Plumbago is a genus of medicinal plants that are used in recent years to induce significant levels of apoptosis in various cancer cells. Purpose: The test substances that are obtained from Plumbago species are studied for their cytotoxicity against U87 cell line in a dose dependent manner and were first subjected to GC-MS study to know the bioactive constituents present in them. Methods: GC-MS was done using ethanol extracts of the roots of both the species. In vitro cytotoxicity of the roots of two species of Plumbago -P. zeylanica (sample I) and P. auriculata (sample II) were tested against U87 cell line. Test samples were taken at concentrations ranging from 400μg/ml to 3.12μg/ml to determine the percentage growth inhibition of both the test substances on U87 cell line. Results: GC-MS analysis on root extracts of P. zeylanica showed the presence of 27 phytochemical constituents and P. auriculata 16 in number .The test substances, Sample I and Sample II exhibited a cytotoxic CTC 50 value of 88.07±4.4 and 23.11±0.9 respectively. Conclusion: P. zeylanica is more effective than P. auriculata in terms of its cytotoxicity as well in the number of useful bioactive compounds.
Sequential peptides corresponding to substance P (6-11) were synthesised on a photocleavable 4-aminomethyl-3-nitrobenzoylaminomethyl polystyrene resin. This photoremovable polymeric support, useful for the synthesis of C-terminal peptide amides, was prepared from 4-bromomethyl-3-nitrobenzoylaminomethyl polystyrene by treatment with potassium phthalimide followed by hydrazinolysis. Amino acid residues were incorporated onto this support following the standard solid-phase methodology of peptide synthesis. The protected peptide amides were cleaved from the resin by photolysis with light of wavelength 350nm. The resin was used for the synthesis of peptides including the partial sequence corresponding to substance P (9-11) which was further subjected to stepwise synthesis to prepare substance P (6-11) in an overall yield of 88~. This approach combines the advantages of the photochemical deprotection of the 4-aminomethyl-3-nitro carboxyl protecting group, the polymer-supported peptide synthesis and the polymer-analogous functionalisation procedure to obtain the C-terminal peptide amide under mild conditions.
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