Phenolic Compound Identification and Antioxidant Capacity of Alperujo Extracts from Region del Maule,Chile

This study was carried out to determinate phenolic, flavonoid content, and antioxidant capacity in methanolic extract from three Alperujo varieties. Alperujo Barnea showed the highest concentration of phenols and flavonoid. The greater hydroxytyrosol content was obtained in the same extract (4.93 ± 0.37 µg/mg extract), whereas the greater tyrosol content (0.23 ± 0.012 µg/mg extract) was found in Arbequina extract. These results were correlated with the greatest radical scavenging and the highest inhibition of lipoperoxidation process observed in Barnea extract (IC₅₀ of 27.9 ± 1.04 µg/mL; IC₅₀ 22.8 ± 3.5 µg/mL, respectively). In spite of differences, alperujo extracts exhibited notable antioxidant capacities.     

Chemical composition of essential oil and antioxidant activity of leaves and stems of Phlomis lurestanica

Essential oils from leaves and stems of Phlomis lurestanica at the flowering stage were extracted by hydrodistillation. The essential oils were analyzed using Gas Chromatography and Gas Chromatography-Mass Spectrometry. Twenty-eight and twenty-five compounds were identified in the stems and leaves, respectively. The main compounds of stems were α-pinene (12.40%), γ-cadinene (10.92%), and γ-elemene (6.46%). Hexadecane (8.97%), 2-dodecnenal (6.57%), and heptadecane (6.32%) were the major constituents in the essential oils of the leaves. The methanol extracts of stems and leaves were evaluated for their antioxidant properties using 2,2-diphenyl-1-picrylhydrazyl and β-carotene/linoleic acid tests. In the 2,2-diphenyl-1-picrylhydrazyl assay, the leaves (IC₅₀ = 1168.9 µg/ml) have stronger antioxidant activity than the stems (IC₅₀ = 1563.6 µg/ml). The extracts of the leaves and stems showed remarkable antioxidant activity in β-carotene/linoleic acid assay (96.2% and 95%, respectively). The total phenol and flavonoid contents of the species were determined using Folin-Ciocalteu and AlCl₃ assays, respectively. The phenol and flavonoid contents of the leaves (301.0 µg/ml and 45.2 µg/ml, respectively) were observed more than the stems (172.3 µg/mg and 18.8 µg/mg, respectively).     

In Vitro Antioxidant and Antiglycation Properties of Methanol Extract and Its Different Solvent Fractions of Musa paradisiaca L. (Cv. Nendran) Inflorescence

Methanolic extract of Musa paradisiaca inflorescence and its different solvent fractions, petroleum ether, ethyl acetate, butanol, and water were studied for their total phenolic and flavonoid content, free radical scavenging, and antiglycation activities, and these properties were compared with standard antioxidant compounds. Ethyl acetate fraction exhibited higher antioxidant and antiglycation properties than other fractions. IC₅₀ values of ethyl acetate fraction for 1,1-diphenyl-2-picrylhydrazyl method, 2,2-azinobis-3 ethylbenzothiazoline-6-sulphonic acid method, superoxide radical scavenging, hydroxyl radical scavenging, nitric oxide radical scavenging, and antiglycation activities were 9.80, 13.50, 26.40, 19.71, 25.73, and 31.00 μ g/ml, respectively. Total phenolic content of ethyl acetate (21.52 mg GAE/g) was significantly higher than other fractions. There was positive linear correlation between antioxidant activity and total phenolic content.      

