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Volumn 11, Issue 1, 2014, Pages 67-75

Antifungal activity of a library of cyclitols and related compounds

Author keywords

Amino acid conjugates; Antifungal activity; Bioautography; Chemoenzymatic; Conduritols; Inositols

Indexed keywords

ALDEHYDE; ANTIFUNGAL AGENT; AZIDOCONDURITOL; AZIDOINOSITOL GLYCOSIDE; BETA AMINO ACID; CYCLITOL; GLYCOSIDE; N (3 BROMO 6 HYDROXY 4,5 ISOPROPYLIDENEDIOXYCYCLOHEX 2 ENYL) N (T BUTOXYCARBONYL)PROLINE; N (T BUTOXYCARBONYL) N (3 BROMO 6 HYDROXY 4,5 ISOPROPYLIDENEDIOXYCYCLOHEX 2 EN 1 YL) 3 (PHENYL)PROPIONAMIDE; N (T BUTOXYCARBONYL) N (3 BROMO 6 HYDROXY 4,5 ISOPROPYLIDENEDIOXYCYCLOHEX 2 EN 1 YL) 4 (METHYL)PENTAMIDE; N (T BUTOXYCARBONYL) N (3 BROMO 6 HYDROXY 4,5 ISOPROPYLIDENEDIOXYCYCLOHEX 2 EN 1 YL) 4 (METHYLSULFANYL)BUTYRAMIDE; N (T BUTOXYCARBONYL) N (3 BROMO 6 HYDROXY 4,5 ISOPROPYLIDENEDIOXYCYCLOHEX 2 EN 1 YL)ACETAMIDE; N (T BUTOXYCARBONYL) N (3 BROMO 6 HYDROXY 4,5 ISOPROPYLIDENEDIOXYCYCLOHEX 2 EN 1 YL)PROPIONAMIDE; UNCLASSIFIED DRUG;

EID: 84889578922     PISSN: 15701808     EISSN: 1875628X     Source Type: Journal    
DOI: 10.2174/15701808113109990036     Document Type: Article
Times cited : (7)

