torsdag 22 mars 2018

Diterpenoidien tutkimusalalta

Diterpenoidit kasvikunnassa voivat sisältää lääkkeellisiä ominaisuuksia , kun ne vain on saatu löydettyä.

Diterpenoids from the Medicinal Plants of Africa

Louis Pergaud Sandjoa, Victor Kueteb, in Medicinal Plant Research in Africa, 2013
3.1

Introduction

Diterpenoids are secondary metabolites containing 20 atoms of carbon derived from the condensation of four isoprenyl units.
 As other terpenoids, they are widespread in the plant kingdom, and most of them biosynthetically derive from geranylgeranyl diphosphate, which forms
  •  acyclic (phytanes), 
  • bicyclic (labdanes, halimanes, clerodanes),
  •  tricyclic (pimaranes, abietanes, cassanes, rosanes, vouacapanes, podocarpanes),
  •  tetracyclic (trachylobanes, kauranes, aphidicolanes, stemodanes, stemaranes, atisanes, gibberellanes), and
  •  macrocyclic diterpenes (taxanes, cembranes, daphnanes, tiglianes, ingenanes) according to the cyclization that occurs [1].

 Diterpenoids are divided into more than 45 classes; they are also found in marine organisms, which provide interesting skeletons (Figure 3.1) such as elisapterane (39).
 Figure 3.1 presents the structural diversity and some of the skeletons of this class of compounds.

Plants produce secondary metabolites in response to some external factors from their biotope. To fight against these, the host plant produces diterpenes, which could represent a problem in the living ecosystem of that species because of the allelopathic activity of some of these terpenoids against surrounding flora [24]

In addition, diterpenoid quinones from the roots of Salvia officinalis were earlier reported to display DNA-damaging effect on colonic and hepatic human cells cultured in vitro, although cytotoxic activity was observed [25]. Nevertheless, these structures are synthesized in the ertheless, these structures are synthesized in the plant cells following a well-established mechanism.Read full chapter

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