Metabolite profiling and inhibitory properties of leaf extracts of Ficus benjamina towards α-glucosidase and α-amylase

The use of antioxidant-rich medicinal plants having the potential to reduce oxidative stress and postprandial hyperglycemic pressure is one of the most promising option for the management of diabetes. This study presents information on metabolite profiling and in vitro anti-diabetic effects of leaf extracts of Ficus benjamina. The DPPH (2, 2-diphenyl-1-picrylhydrazyl radicals) assay was performed to determine the in vitro antioxidant potential of the plant extracts. The anti-diabetic effects were investigated by evaluating inhibitory properties of F. benjamina leaf extracts towards carbohydrate hydrolyzing enzymes, i.e., α-glucosidase and α-amylase, whereas ¹H NMR and UHPLC-QTOF-MS/MS analytical methods were employed for metabolite profiling of F. benjamina leaf extracts. Among 40, 60, 80, and 100% ethanolic leaf extracts of F. benjamina, 80% ethanolic extract exhibited the highest antioxidant activity based upon its DPPH radical scavenging ability (IC₅₀ value: 63.71 ± 2.66 µg/mL). The 80% ethanolic leaf extract of F. benjamina also proved to be the most efficient α-glucosidase and α-amylase inhibitor with IC₅₀ values of 9.65 ± 1.04 µg/mL and 13.08 ± 1.06 µg/mL, respectively; these values were even better than acarbose with α-glucosidase inhibition activity (IC₅₀ = 116.01 ± 3.83 µg/mL) and α-amylase inhibition activity (IC₅₀ = 152.66 ± 7.32 µg/mL). Moreover, a total of 31 metabolites were identified in F. benjamina leaf extract, which may have the potential to contribute to its antioxidant and inhibitory properties against carbohydrate hydrolyzing enzymes. The findings of this study depict F. benjamina leaf extracts as a promising α-glucosidase and α-amylase inhibitor, and therefore, can be utilized for the development of anti-diabetic functional diets/nutra-pharmaceuticals.     

Exploring bioactive fraction of Sargassum wightii: In vitro elucidation of angiotensin-I-converting enzyme inhibition and antioxidant potential

Bioactive fraction of brown algae Sargassum wightii (SWE) was obtained using silica column chromatography and preparative Thin Layer Chromatography (TLC). FT-IR and LC–mass spectrometry ESI analysis revealed presence of various phlorotannins in the SWE. The IC₅₀ value of SWE was found to be 59.91, 51.04, and 55.21 μg/ml for scavenging of 2,2-diphenyl-1-picrylhydrazyl, 2,2-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid), and Ferric Reducing Antioxidant Power assay, respectively. SWE inhibited angiotensin-I-converting enzyme (ACE) in mixed-type manner with IC₅₀ value of 56.96 µg/ml and Ki value of 45 µg/ml. The dual function such as antioxidant and ACE inhibition of SWE warrants further study to understand the antihypertensive potential in vivo.     

ANTIFUNGAL,AFLATOXIN INHIBITORY AND FREE RADICAL‐SCAVENGING ACTIVITIES OF SOME MEDICINAL PLANTS EXTRACTS

ABSTRACT

The antifungal, aflatoxin inhibitory and antioxidant activity of methanol–aqueous extract (2:1) of 62 medicinal plants was explored. Based on the antifungal results, the extracts of 25 plants showed more than 50% antifungal activity and were further investigated for their aflatoxin inhibition and antioxidant properties. Methanol–aqueous extracts of Phyllanthus emblica and Terminalia chebula fruits caused 100% inhibition of aflatoxin production by the toxigenic strain of Aspergillus flavus in semisynthetic medium at 1 mg/mL. In addition, P. emblica (IC₅₀ = 4.1 µg/mL) and T. chebula (IC₅₀ = 6.9 µg/mL) fruits extracts exhibited strong antioxidant activity during the 2,2‐diphenyl‐1‐picrylhydrazyl radical‐scavenging assay in comparison with butylated hydroxytoluene (IC₅₀ = 8.1 µg/mL) and butylated hydroxyanisole (IC₅₀ = 6 µg/mL).

PRACTICAL APPLICATIONS

Based on the results of the present study, methanol–aqueous extracts of Phyllanthus emblica and Terminalia chebula, being endowed with strong antifungal, aflatoxin inhibitory and antioxidant activity, may be recommended as plant‐based preservatives for the enhancement of shelf life of food items and their protection from the undesirable harmful effects of molds, aflatoxin and free radical‐mediated damages.     

