Open Access

Extraction, Isolation, Characterization and DNA Binding Study of Carbazole Alkaloids from Murraya Koenigii (Curry Leaf )

V. Mohanraj, Department of chemistry, Sri Ramakrishna mission Vidyalaya College of Arts and Science, Coimbatore, TN, India. M. Dhandapani, Department of chemistry, Sri Ramakrishna mission Vidyalaya College of Arts and Science, Coimbatore, TN, India. G. Amirthaganesan, profga@yahoo.co.in
Department of chemistry, Sri Ramakrishna mission Vidyalaya College of Arts and Science, Coimbatore, TN, India.
M. Sekar Department of chemistry, Sri Ramakrishna mission Vidyalaya College of Arts and Science, Coimbatore, TN, India.


J. Environ. Nanotechnol., Volume 3, No 1 (2014) pp. 53-59

https://doi.org/10.13074/jent.2014.01.132057

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Abstract

Murraya Koenigii is a medium sized tree belonging to the family rutaceae. The present study aimed to investigate the phytochemical composition of the stem bark of murraya koenigii. The powdered plant material was extracted by maceration with acetone, and the acetone extract was fractionated with petroleum ether and subjected to column chromatography. The structure were established by interpretation of their UV-VIS , 1 H, 13 C, DEPT, 1 H-1 H COSY, 13 C-1 H COSY NMR Spectroscopy and Mass spectrometry. The investigations led to isolation of two constituents were identified, such as Girinimbilol compound can be isolated by petroleum ether, another one compound cannot be isolated by column chromatography. The isolated compound was subjected to DNA binding study with Calf thymus DNA. The binding affinity value is 1.324 x 10 5 m -1 . DNA binding study of the compound isolated from M.Koenigii is the first time reported method. The anti cancer study of the compound in the HeLa cell line with MTT assay method to IC 50 value is 178 μM.

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Reference


Anonymous. Flora of West Bengal, Botanical Survey of India, Kolkata, India, 1, 386 (1997).

Chatterjee, A. and Pakrashi, S. C., The Treatise on Indian Medicinal Plants, National Institute of Science Communication (CSIR) New Delhi, India, 3, 108 (1997).

Harbone, J. B., Phytochemical methods, Chapman and Hall Ltd (1973).

Kureel, S. P., Kapil, R. S. and Popli, S. P. Terpenoid alkaloids from View the Math ML source spreng. - II: The constitution of cyclomahanimbin e, bicyclomahan imbine, and mahanimbidine, Tetrahetron Lett., 44 3857-3862 (1969). 

http://dx.doi.org/10.1016/S0040-4039(01)88531-2

Kureel, S. P., Kapil, R. S. and Popli, S. P., Two novel alkaloids from Murraya koenigii spreng: mahanimbicine and bicyclomahanimbicine, Chem. Ind., 29, 958 (1970).

Marmur, J. and Doty, P., Thermal denaturation of deoxyribonucleic acids, J. Mol. Biol. 3, 585-594 (1961). 

http://dx.doi.org/10.1016/S0022-2836(61)80023-5

Narasimhan, N. S. and Kelkar, S. L., Indian. J. Chem., 14B (1976) 430.

Narasimhan, N. S., paradkar, M. V. and Chitguppi, V. P., Structures of mahanikbin and koenimbin , Tetrahetron Lett., 5501-5504 (1968).  

http://dx.doi.org/10.1016/S0040-4039(00)75545-6

Nayak, A., Mandal, S., Banerjit, A. and Banerji, J., Review on chemistry and pharmacology of Murraya koenigii Spreng (Rutaceae), J. Chem. Pharm. Res., 2(2), 286-299 (2010).

Purthi, J. S., Spices and Condiments, National Book Trust, New Delhi, India, 108 (1976).

Reichmann, M. E., Rice, S. A., Thomas, C. A. and Doty, P., A Further Examination of the Molecular Weight and Size of Desoxypentose Nucleic Acid, J. Am. Chem. Soc., 76,  3047-3053 (1954). 

http://dx.doi.org/10.1021/ja01640a067

Reisch, J., Adebajo, A. C., Aladesanmi, A. J., Adesina, S. K., Bergenthal, D. and Meve, U., Chemotypes of Murraya koenigii growing in Sri Lanka, Planta Medica., 60, 295-296 (1994). 

http://dx.doi.org/10.1055/s-2006-959486

Reisch, J., Goj, O., Wickramasinghe, A., Herath, H. M. T. and Henkel, G., Carbazole alkaloids from seeds of Murraya koenigii, Phytochemistry., 31, 2877-2879 (1992). 

http://dx.doi.org/10.1016/0031-9422(92)83651- E

Tachibana, Y.,  Kikuzak,i H., Lajis, N. H. and Nakatani, N., Antioxidative activity of carbazons from Murraya koenogi leaves, J. Agric. Food Chem., 49, 5589-5594 (2001).

http://dx.doi.org/10.1021/jf010621r

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