Pharmacognosy Magazine

ORIGINAL ARTICLE
Year
: 2020  |  Volume : 16  |  Issue : 5  |  Page : 513--516

A pentacyclic triterpene from Lippia origanoides H.B.K and its cytotoxic activity


Arvind Kumar1, Elizabeth Quintero Rueda2, Jairo Rene Martínez3, Raquel Elvira Ocazionez2, Elena E Stashenko3 
1 Department of Chemistry, Hemwati Nandan Bahuguna Garhwal University, Srinagar, Uttarakhand, India; Centro de Investigacion en Cromatografia y Espectrometria de Masas, CROM.MASS, Universidad Industrial de Santander, Bucaramanga, Colombia
2 Laboratorio de Arbovirus, Centro de Investigaciones en Enfermedades Tropicales (CINTROP), Universidad Industrial de Santander, Bucaramanga, Colombia
3 Centro de Investigacion en Cromatografia y Espectrometria de Masas, CROM-MASS, Universidad Industrial de Santander, Bucaramanga, Colombia

Correspondence Address:
Arvind Kumar
Department of Chemistry, Hemwati Nandan Bahuguna Garhwal University, Garhwal, PO Box 63, Srinagar - 246 174, Uttarakhand

Elena E Stashenko
Centro de Investigacion en Cromatografia y Espectrometria de Masas, CROM-MASS, Universidad Industrial de Santander, Carrera 27, Calle 9, Edificio 45, Bucaramanga-680002
Colombia

Background: Lippia origanoides H. B. K. (Verbenaceae) is an aromatic small shrub appreciated in the traditional systems of medicine. L. origanoides essential oil is an ingredient of commercial poultry feed products and its postdistillation residual biomass is an interesting source of bioactive compounds. During our search for the valorization of this residual biomass, supercritical-CO2(SC-CO2)extraction afforded a mixture that was subjected to an investigation of phytochemicals and of cytotoxicity, which was not reported previously. Objectives: The current study was designed to investigate the phytochemicals from the steam-distilled residual biomass of thymol- and carvacrol-rich L. origanoides chemotypes and to evaluate their in vitro cytotoxic activity. Materials and Methods: Steam-distilled aerial parts of L. origanoides chemotypes were extracted with SC-CO2to obtain a greenish-yellow extract with a strong aromatic odor. The SC-CO2extract was subjected to column chromatography, and the isolate obtained was screened in vitro for cytotoxicity against human normal embryonic kidney 293, MRC-5, THP-1, and XP4PA cell lines, using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. Results: A pentacyclic triterpene, friedelan-3-one (1) was isolated for the first time from L. origanoides chemotypes. The structure of the isolate was elucidated with spectroscopic (ultraviolet, infrared, mass spectra, and nuclear magnetic resonance) techniques. The in vitro cytotoxic activity of the isolated compound was determined. The results showed no significant results against the selected cell lines using the MTT assay. Conclusion: The main significance of the present study was to develop promising routes to utilize the residual biomass for value-addition. This is the first report of friedelan-3-one isolation from the genus Lippia.


How to cite this article:
Kumar A, Rueda EQ, Martínez JR, Ocazionez RE, Stashenko EE. A pentacyclic triterpene from Lippia origanoides H.B.K and its cytotoxic activity.Phcog Mag 2020;16:513-516


How to cite this URL:
Kumar A, Rueda EQ, Martínez JR, Ocazionez RE, Stashenko EE. A pentacyclic triterpene from Lippia origanoides H.B.K and its cytotoxic activity. Phcog Mag [serial online] 2020 [cited 2022 May 22 ];16:513-516
Available from: http://www.phcog.com/article.asp?issn=0973-1296;year=2020;volume=16;issue=5;spage=513;epage=516;aulast=Kumar;type=0