Chemical composition and antioxidant activity of tronchuda cabbage internal leaves

A phytochemical study was undertaken on the internal leaves of tronchuda cabbage (Brassica oleracea L. var. costata DC). Seventeen phenolic compounds were characterized and quantified by reversed-phase HPLC-DAD-ESI-MS ⁿ and HPLC/DAD, respectively: quercetin 3-O-sophoroside-7-O-glucoside, 3-p-coumaroylquinic acid, kaempferol 3-O-sophoroside-7-O-glucoside, kaempferol 3-O-(caffeoyl)-sophoroside-7-O-glucoside, sinapoyl gluc-oside acid, kaempferol 3-O-(sinapoyl)-sophoroside-7-O-glucoside, kaempferol 3-O-(feruloyl)-sophoroside-7-O-glucoside, kaempferol 3-O-(p-coumaroyl)-sophoroside-7-O-glucoside, 4-p-coumaroylquinic acid, sinapic acid, kaempferol 3-O-sophoroside, 3 isomeric forms of 1,2-disinapoylgentiobiose, 1-sinapoyl-2-feruloylgentiobiose, 1,2,2-trisinapoylgentiobiose and 1,2′-disinapoyl-2-ferul-oylgentiobiose. Seven organic acids (aconitic, citric, ascorbic, malic, quinic, shikimic and fumaric acids) were also identified and quantified. The hot water extract of tronchuda cabbage internal leaves was investigated for its capacity to act as a scavenger of DPPH^• radical and reactive oxygen species (superoxide radical, hydroxyl radical and hypochlorous acid), exhibiting antioxidant capacity in a concentration dependent manner against all radicals.     

Flavonoid content of commercial capers (Capparis spinosa, C. sicula and C. orientalis) produced in mediterranean countries

 The flavonol content of commercial capers (pickled flower buds of Capparis spinosa L., C. sicula Veill. in Duham. and C. orientalis Veill. in Duham.) produced in different Mediterranean countries (Spain, Italy, Greece, Turkey and Morocco) has been analysed. The content of quercetin 3-rutinoside, kaempferol 3-rutinoside; and kaempferol 3-rhamnosyl-rutinoside as well as the aglycones (quercetin and kaempferol) were evaluated by HPLC coupled with a diode-array detector. The free aglycones were not detected in the original flower buds, indicating that they were produced during the brining process. In addition, brining extracted most of the kaempferol 3-rhamnosyl rutinoside present in the original buds, this being a minor constituent in pickled capers. The average content of flavonoid glycosides in commercial capers was 5.18 mg/g fresh weight. When this value is converted to the corresponding aglycones (quercetin and kaempferol), capers provide an average of 3.86 mg/g fresh weight. A serving of capers (10 g) will provide 65 mg of flavonoid glycosides or the equivalent 40 mg of quercetin as aglycone. Received: 3 March 2000     

Evolution of ascorbic acid and peroxidase during industrial processing of broccoli

The ascorbic acid content and peroxidase activity of raw, canned and frozen (after blanching times of 60, 90, 120 and 150 s) broccoli florets and stems were determined. The ascorbic acid content represented 1.12 and 0.78 g kg⁻¹ fresh weight in raw florets and stems respectively. After blanching (for different times) and freezing, the ascorbic acid content decreased to values of 0.55–0.56 g kg⁻¹ fresh weight in florets and 0.35–0.36 g kg⁻¹ fresh weight in stems. The industrial processing involved in canning decreased the ascorbic acid content to 0.18 g kg⁻¹ fresh weight in florets. The peroxidase activity observed in the florets and stems of raw broccoli was 308.8 and 278.6 µmol min⁻¹ per 100 g fresh weight respectively. The peroxidase activity remaining in frozen florets varied from 0.9 to 0.2%, while that in stems showed values of between 7.5 and 8.4%. These values for stems were within the range recommended for residual activity after blanching and freezing. The peroxidase activity of canned broccoli florets was practically undetectable. © 2000 Society of Chemical Industry     

Identification and quantitation of flavonols in rowanberry (Sorbus aucuparia L.) juice

Eight flavonols were detected in rowanberry juice, six quercetin and two kaempferol glycosides which were identified as quercetin 3-O-galactoside, quercetin 3-O-glucoside, two quercetin 3-O-dihexosides, quercetin pentose-hexoside and quercetin hexose-pentoside and two kaempferol dihexosides. The total content of identified flavonols in the rowanberry juice was 291 mg L^-1. Quercetin dihexosides contributed 78% to the flavonol content. However, chlorogenic and neochlorogenic acid were the most abundant phenolic compounds in the rowanberry juice (544 and 273 mg L^-1, respectively). From a nutritional point of view, rowanberry juice provides 70 mg of flavonols and 196 mg of chlorogenic acids per serving. HPLC-MSⁿ and HPLC-DAD in combination with solid phase extraction were used to obtain these results.     

