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Volumn 59, Issue 9, 2006, Pages 553-563

New destruxins from the marine-derived fungus Beauveria felina

Author keywords

Beauveria felina; Destruxins; Fungi; Marine microorganisms

Indexed keywords

2,4 5 CHLORO 2,4 DIHYDROXYPENTANOIC ACID; BETA METHYLPROLYLDESTRUXIN E CHLOROHYDRIN; CYCLODEPSIPEPTIDE; DESTRUXIN; DESTRUXIN E CHLOROHYDRIN; ISARIIN B; PHENYLALANYL, N METHYLVALYLDESTRUXIN B; PSEUDODESTRUXIN C; ROSEOCARDIN; ROSEOTOXIN B; UNCLASSIFIED DRUG; VALERIC ACID DERIVATIVE;

EID: 33751253424     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.1038/ja.2006.76     Document Type: Article
Times cited : (41)

References (26)
  • 1
    • 1342311386 scopus 로고    scopus 로고
    • Marine-derived fungi: A chemically and biologically diverse group of microorganisms
    • Bugni TS, 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
  • 2
    • 0036514501 scopus 로고    scopus 로고
    • Secondary metabolites from marine microorganisms
    • Kelecom A. Secondary metabolites from marine microorganisms. An Acad Bras Ciências 74: 151-170 (2002)
    • (2002) An Acad Bras Ciências , vol.74 , pp. 151-170
    • Kelecom, A.1
  • 5
    • 0031929430 scopus 로고    scopus 로고
    • Destruxin-A4 chlorohydrin, a novel destruxin from fungus OS-F68576: Isolation, structure determination, and biological activity as an inducer of erythropoietin
    • Cai P, Smith D, Katz B, Pearce C, Venables D, Houck D. Destruxin-A4 chlorohydrin, a novel destruxin from fungus OS-F68576: isolation, structure determination, and biological activity as an inducer of erythropoietin. J Nat Prod 61: 290-293 (1998)
    • (1998) J Nat Prod , vol.61 , pp. 290-293
    • Cai, P.1    Smith, D.2    Katz, B.3    Pearce, C.4    Venables, D.5    Houck, D.6
  • 7
    • 12144268411 scopus 로고    scopus 로고
    • Marfey's reagent for chiral amino acid analysis: A review
    • Bhushan R, Bruckner H. Marfey's reagent for chiral amino acid analysis: a review. Amino Acids 27: 231-247 (2004)
    • (2004) Amino Acids , vol.27 , pp. 231-247
    • Bhushan, R.1    Bruckner, H.2
  • 8
    • 0033525048 scopus 로고    scopus 로고
    • Stereochemical determination of acyclic structures based on carbon-proton spin-coupling constants. A method of configuration analysis for natural products
    • Matsumori N, Kaneno D, Murata M, Nakamura H, Tachibana K. Stereochemical determination of acyclic structures based on carbon-proton spin-coupling constants. A method of configuration analysis for natural products. J Org Chem 64: 866-876 (1999)
    • (1999) J Org Chem , vol.64 , pp. 866-876
    • Matsumori, N.1    Kaneno, D.2    Murata, M.3    Nakamura, H.4    Tachibana, K.5
  • 9
    • 0033518615 scopus 로고    scopus 로고
    • Absolute configuration of amphidinol 3, the first complete structure determination from amphidionol homologues: Application of a new configuration analysis based on carbon-hydrogen spin-coupling constants
    • Murata M, Matsuoka S, Matsumori N, Paul GK, Tachibana K. Absolute configuration of amphidinol 3, the first complete structure determination from amphidionol homologues: Application of a new configuration analysis based on carbon-hydrogen spin-coupling constants. J Am Chem Soc 121: 870-871 (1999)
    • (1999) J Am Chem Soc , vol.121 , pp. 870-871
    • Murata, M.1    Matsuoka, S.2    Matsumori, N.3    Paul, G.K.4    Tachibana, K.5
  • 10
    • 0032507016 scopus 로고    scopus 로고
    • Are both the (R)- And the (S)-MPA esters really needed for the assignment of the absolute configuration of secondary alcohols by NMR? the use of a single derivative
