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Volumn 6, Issue 9, 2011, Pages 1247-1250

Szentiamide, an N-formylated cyclic depsipeptide from Xenorhabdus szentirmaii DSM 16338T

Author keywords

Cyclodepsipeptide; Formylated; Xenorhabdus

Indexed keywords

ANTIINFECTIVE AGENT; ANTINEOPLASTIC AGENT; DEPSIPEPTIDE; PROTEIN TYROSINE PHOSPHATASE 1B; SZENTIAMIDE; UNCLASSIFIED DRUG; XENOFURANONE A; REPRESSOR PROTEIN; ZNF589 PROTEIN, HUMAN;

EID: 80155169062     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x1100600909     Document Type: Article
Times cited : (29)

References (15)
  • 1
    • 14344266776 scopus 로고    scopus 로고
    • Description of four novel species of Xenorhabdus, family Enterobacteriaceae: Xenorhabdus budapestensis sp. nov., Xenorhabdus ehlersii sp. nov., Xenorhabdus innexi sp. nov., and Xenorhabdus szentirmaii sp. nov
    • (a) Lengyel K, Lang E, Fodor A., Szállás E, Schumann P, Stackebrandt E. (2005) Description of four novel species of Xenorhabdus, family Enterobacteriaceae: Xenorhabdus budapestensis sp. nov., Xenorhabdus ehlersii sp. nov., Xenorhabdus innexi sp. nov., and Xenorhabdus szentirmaii sp. nov. Systematic and Applied Microbiology, 28, 115-122;
    • (2005) Systematic and Applied Microbiology , vol.28 , pp. 115-122
    • Lengyel, K.1    Lang, E.2    Fodor, A.3    Szállás, E.4    Schumann, P.5    Stackebrandt, E.6
  • 2
    • 65349186325 scopus 로고    scopus 로고
    • Entomopathogenic bacteria as a source of secondary metabolites
    • (b) Bode HB. (2009) Entomopathogenic bacteria as a source of secondary metabolites. Current Opinion in Chemical Biology, 13, 224-230;
    • (2009) Current Opinion in Chemical Biology , vol.13 , pp. 224-230
    • Bode, H.B.1
  • 5
    • 47549092029 scopus 로고    scopus 로고
    • Linear and cyclic peptides from the entomopathogenic bacterium Xenorhabdus nematophilus
    • (e) Lang G, Kalvelage T, Peters A, Wiese J, Imhoff JF. (2008) Linear and cyclic peptides from the entomopathogenic bacterium Xenorhabdus nematophilus. Journal of Natural Products, 71, 1074-1077;
    • (2008) Journal of Natural Products , vol.71 , pp. 1074-1077
    • Lang, G.1    Kalvelage, T.2    Peters, A.3    Wiese, J.4    Imhoff, J.F.5
  • 6
    • 3242709451 scopus 로고    scopus 로고
    • Antibiotics from Xenorhabdus spp. and Photorhabdus spp. (enterobacteriaceae): (Review)
    • (f) Li J, Hu K, Webster JM. (1998) Antibiotics from Xenorhabdus spp. and Photorhabdus spp. (Enterobacteriacea) (Review). Chemistry of Heterocyclic Compounds, 34, 1331-1339. (Pubitemid 128698396)
    • (1998) Chemistry of Heterocyclic Compounds , vol.34 , Issue.11 , pp. 1331-1339
    • Li, J.1    Hu, K.2    Webster, J.M.3
  • 9
    • 0029122279 scopus 로고
    • Antimicrobial metabolites from a bacterial symbiont
    • (c) Li J, Chen G, Webster JM. (1995) Antimicrobial metabolites from a bacterial symbiont. Journal of Natural Products, 58, 1081-1086.
    • (1995) Journal of Natural Products , vol.58 , pp. 1081-1086
    • Li, J.1    Chen, G.2    Webster, J.M.3
  • 10
    • 68249107853 scopus 로고    scopus 로고
    • Identification of a new antimicrobial lysine-rich cyclolipopeptide family from Xenorhabdus nematophila
    • (a) Gualtieri M, Aumelas A, Thaler J. (2009) Identification of a new antimicrobial lysine-rich cyclolipopeptide family from Xenorhabdus nematophila. Journal of Antibiotics, 62, 295-302;
    • (2009) Journal of Antibiotics , vol.62 , pp. 295-302
    • Gualtieri, M.1    Aumelas, A.2    Thaler, J.3
  • 11
    • 80555151706 scopus 로고    scopus 로고
    • Herstellung und Verwendung antitumoraler, antibiotischer und insektizider Cyclodepsipeptide
    • Patent DE 10 2009 025 119 A1
    • (b) Imhoff JF, Lang G, Kajahn I, Peters A, Wiese J. (2009) Herstellung und Verwendung antitumoraler, antibiotischer und insektizider Cyclodepsipeptide. Patent DE 10 2009 025 119 A1.
    • (2009)
    • Imhoff, J.F.1    Lang, G.2    Kajahn, I.3    Peters, A.4    Wiese, J.5
  • 12
    • 77953070836 scopus 로고    scopus 로고
    • Insektenpathogene Bakterien als Quelle neuer Naturstoffe
    • Bode HB. (2010) Insektenpathogene Bakterien als Quelle neuer Naturstoffe. Biospektrum, 16, 266-269.
    • (2010) Biospektrum , vol.16 , pp. 266-269
    • Bode, H.B.1
  • 13
    • 33745017396 scopus 로고    scopus 로고
    • Formylation domain: An essential modifying enzyme for the nonribosomal biosynthesis of linear gramicidin
    • DOI 10.1021/ja0611240
    • Schoenafinger G, Schracke N, Linne U, Marahiel MA. (2006) Formylation domain: an essential modifying enzyme for the nonribosomal biosynthesis of linear gramicidin. Journal of the American Chemical Society, 128, 7406-7407. (Pubitemid 43877491)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.23 , pp. 7406-7407
    • Schoenafinger, G.1    Schrecke, N.2    Linne, U.3    Marahiel, M.A.4
  • 15
    • 34147216138 scopus 로고    scopus 로고
    • A high throughput luminescent assay for glycogen synthase kinase-3β inhibitors
    • DOI 10.1089/adt.2006.029
    • (b) Baki A., Bielik A, Molnár L, Szendrei G, Keserü GM. (2007) A high throughput luminescent assay for Glycogen Synthase Kinase-3β Inhibitors. ASSAY and Drug Development Technologies, 5, 75-83. (Pubitemid 46581242)
    • (2007) Assay and Drug Development Technologies , vol.5 , Issue.1 , pp. 75-83
    • Baki, A.1    Bielik, A.2    Molnar, L.3    Szendrei, G.4    Keseru, G.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.