BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

253 related articles for article (PubMed ID: 18081084)

  • 1. Synthesis and antifungal activity of aromatic bis-gamma-lactones analogous to avenaciolide.
    Castelo-Branco PA; Rubinger MM; Alves Lde C; de Barros PM; Pereira SG; de Melo VJ; Pilo-Veloso D; Zambolim L
    Chem Biodivers; 2007 Dec; 4(12):2745-54. PubMed ID: 18081084
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis, characterization, absolute structural determination and antifungal activity of a new chlorinated aromatic avenaciolide analogue.
    Castelo-Branco PA; Rubinger MM; Guilardi S; Leite VM; dos Santos AR; de C Alves L; Lariucci C; Vencato I; Piló-Veloso D; Zambolim L
    Pest Manag Sci; 2009 Jan; 65(1):34-40. PubMed ID: 18785221
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Structure-activity relationship studies on UK-2A, a novel antifungal antibiotic from Streptomyces sp. 517-02. Part 5: Roles of the 9-membered dilactone-ring moiety in respiratory inhibition.
    Usuki Y; Adachi N; Fujita K; Ichimura A; Iio H; Taniguchi M
    Bioorg Med Chem Lett; 2006 Jun; 16(12):3319-22. PubMed ID: 16564168
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Syntheses, crystal structure, spectroscopic characterization and antifungal activity of new N-R-sulfonyldithiocarbimate metal complexes.
    Alves LC; Rubinger MM; Lindemann RH; Perpétuo GJ; Janczak J; Miranda LD; Zambolim L; Oliveira MR
    J Inorg Biochem; 2009 Jul; 103(7):1045-53. PubMed ID: 19505726
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fungistatic activity of bicyclo[4.3.0]-γ-lactones.
    Olejniczak T; Boratyński F; Białońska A
    J Agric Food Chem; 2011 Jun; 59(11):6071-81. PubMed ID: 21520970
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis of (-)-gloeosporone, a fungal autoinhibitor of spore germination using a pi-allyltricarbonyliron lactone complex as a templating architecture for 1,7-diol construction.
    Ley SV; Cleator E; Harter J; Hollowood CJ
    Org Biomol Chem; 2003 Oct; 1(19):3263-4. PubMed ID: 14584786
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthetic method and biological activities of cis-fused alpha-methylene gamma-lactones.
    Higuchi Y; Shimoma F; Ando M
    J Nat Prod; 2003 Jun; 66(6):810-7. PubMed ID: 12828467
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis and determination of the absolute configuration of fugomycin and desoxyfugomycin: CD spectroscopy and fungicidal activity of butenolides.
    Braun M; Hohmann A; Rahematpura J; Bühne C; Grimme S
    Chemistry; 2004 Sep; 10(18):4584-93. PubMed ID: 15378637
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis and biological evaluation of optically active conjugated γ- and δ-lactone derivatives.
    Şardan M; Sezer S; Günel A; Akkaya M; Tanyeli C
    Bioorg Med Chem Lett; 2012 Sep; 22(18):5814-8. PubMed ID: 22902655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structure elucidation of hypocreolide A by enantioselective total synthesis.
    Götz K; Liermann JC; Thines E; Anke H; Opatz T
    Org Biomol Chem; 2010 May; 8(9):2123-30. PubMed ID: 20401389
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolation of (-)-avenaciolide as the antifungal and antimycobacterial constituent of a Seimatosporium sp. Endophyte from the medicinal plant Hypericum perforatum .
    Clark TN; Bishop AI; McLaughlin M; Calhoun LA; Johnson JA; Gray CA
    Nat Prod Commun; 2014 Oct; 9(10):1495-6. PubMed ID: 25522544
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Total synthesis of (+/-) tanikolide.
    Krauss J
    Nat Prod Lett; 2001; 15(6):393-9. PubMed ID: 11838977
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rufuslactone, a new antifungal sesquiterpene from the fruiting bodies of the basidiomycete Lactarius rufus.
    Luo DQ; Wang F; Bian XY; Liu JK
    J Antibiot (Tokyo); 2005 Jul; 58(7):456-9. PubMed ID: 16161484
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Semi-synthesis and biological evaluation of analogues of UK-2A, a novel antifungal antibiotic from Streptomyces sp. 517-02.
    Usuki Y; Mitomo K; Adachi N; Ping X; Fujita K; Sakanaka O; Iinuma K; Iio H; Taniguchi M
    Bioorg Med Chem Lett; 2005 Apr; 15(8):2011-4. PubMed ID: 15808458
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Minor sesquiterpene lactones from Centaurea pullata and their antimicrobial activity.
    Djeddi S; Karioti A; Sokovic M; Stojkovic D; Seridi R; Skaltsa H
    J Nat Prod; 2007 Nov; 70(11):1796-9. PubMed ID: 17979247
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis and Antimicrobial Activity of Methoxy- Substituted γ-Oxa-ε-lactones Derived from Flavanones.
    Gładkowski W; Siepka M; Janeczko T; Kostrzewa-Susłow E; Popłoński J; Mazur M; Żarowska B; Łaba W; Maciejewska G; Wawrzeńczyk C
    Molecules; 2019 Nov; 24(22):. PubMed ID: 31744042
    [TBL] [Abstract][Full Text] [Related]  

  • 17. C3-symmetric trisimidazoline-catalyzed enantioselective bromolactonization of internal alkenoic acids.
    Murai K; Nakamura A; Matsushita T; Shimura M; Fujioka H
    Chemistry; 2012 Jul; 18(27):8448-53. PubMed ID: 22623128
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Citrafungins A and B, two new fungal metabolite inhibitors of GGTase I with antifungal activity.
    Singh SB; Zink DL; Doss GA; Polishook JD; Ruby C; Register E; Kelly TM; Bonfiglio C; Williamson JM; Kelly R
    Org Lett; 2004 Feb; 6(3):337-40. PubMed ID: 14748587
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Bioactive γ-lactones from the fermented broth of Neosartorya sp.
    Yang SS; Wang GJ; Cheng KF; Chen CH; Ju YM; Tsau YJ; Lee TH
    Planta Med; 2010 Oct; 76(15):1701-5. PubMed ID: 20446242
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel sesquiterpene lactone from Centaurea pullata: structure elucidation, antimicrobial activity, and prediction of pharmacokinetic properties.
    Djeddi S; Karioti A; Sokovic M; Koukoulitsa C; Skaltsa H
    Bioorg Med Chem; 2008 Apr; 16(7):3725-31. PubMed ID: 18280170
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.