altilis, 23 and A. communis collected from Indonesia. 24 The compound

total synthesis has also been reported. 25 The compound, 1 was shown to be a potent inhibitor of cathepsin K 25 at an IC50 value of 170 nM. The dendrite elongation inhibition activity of the crude extract, fractions and isolated compound were evaluated by cell culture method by visual observation, estimating the length of dendrites.1 The assay method is most precise and reliable. The melanocyte cells, B16F10 were used for the present study. The cells were cultured in DMEM in the presence of 5% carbon dioxide, 10% serum, pencillin (100 μg/ml), streptomycin (50 μg/ml), amphotericin B (2.5 μg/ml). 1 × 105 cells were seeded in 60 mm cell learn more culture dish and were incubated with and without the test material for 24 h. After 24 h PI3K inhibitor drugs incubation, the cells were examined under an inverted microscope against negative control. The dendrite length was measured and calculated the % inhibition of the cell length (Table 1). The ethyl acetate

fraction and crude methanol extract were shown good dendrite elongation inhibition at 50 μg/ml and isolated compound was showed good activity at same concentration. The present study on the leaves of A. altilis resulted in the isolation of one known compound, 1 ( Fig. 1). Its structure has been identified on the basis of spectroscopic data and comparison with the literature data. The crude methanolic Cell press extract, its fractions and isolated compound were studied for dendrite elongation property and the compound has shown good dendrite elongation inhibition. All authors have none to declare. The authors are thankful to Mr.C.K. Ranganathan, CMD of CavinKare Pvt. Ltd., Chennai for his constant encouragement and providing necessary facilities. “
“Duloxetine is itself a moderate inhibitor of CYP2D6 and therefore may interact with drugs that are extensively metabolized by CYP2D6.

This may lead to clinically significant increases in plasma levels of CYP2D6 substrates that have a narrow therapeutic index (such as Metoprolol, perhexiline, phenothiazines, or flecainide). CYP2D6 is responsible for the metabolism of drugs commonly used to treat various medical conditions; some examples include anti-estrogen, Tamoxifen,1 atypical opioid tramadol,2 anti-arrhythmic amiodarone3 and cyclooxygenase-2 inhibitor celecoxib.4 It is important, therefore, that physicians are aware of the potential for clinically relevant interactions when prescribing antidepressants. Since diabetic patients are vulnerable to diabetic complications like diabetic cardiovascular disorders and diabetic neuropathy, it is very likely that Duloxetine and Metoprolol are concomitantly administered for diabetic neuropathic pain and diabetic cardiovascular disorders respectively.