메뉴 건너뛰기




Volumn 15, Issue 6, 2010, Pages 4294-4308

Design of novel 4-hydroxy-chromene-2-one derivatives as antimicrobial agents

Author keywords

4 Hydroxy coumarins; Antimicrobial activity; Design; Molecular docking; QSAR

Indexed keywords

ANTIINFECTIVE AGENT; COUMARIN; COUMARIN DERIVATIVE;

EID: 77954247703     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules15064294     Document Type: Article
Times cited : (33)

References (33)
  • 1
    • 33745858694 scopus 로고    scopus 로고
    • Antifungal activity of some coumarins obtained from species of Pterocaulon (Asteraceae)
    • Stein, A. C.; Álvarez, S.; Avancini, C.; Zacchinos, S.; von Poser, G. Antifungal activity of some coumarins obtained from species of Pterocaulon (Asteraceae). J. Ethnopharmacol. 2006, 107, 95-98.
    • (2006) J. Ethnopharmacol. , vol.107 , pp. 95-98
    • Stein, A.C.1    Álvarez, S.2    Avancini, C.3    Zacchinos, S.4    Von Poser, G.5
  • 3
    • 66349085909 scopus 로고    scopus 로고
    • Synthesis and molecular descriptor characterization of novel 4-hydroxy-chromene-2-one derivatives as antimicrobial agents
    • Mladenovic, M.; Vukovic, N.; Niciforovic, N.; Sukdolak, S.; Solujic, S. Synthesis and molecular descriptor characterization of novel 4-hydroxy-chromene-2-one derivatives as antimicrobial agents. Molecules 2009, 14, 1495-1512.
    • (2009) Molecules , vol.14 , pp. 1495-1512
    • Mladenovic, M.1    Vukovic, N.2    Niciforovic, N.3    Sukdolak, S.4    Solujic, S.5
  • 4
    • 53149139920 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of some novel 2-aminothiayole derivatives of 4-hydroxy-chromene-2-one
    • Vukovic, N.; Sukdolak, S.; Solujic, S.; Miloševic, T. Synthesis and antimicrobial evaluation of some novel 2-aminothiayole derivatives of 4-hydroxy-chromene-2-one. Arch. Pharm. Chem. Life Sci. 2008, 341, 491-496.
    • (2008) Arch. Pharm. Chem. Life Sci. , vol.341 , pp. 491-496
    • Vukovic, N.1    Sukdolak, S.2    Solujic, S.3    Miloševic, T.4
  • 5
    • 0033103874 scopus 로고    scopus 로고
    • Antibacterial activity of simple coumarins structural requirements for biological activity
    • Kayser, O.; Koldrziey, H. Antibacterial activity of simple coumarins structural requirements for biological activity. Z. Naturforch. 1999, 54 c, 169-174.
    • (1999) Z. Naturforch , vol.54 , pp. 169-174
    • Kayser, O.1    Koldrziey, H.2
  • 6
    • 33846594197 scopus 로고    scopus 로고
    • Quantum chemical studies on structure activity relationship of natural product polyacetylenes
    • Zloh, M.; Bucar, F.; Gibbons, S. Quantum chemical studies on structure activity relationship of natural product polyacetylenes. Theor. Chem. Acc. 2007, 117, 247-252.
    • (2007) Theor. Chem. Acc. , vol.117 , pp. 247-252
    • Zloh, M.1    Bucar, F.2    Gibbons, S.3
  • 7
    • 21944434729 scopus 로고    scopus 로고
    • QSAR study of inibition by coumarins of IQ induced mutation in S. typhimurium TA98
    • Okamoto, A. K.; Gaudio, A. C.; dos Santos Marques, A.; Takahata, Y. QSAR study of inibition by coumarins of IQ induced mutation in S. typhimurium TA98. J. Mol. Struc. Theochem. 2005, 725, 231-238.
    • (2005) J. Mol. Struc. Theochem , vol.725 , pp. 231-238
    • Okamoto, A.K.1    Gaudio, A.C.2    Dos Marques, S.A.3    Takahata, Y.4
  • 8
    • 63449137987 scopus 로고    scopus 로고
    • Antimicrobial and antioxidant activities of coumarins from the roots of Ferulago campestris (Apiaceae)
    • Basile, A.; Sorbo, S.; Spadaro, V.; Bruno, M.; Maggio, A.; Faraone, N.; Rosselli, S. Antimicrobial and antioxidant activities of coumarins from the roots of Ferulago campestris (Apiaceae). Molecules 2009, 14, 939-952.
    • (2009) Molecules , vol.14 , pp. 939-952
    • Basile, A.1    Sorbo, S.2    Spadaro, V.3    Bruno, M.4    Maggio, A.5    Faraone, N.6    Rosselli, S.7
  • 9
    • 69549108156 scopus 로고    scopus 로고