Analysis of the Major Flavonol Glycosides Present in Four Varieties of Onion (Allium cepa) and Changes in Composition Resulting from Autolysis

The major flavonoids of mature onion bulb were confirmed as the 3,4′-O-diglucoside (Qdg) and 4′-O-monoglucoside (Qmg) of quercetin using a combination of chromatographic comparisons, mass spectrometry and nuclear magnetic resonance spectroscopy. These two components account for over 85% of the total flavonoids in three varieties of onion with Qdg as the main component. Quercetin is detected in these long stored onions but only at low levels of less than 2% of the total. The remaining flavonoid fraction (approx 15%) comprises upto 17 different components of which quercetin-3-O-glucoside and isorhamnetin glucoside are prominent members although each contribute less than 1% of the total flavonoid fraction. There are significant differences in the levels of Qdg and Qmg between the four different onion varieties analysed; Qdg varying from 50–1300 mg kg^-1 fresh onion tissue and Qmg from 36–394 mg kg^-1. Maceration of the tissue for the three varieties tested led to a loss of Qdg and the appearance of Qmg and free quercetin. In the variety Rijnsburger 50% of the Qdg was degraded in 5 h and had completely disappeared after 24 h. These changes in Qdg can be quantitatively explained by increases in Qmg and free quercetin. The possible significance of quercetin glycosides in the diet is discussed. © 1997 SCI     

Flavonoid and chlorogenic acid profiles of English cider apples

The phenolics in 20 apple cultivars comprising 19 English cider apple varieties and one dessert apple variety were analysed by high‐performance liquid chromatography/tandem mass spectrometry. The cider varieties contained higher levels than the dessert apple and the peel was richer in phenolics than the flesh. The phenolic concentrations ranged between 230 and 4920 mg kg^?1 fresh weight in the flesh and between 546 and 6306 mg kg^?1 fresh weight in the peel. Fifteen compounds from five different phenolic groups, flavan‐3‐ols, flavonols, anthocyanins, hydroxycinnamates and dihydrochalcones, were detected. The major components in the flesh were 5‐O‐caffeoylquinic acid, procyanidin B2 and (?)‐epicatechin, while (?)‐epicatechin and quercetin glycosides predominated in the peel. Copyright © 2007 Society of Chemical Industry     

Flavonoid glycosides from cowpea seeds (Vigna sinensis K.) inhibit LDL oxidation

Six flavonoid glycosides were isolated from the n-butanol fraction of cowpea seeds (Vigna sinensis K.) through silica gel (SiO₂) and octadecyl silica gel (ODS) column chromatographies. Based on their chemical structures determined via interpretation of spectroscopic data including NMR, MS, and IR, the compounds were identified as kaempferol 3-O-β-d-sophoroside (1), quercetin 3-O-β-d-sophoroside (2), isoquercitrin (3), hyperin (4), catechin 7-O-β-d-glucopyranoside (5), and quercetin 3-O-β-Dglucopyranosyl( 1→6)-O-β-d-galactopyranoside (6). This is the first report of the isolation of these flavonoids from this plant. Among these flavonoids, compound 2, 5, and 6 significantly inhibited LDL oxidation exhibiting 96.0±0.1 (IC₅₀: 3.9 μM), 96.8±1.7 (IC₅₀: 2.9 μM), and 97.4±0.1% (IC₅₀: 3.5 μM) inhibition, respectively, at a concentration of 40 μM.     

