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Armando Zarrelli - One of the best experts on this subject based on the ideXlab platform.

  • Bioactivity of phenanthrenes from Juncus acutus on Selenastrum capricornutum.
    Journal of Chemical Ecology, 2004
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Twenty-five 9,10-Dihydrophenanthrenes, four phenanthrenes, a dihydrodibenzoxepin, and a pyrene, isolated from the wetland plant Juncus acutus, were tested to detect their effects on the green alga Selenastrum capricornutum. Nine of the compounds were isolated and identified for the first time. Most of the compounds caused inhibition of algal growth. The 9,10-Dihydrophenanthrenes 1, 5, 21, and 22 were the most active.

  • phenanthrenoids from the wetland juncus acutus
    Phytochemistry, 2002
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Antonio Fiorentino, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Abstract Nine 9,10-Dihydrophenanthrenes, three phenanthrenes and a related pyrene have been isolated from the wetland plant Juncus acutus. The structures have been attributed by means of their spectral data and chemical correlation. 5-(1-Ethoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene and 5-(1-phytoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene, 2,7-dihydroxy-1-methyl-5-vinylphenanthrene, 2,7-dimethoxy-1,6-dimethyl-5-vinylphenanthrene and 2,7-dihydroxy-1,6-dimethylpyrene are described for the first time. Many of the compounds showed in vitro phytotoxicity against Selenastrum capricornutum, a microalga used in aquatic tests.

  • phenanthrenoids from the wetland juncus acutus
    Phytochemistry, 2002
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Nine 9,10-Dihydrophenanthrenes, three phenanthrenes and a related pyrene have been isolated from the wetland plant Juncus acutus. The structures have been attributed by means of their spectral data and chemical correlation. 5-(1-Ethoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene and 5-(1-phytoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene, 2,7-dihydroxy-1-methyl-5-vinylphenanthrene, 2,7-dimethoxy-1,6-dimethyl-5-vinylphenanthrene and 2,7-dihydroxy-1,6-dimethylpyrene are described for the first time. Many of the compounds showed in vitro phytotoxicity against Selenastrum capricornutum, a microalga used in aquatic tests.

  • effusides i v 9 10 Dihydrophenanthrene glucosides from juncus effusus
    Phytochemistry, 1995
    Co-Authors: Marina Della Greca, Pietro Monaco, Lucio Previtera, Antonio Fiorentino, Armando Zarrelli
    Abstract:

    Five 9,10-Dihydrophenanthrene glucosides, named effusides I-V, have been isolated from the methanolic extract of Juncus effusus. Structures have been determined on spectroscopic grounds.

Lucio Previtera - One of the best experts on this subject based on the ideXlab platform.

  • Bioactivity of phenanthrenes from Juncus acutus on Selenastrum capricornutum.
    Journal of Chemical Ecology, 2004
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Twenty-five 9,10-Dihydrophenanthrenes, four phenanthrenes, a dihydrodibenzoxepin, and a pyrene, isolated from the wetland plant Juncus acutus, were tested to detect their effects on the green alga Selenastrum capricornutum. Nine of the compounds were isolated and identified for the first time. Most of the compounds caused inhibition of algal growth. The 9,10-Dihydrophenanthrenes 1, 5, 21, and 22 were the most active.

  • phenanthrenoids from the wetland juncus acutus
    Phytochemistry, 2002
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Antonio Fiorentino, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Abstract Nine 9,10-Dihydrophenanthrenes, three phenanthrenes and a related pyrene have been isolated from the wetland plant Juncus acutus. The structures have been attributed by means of their spectral data and chemical correlation. 5-(1-Ethoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene and 5-(1-phytoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene, 2,7-dihydroxy-1-methyl-5-vinylphenanthrene, 2,7-dimethoxy-1,6-dimethyl-5-vinylphenanthrene and 2,7-dihydroxy-1,6-dimethylpyrene are described for the first time. Many of the compounds showed in vitro phytotoxicity against Selenastrum capricornutum, a microalga used in aquatic tests.

  • phenanthrenoids from the wetland juncus acutus
    Phytochemistry, 2002
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Nine 9,10-Dihydrophenanthrenes, three phenanthrenes and a related pyrene have been isolated from the wetland plant Juncus acutus. The structures have been attributed by means of their spectral data and chemical correlation. 5-(1-Ethoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene and 5-(1-phytoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene, 2,7-dihydroxy-1-methyl-5-vinylphenanthrene, 2,7-dimethoxy-1,6-dimethyl-5-vinylphenanthrene and 2,7-dihydroxy-1,6-dimethylpyrene are described for the first time. Many of the compounds showed in vitro phytotoxicity against Selenastrum capricornutum, a microalga used in aquatic tests.

  • effusides i v 9 10 Dihydrophenanthrene glucosides from juncus effusus
    Phytochemistry, 1995
    Co-Authors: Marina Della Greca, Pietro Monaco, Lucio Previtera, Antonio Fiorentino, Armando Zarrelli
    Abstract:

    Five 9,10-Dihydrophenanthrene glucosides, named effusides I-V, have been isolated from the methanolic extract of Juncus effusus. Structures have been determined on spectroscopic grounds.

  • 9,10-Dihydrophenanthrene Glucosides from Juncus effusus
    Natural Product Letters, 1995
    Co-Authors: Marina Della Greca, Pietro Monaco, Antonio Molinaro, Antonio Fiorentino, Lucio Previtera
    Abstract:

    Abstract Four 9,10-Dihydrophenanthrene glucosides have been isolated from Juncus effusus and their structures confirmed on spectroscopic grounds and by semisynthesis. The results of a cytotoxic assay are also reported.

