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Volumn 62, Issue 7-8, 2007, Pages 477-482

Preliminary evaluation of antimicrobial activity of diastereomeric cis/trans-3-aryl(heteroaryl)-3,4-dihydroisocoumarin-4-carboxylic acids

Author keywords

Antibacterial; Antifungal; Homophthalic anhydride; Isocoumarin

Indexed keywords

BACTERIA (MICROORGANISMS); STAPHYLOCOCCUS AUREUS;

EID: 34548655263     PISSN: 09395075     EISSN: None     Source Type: Journal    
DOI: 10.1515/znc-2007-7-804     Document Type: Article
Times cited : (11)

References (22)
  • 1
    • 1342324005 scopus 로고    scopus 로고
    • cis/trans- Isochromanones. DMAP induced cycloaddition of homophthalic anhydride and aldehydes
    • Bogdanov M. G. and Palamareva M. D. (2004), cis/trans- Isochromanones. DMAP induced cycloaddition of homophthalic anhydride and aldehydes. Tetrahedron 60, 2525-2530.
    • (2004) Tetrahedron , vol.60 , pp. 2525-2530
    • Bogdanov, M.G.1    Palamareva, M.D.2
  • 2
    • 5144226969 scopus 로고    scopus 로고
    • Configuration and conformational equilibrium of (+/-)-trans-1-oxo-3-thiophen-2-yl-isochroman-4-carboxylic acid methyl ester
    • Bogdanov M. G., Todorov I. S., Manolova P. G., Cheshmedzhieva D. V., and Palamareva M. D. (2004), Configuration and conformational equilibrium of (+/-)-trans-1-oxo-3-thiophen-2-yl-isochroman-4-carboxylic acid methyl ester. Tetrahedron Lett. 45, 8383-8386.
    • (2004) Tetrahedron Lett , vol.45 , pp. 8383-8386
    • Bogdanov, M.G.1    Todorov, I.S.2    Manolova, P.G.3    Cheshmedzhieva, D.V.4    Palamareva, M.D.5
  • 3
    • 34250204448 scopus 로고    scopus 로고
    • Bogdanov M. G., Gocheva B. T., Dimitrova D. B., and Palamareva M. D. (2007), New isochromans. 1. Synthesis and antimicrobial activity of 4-substituted (±)-1H-spiro[benzo(c)pyran-3(4H),1′- cyclohexane]-1-ones. J. Het. Chem. 44, 673-677.
    • Bogdanov M. G., Gocheva B. T., Dimitrova D. B., and Palamareva M. D. (2007), New isochromans. 1. Synthesis and antimicrobial activity of 4-substituted (±)-1H-spiro[benzo(c)pyran-3(4H),1′- cyclohexane]-1-ones. J. Het. Chem. 44, 673-677.
  • 4
    • 33745960002 scopus 로고    scopus 로고
    • Reaction between glutaric anhydride and N-benzylidenebenzylamine, and further transformations to new substituted piperidin-2-ones
    • Burdzhiev N. T. and Stanoeva E. R. (2006), Reaction between glutaric anhydride and N-benzylidenebenzylamine, and further transformations to new substituted piperidin-2-ones. Tetrahedron 62, 8318-8326.
    • (2006) Tetrahedron , vol.62 , pp. 8318-8326
    • Burdzhiev, N.T.1    Stanoeva, E.R.2
  • 5
    • 34548624181 scopus 로고    scopus 로고
    • In vitro cytotoxicity of some natural and semi-synthetic isocoumarins from Paepalanthus bromelioides
    • Devienne K. F., Raddi M. S. G., Varanda E. A., and Vilegas W. (2002), In vitro cytotoxicity of some natural and semi-synthetic isocoumarins from Paepalanthus bromelioides. Z. Naturforsch. 52c, 240-244.
    • (2002) Z. Naturforsch , vol.52 c , pp. 240-244
    • Devienne, K.F.1    Raddi, M.S.G.2    Varanda, E.A.3    Vilegas, W.4
  • 6
    • 18144416167 scopus 로고    scopus 로고
    • Structure-antimicrobial activity of some natural isocoumarins and their analogues
    • Devienne K. F., Raddi M. S. G., Coelho R. G., and Vilegas W. (2005), Structure-antimicrobial activity of some natural isocoumarins and their analogues. Phytomedicine 12, 378-381.
    • (2005) Phytomedicine , vol.12 , pp. 378-381
    • Devienne, K.F.1    Raddi, M.S.G.2    Coelho, R.G.3    Vilegas, W.4
  • 7
    • 1342313257 scopus 로고
    • Knoevenagel condensation in the homophthalic acid series. A synthesis of zearalenone