Essential oil composition,total phenolic content,antioxidant and antibiofilm activities of four Origanum species from southeastern Turkey

This study reports a comparative screening of four species of Origanum in Turkey, based on their essential oil composition, total phenolic content, antioxidant and antibiofilm activities. The major components of essential oils were p-cymene, linalool, and thymol. The total phenolic contents differed from 3.81 to 47.54 mg of GAE/g of extract. The concentrations of flavonoids varied from 12.74 to 58.39 mg of Ru/g of extract. Antioxidant activity was determined in vitro using DPPH reagent and expressed as concentration of each extract required to inhibit radical by 50% (IC₅₀) values that ranged from 16.03 to 48.94 μg/ml. Our results indicated that chloroform extracts of species O. majorana and O. onites, with a total content of polyphenols (47.54 mg of GAE/g and 45.17 mg of GAE/g, respectively) and an IC₅₀ of 16.03 μg/ml and 16.89 μg/ml, respectively were more antioxidant. Among the essential oil concentrations tested, maximum antibiofilm activity was found as 92.24% against M. luteus NRRL-B 1013 by O. majorana essential oil at 50 mg/ml.     

In vitro evaluation of the antioxidant activities in the differentially processed seeds from underutilized legume, Bauhinia vahlii Wight & Arn

Antioxidant potential and total phenolics content of 70% acetone extracts of the raw and processed seeds of Bauhinia vahlii were evaluated. The extract of raw seeds contained higher levels of total phenolics (30.8 g/100 g) and tannins (19.6 g/100 g) compared to dry heated and soaking followed by autoclaving seed extracts. Extracts were screened for antioxidant and free radical scavenging activities using various chemical and in vitro model systems. In all the models, except DPPH radical scavenging activity, the extract from raw seeds manifested the strongest antioxidant activity than that from processed seeds. In β-carotene/linoleic acid emulsion system and superoxide scavenging activity, the raw seed extract registered more activity when compared to the standards (butylated hydroxyanisole and α-tocopherol). Whereas, the extract from dry heated seed exhibited higher DPPH^· scavenging activity (IC₅₀ 70.77 μg/mL) than the raw seeds (IC₅₀ 74.4 μg/mL). This study has to some extent validated the antioxidant potential of the seeds of B. vahlii.     

Phenolic composition,antioxidant, antibacterial,larvacidal against Culex pipiens,and cytotoxic activities of Hyacinthella lineata steudel extracts

This study reports the phenolic composition, antioxidant, antibacterial, larvacidal, and cytotoxic activity of methanol and acetone extracts of Hyacinthella lineata leaves and bulbs. The phenolic composition of H. lineata was determined by HPLC. The most abundant component was gallic acid (421.9µg/g). The β-carotene/DPPH/ABTS/FRAP decoloration method was used to estimate the total antioxidant activity. The total antioxidant activity was the highest for bulb-methanol fraction (65.41 ± 0.05%). The total phenolic content for leaves-methanol extract of the plant was determined as 6.56 ± 4.027mg/mL gallic acid equivalents. Analysis of the antibacterial activity showed that the methanolic-bulb extract are efficient against gram positive and gram negative bacteria. The cytotoxic effect on Artemia salina was assessed by Brine shrimp assay. Brine shrimp lethality assay showed that LC₅₀ values of HBM were obtained as 4.105 ± 2.42μg/ml. The bulb extract of H. lineata showed the highest larvicidal activity against Cx pipiens with value LC₅₀ (64.3275μg/ml). This study suggested that H. lineata may be used as a potential source of antioxidant, and for their biological activity, cytotoxic and antimicrobial properties.     