Pietro Monaco - One of the best experts on this subject based on the ideXlab platform.

  • Bioactivity of phenanthrenes from Juncus acutus on Selenastrum capricornutum.
    Journal of Chemical Ecology, 2004
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Twenty-five 9,10-Dihydrophenanthrenes, four phenanthrenes, a dihydrodibenzoxepin, and a pyrene, isolated from the wetland plant Juncus acutus, were tested to detect their effects on the green alga Selenastrum capricornutum. Nine of the compounds were isolated and identified for the first time. Most of the compounds caused inhibition of algal growth. The 9,10-Dihydrophenanthrenes 1, 5, 21, and 22 were the most active.

  • phenanthrenoids from the wetland juncus acutus
    Phytochemistry, 2002
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Antonio Fiorentino, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Abstract Nine 9,10-Dihydrophenanthrenes, three phenanthrenes and a related pyrene have been isolated from the wetland plant Juncus acutus. The structures have been attributed by means of their spectral data and chemical correlation. 5-(1-Ethoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene and 5-(1-phytoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene, 2,7-dihydroxy-1-methyl-5-vinylphenanthrene, 2,7-dimethoxy-1,6-dimethyl-5-vinylphenanthrene and 2,7-dihydroxy-1,6-dimethylpyrene are described for the first time. Many of the compounds showed in vitro phytotoxicity against Selenastrum capricornutum, a microalga used in aquatic tests.

  • phenanthrenoids from the wetland juncus acutus
    Phytochemistry, 2002
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Nine 9,10-Dihydrophenanthrenes, three phenanthrenes and a related pyrene have been isolated from the wetland plant Juncus acutus. The structures have been attributed by means of their spectral data and chemical correlation. 5-(1-Ethoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene and 5-(1-phytoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene, 2,7-dihydroxy-1-methyl-5-vinylphenanthrene, 2,7-dimethoxy-1,6-dimethyl-5-vinylphenanthrene and 2,7-dihydroxy-1,6-dimethylpyrene are described for the first time. Many of the compounds showed in vitro phytotoxicity against Selenastrum capricornutum, a microalga used in aquatic tests.

  • effusides i v 9 10 Dihydrophenanthrene glucosides from juncus effusus
    Phytochemistry, 1995
    Co-Authors: Marina Della Greca, Pietro Monaco, Lucio Previtera, Antonio Fiorentino, Armando Zarrelli
    Abstract:

    Five 9,10-Dihydrophenanthrene glucosides, named effusides I-V, have been isolated from the methanolic extract of Juncus effusus. Structures have been determined on spectroscopic grounds.

  • 9,10-Dihydrophenanthrene Glucosides from Juncus effusus
    Natural Product Letters, 1995
    Co-Authors: Marina Della Greca, Pietro Monaco, Antonio Molinaro, Antonio Fiorentino, Lucio Previtera
    Abstract:

    Abstract Four 9,10-Dihydrophenanthrene glucosides have been isolated from Juncus effusus and their structures confirmed on spectroscopic grounds and by semisynthesis. The results of a cytotoxic assay are also reported.

Marina Dellagreca - One of the best experts on this subject based on the ideXlab platform.

  • Bioactivity of phenanthrenes from Juncus acutus on Selenastrum capricornutum.
    Journal of Chemical Ecology, 2004
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Twenty-five 9,10-Dihydrophenanthrenes, four phenanthrenes, a dihydrodibenzoxepin, and a pyrene, isolated from the wetland plant Juncus acutus, were tested to detect their effects on the green alga Selenastrum capricornutum. Nine of the compounds were isolated and identified for the first time. Most of the compounds caused inhibition of algal growth. The 9,10-Dihydrophenanthrenes 1, 5, 21, and 22 were the most active.

  • phenanthrenoids from the wetland juncus acutus
    Phytochemistry, 2002
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Antonio Fiorentino, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Abstract Nine 9,10-Dihydrophenanthrenes, three phenanthrenes and a related pyrene have been isolated from the wetland plant Juncus acutus. The structures have been attributed by means of their spectral data and chemical correlation. 5-(1-Ethoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene and 5-(1-phytoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene, 2,7-dihydroxy-1-methyl-5-vinylphenanthrene, 2,7-dimethoxy-1,6-dimethyl-5-vinylphenanthrene and 2,7-dihydroxy-1,6-dimethylpyrene are described for the first time. Many of the compounds showed in vitro phytotoxicity against Selenastrum capricornutum, a microalga used in aquatic tests.

  • phenanthrenoids from the wetland juncus acutus
    Phytochemistry, 2002
    Co-Authors: Marina Dellagreca, Pietro Monaco, Lucio Previtera, Marina Isidori, Margherita Lavorgna, Armando Zarrelli
    Abstract:

    Nine 9,10-Dihydrophenanthrenes, three phenanthrenes and a related pyrene have been isolated from the wetland plant Juncus acutus. The structures have been attributed by means of their spectral data and chemical correlation. 5-(1-Ethoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene and 5-(1-phytoxy-ethyl)-2-hydroxy-7-methoxy-1,8-dimethyl-9,10-Dihydrophenanthrene, 2,7-dihydroxy-1-methyl-5-vinylphenanthrene, 2,7-dimethoxy-1,6-dimethyl-5-vinylphenanthrene and 2,7-dihydroxy-1,6-dimethylpyrene are described for the first time. Many of the compounds showed in vitro phytotoxicity against Selenastrum capricornutum, a microalga used in aquatic tests.

Takakazu Yamamoto - One of the best experts on this subject based on the ideXlab platform.