The aim of this work was to investigate the changes in total phenolic compounds content and free radical scavenging abilities against the stable 2,2-diphenyl-1picrylhydrazyl (DPPH assay) during soaking and germination of three cereal grains; wheat (Sids 1), corn (H310 White) and sorghum (Giza 15). Total phenolic compounds in wheat, sorghum and corn raw grains were 381.4, 288.5 and 204 mg/100g, respectively. Soaking and germination processes showed significant decrease in total phenolic compounds. Losses of total phenols during soaking for 12 hr were 15.18, 14.9 and 5.96 % of its initial values in wheat, sorghum and corn raw materials, respectively. Germination process for 48 hr led to decrement of total phenols ranged from 39.3-43.95 % of its initial values in studied raw cereal grains. The DPPH radical scavenging activity decreased during soaking and germination processes of cereal grains. MATERIALS AND METHODS Materials: Grains: Three cereal grains, including wheat (Triticum aestivum L.) Sids 1, corn (Zea maiys L.) Hybrid 310 and sorghum (Sorghum bicolor L.) Giza 15 collected from Sohag Governorate, Egypt. Chemicals: DPPH (2, 2-diphenyl-1-picrylhydrazyl), 6-hydroxy-2, 5, 7, Folin-Ciocalteau reagent, acetic acid were purchased from Sigma-Aldrich (St. Louis, MO). Methanol, ethanol, hexane, and ethyl acetate were HPLC grade. Technological processes: Soaking: Grains samples were soaked in water (1:5, w/v) at room temperature for 12 hr, water was changed every 6 hr (Abdel-Gawad, 1993). Germination: Soaked grains samples were geminated in betry dishes coating with moistened filter paper at room temperature for 12, 24, 36 and 48 hr (Youssef et al., 1987). Milling: All soaked and germinated grains were dried then conditioned by rising its moisture content up to 14 %, then left for 24 hr as tempering time. Milling was run in a Buhler experimental mill (type 212) by progressively receiving the whole flour (Sorour, M. A 1997). Analytical methods: Moisture, protein, fat and ash contents was determined according to AOAC (2000). Total carbohydrate content of grains was calculated by difference. Potassium, calcium, iron, and zanic were determind using Perkin Elmer Atomic Absorption Spectero-photometer 2380. Phosphorus content was determind by Specter-photometer according to AOAC (1980). Extraction of total antioxidants: Ten grams of dry sample were ground fine using a coffee grinder, then weighed and transferred into a test tube (25 x 150 mm). For extraction; 40 mL of methanol were added in a test tube and vortexes to mix with the sample well triplicate. The test tubes were capped and placed in a 60˚C water bath for 20 min. The tubes were vortexed twice during the incubation. Then, the solvent layer from each tube was separated by centrifugation at 2000 rpms for 15 min. The solvent supernatant was transferred to clean, previously weighed and labeled test tubes. The residue was mixed with 20 mL of the same solvent again and vortexed. The solvent supernatant was combined with the previous one. The tube with supernatant was then...