ArticlesAbstractPharmacognosy Research,2011,3,2,143-145.DOI:10.4103/0974-8490.81964Published:June 2011Type:Short CommunicationAuthors:Gottumukkala Venkateswara Rao, T. Mukhopadhyay, T. Annamalai, N. Radhakrishnan, and M. R. Sahoo Author(s) affiliations:Gottumukkala Venkateswara Rao, T. Mukhopadhyay, T. Annamalai, N. Radhakrishnan, M. R. Sahoo CavinKare Research Centre, Ekkattuthangal, Chennai – 600 032, India. Abstract:Bioassay-guided isolation of methanolic extract of the leaves of Origanum vulgare Linn., yielded two protocatechuic acid ester derivatives, origanol A (1) and origanol B (2) along with ursolic acid (3), oleanolic acid (4), β-sitosterol (5), and triacontanol (6). Structures of the compound were established based on physical and spectral data (UV, IR, 1H and 13C NMR and mass). Origanol A (1) showed significant mushroom tyrosinase inhibition activity. Keywords:Origanol A and B, Origanum vulgare Linn., Triterpene acids, Tyrosinase inhibition, β-sitosterolView:PDF (531.98 KB) PDF Thumbnails Document Outline Search Document Find Toggle Sidebar Previous Next Page: Fullscreen Print Download Current View Zoom Out Zoom In Automatic Zoom Actual Size Fit Page Full Width 50% 75% 100% 125% 150% 200% More Information Less Information Close Click here to download the PDF file. Images Chemical Constituents and Biological Studies of Origanum vulgare Linn. KeywordsOriganol A and BOriganum vulgare Linn.Triterpene acidsTyrosinase inhibitionβ-sitosterol ‹ An in vitro Evaluation of the Anthelmintic Activity of Hedychium spichatum Rhizomes and Zingiber zerumbet Rhizomes on the Pheritima Posthuma model: A Comparative Study up Monograph: Ochrocarpus longifolius ›