Phenolic compounds,lycopene and antioxidant activity in commercial varieties of tomato (Lycopersicum esculentum)

Nine commercial varieties of tomato (Rambo, Senior, Ramillete, Liso, Pera, Canario, Durina, Daniella and Remate) produced in Spain were analysed for their lycopene content, content of phenolic compounds and antioxidant capacity. The phenolic compounds were characterised as flavonoids (quercetin, kaempferol and naringenin) and hydroxycinnamic acids (caffeic, chlorogenic, ferulic and p‐coumaric acids). Antioxidant activity was measured using the DPPH and ABTS assays. The concentrations of lycopene and the various phenolic compounds as well as the antioxidant activity were significantly influenced by the tomato variety. Quercetin, the most abundant flavonoid, was found in concentrations ranging between 7.19 and 43.59 mg kg^?1 fresh weight, while naringenin levels were lower than 12.55 mg kg^?1. The most abundant hydroxycinnamic acid was chlorogenic acid, with values ranging from 14 to 32 mg kg^?1 fresh weight, followed by caffeic acid, while p‐coumaric and ferulic acids showed similar concentrations lower than 5 mg kg^?1. The highest content of lycopene was found in Ramillete, Pera and Durina (>50 mg kg^?1 fresh weight), while the concentration in the other varieties was between 50 and 30 mg kg^?1, with the exception of Liso (less than 20 mg kg^?1). The antioxidant activity of tomato extracts varied with the tomato variety and the assay method used. Individual compounds found to be significantly related to antioxidant capacity were lycopene and ferulic and caffeic acids, but not quercetin and chlorogenic acid. © 2002 Society of Chemical Industry     

Effects of cultivar,lifting time and nitrogen fertiliser level on quercetin content in onion (Allium cepa L.) at lifting

Commercial cultivars of onion (Allium cepa L.) were grown at Torslunda research station, Sweden with different levels of nitrogen fertiliser and lifted at different growth stages. Soon after lifting, before any drying or curing, tissue from the fleshy edible part of onions was extracted in ethanol and the raw extracts were analysed by high‐performance liquid chromatography without any previous hydrolysis. It was confirmed that the main flavonoid compounds were quercetin monoglucoside and quercetin diglucoside, whereas only trace amounts of quercetin aglycone and other flavonoids were found. The greatest variation in quercetin content, in the range 100–500 mg kg^?1 fresh weight, occurred between years. The concentration of quercetin glucosides in the onions was strongly correlated (R² = 0.98) with the total amount of global radiation in August. Individual onions with fallen leaves had significantly higher concentrations of quercetin glucosides than individuals in the same row with erect leaves. Only minor differences were found between the three cultivars analysed. Higher levels of nitrogen fertiliser had only minor effects on onion yield and size and resulted in lower or equal amounts of quercetin glucosides. Nitrogen leakage from the soil, a potential source of environmental problems, could therefore be minimised by avoiding high nitrogen fertiliser levels with almost no effect on onion flavonol content. Late lifting of onions (80% fallen leaves) resulted in up to 45% higher concentrations of quercetin glucosides compared with early lifting (50% fallen leaves). Copyright © 2006 Society of Chemical Industry     

Chemical and antioxidative assessment of dietary turnip (Brassica rapa var. rapa L.)

The phenolic compounds and organic acids of turnip (Brassica rapa var. rapa L.) edible parts (leaves and stems, flower buds and roots) were determined by HPLC–DAD and HPLC–UV, respectively. The results revealed a profile composed of 14 phenolics (3-p-coumaroylquinic, caffeic, ferulic and sinapic acids, kaempferol 3-O-sophoroside-7-O-glucoside, kaempferol 3-O-sophoroside-7-O-sophoroside, kaempferol 3-O-(feruloyl/caffeoyl)-sophoroside-7-O-glucoside, kaempferol 3,7-O-diglucoside, isorhamnetin 3,7-O-diglucoside, kaempferol 3-O-sophoroside, 1,2-disinapoylgentiobiose, 1,2′-disinapoyl-2-feruloylgentiobiose, kaempferol 3-O-glucoside and isorhamnetin 3-O-glucoside) and six organic acids (aconitic, citric, ketoglutaric, malic, shikimic and fumaric acids). The quantification of the identified compounds showed kaempferol 3-O-sophoroside-7-O-glucoside, kaempferol 3-O-(feruloyl/caffeoyl)-sophoroside-7-O-glucoside, isorhamnetin 3,7-O-diglucoside and isorhamnetin 3-O-glucoside as the main phenolics, and malic acid as the organic acid present in highest amounts. A screening of the antioxidative potential was also performed by means of the DPPH radical scavenging assay. Turnip flower buds exhibited the strongest antioxidant capacity.     

