EventsThe 21st International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session B. Bioorganic, Medicinal and Natural Products Chemistry of the event The 21st International Electronic Conference on Synthetic Organic Chemistry
Published date
03 Nov, 2017
Citation
Manik Ghosh, Siva Ganesh Mavuduru, Komal Kriti, Amar Nath Mishra, ISOLATION OF ANTICANCER AGENTS FROM Tabernaemontana divaricata (L.) R. Br. ex Roem. & Schult. , in Proceedings of The 21st International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2017, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-21-04813
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ISOLATION OF ANTICANCER AGENTS FROM Tabernaemontana divaricata (L.) R. Br. ex Roem. & Schult.

Komal Kriti 1
Amar Nath Mishra 2
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1. Department of Pharmaceutical Sciences and Technology, Birla Institute of Technology, Mesra, Ranchi, Jharkhand (835215), INDIA
2. Department of Chemical Engineering and Technology, Birla Institute of Technology, Mesra, Ranchi, Jharkhand (835215), INDIA
Abstract

Treatment of breast cancer is not easy because of the complexity in molecular physiology. Surgery, chemotherapy and radiation therapy includes different sources of treating breast cancer. The systemic chemotherapy faces lot of challenges, mainly adverse effects. So, there is a need of newer drugs to be developed against breast cancer. The present work tries to justify the folklore claims of Tabernaemontana divaricata (L.) R. Br. ex Roem. & Schult. through a sound scientific background using modern analytical tools. It was found that phytoconstituents of the plant showed good docking score against 3ERT protein. The petroleum ether extract and chloroform extract showed anticancer activity. Petroleum ether extract was found to have GI50 value of 18.7µg/ml. Phytochemical Studies lead to the isolation of two compounds, 1 and 2. These compounds, isolated from the leaves were studied and characterized tentatively with the help of modern analytical tools like FTIR, 1H NMR and MS. Based upon spectral studies, compound 1 was characterized as 2-(1,6a,6b,9,9,12a,14b-heptamethyl 1, 2, 4a, 5, 6, 6a, 6b, 7, 9, 10, 11, 12, 12a, 12b, 13, 14b-hexadecahydropicen-3-yl) propan-2-yl nonanoate. Compound 2 was found to be not pure enough to be characterized. The isolated compounds were also tested for their anti-proliferative activity against breast cancer.

Keywords
Anticancer
Tabernaemontana divaricata
Isolation
Phytoconstituents
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