5D. regia contains large amount of terpenoids, polyphenolic compounds, tannins, cardiac glycosides and anthroquinones. 6 The D. regia flowers are used in antimicrobial, antibacterial, anti-inflammatory

activities. 7 Trees are released by terpenes more actively in warmer weather, acting as a natural form of cloud seeding then, it reflects Lapatinib cell line sunlight, allowing the forest to regulate the temperature.4 A large of medicinal plants and its phytoconstituents have shown beneficial therapeutic potentials and a majority of Indian medicinal plants are evaluated for such properties.8 With this background, the aim of present study was carried out to predict the fraction having oleananoic acid acetate and evaluation of antibacterial activity. The leaves of the plant D. regia collected from Thanjavur district and authenticated by Dr. John Britto, Rapinet Herbarium, St. Joseph’s College, Tiruchirappalli. The leaves were cleaned, dried in shadow and crushed into powder. The powdered sample was extracted with 95% ethanol by using cold method extraction in room temperature for one week. The 95% ethanol extract was filtered,

distilled and concentrated VE-821 in vivo to obtain the solid greenish residue. The 95% ethanol extract was further fractionated successively with petroleum ether, n-hexane, chloroform, ethyl acetate, ethanol, n-butanol and methanol. The solvents were recovered under reduced pressure. Ethyl acetate soluble part (5.8 g) was subjected to silica gel (70–130 mesh) Column chromatography (60 cm × 4.5 cm). The ethyl acetate soluble part eluted gradient with Ethyl acetate, Ethyl acetate:Methanol mixtures (4.05:0.05, 4:1), Methanol. The eluents were collected and the progress of separation heptaminol was noted by micro thin layer chromatography using Ethyl acetate:Methanol (4.75:0.25) solvent system

and iodine vapor as detecting agent. 4:1 Ethyl acetate: Methanol fraction were purified and recrystallized by methanol. A white solid powder obtained, which was characterized by spectroscopic studies (FT-IR, NMR, EI-MS, ESI-MS) (Negative mode). FT-IR (Fourier Transform- Infra red) spectra were obtained using Perkin Elmer FR-IR 450–4000 in KBr disc and absorption peaks in terms of wave numbers (cm−1). EI-MS (electron impact mass spectrum) were recorded on Jeol instrument and ESI-MS (electron spray ionization mass spectrum) in negative mode, were recorded on Thermo LCQ instrument. NMR (Nuclear magnetic resonance) was acquired on Brucker at 400 MHz (1H) and 100 MHz (13C). Chemical shifts were recorded as δ value (ppm) and chloroform as an inert solvent. Streptococcus mitis and Lactobacillus sp bacteria included in the study. All the cultures were obtained in pure form from the culture collection of Institute of Microbial Technology (IMTECH), Chandigarh, India. 36 g of Muller Hinton Media was mixed with distilled water and then sterilized in autoclave at 151 b pressure for 15 min.