Effect of industrial processing on chlorophyll content of broccoli

Chlorophylls a and b and pheophytins a and b were quantitaty determined in raw, frozen (after blanching for 60, 120 or 150 s) and canned florets and stems of broccoli. The chlorophyll a and b contents were 0.11 and 0.043 g kg⁻¹ fresh weight respectively in raw florets and 0.036 and 0.018 g kg⁻¹ respectively in stems. About 37.8% and 61.1% losses were incurred during the freezing process in florets and stems respectively, and 98.5% after canning as a consequence of industrial processing. After different blanching times the losses of chlorophyll a in frozen florets varied between 17.7 and 66.4%, while the losses of chlorophyll b varied between 23.2 and 48.8%. In the losses ranged from 55.5 to 75% and from 50 to 88.9% for chlorophylls a and b respectively. These losses resulted in an increase in pheophytin a and b levels in both florets and stems. © 2000 Society of Chemical Industry     

Antioxidative and anti-inflammatory effect of quercetin and its glycosides isolated from mampat (Cratoxylum formosum)

In this study, quercetin, quercetin-3-O-β-d-glucopyranoside (isoquercitrin), quercetin-3-O-β-d-galactopyranoside (hyperin), and quercertin-3-O-α-l-rhamnoside (quercitrin) from mampat (Cratoxylum formosum) were isolated and their antioxidative and anti-inflammatory activities were investigated. Quercetin displayed weaker antioxidant activity than its glycosides, while the cellular antioxidant capacity of quercetin and hyperin was stronger than that of isoquercitrin and quercitrin, indicating that the higher cell-membrane permeability of quercetin and hyperin than isoquercitrin and quercitrin was due to the different hydrophobicity and the specific membrane receptor for galactose. The anti-inflammatory activity of quercetin was shown to be higher to its glycosides in nitric oxide (NO) production, inducible nitric oxide synthase (iNOS) expression, and nuclear factor (NF)-κB activation, suggesting that quercetin inhibits NO production in LPS-stimulated RAW 264.7 cells via control of iNOS expression with attenuation of NF-κB activation. The data obtained in this study illustrates that the presence and kind of monosaccharide in quercetin glycosides may play a critical role in their cellular antioxidant and anti-inflammatory activities.     

The effect of temperature and radiation on flavonol aglycones and flavonol glycosides of kale (Brassica oleracea var. sabellica)

The winter crop kale has a complex profile of different glycosylated and acylated flavonol glycosides which may be affected by global warming. To the best of our knowledge, compound–climate relationships for flavonol aglycones and flavonol glycosides were established for the first time. The investigated 10 major flavonol glycosides responded structure-dependent in the investigated temperature range between 0 and 12 °C and the photosynthetic active radiation range between 4 and 20 mol m⁻² d⁻¹, e.g. the decrease in temperature led to an increase in sinapic acid monoacylated and diacylated quercetin glycosides, while the sinapic acid monoacylated kaempferol glycosides showed a maximum at 4.5 °C. Furthermore, the hydroxycinnamic acid residues and the different number of glucose moieties in the 7-O position affected the response of kaempferol triglucosides. Consequently, global warming would result in lower concentrations of antioxidant-relevant quercetin glycosides in winter crops, suggesting a production at e.g. higher altitudes due to lower temperature.     

Antioxidative properties and flavonoid composition of Chenopodium quinoa seeds cultivated in Japan

To evaluate the nutritional advantages of quinoa seeds (Chenopodium quinoa Willd.) cultivated in Japan, antioxidative properties and flavonoid composition were determined and compared to corresponding data for conventionally-used cereals and pseudo-cereals, including quinoa seeds from South America. The antioxidant activities of these grains against DPPH radicals were strongly associated with the total phenolic content of the tested samples. The crude extracts of quinoa seeds cultivated in Japan exhibited higher antioxidative effects than those from South America and other cereals, excluding buckwheat. Four flavonol glycosides were isolated and identified from the Japanese quinoa seeds, and the chemical composition of the flavonoids – quercetin and kaempferol 3-O-(2″,6″-di-O-α-rhamnopyranosyl)-β-galactopyranosides (1 and 4), quercetin 3-O-(2″,6″-di-O-α-rhamnopyranosyl)-β-glucopyranoside (2), and quercetin 3-O-(2″-O-β-apiofuranosyl-6″-O-α-rhamnopyranosyl)-β-galactopyranoside (3) – was evaluated through quantitative determination. Trioside 2 was isolated for the first time from quinoa seeds. These glycosides were not detected in extracts from any of the tested grains except quinoa. The aglycone quercetin content of the Japanese quinoa seeds is higher than in the seeds from South America and buckwheat. The amounts of quercetin and kaempferol formed via acidic hydrolysis in quinoa are much higher than those of conventionally-used edible plants. The quinoa seeds cultivated in Japan are the most effective functional foodstuff – in terms of being a source of antioxidative and bioactive flavonoids – among cereals and pseudo-cereals.     

