Planta Med 1981; 41(2): 150-160
DOI: 10.1055/s-2007-971692
Research Articles

© Hippokrates Verlag Stuttgart

Secoiridoids and Xanthones in the Genus Centaurium

Part III1: Decentapicrins A, B and C, New M-hydroxybenzoyl Esters of Sweroside from Centaurium littorale W. G. van der Sluis, R. P. Labadie
  • Farmaceutisch Laboratorium, Rijksuniversiteit Utrecht, Utrecht, the Netherlands
1 Part II, see [4] Parts of these studies were presented at the International Research Congress on Natural Products as Medicinal Agents in Strasbourg, France, July 6-11, 1980 (see Planta Medica 39, 268 (1980)).
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Publication History

Publication Date:
29 March 2007 (online)

Abstract

Two new acyl secoiridoid glucosides, named decentapicrins A and B, accumulating in the fruits of Centaurium littorale GILMOUR spp. littorale, have been isolated by means of preparative column chromatography. Another new compound, named decentapicrin C, could also be detected but in minute amounts and was prepared from decentapicrin B.

The close interrelation between these three compounds and the strongly bitter centapicrin (Ia) and desacetylcentapicrin (Ib), accumulating in the fruits of Centaurium erythraea RAFN. [1, 2], have been demonstrated by means of TLC analysis of the products obtained under alkaline treatment.

Under these conditions not only hydrolysis, but also acyl migrations, took place.

Decentapicrin A is partly converted into desacetylcentapicrin (Ib) and decentapicrin C; decentapicrin B is converted into decentapicrin C.

On the basis of this chemical information and spectroscopical data (1H-NMR, 13C-NMR, UV and IR) the structures of decentapicrins A, B and C are postulated to be Ic, Id and Ie respectively.

The single acylation at C3-OH and C4-OH of the glucose moiety as shown in the structures of decentapicrins A and B is new in iridoid chemistry.

Unlike centapicrin (Ia) and desacetylcentapicrin (Ib) the new compounds decentapicrins A, B and C are only weak bitter principles like sweroside (I).

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