2). The reduction of Fe3+ ions can be assed by this reducing model for antioxidants. All the extracts were subjected for reducing activity. Water extract showed significant reducing activity when compared to that of other extracts (Table 3; Fig. 3). Hydrogen peroxide is a weak click here oxidizing agent and can inactivate a few enzymes directly, usually by oxidation of essential thiols (–SH) groups. Hydrogen peroxide crosses cell membrane and reacts

with ferric and copper ions, which shows toxic effects. Extracts have the good hydrogen peroxide scavenging activity.5 The total antioxidant capacity of the extracts was found to be 49; 68; 74 mg ascorbic acid equivalent at 500 μg/ml extracts concentration. The good antioxidant activity might be attributed to the presence of Phytochemicals like phenols and tannins (Table 4; Fig. 4). The alcoholic and benzene extracts showed significant activity when compared with aqueous and pet-ether extracts (Table 5). An increasing demand for natural additives has shifted the attention from synthetic to natural antioxidants. As leafy vegetables are found to be good source of antioxidants and the present study

is to examine the antioxidant potential and antimicrobial activity of leaf extracts of P. tirupatiensis. Many plants often contain substantial amounts of antioxidants including vitamins C and E, carotenoids, flavonoids, phenols and tannins etc. and thus can be utilized to scavenge

the excess free Selleckchem PI3K inhibitor radicals from the body. All authors have none to declare. The authors are grateful to Prof. G. Bagyanarayana, Vice-Chancellor and Prof. K. Venkata Chalam, Registrar, Palamuru University for their encouragement and support. “
“A survey of the literature reveals that, pyrimidine, iminopyrimidine1, 2, 3, 4 and 5 and fused benzothiazole hetrocycles4, 5 and 6 exhibit effective pharmacophore nearly activity. M.F.G. Stevens et al7, 8, 9 and 10 reported the compounds containing benzothiazole possess antitumor activity against renal, ovarian and breast cancer cell line. Domino et al11 and 12 reported the use of 2-amino benzothiazoles as central muscles relaxant. Jimonet and his research group12 reported syntheses and pharmacological activity of 3-substituted-2-imino benzothiazolines which were found to be three times more potent than Riluzole, a blocker of excitatory amino acids mediated neurotransmission. E. Brantsly et.al13 reported the fluorinated 2-(4-amino-3-methyl phenyl) benzothiazole induced to CYP1A1 expression, become metabolized and bind to macromolecules in sensitive Human Cancer cells. Recently, Survarna Kini and her research group14 synthesized novel benzothiazole derivatives and evaluated against Human Cervical Cancer cell lines.