Developmental changes in the concentration and composition of flavonoids in skin of a red and a green apple cultivar

Flavonoids from the skin of Granny Smith, a green apple cultivar, and Splendour, a red apple cultivar, were quantified by high-performance liquid chromatography for two seasons (1989–1990 and 1990–1991). Both cultivars contained a similar composition and concentration of quercetin glycosides and proanthocyanidins. Splendour also synthesised cyanidin glycosides during ripening. Quercetin glycosides and proanthocyanidins were highest in the skin of very young fruit of Granny Smith and decreased by 50% during fruit development. In Splendour, concentrations of quercetin glycosides and proanthocyanidins in the skin decreased by 50% from early to mid-season but then increased during ripening. Cyanidin glycosides in Splendour increased to about 1 mg g^-1 fresh weight during ripening. There were significant differences between the two cultivars but not between years. Total amount of flavonoids increased throughout the season as fruit surface area increased. For Granny Smith there was an estimated net synthesis per apple of 0.16 mg day^-1 quercetin glycosides, 0.1 mg day^-1 proanthocyanidins and for Splendour a net synthesis per apple of 0.28 mg day^-1 quercetin glycosides, 0.21 mg day^-1 proanthocyanidins and during ripening 0.21 mg day^-1 cyanidin glycosides. Relative proportions of major quercetin glycosides and proanthocyanidins were stable during fruit development. For Splendour, however, cyanidin glycoside synthesis was accompanied by a corresponding increase in quercetin glycoside and proanthocyanidin synthesis. The data suggest a coordinate regulation of enzymes in the flavonoid biosynthetic pathway during fruit development.     

Selenium increases chlorogenic acid,chlorophyll and carotenoids of Lycium chinense leaves

BACKGROUND: Leaves of Lycium chinense L. are widely used in traditional Chinese medicine and as functional food in China and south‐east Asia. Polyphenols are important active compounds in leaves of L. chinense L, but their compositions are still not very clear. Selenium has been reported to increase some components of plants. In this study, the composition of polyphenols of L. chinense leaves were analysed, and the effects of selenium on the polyphenols and other components were studied. RESULTS: The main polyphenols were identified as rutin, chlorogenic acid, quercetin, kaempferol and apigenin‐7‐O‐(6′‐O‐acetyl) glucose‐rhamnose. Chlorogenic acid showed the highest average content of 78.36 g kg^?1. Rutin, quercetin and kaempferol were determined at low contents from 3.85 g kg^?1 to 7.08 g kg^?1. Correlation coefficients between selenium and chlorogenic acid, chlorophyll a, chlorophyll b and carotenoids were: R² = 0.963 (P = 0.002), 0.943 (P = 0.005), 0.957 (P = 0.003) and 0.943 (P = 0.005), respectively. Selenium (0.01–0.05 g kg^?1) significantly increased chlorogenic acid, chlorophyll and carotenoids by 200–400% and reduced rutin by 400–900%. CONCLUSION: L. chinense can be an alternative source of chlorogenic acid. Selenium significantly increased chlorogenic acid, chlorophyll a, chlorophyll b and carotenoids, hence increasing the medicinal value of L. chinense leaves. Rutin, quercetin, kaempferol and apigenin‐7‐O‐(6′‐O‐acetyl) glucose‐rhamnose proved to be not significantly influenced by selenium. Copyright © 2012 Society of Chemical Industry     

Study of flavonoids in aqueous spinach extract using positive electrospray ionisation tandem quadrupole mass spectrometry