References (32)
  • 2
    • 35748935537 scopus 로고    scopus 로고
    • Recent advances and challenges in the treatment of invasive fungal infections
    • Shao, P.L.; Huang, L.M.; P.R., H. Recent advances and challenges in the treatment of invasive fungal infections. Int. J. Antimicrob. Ag., 2007, 30, 487-495.
    • (2007) Int. J. Antimicrob. Ag. , vol.30 , pp. 487-495
    • Shao, P.L.1    Huang, L.M.2
  • 4
    • 4444312095 scopus 로고    scopus 로고
    • Cyclitols: Conduritols and related compounds
    • DOI 10.2174/1385272043370069
    • Gultekin, M.S.; Celik, M.; Balci, M. Cyclitols: Conduritols and related compounds. Curr. Org. Chem., 2004, 13, 1159-1186. (Pubitemid 39162404)
    • (2004) Current Organic Chemistry , vol.8 , Issue.13 , pp. 1159-1186
    • Gultekin, M.S.1    Celik, M.2    Balci, M.3
  • 5
    • 0025675652 scopus 로고
    • Glycoside hydrolases: Mechanistic information from studies with reversible and irreversible inhibitors
    • Legler, G. Glycoside hydrolases: mechanistic information from studies with reversible and irreversible inhibitors. Adv. Carbohydr. Chem. Biochem., 1990, 48, 319-384.
    • (1990) Adv. Carbohydr. Chem. Biochem. , vol.48 , pp. 319-384
    • Legler, G.1
  • 6
    • 0000519434 scopus 로고
    • Conduritols and related compounds
    • Balci, M.; Sutbeyaz, Y.; Secen, H. Conduritols and related compounds. Tetrahedron, 1990, 46, 3715-3742.
    • (1990) Tetrahedron , vol.46 , pp. 3715-3742
    • Balci, M.1    Sutbeyaz, Y.2    Secen, H.3
  • 7
    • 0024453294 scopus 로고
    • Inositol phosphates and cell signalling
    • DOI 10.1038/341197a0
    • Berridge, M.J.; Irvine, R.F. Inositol phosphates and cell signalling. Nature., 1989, 341, 197-205. (Pubitemid 19231718)
    • (1989) Nature , vol.341 , Issue.6239 , pp. 197-205
    • Berridge, M.J.1    Irvine, R.F.2
  • 8
    • 85044699708 scopus 로고    scopus 로고
    • Biologically active myo-inositol phosphates
    • Stepanov, A.E.; Shvets, V.I. Biologically Active myo-Inositol Phosphates. Bioorg. Khim., 1996, 22, 737-744.
    • (1996) Bioorg. Khim. , vol.22 , pp. 737-744
    • Stepanov, A.E.1    Shvets, V.I.2
  • 9
    • 79953308533 scopus 로고    scopus 로고
    • Expanding cyclitol structural diversity by biocatalysis and metalocatalysis. A click chemistry approach
    • De La Sovera, V.; Bellomo, A.; Pena, J.M.; Gonzalez, D.; Stefani, H.A. Expanding cyclitol structural diversity by biocatalysis and metalocatalysis. A click chemistry approach. Mol. Divers., 2011, 15, 163-172.
    • (2011) Mol. Divers. , vol.15 , pp. 163-172
    • De La Sovera, V.1    Bellomo, A.2    Pena, J.M.3    Gonzalez, D.4    Stefani, H.A.5
  • 10
    • 76649101463 scopus 로고    scopus 로고
    • Novel deoxy-selenylconduritols: Chemoenzymatic synthesis and biological evaluation
    • Bellomo, A.; Bertucci, A.; Stefani, H.; Vázquez, A.; Gonzalez, D. Novel deoxy-selenylconduritols: chemoenzymatic synthesis and biological evaluation. Tetrahedron: Asymmetry., 2009, 20, 2673- 2676.
    • (2009) Tetrahedron: Asymmetry. , vol.20 , pp. 2673-2676
    • Bellomo, A.1    Bertucci, A.2    Stefani, H.3    Vázquez, A.4    Gonzalez, D.5
  • 11
    • 70349236170 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of glycosyl-deoxyinositol derivatives. First example of a fagopyritol β-analogue containing an aminoinositol unit
    • Bellomo, A.; Bonilla, J.B.; López-Prados, J.; Martín-Lomas, M.; Gonzalez, D. Chemoenzymatic synthesis of glycosyl-deoxyinositol derivatives. First example of a fagopyritol β-analogue containing an aminoinositol unit. Tetrahedron: Asymmetry, 2009, 20, 2061- 2064.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 2061-2064
    • Bellomo, A.1    Bonilla, J.B.2    López-Prados, J.3    Martín-Lomas, M.4    Gonzalez, D.5
  • 12
    • 57649183892 scopus 로고    scopus 로고
    • Enantiospecific synthesis and insect feeding activity of sulfurcontaining cyclitols
    • Bellomo, A.; Camarano, S.; Rossini, C.; Gonzalez, D. Enantiospecific synthesis and insect feeding activity of sulfurcontaining cyclitols. Carbohydr. Res., 2009, 344, 44-51.
    • (2009) Carbohydr. Res. , vol.344 , pp. 44-51
    • Bellomo, A.1    Camarano, S.2    Rossini, C.3    Gonzalez, D.4
  • 13
    • 67649967520 scopus 로고    scopus 로고
    • Consecutive biocatalysis-palladium catalysis II: Synthesis of conduritol-alkyne conjugates