Plum cultivars grown in Himalayan temperate conditions: physicochemical,antioxidant and antiproliferative activity against three cancer cell lines

Six plum cultivars were evaluated in terms of physicochemical attributes (fruit and stone length, breadth, thickness, weight, fruit moisture content, ash, pH, fruit color, firmness, total soluble solids, total sugars, reducing sugars and titrable acidity), nutraceutical potential i.e., ascorbic acid, β carotene, anthocyanin, total phenol content, total antioxidant activity (DPPH, FRAP) and antiproliferative potential against human breast cancer cell line (MCF7), neuroblastoma (IMR32) and colon cancer cell line (HCT116). The hydroxycinnamates and flavon-3-ols dominated the phenolic profile. Red fleshed plum cultivar Krassivica showed significantly greater antioxidant activity as shown by lowest IC₅₀ value (1.04 mg/mL) for DPPH assay and FRAP value (13.63 µMFe²⁺/g). Significant inhibition of all the three cancer cells was observed in a dose dependent manner after exposure to plum extracts. For IMR32, MCF7 and HCT116 lowest IC₅₀ value of 67.90, 51.48 and 71.10 µg/mL was observed in Krassivica. Thus, Krassivica can be introduced as a cultivar with good physicochemical characteristics and high neutraceutical potential, making it a preferable choice for fresh use and processing.     

Antioxidant and melanogenesis‐inhibitory activities of collagen peptide from jellyfish (Rhopilema esculentum)

BACKGROUND: Jellyfish collagen was hydrolysed with trypsin and properase E, and jellyfish collagen peptide (JCP) was purified from the enzymatic hydrolysate using ion exchange chromatography and gel filtration. The antioxidant activity of JCP in a linoleic acid emulsion system, its superoxide anion‐ and hydroxyl radical‐scavenging activities and its copper‐chelating ability were evaluated in vitro. Initial investigations of JCP's ability to inhibit melanogenesis were carried out using cultured B16 melanoma cells. RESULTS: The molecular weight distribution of JCP was from 400 to 1200 Da. Amino acid analysis showed that JCP was rich in Gly, Pro, Ser, Ala, Glu and Asp and had a total hydrophobic amino acid content of 384.2 g kg^?1. JCP showed high antioxidant activity (IC₅₀147.8 µg mL^?1), superoxide anion‐scavenging activity (IC₅₀21.9 µg mL^?1), hydroxyl radical‐scavenging activity (IC₅₀16.7 µg mL^?1) and copper‐chelating ability (IC₅₀88.7 µg mL^?1) in vitro. It also significantly inhibited intracellular tyrosinase activity, decreased melanin content and enhanced glutathione synthesis (P < 0.05). Furthermore, JCP decreased intracellular cAMP levels and suppressed tyrosinase mRNA expression. CONCLUSION: Based on the results of this study, JCP exerts anti‐melanogenic actions via its antioxidant properties and copper‐chelating ability. JCP could be used as a natural skin‐lightening agent in the medicine and food industries. Copyright © 2009 Society of Chemical Industry     

Application of GC, GC-MSD, ICP-MS and Spectrophotometric Methods for the Determination of Chemical Composition and In Vitro Bioactivities of Chroogomphus rutilus: The Edible Mushroom Species

Chemical composition of Chroogomphus rutilus, the edible mushroom species, was analyzed by using gas chromatography (GC), gas chromatography mass spectrometry (GC-MSD) and inductively coupled plasma mass spectrometry (ICP-MS). The silylated extract affords 19 components. Xylitol (56.28 %), glucitol (11.08 %), fumaric acid (10.92 %) and mannitol (6.79 %) were identified as the major compounds. The methylated extract possessed 13 fatty acids, and linoleic acid (41.61 %) and oleic acid (35.87 %) were the majors. In addition, the mineral and the heavy metal contents were tested for nine minerals and 12 heavy metals by using ICP-MS. In addition, the extracts were evaluated for cholinesterase inhibitory effects against acetyl-cholinesterase and butyrylcholinesterase which are the chief enzymes of Alzheimer’s disease. The antioxidative effect of the extracts was also determined by using five complimentary assays. Moreover, the hexane extract (IC₅₀, 2.22?±?0.13 μg/ml) and the ethyl acetate extract (IC₅₀, 2.28?±?0.18 μg/ml) exhibited a good lipid peroxidation inhibitory activity while the methanol extract demonstrated good butyrylcholinesterase inhibitory activity (IC₅₀, 45.5?±?1.1 μg/ml). In addition, total phenol and flavonoid contents of the extracts were also determined as pyrocatechol and quercetin equivalents, respectively. Because of its high antioxidant activity, C. rutilus might protect people against lipid peroxidation and free radical damage when consumed. It can be also used in food industry as preservative agents or extension of the shelf-life of foods. Since methanol extract indicated remarkable inhibitory activity being close to that of galantamine, it may be also useful as moderate cholinesterase inhibitory agents, particularly against butyrylcholinesterase.     

