Two new 5-deoxyflavan-3,4-diol glucosides from roots of Albizia chevalieri

Abdou Tchoukoua; Turibio Kuiate Tabopda; Shota Uesugi; Ken ichi Kimura; Eunsang Kwon; Hiroyuki Momma; Bonaventure Tchaleu Ngadjui; Takuya Koseki; Yoshihito Shiono

doi:10.1002/mrc.4504

Two new 5-deoxyflavan-3,4-diol glucosides from roots of Albizia chevalieri

Abdou Tchoukoua, Turibio Kuiate Tabopda, Shota Uesugi, Ken ichi Kimura, Eunsang Kwon, Hiroyuki Momma, Bonaventure Tchaleu Ngadjui, Takuya Koseki, Yoshihito Shiono

理学研究科・附属巨大分子解析研究センター

研究成果: Article › 査読

4 被引用数 (Scopus)

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Phytochemical investigation of the roots of Albizia chevalieri led to the isolation of two new 5-deoxyflavan-3,4-diol glucosides from roots of A. chevalieri, Chevalieriflavanosides A and B. Their structures were established by 2D NMR techniques, UV, IR, CD, and mass spectrometry. Cytotoxicity of the two compounds was evaluated against acute promyelocytic leukemia HL60 cells. The antibacterial activities of 1 and 2 also were evaluated against Pseudomonas aeruginosa and Staphylococcus aureus using the agar diffusion test.

本文言語	English
ページ（範囲）	893-896
ページ数	4
ジャーナル	Magnetic Resonance in Chemistry
巻	54
号	11
DOI	https://doi.org/10.1002/mrc.4504
出版ステータス	Published - 2016 11月 1

ASJC Scopus subject areas

化学 (全般)
材料科学（全般）

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10.1002/mrc.4504

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title = "Two new 5-deoxyflavan-3,4-diol glucosides from roots of Albizia chevalieri",

abstract = "Phytochemical investigation of the roots of Albizia chevalieri led to the isolation of two new 5-deoxyflavan-3,4-diol glucosides from roots of A. chevalieri, Chevalieriflavanosides A and B. Their structures were established by 2D NMR techniques, UV, IR, CD, and mass spectrometry. Cytotoxicity of the two compounds was evaluated against acute promyelocytic leukemia HL60 cells. The antibacterial activities of 1 and 2 also were evaluated against Pseudomonas aeruginosa and Staphylococcus aureus using the agar diffusion test.",

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AU - Tchoukoua, Abdou

AU - Kuiate Tabopda, Turibio

AU - Uesugi, Shota

AU - Kimura, Ken ichi

AU - Kwon, Eunsang

AU - Momma, Hiroyuki

AU - Ngadjui, Bonaventure Tchaleu

AU - Koseki, Takuya

AU - Shiono, Yoshihito

PY - 2016/11/1

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N2 - Phytochemical investigation of the roots of Albizia chevalieri led to the isolation of two new 5-deoxyflavan-3,4-diol glucosides from roots of A. chevalieri, Chevalieriflavanosides A and B. Their structures were established by 2D NMR techniques, UV, IR, CD, and mass spectrometry. Cytotoxicity of the two compounds was evaluated against acute promyelocytic leukemia HL60 cells. The antibacterial activities of 1 and 2 also were evaluated against Pseudomonas aeruginosa and Staphylococcus aureus using the agar diffusion test.

AB - Phytochemical investigation of the roots of Albizia chevalieri led to the isolation of two new 5-deoxyflavan-3,4-diol glucosides from roots of A. chevalieri, Chevalieriflavanosides A and B. Their structures were established by 2D NMR techniques, UV, IR, CD, and mass spectrometry. Cytotoxicity of the two compounds was evaluated against acute promyelocytic leukemia HL60 cells. The antibacterial activities of 1 and 2 also were evaluated against Pseudomonas aeruginosa and Staphylococcus aureus using the agar diffusion test.

KW - Albizia chevalieri

KW - C

KW - H

KW - Leguminosae

KW - NMR

KW - cytotoxicity

KW - flavan-3,4-diols

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Two new 5-deoxyflavan-3,4-diol glucosides from roots of Albizia chevalieri

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