    • Bellomo, A.; Weber, M.; Gonzalez, D.; Stefani, H. A. Consecutive biocatalysis-palladium catalysis II: Synthesis of conduritol-alkyne conjugates. Catal. Commun., 2009, 10, 1647-1650.
    • (2009) Catal. Commun. , vol.10 , pp. 1647-1650
    • Bellomo, A.1    Weber, M.2    Gonzalez, D.3    Stefani, H.A.4
  • 14
    • 39749194858 scopus 로고    scopus 로고
    • Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach
    • Bellomo, A.; Gonzalez, D.; Stefani, H.A. Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach. J. Organomet. Chem., 2008, 693, 1136-1142.
    • (2008) J. Organomet. Chem. , vol.693 , pp. 1136-1142
    • Bellomo, A.1    Gonzalez, D.2    Stefani, H.A.3
  • 15
    • 35148863199 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis and biological evaluation of (-)-conduramine C-4
    • DOI 10.1080/00397910701555725, PII 782879366
    • Bellomo, A.; Giacomini, C.; Brena, B.; Seoane, G.; Gonzalez, D. Chemoenzymatic synthesis and biological evaluation of (-)- conduramine C-4. Synthetic Commun., 2007, 37, 3509-3518. (Pubitemid 47537109)
    • (2007) Synthetic Communications , vol.37 , Issue.20 , pp. 3509-3518
    • Bellomo, A.1    Giacomini, C.2    Brena, B.3    Seoane, G.4    Gonzalez, D.5
  • 16
    • 33947582664 scopus 로고    scopus 로고
    • Diasterodivergent synthesis of optically pure vinyl episulfides and β-hydroxy thiocyanates from a bacterial metabolite
    • DOI 10.1016/j.tetlet.2007.02.113, PII S0040403907004054
    • Bellomo, A.; Gonzalez, D. Diasterodivergent synthesis of optically pure vinyl episulfides and ?-hydroxy thiocyanates from a bacterial metabolite. Tetrahedron Lett., 2007, 48, 3047-3051. (Pubitemid 46483591)
    • (2007) Tetrahedron Letters , vol.48 , Issue.17 , pp. 3047-3051
    • Bellomo, A.1    Gonzalez, D.2
  • 17
    • 33644679572 scopus 로고    scopus 로고
    • Catalytic thiolysis of chemoenzymatically derived vinylepoxides. Efficient synthesis of homochiral phenylthioconduritol F
    • DOI 10.1016/j.tetasy.2006.01.024, PII S0957416606000668
    • Bellomo, A.; Gonzalez, D. Catalytic thiolysis of chemoenzymatically derived vinylepoxides. Efficient synthesis of homochiral phenylthioconduritol F. Tetrahedron: Asymmetry., 2006, 17, 474-478. (Pubitemid 43330794)
    • (2006) Tetrahedron Asymmetry , vol.17 , Issue.3 , pp. 474-478
    • Bellomo, A.1    Gonzalez, D.2
  • 18
    • 3042651952 scopus 로고    scopus 로고
    • Concise chemoenzymatic synthesis of epi-inositol
    • DOI 10.1016/j.carres.2004.04.011, PII S0008621504001855
    • Vitelio, C.; Bellomo, A.; Brovetto, M.; Seoane, G.; Gonzalez, D. Concise chemoenzymatic synthesis of epi-inositol. Carbohydr. Res., 2004, 339, 1773-1778. (Pubitemid 38829505)
    • (2004) Carbohydrate Research , vol.339 , Issue.10 , pp. 1773-1778
    • Vitelio, C.1    Bellomo, A.2    Brovetto, M.3    Seoane, G.4    Gonzalez, D.5
  • 19
    • 84889583995 scopus 로고    scopus 로고
    • Clinical and Laboratory Standards Institute. Reference method for broth dilution antifungal susceptibility testing of yeasts; Approved standard, 3rd ed, CLSI document M27-A3, Clinical and Laboratory Standards Institute, Wayne, PA 2008.
    • Clinical and Laboratory Standards Institute. Reference method for broth dilution antifungal susceptibility testing of yeasts; Approved standard, 3rd ed, CLSI document M27-A3, Clinical and Laboratory Standards Institute, Wayne, PA 2008.
  • 20
    • 79960604537 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of inositols, conduritols, and cyclitol analogues
    • Duchek, J.; Adams, D.R.; Hudlicky, T. Chemoenzymatic Synthesis of Inositols, Conduritols, and Cyclitol Analogues. Chem. Rev., 2011, 111, 4223-4258.
    • (2011) Chem. Rev. , vol.111 , pp. 4223-4258
    • Duchek, J.1    Adams, D.R.2    Hudlicky, T.3
  • 21
    • 62449130187 scopus 로고    scopus 로고
    • Celebrating 20 years of synlett - Special account on the merits of biocatalysis and the impact of arene cis- dihydrodiols on enantioselective synthesis
    • Reed, J.W.; Hudlicky, T. Celebrating 20 Years of Synlett - Special Account On the Merits of Biocatalysis and the Impact of Arene cis- Dihydrodiols on Enantioselective Synthesis. Synlett., 2009, 685- 703.
    • (2009) Synlett. , pp. 685-703
    • Reed, J.W.1    Hudlicky, T.2
  • 22
    • 0001846314 scopus 로고    scopus 로고
    • Enzymatic dihydroxylation of aromatics in enantioselective synthesis: Expanding asymmetric methodology