Chemical and biological variability of hot pepper fruits (Capsicum annuum var. acuminatum L.) in relation to maturity stage

The aim of the present work was to evaluate the chemical composition and the radical-scavenging and antioxidant activities of hot pepper fruits (Capsicum annuum L. var. acuminatum) at three maturity stages (small green, green and red). GC–MS analysis of n-hexane and chloroform fractions showed a different composition between the three stages of ripening. The first stage of maturation (small green) showed the highest radical-scavenging activity (IC₅₀ of 129 μg/ml). Using the bovine brain peroxidation assay, the methanolic extract of green pepper showed significant antioxidant activity (IC₅₀ of 522 μg/ml). Addition of methanolic extract of red and green pepper inhibited oxidation of linoleic acid. Methanolic extract of red pepper showed greater antioxidative potency than the others (IC₅₀ of 3 μg/ml). The different composition of lipophilic compounds and the various amount of phenolics, showed in the three stage of ripening of C. annuum var. acuminatum fruits, modifies the antioxidant activity.     

Characterization of aromatic compounds and biological activities of essential oils from Tunisian aromatic plants

The aromatic compounds and biological activities of essential oils from six Tunisian aromatic plants including Artemisia herba-alba, Rosmarinus officinalis, Thymus capitatus, Mentha piperita, Ocimum basilicum and Artemisia absinthium were investigated. Hydro-distillation was used to extract essential oil from these plants. The identification of compounds from essential oils was performed using GC–MS analysis. Camphor (28.47%) was the major compound of A. absinthium essential oil. High contents of verbenone (20.99%) and camphor (19.72%) were found in R. officinalis. In the case of T. capitatus, carvacrol (81.09%), gamma terpinene (6.61%) and caryophyllene (4.87%) were identified as the major compounds. While eugenol (24.69%), linalool (18.00%) were characteristic compounds of O. basilicum essential oil, camphor (39.10%) and farnesol (14.25%) together with bornyl acetate (12.31%) were the main constituents of A. absinthium. These oils were also subjected to a screening for their antioxidant activity and essential oil from A. absinthium showed a greater antioxidant activity (IC₅₀?=?0.0063 mg/mL) compared to the standard Vitamin E (IC₅₀?=?0.019 mg/mL). The antibacterial activities of the oils against seven pathogenic strains, Pseudomonas aeruginosa, Bacillus cereus, Salmonella, Klebsiella pneumoniae, Escherichia coli, Staphylococcus aureus, Enterococcus faecalis and Micrococcus luteus, were tested. The highest and broadest activity was shown by M. piperita; however, Ocimum basilicum was inactive against all strains. Essential oils were also evaluated for antidiabetic and anti-acetylcholinesterase activities. The IC₅₀ values of A. herba-alba and O. basilicum against α-amylase were respectively 17.76 and 16.32 µg/mL suggesting a powerful anti-diabetic effect comparable to that of acarbose (IC₅₀?=?14.88 µg/mL). R. officinalis, M. piperita and A. absinthium exhibited an interesting acetylcholinesterase inhibition with IC₅₀ equal to 22, 24 and 58 µg/mL respectively.     

Antioxidant and tyrosinase inhibitory activities of different parts of guava (<Emphasis Type="Italic">Psidium guajava</Emphasis> L.)

