메뉴 건너뛰기




Volumn 6, Issue 12, 2011, Pages 1821-1824

New antifungal cholestane and aldehyde derivatives from the red alga Laurencia papillosa

Author keywords

Aldehyde; Antifungal activity; Cholestane derivatives; Laurencia papillosa; Red alga

Indexed keywords

2 (TRIDEC 2 EN 2 YL)HEPTADEC 2 ENAL; 3ALPHA,6ALPHA DIHYDROXY 5BETA CHOLESTAN 12 ONE; 6BETA HYDROXYCHOLEST 4 EN 3 ONE; ALDEHYDE DERIVATIVE; ALGAL EXTRACT; ANTIFUNGAL AGENT; CHLOROFORM; CHOLESTANE DERIVATIVE; KETOCONAZOLE; LAURENCIA PAPILLOSA EXTRACT; METHANOL; UNCLASSIFIED DRUG;

EID: 83455211117     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x1100601208     Document Type: Article
Times cited : (19)

References (18)
  • 1
    • 28444447038 scopus 로고    scopus 로고
    • New cytotoxic sesquiterpenes from the red algae Laurencia obtusa and Laurencia microcladia
    • (a) Kladi M, Xenaki H, Vagias C, Papazafiri P, Roussis V. (2006) New cytotoxic sesquiterpenes from the red algae Laurencia obtusa and Laurencia microcladia. Tetrahedron, 62, 182-189;
    • (2006) Tetrahedron , vol.62 , pp. 182-189
    • Kladi, M.1    Xenaki, H.2    Vagias, C.3    Papazafiri, P.4    Roussis, V.5
  • 4
    • 0043068060 scopus 로고    scopus 로고
    • Potent antibacterial activity of halogenated metabolites from Malaysian red alga, Laurencia maiuscula (Rhodomelaceae, Ceramiales)
    • (d) Vairappan CS. (2003) Potent antibacterial activity of halogenated metabolites from Malaysian red alga, Laurencia maiuscula (Rhodomelaceae, Ceramiales). Biomolecular Engineer, 20, 255-259.
    • (2003) Biomolecular Engineer , vol.20 , pp. 255-259
    • Vairappan, C.S.1
  • 5
    • 77954095392 scopus 로고    scopus 로고
    • Sesquiterpenes of the Brazilian marine red alga Laurencia filiformis (Rhodophyta, Ceramiales)
    • (a) Bruno LA, Beatriz GF, Mutue TF, Valéria LT. (2008) Sesquiterpenes of the Brazilian marine red alga Laurencia filiformis (Rhodophyta, Ceramiales). Natural Product Communications, 3, 1653-1654;
    • (2008) Natural Product Communications , vol.3 , pp. 1653-1654
    • Bruno, L.A.1    Beatriz, G.F.2    Mutue, T.F.3    Valéria, L.T.4
  • 6
    • 66849095178 scopus 로고    scopus 로고
    • Laurencia filiformis: Phytochemical profiling by conventional and HPLC-NMR approaches
    • (b) Dias DA, White JM, Urban S. (2009) Laurencia filiformis: Phytochemical profiling by conventional and HPLC-NMR approaches. Natural Product Communications, 4, 157-172;
    • (2009) Natural Product Communications , vol.4 , pp. 157-172
    • Dias, D.A.1    White, J.M.2    Urban, S.3
  • 7
    • 34250815151 scopus 로고    scopus 로고
    • New sesquiterpenes from the red alga Laurencia microcladia
    • DOI 10.1016/j.tet.2007.05.051, PII S0040402007009118
    • (c) Kladi M, Vagias C, Papazafiri P, Furnari G, Serio D, Roussis V. (2007). New sesquiterpenes from the red alga Laurencia microcladia. Tetrahedron, 63, 7606-7611. (Pubitemid 46970778)
    • (2007) Tetrahedron , vol.63 , Issue.32 , pp. 7606-7611
    • Kladi, M.1    Vagias, C.2    Papazafiri, P.3    Furnari, G.4    Serio, D.5    Roussis, V.6
  • 8
    • 77958495794 scopus 로고    scopus 로고
    • 3β, 7β-Dihydroxy-5α-cholestan-11-one: A new oxidation pattern of cholestane skeleton from Laurencia papillosa