    • Latypov SK, Seco JM, Quiñoá E, Riguera R. Are both the (R)- and the (S)-MPA esters really needed for the assignment of the absolute configuration of secondary alcohols by NMR? The use of a single derivative. J Am Chem Soc 120: 877-882 (1998)
    • (1998) J Am Chem Soc , vol.120 , pp. 877-882
    • Latypov, S.K.1    Seco, J.M.2    Quiñoá, E.3    Riguera, R.4
  • 11
    • 0031993816 scopus 로고    scopus 로고
    • Sensitivity- and gradient-enhanced hetero (ω1) half-filtered TOCSY experiment for measuring long-range heteronuclear coupling constants
    • Uhrin D, Batta G, Hruby VJ, Barlow PN, Kover KE. Sensitivity- and gradient-enhanced hetero (ω1) half-filtered TOCSY experiment for measuring long-range heteronuclear coupling constants. J Mag Res 130: 155-161 (1998)
    • (1998) J Mag Res , vol.130 , pp. 155-161
    • Uhrin, D.1    Batta, G.2    Hruby, V.J.3    Barlow, P.N.4    Kover, K.E.5
  • 12
    • 0037111707 scopus 로고    scopus 로고
    • Structure and absolute stereochemistry of phomidolide, a new toxic metabolite from the marine cyanobacterium Phormidium sp
    • Williamson RT, Boulanger A, Vulpanovici A, Roberts MA, Gerwick WH. Structure and absolute stereochemistry of phomidolide, a new toxic metabolite from the marine cyanobacterium Phormidium sp. J Org Chem 67: 7927-7936 (2002)
    • (2002) J Org Chem , vol.67 , pp. 7927-7936
    • Williamson, R.T.1    Boulanger, A.2    Vulpanovici, A.3    Roberts, M.A.4    Gerwick, W.H.5
  • 13
    • 0030569509 scopus 로고    scopus 로고
    • Study of structure-activity correlation in destruxins, a class of cyclodepsipeptides possessing suppressive effect on the generation of hepatitis B virus surface antigen in human hepatoma cells
    • Yeh SF, Pan W, Ong GT, Chiou AJ, Chuang CC, Chiou SH, Wu SH. Study of structure-activity correlation in destruxins, a class of cyclodepsipeptides possessing suppressive effect on the generation of hepatitis B virus surface antigen in human hepatoma cells. Biochem Biophys Res Commun 229: 65-72 (1996)
    • (1996) Biochem Biophys Res Commun , vol.229 , pp. 65-72
    • Yeh, S.F.1    Pan, W.2    Ong, G.T.3    Chiou, A.J.4    Chuang, C.C.5    Chiou, S.H.6    Wu, S.H.7
  • 14
    • 0036305819 scopus 로고    scopus 로고
    • Structure elucidation of a new cyclic hexadepsipeptide from Beauveria felina
    • Kim HS, Jung MH, Ahn S, Lee CW, Kim SN, Ok JH. Structure elucidation of a new cyclic hexadepsipeptide from Beauveria felina. J Antibiot 55: 598-601 (2002)
    • (2002) J Antibiot , vol.55 , pp. 598-601
    • Kim, H.S.1    Jung, M.H.2    Ahn, S.3    Lee, C.W.4    Kim, S.N.5    Ok, J.H.6
  • 16
    • 0035024178 scopus 로고    scopus 로고
    • Pseudodestruxins A and B: New cyclic depsipeptides from the Coprophilous fungus Nigrosabulum globosum
    • Che Y, Swenson DC, Gloer JB, Koster B, Malloch D. Pseudodestruxins A and B: new cyclic depsipeptides from the Coprophilous fungus Nigrosabulum globosum. J Nat Prod 64: 555-558 (2001)
    • (2001) J Nat Prod , vol.64 , pp. 555-558
    • Che, Y.1    Swenson, D.C.2    Gloer, J.B.3    Koster, B.4    Malloch, D.5
  • 17
    • 0016481532 scopus 로고
    • Purification and characterization of roseotoxin B, a toxic cyclodepsipeptide from Trichothecium roseum
    • Engstrom GW, DeLance JV, Richard JL, Baetz AL. Purification and characterization of roseotoxin B, a toxic cyclodepsipeptide from Trichothecium roseum. J Agric Food Chem 23: 244-253 (1975)
    • (1975) J Agric Food Chem , vol.23 , pp. 244-253
    • Engstrom, G.W.1    DeLance, J.V.2    Richard, J.L.3    Baetz, A.L.4
  • 18
    • 0031455066 scopus 로고    scopus 로고
    • Roseocardin, a novel cardiotonic cyclodepsipeptide from Trichothecium roseum TT103
