GC-MS analysis of the ethanol extracts of Dyschoriste littoralis Nees. (Acanthaceae)
DOI:
https://doi.org/10.56511/JIPBS.2018.v5.i01.pp113-116Abstract
In the present study, ethanol extracts from Dyschoriste littoralis Nees. were subjected to GC-MS analysis to study the important phytochemical constituents responsible for the various pharmacological activities. The crude extracts of ethanol were obtained by soxlet method. The GC-MS analysis of ethanol extract from D. littoralis revealed the presence of nine phytocompounds in the underground part and twenty six compounds in the aerial parts. The compounds were identified by comparing their retention time and peak area with that of literature and by interpretation of mass spectra. acetyl chloride, dichloro (CHCl2COCl) (Rt 9.49); Ethane, 1,1-diethoxy- and Methoxymethyl isothiocyanate are prominent compounds in underground part. Three major phytochemical constituent’s mass spectra in aerial part are Ethyl Acetate, (3-Methyl-oxiran-2-yl)-methanol, Hydroperoxide and 1-methylbutyl
Keywords:
Dyschoriste littoralis, bioactive compound, Gas Chromatography (GC), Mass Spectroscopy (MS)Downloads
References
Hemant Kumar Sharma, Veerachamy Alagarsamy: In-vitro antimicrobial activity of various extracts of Dyschoriste littoralis Nees. International J. Phytopharmacology 2013; 4(3): 212-216.
Momin MA, Bellah SF, Rahman SM, Rahman AA, Murshid GM, Emran TB: Phytopharmacological evaluation of ethanol extract of Sida cordifolia L. roots. Asian Pac J. Trop. Biomed 2014; 4(1): 18-24.
Farid MM, Hussein SR, Ibrahim LF, Desouky MA, Elsayed AM, Oqlah AA, et al.: Cytotoxic activity and phytochemical analysis of Arum palaestinum Boiss. Asian Pac J Trop Biomed 2015; 5(11): 944-7.
Guo F, Feng L, Huang C, Ding H, Zhang X, Wang Z, et al.: Phenylflavone derivatives from Broussonetia papyrifera inhibit the Figure 2. Chromatogram for D. littoralis underground part of ethanol extract D. littoralis Chemical compound Hydroxylamine, 0 - (2 - methylpropyl) - - methyl - - (2 - propynyloxy) - Hexene, 4 - methyl - Propene, 2 - methyl - - methyl - Acetyl chloride, dichloro - Hexadiyne - diethoxy - Methoxymethyl isothiocyanate - 4 - yne, 2 - methyl - Pyrano(3,2 - b)pyridine Thiocyanic acid, 2 - propynyl ester 2 - bromo - Cyclohexanone, 2,5 - dimethyl - 2 - (1 - methanol) growth of breast cancer cells in vitro and in vivo. Phytochem Lett 2013; 6(3): 331-6.
Jayapriya G, Gricilda Shoba F: GC-MS analysis of bio-active compounds in methanolic leaf extracts of Justicia adhatoda (Linn.) Journal of Pharmacognosy and Phytochemistry 2015; 4(1): 113-117.
Gamble JS: Acanthaceae In: Flora of the Presidency of Madras London: West, Newman and Adlard 1915-1936.
Matthew KM: The Flora of Tamil Nadu Carnatic Vol I, The Rapinat Herbarium, Tiruchirappali, Vol – I. 1983 – 1988.
Brown KK , Hampton MB : Biological targets of isothiocyanates. Biochim. Biophys. Acta. 2011; 1810(9):888-94.
Ajmal R. Bhat, Rajendra S. Dongre, Rupali S. Selokar: Potent in-vitro antibacterial and antifungal activities of pyrano [2,3-D] pyrimidine derivatives with quantitative yield. Int. J. Pharm. Bio. Sci. 2014; 5(1): 422 – 430.
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Copyright (c) 2018 Rajasekar P., Subha S., Saravana Ganthi A

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