    • Hudlicky, T.; Gonzalez, D.; Gibson, D.T. Enzymatic dihydroxylation of aromatics in enantioselective synthesis: Expanding asymmetric methodology. Aldrichim. Acta., 1999, 32, 35-62.
    • (1999) Aldrichim. Acta. , vol.32 , pp. 35-62
    • Hudlicky, T.1    Gonzalez, D.2    Gibson, D.T.3
  • 23
    • 0035711112 scopus 로고    scopus 로고
    • Aromatic dioxygenases: Molecular biocatalysis and applications
    • DOI 10.1016/S0958-1669(01)00264-6
    • Boyd, D. R.; Sharma, N.D.; Allen, C.C.R. Aromatic dioxygenases: molecular biocatalysis and applications. Curr. Op. Biotechnol., 2001, 12, 564-573. (Pubitemid 34146507)
    • (2001) Current Opinion in Biotechnology , vol.12 , Issue.6 , pp. 564-573
    • Boyd, D.R.1    Sharma, N.D.2    Allen, C.C.R.3
  • 24
    • 0024988763 scopus 로고
    • Microbial oxidation of chloroaromatics in the enantiodivergent synthesis of pyrrolizidine alkaloids: Trihydroxyheliotridanes
    • DOI 10.1021/jo00302a037
    • Hudlicky, T.; Luna, H.; Price, J.D.; Rulin, F. Microbial oxidation of chloroaromatics in the enantiodivergent synthesis of pyrrolizidine alkaloids: trihydroxyheliotridanes. J. Org. Chem., 1990, 55, 4683-4687. (Pubitemid 20274272)
    • (1990) Journal of Organic Chemistry , vol.55 , Issue.15 , pp. 4683-4687
    • Hudlicky, T.1    Luna, H.2    Price, J.D.3    Rulin, F.4
  • 26
    • 0029102006 scopus 로고
    • Use of specific dyes in the detection of antimicrobial compounds from crude plant extracts using a thin layer chromatography agar overlay technique
    • Saxena, Q.; Farmer, S.; Towers, G.H.N.; Hancock, R.E.W. Use of specific dyes in the detection of antimicrobial compounds from crude plant extracts using a thin layer chromatography agar overlay technique. Phytochem. Analysis., 1995, 6, 125-129.
    • (1995) Phytochem. Analysis. , vol.6 , pp. 125-129
    • Saxena, Q.1    Farmer, S.2    Towers, G.H.N.3    Hancock, R.E.W.4
  • 27
    • 84986959314 scopus 로고
    • A bioautographic agar overlay method for the detection of antifungal compounds from higher plants
    • Rahalison, L.; Hamburger, M.; Hostettman, K.; Monod, M.; Frenk, E. A bioautographic agar overlay method for the detection of antifungal compounds from higher plants. Phytochem. Analysis., 1991, 2, 199-203.
    • (1991) Phytochem. Analysis. , vol.2 , pp. 199-203
    • Rahalison, L.1    Hamburger, M.2    Hostettman, K.3    Monod, M.4    Frenk, E.5
  • 29
    • 2942703994 scopus 로고    scopus 로고
    • A quantitative structure-antifungal activity relationship study of oxygenated aromatic essential oil compounds using data structuring and PLS regression analysis
    • DOI 10.1007/s00894-003-0174-5
    • Voda, K.; Boh, B.; Vrtacnik, M.A quantitative structure-antifungal activity relationship study of oxygenated aromatic essential oil compounds using data structuring and PLS regression analysis J. Mol. Model., 2004, 10, 76-84. (Pubitemid 38787179)
    • (2004) Journal of Molecular Modeling , vol.10 , Issue.1 , pp. 76-84
    • Voda, K.1    Boh, B.2    Vrtacnik, M.3
  • 30
    • 0038159878 scopus 로고    scopus 로고
    • Systemic mycoses in the immunocompromised host: An update in antifungal therapy
    • DOI 10.1053/jhin.2002.1278, PII S0195670102912788
    • Kontoyiannis, D.; Mantadakis, E.; Samonis, G. Systemic mycoses in the immunocompromised host: an update in antifungal therapy. J. Hosp. Inf., 2003, 53, 243-258. (Pubitemid 38002036)
    • (2003) Journal of Hospital Infection , vol.53 , Issue.4 , pp. 243-258
    • Kontoyiannis, D.P.1    Mantadakis, E.2    Samonis, G.3
  • 31
    • 0242386559 scopus 로고    scopus 로고
    • Treatment of opportunistic mycoses: How long is long enough?
    • DOI 10.1016/S1473-3099(03)00802-8
    • Singh, N. Treatment of opportunistic mycoses: how long is long enough? Lancet Infect. Dis., 2003, 3, 703-708. (Pubitemid 37345348)
    • (2003) Lancet Infectious Diseases , vol.3 , Issue.11 , pp. 703-708
    • Singh, N.1
  • 32
    • 33846466508 scopus 로고    scopus 로고
    • Epidemiology of invasive candidiasis: A persistent public health problem
    • DOI 10.1128/CMR.00029-06
    • Pfaller, M.A.; Diekema, D.J. Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem. Clin. Microbiol. Rev., 2007, 20, 133-163. (Pubitemid 46167771)
    • (2007) Clinical Microbiology Reviews , vol.20 , Issue.1 , pp. 133-163
    • Pfaller, M.A.1    Diekema, D.J.2


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