    • Girotra N. N. and Wendler N. L. (1976), Knoevenagel condensation in the homophthalic acid series. A synthesis of zearalenone. J. Org. Chem. 34, 3192-3194.
    • (1976) J. Org. Chem , vol.34 , pp. 3192-3194
    • Girotra, N.N.1    Wendler, N.L.2
  • 8
    • 0022980472 scopus 로고
    • Naturally occurring isocoumarins
    • Hill R. A. (1986), Naturally occurring isocoumarins. Fortschr. Chem. Org. Naturst. 49, 1-78.
    • (1986) Fortschr. Chem. Org. Naturst , vol.49 , pp. 1-78
    • Hill, R.A.1
  • 9
    • 0037716831 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activities of some isocoumarin and dihydroisocoumarin derivatives
    • Hussain M., Hussain M. T., Rama N. H., Hameed S., Malik A., and Khan K. M. (2003), Synthesis and antimicrobial activities of some isocoumarin and dihydroisocoumarin derivatives. Nat. Prod. Res. 17, 207-214.
    • (2003) Nat. Prod. Res , vol.17 , pp. 207-214
    • Hussain, M.1    Hussain, M.T.2    Rama, N.H.3    Hameed, S.4    Malik, A.5    Khan, K.M.6
  • 11
    • 34548630732 scopus 로고    scopus 로고
    • Applications of spin-spin couplings
    • Kamienska-Trela K. and Wojcik J. (2006), Applications of spin-spin couplings. Nucl. Magn. Res. 35, 152-198.
    • (2006) Nucl. Magn. Res , vol.35 , pp. 152-198
    • Kamienska-Trela, K.1    Wojcik, J.2
  • 12
    • 33745516557 scopus 로고    scopus 로고
    • Synthesis of new trans-2-benzyl-3-(furan-2-yl)-4-substituted-1,2,3,4- tetrahydroisoquinolinones
    • Kandinska M. I., Kozekov I. D., and Palamareva M. D. (2006), Synthesis of new trans-2-benzyl-3-(furan-2-yl)-4-substituted-1,2,3,4- tetrahydroisoquinolinones. Molecules 11, 403-414.
    • (2006) Molecules , vol.11 , pp. 403-414
    • Kandinska, M.I.1    Kozekov, I.D.2    Palamareva, M.D.3
  • 13
    • 33748815663 scopus 로고    scopus 로고
    • Total synthesis of the toxin oosponol and of structural analogues and investigation of their antibiotic activities
    • Kovacs T., Sonnenbichler I., and Sonnenbichler J. (1997), Total synthesis of the toxin oosponol and of structural analogues and investigation of their antibiotic activities. Justus Liebigs Ann. Chem. 4, 773-777.
    • (1997) Justus Liebigs Ann. Chem , vol.4 , pp. 773-777
    • Kovacs, T.1    Sonnenbichler, I.2    Sonnenbichler, J.3
  • 14
    • 0032477689 scopus 로고    scopus 로고
    • Immunomodulatory activity of thunberginol A and related compounds isolated from Hydrangeae Dulcis Folium on splenocyte proliferation activated by mitogens
    • Matsuda H., Shimoda H., Yamahara J., and Yoshikawa M. (1998), Immunomodulatory activity of thunberginol A and related compounds isolated from Hydrangeae Dulcis Folium on splenocyte proliferation activated by mitogens. Biorg. Med. Chem. Lett. 8, 215-220.
    • (1998) Biorg. Med. Chem. Lett , vol.8 , pp. 215-220
    • Matsuda, H.1    Shimoda, H.2    Yamahara, J.3    Yoshikawa, M.4
  • 15
    • 0033041711 scopus 로고    scopus 로고
    • Structure-requirements of isocoumarins, phthalides, and stilbenes from Hydrangeae Dulcis Folium for inhibitory activity on histamine release from rat peritoneal mast cells
    • Matsuda H., Shimoda H., and Yoshikawa M. (1999), Structure-requirements of isocoumarins, phthalides, and stilbenes from Hydrangeae Dulcis Folium for inhibitory activity on histamine release from rat peritoneal mast cells. Bioorg. Med. Chem. Lett. 7, 1445-1450.
    • (1999) Bioorg. Med. Chem. Lett , vol.7 , pp. 1445-1450
    • Matsuda, H.1    Shimoda, H.2    Yoshikawa, M.3
  • 16
    • 0347419646 scopus 로고    scopus 로고
    • The synthesis of isocoumarins over the last decade. A review
    • Napolitano E. (1997), The synthesis of isocoumarins over the last decade. A review. Org. Prep. Proced. Int. 29, 631-664.
