Planta Med 2011; 77(9): 882-887
DOI: 10.1055/s-0030-1250648
Biological and Pharmacological Activity
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Gastroprotective Effect and Cytotoxicity of Carnosic Acid Derivatives

Cristina Theoduloz1 , Mariano Walter Pertino2 , Jaime A. Rodríguez1 [*] , Guillermo Schmeda-Hirschmann2
  • 1Laboratorio de Cultivo Celular, Facultad de Ciencias de la Salud, Universidad de Talca, Talca, Chile
  • 2Laboratorio de Química de Productos Naturales, Instituto de Química de Recursos Naturales, Universidad de Talca, Talca, Chile
Further Information

Publication History

received August 26, 2010 revised Nov. 17, 2010

accepted Nov. 28, 2010

Publication Date:
14 January 2011 (online)

Abstract

Carnosic acid (CA) is the main phenolic diterpene of rosemary (Rosmarinus officinalis L., Lamiaceae) and presents gastroprotective effect in vitro and in vivo. To determine structure-activity relationships, seventeen esters and ethers of CA were prepared, comprising aliphatic, aromatic, and heterocyclic compounds. The naturally occurring 12-O-methylcarnosic acid (14) was also included in the study. The compounds were evaluated for their gastroprotective activity in the HCl/EtOH-induced gastric lesions model in mice, and for cytotoxicity in human adenocarcinoma AGS cells, Hep G2 hepatocellular carcinoma cells, and human lung fibroblasts. At 10 mg/kg, some of the CA derivatives (5, 8, 9, 12, 14, and 18) were more effective preventing gastric lesions than the reference compound lansoprazole at the same dose. The dibenzoate 9, diindoleacetate 12, and the derivative 18 showed the best gastroprotective effect combined with the lowest cytotoxicity.

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1 Dedicated to the memory of Prof. Jaime A. Rodríguez.

Guillermo Schmeda-Hirschmann

Laboratorio de Química de Productos Naturales
Instituto de Química de Recursos Naturales
Universidad de Talca

2 Norte 685

Casilla 747, Talca

Chile

Phone: +56 71 20 02 88

Fax: +56 71 20 15 73

Email: schmeda@utalca.cl

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