    • Coumarins from Angelica lucida L.-Antibacterial activities
    • Widelski, J.; Popova, M.; Graikou, K.; Glowniak, K.; Chinou, I. Coumarins from Angelica lucida L.-Antibacterial activities. Molecules 2009, 14, 2729-2734.
    • (2009) Molecules , vol.14 , pp. 2729-2734
    • Widelski, J.1    Popova, M.2    Graikou, K.3    Glowniak, K.4    Chinou, I.5
  • 11
    • 51849182933 scopus 로고
    • Synthesis of some coumarin derivatives and their antimicrobial activity
    • Hishmit, O. H.; Miky, A. A. J.; Farrag, A. A.; Fadl-Allah, E. M. Synthesis of some coumarin derivatives and their antimicrobial activity. Arch. Pharm. Res. 1989, 12, 181-185.
    • (1989) Arch. Pharm. Res. , vol.12 , pp. 181-185
    • Hishmit, O.H.1    Miky, A.A.J.2    Farrag, A.A.3    Fadl-Allah, E.M.4
  • 12
    • 70149097993 scopus 로고    scopus 로고
    • QSAR, synthesis and biological activity studies of some thiazolidines derivatives
    • Sharma, M. C.; Sahu, N. K.; Kohali, D. V.; Chaturvedi, S. C.; Sharma, S. QSAR, synthesis and biological activity studies of some thiazolidines derivatives. DJNB 2009, 4, 223-232.
    • (2009) DJNB , vol.4 , pp. 223-232
    • Sharma, M.C.1    Sahu, N.K.2    Kohali, D.V.3    Chaturvedi, S.C.4    Sharma, S.5
  • 13
    • 0029978822 scopus 로고    scopus 로고
    • The nature of inhibition of DNA gyrase by the coumarins and the cyclothialidines by X-ray crystallography
    • Lewis, J. R.; Singh, M. P. O.; Smith, V. C.; Skarzynski, T.; Maxwell, A.; Wonacott, J. A.; Wigley, B. D. The nature of inhibition of DNA gyrase by the coumarins and the cyclothialidines by X-ray crystallography. EMBO J. 1996, 15, 1412-1240.
    • (1996) EMBO J. , vol.15 , pp. 1412-1240
    • Lewis, J.R.1    Singh, M.P.O.2    Smith, V.C.3    Skarzynski, T.4    Maxwell, A.5    Wonacott, J.A.6    Wigley, B.D.7
  • 14
    • 77954292930 scopus 로고    scopus 로고
    • Optimization of chromatographic conditions in thin layer chromatography of flavonoids and phenolic acids
    • Šaric-Medic, M.; Mornar, A.; Crnjevic-Badovinac, T.; Josprica, I. Optimization of chromatographic conditions in thin layer chromatography of flavonoids and phenolic acids. Croat. Chem. Acta 2004, 77, 367-370.
    • (2004) Croat. Chem. Acta , vol.77 , pp. 367-370
    • Šaric-Medic, M.1    Mornar, A.2    Crnjevic-Badovinac, T.3    Josprica, I.4
  • 15
    • 41349091302 scopus 로고    scopus 로고
    • Synthesis, computational study and cytotoxic activity of new 4-hydroxycoumarin derivatives
    • Stanchev, S.; Momekov, G.; Jensen, F.; Manolov, I. Synthesis, computational study and cytotoxic activity of new 4-hydroxycoumarin derivatives. Eur. J. Med. Chem. 2008, 43, 694-706.
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 694-706
    • Stanchev, S.1    Momekov, G.2    Jensen, F.3    Manolov, I.4
  • 18
    • 0000130397 scopus 로고
    • The quantitative analysis of structure-activity relationships
    • 5th ed.; Wolff, M. E., Ed.; John Wiley & Sons: New York, NY, USA
    • Kubinyi, H. The Quantitative Analysis of Structure-Activity Relationships. In Burger's Medicinal Chemstry and Drug Discovery, Principles and Practice, 5th ed.; Wolff, M. E., Ed.; John Wiley & Sons: New York, NY, USA, 1995; Volume 3, pp. 497-571.
    • (1995) Burger's Medicinal Chemstry and Drug Discovery, Principles and Practice , vol.3 , pp. 497-571
    • Kubinyi, H.1
  • 20
    • 37449001930 scopus 로고    scopus 로고
    • A novel indicator plant to test the hypersensitivity of phytopathogenic bacteria
    • Umesha, S.; Richardson, P. A.; Kong, P. Hong, C. X. A novel indicator plant to test the hypersensitivity of phytopathogenic bacteria. J. Microbiol. Meth. 2008, 72, 95-97.
    • (2008) J. Microbiol. Meth. , vol.72 , pp. 95-97
    • Umesha, S.1    Richardson, P.A.2    Kong, P.3    Hong, C.X.4
  • 22
    • 77954292489 scopus 로고    scopus 로고