The antioxidant and the tyrosinase inhibitory activities of 4 different solvents (acetone, ethanol, methanol, and water) for preparation of extracts from guava (branch, fruit, leaf, and seed) were evaluated by measuring total phenolic contents (TPC), DPPH radical scavenging activity, ABTS radical scavenging activity, reducing power (RP), and tyrosinase inhibitory activity. The extracts of branch and leaf showed relatively higher antioxidant properties than those of fruit and seed. The highest TPC (141.28 mg/g gallic acid equivalents), DPPH radical scavenging activity (IC₅₀=34.01 μg/mL), ABTS radical scavenging activity (IC₅₀=3.23 μg/mL), and RP (IC₅₀= 75.63 μg/mL) were found in acetone extract of leaf, while water extract of seed had the lowest antioxidant activity. The tyrosinase inhibitory activity of ethanol extract from guava leaf was 69.56%, which was the highest activity among the extracts. These results indicate that useful bioactive substances exist in the guava branch as well as leaf extracts.     

A dietary antioxidant supplementation of Jamaican cherries (<Emphasis Type="Italic">Muntingia calabura</Emphasis> L.) attenuates inflammatory related disorders

The polyphenolic extract from Jamaican cherries (Muntingia calabura L.) was screened for its antioxidant and anti-inflammatory activities. The extract contained considerable amounts of vitamin C (33.6 mg AAE/g extract) and E (14.7 mg TE/g extract), total phenolics (121.1 mg GAE/g extract), flavonoids (173.2 mg RE/g extract), and anthocyanins (82.4 mg CGE/g extract) estimated through standard spectrophotometric methods. The extract also revealed the presence of volatile compounds such as phytol (26.26%), n-hexadecanoic acid (11.97%), cyclopropaneoctanoic acid (10.26%), γ-sitosterol (11.15%), stigmasterol (7.20%), and campesterol (4.47%) as main constituents in the extract. The polyphenol extract demonstrated DPPH radical scavenging activity (IC₅₀ 10.6±0.6 μg/mL) and effectively inhibited hydroxyl (IC₅₀ 24.9±3.3 μg/mL), and nitric oxide (IC₅₀ 15.01±1.2 μg/mL) radicals in vitro. The extract also exhibited anti-inflammatory activity in a dose dependent manner by significantly (p<0.01) inhibiting carrageenan induced paw edema and reducing the weight of granuloma in cotton pellet-induced granuloma model in rats. Results indicated that Jamaican cherries could be a potential source of nutrient supplement with anti-inflammatory and antioxidant properties and require promotion of their consumption for public health benefits.     

Assessment of phenolic profile of Turkish honeys

In this study, phenolic profile and antioxidant activity of 60 Turkish honey samples of nineteen different floral origins were evaluated by ultra-performance liquid chromatography with electrospray ionization coupled to tandem mass spectrometry, providing the identification of 32 phenolic compounds. Thyme (1051.58 mg/kg), pine (994.18 mg/kg), carob (935.03 mg/kg), eucalyptus (814.46 mg/kg), rhododendron (680.71 mg/kg), heather (562.59 mg/kg), cedar (561.83 mg/kg), and euphorbia (501.64 mg/kg) present significantly high phenolic content. Moreover ferulic, homogentisic, gentisic, syringic, 3,4-dihydroxybenzoic, caffeic, vanillic, p-coumaric, 4-hydroxy benzoic, and trans-2-hydroxy cinnamic acids were the most abundant of the determined compounds. The antioxidant activities of the honeys were evaluated by β-carotene-linoleic acid inhibition, DPPH free radical scavenging activity and ABTS⁺ cation radical scavenging activity which were measured as IC₅₀: 10.87 – 48.23 µg/mL, SC₅₀: 54.33 – 99.40 µg/mL and SC₅₀: 10.33 – 41.20 µg/mL, respectively. Phenolic compounds are considered antioxidant constituents, and they could be stated as components that account for antioxidant activity in Turkish honeys.     

