2 The phytochemicals

analyzed were saponins, flavonoids, glycosides, tannins, A-1210477 purchase phenols, phlobatannins, proteins, terpenoids, alkaloids, steroids and amino acids. About 0.5 g of dried powdered sample of plant was boiled in 10 ml distilled water in test tube and then filtered. A few drops 0.1% of FeCl3 solution were added to the filtrate. Blue–black precipitate indicated the presence of tannins and phenols. 2 ml of 2 N HCl was added to 5 ml aqueous extract and the solution was heated with stirring in a water bath for 10 min. The cooled solution was filtered and a few drops of Dragendorff’s reagent were added. Reddish-brown precipitate indicated the presence of alkaloid. About 1 g of dried powdered sample was boiled with 10 ml distilled water. Frothing persistence indicated the presence of saponins. 5 ml of aqueous extract was

mixed with 2 ml of chloroform and few drops concentrated H2SO4 was carefully added to form a layer. Blue/green ring indicated the terpenoids are present. About 0.5 g of dried powdered plant sample was mixed with 10 ml CHCl3 and filtered then added 1 ml acetic anhydride and few drops of concentrated H2SO4 to the filtrate. Green ring indicated the presence of steroids. About 0.5 g of dried powdered plant sample was boiled in 10 ml ethanol and filtered. Few this website pieces of magnesium ribbon and few drops of concentrated HCl were carefully added to the filtrate. Red color indicated the presence of flavonoids. About 2 ml of aqueous extract was boiled with 2 ml 1% HCl. Deposition of a red color indicated the presence of phlobatannins. 1 ml glacial acetic acid, few drops FeCl3 and few drops concentrated H2SO4were added to 2 ml aqueous extract. Green/blue precipitate indicated the presence of glycosides. 5–6 drops of ninhydrin reagent were added in 2 ml of aqueous extract and heated in boiling water bath for about 5 min. Purple coloration indicated the presence of amino acid. 5–6 drops of 5% NaOH and 5–7 drops of 1% Cu(SO4)2 were added in 2 ml aqueous extract.

Violet color indicated the presence of proteins. Water is universal solvent, used to extract plant products. However traditional healers use primarily water extract.11 The results of phytochemical Terminal deoxynucleotidyl transferase screening of stems, flowers, leaves and roots of T. dioica show that steroids and phlobatannins are present in all part of plants; tannins, phenols and flavonoids are present in flowers, leaves and roots; terpenoids and saponins are present in stems, flowers and leaves. However, proteins, alkaloids, glycosides and amino acids were not detected in any part of plant as shown in Table 1. The presence of above phytochemicals may show therapeutic activities of T. dioica. Previous studies on plants showed that, flavonoids is likely to be accountable for pharmacological and biochemical actions viz., antioxidant, anti-allergic, anti-inflammatory, hepatoprotective, anti-carcinogenic, anti-viral and anti-thrombotic activities.