    • Software Spartan 2002 for Windows. Wavefunction, Inc., 18401 Von Karman Ave. Ste. 370, Irvine, CA 92612-8542, USA
    • Software Spartan 2002 for Windows. Wavefunction, Inc., 18401 Von Karman Ave. Ste. 370, Irvine, CA 92612-8542, USA, 2002.
    • (2002)
  • 24
    • 77954296395 scopus 로고    scopus 로고
    • MOPAC 2009. Stewart Computational Chemistry: Colorado Springs, CO, USA
    • Stewart, J. J. P. MOPAC 2009. Stewart Computational Chemistry: Colorado Springs, CO, USA, http://www.openMOPAC.net.
    • Stewart, J.J.P.1
  • 25
    • 0036284090 scopus 로고    scopus 로고
    • VEGA: A versatile program to convert, handle and virtualize molecular structure on Windows-based PCs
    • Pedretti, A.; Villa, A.; Vistoli. G. VEGA: A versatile program to convert, handle and virtualize molecular structure on Windows-based PCs. J. Mol. Graph. 2002, 21, 47-49.
    • (2002) J. Mol. Graph , vol.21 , pp. 47-49
    • Pedretti, A.1    Villa, A.2    Vistoli, G.3
  • 27
    • 57949115339 scopus 로고    scopus 로고
    • Synthesis and QSAR modeling of 2-acetyl-2-ethoxycarbonyl-1-[4 (4'-arylazo)-phenyl]-N, N-dimethylaminophenyl aziridines as potential antibacterial agents
    • Sharma, P.; Kumar, A.; Upadhyay, S.; Sahu, V.; Singh, J. Synthesis and QSAR modeling of 2-acetyl-2-ethoxycarbonyl-1-[4 (4'-arylazo)-phenyl]-N, N-dimethylaminophenyl aziridines as potential antibacterial agents. Eur. J. Med. Chem. 2009, 44, 251-259.
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 251-259
    • Sharma, P.1    Kumar, A.2    Upadhyay, S.3    Sahu, V.4    Singh, J.5
  • 28
    • 77954252229 scopus 로고    scopus 로고
    • Chem3D Ultra 10.0, ChemOffice Ultra, 100 Cambridge Park Drive Cambridge, MA 02140, USA, 2006
    • Chem3D Ultra 10.0, ChemOffice Ultra, 2006; Cambridge Scientific Software: CambridgeSoft Corporate Headquarters, 100 Cambridge Park Drive Cambridge, MA 02140, USA, 2006.
    • (2006) Cambridge Scientific Software: CambridgeSoft Corporate Headquarters
  • 29
    • 36749043324 scopus 로고    scopus 로고
    • Design and QSAR study of analogs of a-tocopherol with enhanced antiproliferative activity against human breast adenocarcinoma cells
    • Nikolic, K. M.; Design and QSAR study of analogs of a-tocopherol with enhanced antiproliferative activity against human breast adenocarcinoma cells. J. Mol. Graph. Model. 2008, 26, 868-873.
    • (2008) J. Mol. Graph. Model , vol.26 , pp. 868-873
    • Nikolic, K.M.1
  • 30
    • 77954267817 scopus 로고    scopus 로고
    • Origin Pro 8. Origin Lab Corporation: Northampton, MA, USA
    • Origin Pro 8. Origin Lab Corporation: Northampton, MA, USA, 2009.
    • (2009)
  • 31
    • 0037062576 scopus 로고    scopus 로고
    • DNA gyrase interaction with coumarin-based inhibitors: The role of the hydroxybenzoate isopentenyl moiety and the 5'-methyl group of the noviose
    • Lafitte, D.; Lamour, V.; Tsvetkov, P. O.; Makarov, A. A.; Klich, M.; Deprez, P.; Moras, D.; Briand, C.; Gilli, R. DNA gyrase interaction with coumarin-based inhibitors: the role of the hydroxybenzoate isopentenyl moiety and the 5'-methyl group of the noviose. Biochemistry 2002, 41, 7217-7223.
    • (2002) Biochemistry , vol.41 , pp. 7217-7223
    • Lafitte, D.1    Lamour, V.2    Tsvetkov, P.O.3    Makarov, A.A.4    Klich, M.5    Deprez, P.6    Moras, D.7    Briand, C.8    Gilli, R.9
  • 33
    • 0030203710 scopus 로고    scopus 로고
    • Distributed automated docking of flexible ligands to proteins: Parallel applications of AutoDock 2.4
    • Morris, M. G.; Goodsell, S. D.; Huey, R.; Olson, J. A. Distributed automated docking of flexible ligands to proteins: Parallel applications of AutoDock 2.4. J. Comp. Aid. Mol. Des. 1996, 10, 293-304.
    • (1996) J. Comp. Aid. Mol. Des. , vol.10 , pp. 293-304
    • Morris, M.G.1    Goodsell, S.D.2    Huey, R.3    Olson, J.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.