    • Tsunoo A, Kamijo M, Taketomo N, Sato Y, Ajisaka K. Roseocardin, a novel cardiotonic cyclodepsipeptide from Trichothecium roseum TT103. J Antibiot 50: 1007-1013 (1997)
    • (1997) J Antibiot , vol.50 , pp. 1007-1013
    • Tsunoo, A.1    Kamijo, M.2    Taketomo, N.3    Sato, Y.4    Ajisaka, K.5
  • 19
    • 0019814048 scopus 로고
    • New insecticidal cyclodepsipeptides from the fungus Isaria felina. I. Production, isolation and insecticidal properties of isariins B, C and D
    • Baute R, Deffieux G, Merlet D, Baute MA, Neveu A. New insecticidal cyclodepsipeptides from the fungus Isaria felina. I. Production, isolation and insecticidal properties of isariins B, C and D. J Antibiot 34: 1261-1265 (1981)
    • (1981) J Antibiot , vol.34 , pp. 1261-1265
    • Baute, R.1    Deffieux, G.2    Merlet, D.3    Baute, M.A.4    Neveu, A.5
  • 20
    • 0019839703 scopus 로고
    • New insecticidal cyclodepsipeptides from the fungus Isaria felina. II. Structure elucidation of isariins B, C and D
    • Deffieux G, Merlet D, Baute R, Bourgeois Q, Baute MS, Neveu A. New insecticidal cyclodepsipeptides from the fungus Isaria felina. II. Structure elucidation of isariins B, C and D. J Antibiot 34: 1266-1270 (1981)
    • (1981) J Antibiot , vol.34 , pp. 1266-1270
    • Deffieux, G.1    Merlet, D.2    Baute, R.3    Bourgeois, Q.4    Baute, M.S.5    Neveu, A.6
  • 21
    • 0022206304 scopus 로고
    • Rapid preparation of DNA from filamentous fungi
    • Raeder J, Broda P. Rapid preparation of DNA from filamentous fungi. Lett Appl Microbiol 1: 17-20 (1985)
    • (1985) Lett Appl Microbiol , vol.1 , pp. 17-20
    • Raeder, J.1    Broda, P.2
  • 22
    • 0027968068 scopus 로고
    • Improving the sensitivity of progressive multiple alignment through sequence weighting, positions-specific gap penalties and weight matrix choice
    • Thompson JD, Higgins DG, Gibson TJ, Clustal W. Improving the sensitivity of progressive multiple alignment through sequence weighting, positions-specific gap penalties and weight matrix choice. Nucl Acids Res 22: 4673-4680 (1994)
    • (1994) Nucl Acids Res , vol.22 , pp. 4673-4680
    • Thompson, J.D.1    Higgins, D.G.2    Gibson, T.J.3    Clustal, W.4
  • 23
    • 0036139211 scopus 로고    scopus 로고
    • MEGA2: Molecular Evolutionary Genetics Analysis software, Arizona State University, Tempe, Arizona, USA
    • Kumar S, Tamura K, Jakobsen IB, Nei M. MEGA2: Molecular Evolutionary Genetics Analysis software, Arizona State University, Tempe, Arizona, USA. Bioinform 17: 1244-1245 (2001)
    • (2001) Bioinform , vol.17 , pp. 1244-1245
    • Kumar, S.1    Tamura, K.2    Jakobsen, I.B.3    Nei, M.4
  • 24
    • 0019296687 scopus 로고
    • A simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences
    • Kimura M. A simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 16: 111-120 (1980)
    • (1980) J Mol Evol , vol.16 , pp. 111-120
    • Kimura, M.1
  • 25
    • 0034670511 scopus 로고    scopus 로고
    • Synthesis of dideuterated and enantiomers of monodeuterated tridecanoic acids at C-9 and C-10 positions
    • Abad J-L, Fabrias G, Camps F. Synthesis of dideuterated and enantiomers of monodeuterated tridecanoic acids at C-9 and C-10 positions. J Org Chem 65: 8582-8588 (2000)
    • (2000) J Org Chem , vol.65 , pp. 8582-8588
    • Abad, J.-L.1    Fabrias, G.2    Camps, F.3
  • 26
    • 0026040063 scopus 로고
    • A simple method for the microscale preparation of Mosher's acid chloride
    • Ward DE, Rhee CK. A simple method for the microscale preparation of Mosher's acid chloride. Tetrahedron Lett 32: 7165-7166 (1991)
    • (1991) Tetrahedron Lett , vol.32 , pp. 7165-7166
    • Ward, D.E.1    Rhee, C.K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.