Isolation and absolute stereochemistry of coussaric acid,a new bioactive triterpenoid from the stems of Coussarea brevicaulis |
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Authors: | Su Bao-Ning Kang Young-Hwa Pinos Rosa Elena Santarsiero Bernard D Mesecar Andrew D Soejarto D Doel Fong Harry H S Pezzuto John M Kinghorn A Douglas |
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Affiliation: | Program for Collaborative Research in the Pharmaceutical Sciences and Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, Chicago, IL 60612, USA. |
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Abstract: | ![]() Coussaric acid (1), a triterpenoid based on an ursane skeleton, and an oleanane-type triterpene acid, 3-epi-spathodic acid (2), as well as four known compounds, barbinervic acid, scutellaric acid, stigmasterol and stigmasterol glucoside, have been isolated from an EtOAc-soluble extract of the stems of Coussarea brevicaulis. The structures of compounds 1 and 2 were elucidated on the basis of spectroscopic investigation, and single-crystal X-ray crystallography was used to confirm the structure of 1. The absolute stereochemistry of 1 was established by chemical transformations and by the Mosher ester procedure. The potential of the isolates and chemical transformation products to induce quinone reductase was evaluated in mouse Hepa lclc7 hepatoma cells. |
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Keywords: | Coussarea brevicaulis Rubiaceae Coussaric acid Single-crystal X-ray analysis Chemical transformation Mosher ester method Quinone reductase induction assay |
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