    • (a) Al-lihaibi SS, Ayyad SN, Al-wessabi EO, Alarif WM. (2010) 3β, 7β-Dihydroxy-5α-cholestan-11-one: A new oxidation pattern of cholestane skeleton from Laurencia papillosa. Biochemical Systematics and Ecology, 38, 861-863;
    • (2010) Biochemical Systematics and Ecology , vol.38 , pp. 861-863
    • Al-lihaibi, S.S.1    Ayyad, S.N.2    Al-wessabi, E.O.3    Alarif, W.M.4
  • 9
    • 0002819598 scopus 로고
    • The trace sterols of the red alga Laurencia papillosa investigated by open tubular capillary column gas chromatography
    • (b) Lisboa BP, Ganshow LI, Halket JM, Pinheiro-Joventio F.(1982) The trace sterols of the red alga Laurencia papillosa investigated by open tubular capillary column gas chromatography. Compound Biochemical Physiology, 73B, 257-264;
    • (1982) Compound Biochemical Physiology , vol.73 B , pp. 257-264
    • Lisboa, B.P.1    Ganshow, L.I.2    Halket, J.M.3    Pinheiro-Joventio, F.4
  • 11
    • 0000616740 scopus 로고
    • (E)-2-Tridecyl-2-heptadecenal, an unusual metabolite from the red alga Laurencia species
    • (a) Suzuki M, Kurosawa E, Kurata K. (1987) (E)-2-Tridecyl-2-heptadecenal, an unusual metabolite from the red alga Laurencia species. Bulletin of the Chemical Society of Japan. 60, 3793-3794;
    • (1987) Bulletin of the Chemical Society of Japan , vol.60 , pp. 3793-3794
    • Suzuki, M.1    Kurosawa, E.2    Kurata, K.3
  • 12
    • 1842830724 scopus 로고    scopus 로고
    • Antibiotic longchain and α,β-unsaturated aldehydes from the culture of the marine fungus Cladosporium sp
    • (b) Gallo ML, Seldes AM, Cabrera GM. (2004) Antibiotic longchain and α,β-unsaturated aldehydes from the culture of the marine fungus Cladosporium sp., Biochemical Systematics and Ecology, 32, 545-551;
    • (2004) Biochemical Systematics and Ecology , vol.32 , pp. 545-551
    • Gallo, M.L.1    Seldes, A.M.2    Cabrera, G.M.3
  • 13
    • 0014123945 scopus 로고
    • New evidence for the structure of myxinol
    • (c) Anderson IG, Haslewood AD. (1967) New evidence for the structure of myxinol. Biochemistry Journal, 104, 1061-1063;
    • (1967) Biochemistry Journal , vol.104 , pp. 1061-1063
    • Anderson, I.G.1    Haslewood, A.D.2
  • 15
    • 33845933692 scopus 로고    scopus 로고
    • 4,5-Epoxy cholestane-3,6- Diols: Templates for generating the full set of eight cholestane -3, 5, 6- triol stereoisomerisms in multigram scales, but not for cholestane- 3, 4, 6- triol
    • (a) Zhao K, Wang Y, Han L. (2007) 4,5-Epoxy cholestane-3,6- diols: templates for generating the full set of eight cholestane -3, 5, 6- triol stereoisomerisms in multigram scales, but not for cholestane- 3, 4, 6- triol. Steroids, 72, 95-104;
    • (2007) Steroids , vol.72 , pp. 95-104
    • Zhao, K.1    Wang, Y.2    Han, L.3
  • 16
  • 18
    • 0032853292 scopus 로고    scopus 로고
    • Morinins H-K, four novel phenylpropanol ester lipid metabolites from Morina chinensis
    • DOI 10.1021/np990145n
    • (b) Su B-N, Takaishi Y, Morinins H-K. (1999) Four novel phenylpropanol ester lipid metabolites from Morina chinesis, Journal of Natural Products, 62, 1325-1327. (Pubitemid 29463341)
    • (1999) Journal of Natural Products , vol.62 , Issue.9 , pp. 1325-1327
    • Su, B.-N.1    Takaishi, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.