scopus 로고
    • Cell signaling pathways and iron chelation in the neurorestorative activity of green tea polyphenols: Special reference to epigallocatechin gallate (EGCG)
    • S.A. Mandel, T. Amit, L. Kalfon, L. Reznichenko, O. Weinreb, and M.B. Youdim Cell signaling pathways and iron chelation in the neurorestorative activity of green tea polyphenols: special reference to epigallocatechin gallate (EGCG) J Alzheimers Dis 15 2008 211 222
    • (2008) J Alzheimers Dis , vol.15 , pp. 211-222
    • Mandel, S.A.1    Amit, T.2    Kalfon, L.3    Reznichenko, L.4    Weinreb, O.5    Youdim, M.B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.