覆盆子不同多酚组成及抗氧化、抗糖尿病活性

为阐明覆盆子不同形态多酚抗氧化和抗糖尿病活性差异,采用不同溶剂和方法提取覆盆子中的水溶、醇溶、游离和结合多酚,比较不同提取物的总酚、总黄酮和可水解单宁含量差异,测定其自由基清除能力、α-葡萄糖苷酶抑制和抗糖基化能力,并采用质谱技术测定活性最佳样品的主要化学成分。结果表明：覆盆子醇溶性多酚提取物的总酚和可水解单宁含量最高,分别为414.95、182.47 μg/mg（以每毫克提取物中所含没食子酸当量表示）,同时具有最高的1,1-二苯基-2-三硝基苯肼自由基清除能力、2,2’-联氮-双(3-乙基苯并噻唑啉-6-磺酸)阳离子自由基清除能力、α-葡萄糖苷酶活性抑制能力,半抑制浓度分别为40.68、23.90 μg/mL和1.65 μg/mL。结合多酚提取物的总黄酮含量和抗糖基化能力最强。共从醇溶性多酚中初步鉴定出31 个化合物,单宁类和黄酮类化合物为其主要活性成分。因此,提取游离多酚和水溶性成分后的覆盆子残渣具有进一步利用、开发高活性抗氧化和抗糖尿病活性成分的应用价值。     

Chemical composition and in vitro antioxidant studies on Syzygium cumini fruit

Syzygium cumini, widely known as Jamun, is a tropical tree that yields purple ovoid fleshy fruit. Its seed has traditionally been used in India for the treatment of diabetes. Based on the available ethno‐pharmacological knowledge, further studies were extended to understand the chemical composition and antioxidant activities of three anatomically distinct parts of fruit: the pulp, kernel and seed coat. Fruit parts, their corresponding ethanol extracts and residues were evaluated for chemical composition. The alcoholic extract was evaluated for its antioxidant potential against DPPH^?, OH^?, O₂^?? and lipid peroxidation. The whole fruit consisted of 666.0 ± 111.0 g kg^?1 pulp, 290.0 ± 40.0 g kg^?1 kernel and 50.0 ± 15.0 g kg^?1 seed coat. Fresh pulp was rich in carbohydrates, protein and minerals. Total fatty matter was not significant in all three parts of fruit. Detailed mineral analysis showed calcium was abundant in all fruit parts and extracts. Total phenolics, anthocyanins and flavonoid contents of pulp were 3.9 ± 0.5, 1.34 ± 0.2 and 0.07 ± 0.04 g kg^?1, respectively. Kernel and seed coat contained 9.0 ± 0.7 and 8.1 ± 0.8 g kg^?1 total phenolics respectively. Jamun pulp ethanol extract (PEE), kernel ethanol extract (KEE) and seed coat ethanol extract (SCEE) showed a high degree of phenolic enrichment. DPPH radical scavenging activity of the samples and standards in descending order was: gallic acid > quercetin > Trolox > KEE > BHT > SCEE > PEE. Superoxide radical scavenging activity (IC₅₀) of KEE was six times higher (85.0 ± 5.0 µg mL^?1) compared to Trolox (540.0 ± 5.0 µg mL^?1) and three times compared to catechin (296.0 ± 11.0 µg mL^?1). Hydroxyl radical scavenging activity (IC₅₀) of KEE was 151.0 ± 5.0 µg mL^?1 which was comparable with catechin (188.0 ± 6.0 µg mL^?1). Inhibition of lipid peroxidation of the extracts was also studied and their activity against peroxide radicals were lower than that of standard compounds (BHT, 79.0 ± 4.0 µg mL^?1; quercetin, 166.0 ± 13.0 µg mL^?1; Trolox, 175.0 ± 4.0 µg mL^?1; PEE, 342.0 ± 17.0 µg mL^?1; KEE, 202.0 ± 13.0 µg mL^?1 and SCEE, 268.0 ± 13.0 µg mL^?1. Copyright © 2007 Society of Chemical Industry