Taxifolin

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Akiyo Sakushima - One of the best experts on this subject based on the ideXlab platform.

  • structural studies of zoospore attractants from trachelospermum jasminoides var pubescens Taxifolin 3 o glycosides
    Phytochemical Analysis, 2006
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

  • Structural Studies of Zoospore Attractants from Trachelospermum jasminoides var. pubescens: Taxifolin 3‐O‐glycosides
    Phytochemical analysis : PCA, 2005
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

Shinzo Hosoi - One of the best experts on this subject based on the ideXlab platform.

  • structural studies of zoospore attractants from trachelospermum jasminoides var pubescens Taxifolin 3 o glycosides
    Phytochemical Analysis, 2006
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

  • Structural Studies of Zoospore Attractants from Trachelospermum jasminoides var. pubescens: Taxifolin 3‐O‐glycosides
    Phytochemical analysis : PCA, 2005
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

Shiro Kuninaga - One of the best experts on this subject based on the ideXlab platform.

  • structural studies of zoospore attractants from trachelospermum jasminoides var pubescens Taxifolin 3 o glycosides
    Phytochemical Analysis, 2006
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

  • Structural Studies of Zoospore Attractants from Trachelospermum jasminoides var. pubescens: Taxifolin 3‐O‐glycosides
    Phytochemical analysis : PCA, 2005
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

Eri Shimizu - One of the best experts on this subject based on the ideXlab platform.

  • structural studies of zoospore attractants from trachelospermum jasminoides var pubescens Taxifolin 3 o glycosides
    Phytochemical Analysis, 2006
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

  • Structural Studies of Zoospore Attractants from Trachelospermum jasminoides var. pubescens: Taxifolin 3‐O‐glycosides
    Phytochemical analysis : PCA, 2005
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

Kosei Ohno - One of the best experts on this subject based on the ideXlab platform.

  • structural studies of zoospore attractants from trachelospermum jasminoides var pubescens Taxifolin 3 o glycosides
    Phytochemical Analysis, 2006
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.

  • Structural Studies of Zoospore Attractants from Trachelospermum jasminoides var. pubescens: Taxifolin 3‐O‐glycosides
    Phytochemical analysis : PCA, 2005
    Co-Authors: Shinzo Hosoi, Eri Shimizu, Kosei Ohno, Ryozo Yokosawa, Shiro Kuninaga, Maksut Coskun, Akiyo Sakushima
    Abstract:

    (2S, 3S)-Taxifolin 3-O-arabinoside, a new dihydroflavonol glycoside, together with the known substances, (2R 3R)-Taxifolin 3-O-arabinoside, astragalin, isoquercitrin, and cosmosiin, were isolated from the leaves of Trachelospermum jasminoides var. pubescens. Structural elucidation was carried out by spectroscopic methods, and the absolute configurations of C-2 and C-3 in Taxifolin 3-O-arabinosides were determined on the basis of circular dichroism. Unlike the dihydroflavonol glycosides, (2R 3R)-Taxifolin 3-O-glucoside and (2R, 3R-Taxifolin 3-O-arabinoside, the novel (2S, 3S)-Taxifolin 3-O-arabinoside is not effective as a zoospore attractant of the plant pathogenic fungus Aphanomyces cochlioides.