Salicornia brachiata: Isolation of 7-0-β -D-glucopyranosyl-6-methoxychromone and 7-Hydroxy-6-methoxychromone from Ethanolic Plant Extract and Antimicrobial Studies

Chakrapani Patnaik, Bibhu Prasad Sahu, Panchanan Gouda


The compounds 7-0-β -D-glucopyranosyl-6-methoxychromone and 7-Hydroxy-6-methoxychromone have been isolated and identified from ethanolic extract of the whole plant of Salicornia brachiata. Structures were established by chemical and spectroscopic methods. Antimicrobial Activity of the isolated compound7-0-β -D-glucopyranosyl-6-methoxychromone against some microbes has been tested and reported.

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S. Deepa et al. International Journal of Research in Pharmaceutical Sciences 4: 512-517, (2013).

D.H. Lu et alLWT Food Science and Technology, 43: 519-524, (2010).

K.Padmakumar and K. Ayyakkannu Indian J. Vir. 1997, 13: 33-36.

M.Premnathan, K. Chandra, S.KBajpai and K.Kathiresan. Botanica Marina. 1992, 35: 321-324.

Ghosh P K, Reddy M P, Pandya J P, Patolia J S. U S Patent 929809 2005; 6.

A.M. Rizk. The Phytochemistry of the Flora of Qatar. University of Qatar, Doha, Qatar, Scientific and Applied Research Centre. 1986.

S. Deepa, N. Sripriya. Shankar and B. Chandrasekaran, International Journal of Pharmacy and Pharmaceutical Sciences, 2014, 6(6), 430-432.

D.I Park. 2000; Korea Patent 2000-0074066.

M.H.Rhee, H.J. Park, and J.Y. Cho, (2009). Journal of Medicinal Plants Research, 3: 548-555 and the references cited herein.

H.M.Radwan, N.M.Nazif, and L.M.Abou-Setta, (2007). Research Journal of Medicine and Medical Sciences, 2: 72-78.

N.K. Udaya Prakash et. al.. International Journal of Pharmacy Pharmaceutical Sciences. 2013a;5:88-91

T. Manikandan, T. Neelakandan, G. Usha Rani. Journal of Phytology. 2009; 1:441-443.

C.P.Khare, (2007). Indian medicinal plants, Springer Science and Business Media, LLC, 1st ed., New York.

B. Borkowski, and K.Drost, (1965). Alkaloide aus Salicornia herbacea L. Pharmazie, 20: 390-393.

H. Chiji, T. Aiba and M. Izawa (1978): Agricultural Biology and Chemistry, 42: 159-1654.

Y. Arakawa, H. Chiji and M. Izawa (1983). Agricultural Biology and Chemistry, 47: 2029-2033.

Y. Arakawa, Y. Asada, H.Ishida, H. Chiji and M. Izawa, (1982). Journal of the Faculty of Agriculture, Hokkaido University, 6: 11-12.

M. Geslin, and J.F. Verbist, (1985). Journal of Natural Products, 48: 111-113.

G. Liebezeit, (2008): Senckenbergianan Maritima, 38: 1-30; and the reference cited herein.

M. Yin, Chemistry of Natural Compounds, 48: 258-261.

T.A.Salt and J.H.Adler (1985). Diversity of sterol composition in the family Chenopodiaceae. Lipids, 9: 594-601.

Q. Wang Fitoterapia, 83: 742-749 and the reference cited herein.

Y.S.Lee, S.L,Hye, H.S. Kuk, B.K.Kim, and S.Lee. (2004). Constituents of the halophyte Salicornia herbacea. Archives Pharmacal Research, 27: 1034-1036.

A.J.Davy, G.F.Bishop and C.S.B. Costa (2001). Journal of Ecology, 89: 681-707.

B.P.Sahu, P. Gouda and C.Patnaik, IJARSET, Vol. 3, Issue 6 ,, PP. 2219-2224, (2016).

B.P.Sahu, P. Gouda and C.Patnaik, Journal of Chemistry and Chemical Sciences, Vol.6(6), 574-585, (2016).

A. J. Patnaik, P. P. Gouda, P. Gouda and C. Patnaik, Journal of Chemistry and Chemical Sciences, Vol.6(6), 563-573, (2016).



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