Elsevier

Phytochemistry

Volume 22, Issue 5, 1983, Pages 1253-1256
Phytochemistry

Flavonoids from Dodonaea viscosa

https://doi.org/10.1016/0031-9422(83)80234-9Get rights and content

Abstract

An investigation of Dodonaea viscosa afforded a new flavonoid having an isoprenoid side chain along with the seven known flavonoids: 5-hydroxy-3,6,

References (16)

  • M. Goudard et al.

    Phytochemistry

    (1978)
  • L. Southwick et al.

    Phytochemistry

    (1972)
  • E. Wollenweber et al.

    Biochimie

    (1971)
  • S.E. Flores et al.

    Tetrahedron

    (1958)
  • H. Rosler et al.

    Phytochemistry

    (1971)
  • T.G. Payne et al.

    Tetrahedron

    (1973)
  • K. Sachdev et al.

    Indian J. Chem.

    (1982)
  • A. Mears et al.

    Phytochemistry

    (1972)
There are more references available in the full text version of this article.

Cited by (63)

  • Biological and phytochemicals review of Omani medicinal plant Dodonaea viscosa

    2019, Journal of King Saud University - Science
    Citation Excerpt :

    The previously reported phytochemical studies showed that the plant contains different nitrogenous cyclic compounds, various types of flavonoids, volatile oils, immune modulator ingredients, saponins, primary and secondary cyclic and acyclic phenols, tannins, gum, cardiac glycosides, carbohydrate and sugar (Venkatesh et al., 2008; Shafek et al., 2015; Ramya et al., 2011; Jeya et al., 2014; Jawahar et al., 2004; Kumar et al., 2013a). Various groups of chemical compounds were isolated from the selected plant parts which were reported earlier by the researchers (Sachdev and Kulshreshtha, 1983, 1984, 1982; Mata et al., 1991; Wabo et al., 2012; Lai-Bin et al., 2012; Akhtar et al., 2012a, 2012b; Abdel-Mogib et al., 2010; Khan et al., 1988; Dominguez et al., 1980; Dreyer, 1978; Zeza et al., 1985). Not all groups of compounds were isolated from one part of this plant.

  • Antimicrobial flavonoids and diterpenoids from Dodonaea angustifolia

    2014, South African Journal of Botany
    Citation Excerpt :

    The MICs of the test microorganisms was similarly determined by the agar well-diffusion method and is defined as the lowest concentrations of the compounds that visually showed no growth compared with growth in control wells. Chromatographic separation of surface exudates of the leaves of D. angustifolia led to isolation of flavonoids: 5-hydroxy-3,4′,7-trimethoxyflavone (1) (Dreyer, 1978), 3,5-dihydroxy-4′,7-dimethoxyflavone (2) (Dreyer, 1978), 5,7-dihydro-3,4′,6-trimethoxyflavone (3, santin) (Abdel-Mogib et al., 2001), 4′,5-dihydroxy-3,7-dimethoxyflavone (4, kumatakenin) (Sarmento da Silva, 2002), 3,4′,5-trihydroxy-7-methoxyflavone (5, rhamnocitrin) (Valant-Vetschera et al., 2003), 4′,5,7-trihydroxy-3-methoxyflavone (6, isokaempferide) (Dreyer, 1978), 3,4′,5,7-tetrahydroxy-6-methoxyflavone (7) (Valant-Vetschera et al., 2003), 5,7-dihydroxyflavanone (8, pinocembrin) (Sachdev and Kulshreshtha, 1983) and diterpenoids: dodonic acid (9) (Sachdev and Kulshreshtha, 1984), 2β-hydroxyhardwickiic acid (10) (Jefferies et al., 1973; Anis et al., 2001) and (ent-3β,8α)-15,16-epoxy-13(16),14-labdadiene-3,8-diol (11) (Dawson et al., 1966) (Fig. 1). Five of the compounds, two flavonoids (6, 7) and three diterpenoids (9, 10 and 11) are reported for the first time from this species.

  • Labdane-type diterpenes and flavones from Dodonaea viscosa

    2012, Fitoterapia
    Citation Excerpt :

    However, the active anti-inflammatory constituents were not identified. Phytochemical investigations of this plant have resulted in the isolation and identification of various flavonoids [10–13], clerodane derivatives [11,12,14] and saponins [15]. In our ongoing search for potential anti-inflammatory compounds from the medicinal plants in the tropics, we investigated the aerial parts of D. viscosa.

View all citing articles on Scopus

CDRI communication No. 3175.

View full text