    • (1997) Org. Prep. Proced. Int , vol.29 , pp. 631-664
    • Napolitano, E.1
  • 17
    • 0019849474 scopus 로고
    • Antifungal activity of oosponol, oospolactone, phyllodulcin, hydrangenol, and some other related compounds
    • Nozawa K., Yamada M., Tsuda Y., Kawai K., and Nakajima S. (1981a), Antifungal activity of oosponol, oospolactone, phyllodulcin, hydrangenol, and some other related compounds. Chem. Pharm. Bull. 29, 2689-2691.
    • (1981) Chem. Pharm. Bull , vol.29 , pp. 2689-2691
    • Nozawa, K.1    Yamada, M.2    Tsuda, Y.3    Kawai, K.4    Nakajima, S.5
  • 18
    • 0019815008 scopus 로고
    • Syntheses of antifungal isocoumarins. III. Synthesis and antifungal activity of 3-aryl-3,4-dihydro-4-substituted isocoumarins
    • Nozawa K., Yamada M., Tsuda Y., Kawai K., and Nakajima S. (1981b), Syntheses of antifungal isocoumarins. III. Synthesis and antifungal activity of 3-aryl-3,4-dihydro-4-substituted isocoumarins. Chem. Pharm. Bull. 29, 3486-3493.
    • (1981) Chem. Pharm. Bull , vol.29 , pp. 3486-3493
    • Nozawa, K.1    Yamada, M.2    Tsuda, Y.3    Kawai, K.4    Nakajima, S.5
  • 19
    • 0344514158 scopus 로고    scopus 로고
    • Asymmetric total synthesis and stereochemical elucidation of the antitumor agent PM-94128
    • Patel S. K., Murat K., Py S., and Vallee Y. (2003), Asymmetric total synthesis and stereochemical elucidation of the antitumor agent PM-94128. Org. Lett. 5, 4081-4084.
    • (2003) Org. Lett , vol.5 , pp. 4081-4084
    • Patel, S.K.1    Murat, K.2    Py, S.3    Vallee, Y.4
  • 20
    • 0021982007 scopus 로고
    • 1H-2-Benzopyran derivatives, microbial products with pharmacological activity. Conversion into orally active derivatives with antiinflammatory and antiulcer activities
    • Shimojima Y., Shirai T., Baba T., and Hayashi H. (1985), 1H-2-Benzopyran derivatives, microbial products with pharmacological activity. Conversion into orally active derivatives with antiinflammatory and antiulcer activities. J. Med. Chem. 28, 3-9.
    • (1985) J. Med. Chem , vol.28 , pp. 3-9
    • Shimojima, Y.1    Shirai, T.2    Baba, T.3    Hayashi, H.4
  • 21
    • 0029756586 scopus 로고    scopus 로고
    • Cercophorins A-C: Novel Antifungal and cytotoxic metabolites from the coprophilous fungus Cercophora areolata
    • Whyte A. C., Gloer J. B., Scott J. A., and Malloch D. (1996), Cercophorins A-C: Novel Antifungal and cytotoxic metabolites from the coprophilous fungus Cercophora areolata. J. Nat. Prod. 59, 765-769.
    • (1996) J. Nat. Prod , vol.59 , pp. 765-769
    • Whyte, A.C.1    Gloer, J.B.2    Scott, J.A.3    Malloch, D.4
  • 22
    • 0029766946 scopus 로고    scopus 로고
    • Development of bioactive functions in Hydrangeae Dulcis Folium. V. On the antiallergic and antimicrobial principles of Hydrangeae Dulcis Folium. (2). Thunberginols C, D, and E, thunberginol G 3′-O-glucoside, (-)-hydrangenol 4′-O-glucoside, and (+)-hydrangenol 4′-O-glucoside
    • Yoshikawa M., Matsuda H., Shimoda H., Shimada H., Harada E., Naitoh Y., Miki A., Yamahara J., and Murakami N. (1996), Development of bioactive functions in Hydrangeae Dulcis Folium. V. On the antiallergic and antimicrobial principles of Hydrangeae Dulcis Folium. (2). Thunberginols C, D, and E, thunberginol G 3′-O-glucoside, (-)-hydrangenol 4′-O-glucoside, and (+)-hydrangenol 4′-O-glucoside. Chem. Pharm. Bull. 44, 1440-1447.
    • (1996) Chem. Pharm. Bull , vol.44 , pp. 1440-1447
    • Yoshikawa, M.1    Matsuda, H.2    Shimoda, H.3    Shimada, H.4    Harada, E.5    Naitoh, Y.6    Miki, A.7    Yamahara, J.8    Murakami, N.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.