The presence of three flavonols (quercetin, kaempferol, myricetin) and two flavones (apigenin, luteolin) were investigated in the extract of fresh spinach leaves. Aqueous spinach extracts were prepared with a leaf/water ratio of 1:2 at 80 °C for 30 min stirring. Ferric ammonium sulphate method was used for measuring total polyphenols in the extracts and expressed as catechins and tannic acid equivalents. The flavonoids glycosides in the extract were hydrolysed to their aglycons with 1.2 M HCl in boiling 50% water methanol solution. The resulting aglycons were identified and quantified by a C18 reverse phase high-performance liquid chromatography (RP-HPLC). Furthermore, the results were confirmed by HPLC coupled to an electrospray ionisation tandem triple-quadrupole mass spectrometer ESI-MS performing low-energy collision induced dissociation (CID-MS/MS) in the collision cell (HPLC-ESI-MS/MS). Analyses were made in the multiple reaction monitory (MRM) mode. Results showed that total polyphenols contents in fresh spinach leaves were 270 mg kg⁻¹ and 390 mg kg⁻¹ as tannic acid and catechin equivalents, respectively, in which, major flavonoids aglycons were apigenin (170 mg kg⁻¹), quercetin (50 mg kg⁻¹) and kaempferol (30 mg kg⁻¹).     

Chemical,rheological and sensory characteristics of sweet spreads made from by-products of soya bean and maize

Sweet maize cob (SMC) and black soya bean seed coat (BSC) were used to prepare a sweet spread. Chemical composition of the prepared spread and its rheological and sensory characteristics were investigated. The results were compared with those of commercial plum and raspberry jams and spreads. Spreads made from SMC and BSC had the highest content of proteins, total fibres, hemicellulose and cellulose. In relation to fruit jams, they are distinguished by the presence and content of p-coumaric, ferulic and 3,4-dihydroxybenzoic acids, as well as of flavonoids such as catechin and quercetin. SMC spread with 3.2% of BSC had the highest content of total anthocyanins (666.75 mg CGE kg⁻¹) (cyanidin 3-glucoside equivalent). Cyanidin-3-glucoside (Cy-3-Glu) was the most abundant anthocyanins in SMC/BSC containing spreads, while in raspberry jam, that was cyanidin-3-sophoroside (Cy-3-Sop). According to chemical, rheological and sensory properties, SMC/BSC containing spreads could be competitive with fruit jams and spreads.     

Isolation and identification of compounds from the ethanolic extract of flowers of the tea (Camellia sinensis) plant and their contribution to the antioxidant capacity

While beneficial health properties of tea leaves have been extensively studied, less attention has been given to that of flowers of the tea (Camellia sinensis) plant. In this work, the ethanolic extract and its ethyl acetate-soluble fraction (EEA) from the tea flowers were found to possess the potent antioxidant activity using 2, 2-diphenyl-1-picrylhydrazyl (DPPH) free radical-scavenging assay. The compounds present in EEA had comparatively strong DPPH scavenging activity and strongly contributed to the antioxidant activity of the tea flowers. From EEA, besides eight catechins, five flavonol glycosides were isolated and their structures were elucidated on the basis of mass spectrometry and nuclear magnetic resonance spectroscopy as myricetin 3-O-β-d-galactopyranoside, quercetin 3-O-β-d-galactopyranoside, kaempferol 3-O-β-d-galactopyranoside, kaempferol 3-O-β-d-glucopyranoside, and kaempferol 3-O-[α-l-rhamnopyranosyl-(1-6)-β-d-glucopyranoside]. In addition, epigallocatechin gallate and epicatechin gallate were found as the major active components responsible for the antioxidant activity of tea flowers through the use of a combination of preparative liquid chromatography separation and DPPH assay.     

The Nutritive Value of Mango Seed Kernels for Starting Chicks

Raw mango ( Mangifera indica L) seed kernels were found to contain tannins (56·5 g kg⁻¹ DM), cyanogenic glucosides (64 mg kg⁻¹ DM), oxalates (42 mg kg⁻¹ DM) and trypsin inhibitory activity (20 TIU g⁻¹ DM). The contents of these anti-nutritive factors were lowered by both soaking and boiling treatments, but boiling was more effective. The in vitro protein digestibility (26·3%) and apparent metabolisable energy (7·88 MJ kg⁻¹ DM) values of raw kernels were low, and these parameters were improved by soaking and boiling. The observed improvements paralleled reductions in tannin contents, indicating that tannins are largely responsible for the poor nutritive value of raw kernels. In experiment 1, diets containing 0, 50, 100, 150 and 200 g kg⁻¹ raw mango seed kernels that replaced maize were fed to 7-day-old White Leghorn cockerels for 14 days. Inclusion of more than 50 g kg⁻¹ raw kernels lowered ( P< 0·05) the weight gains, feed intake and feed efficiency of chicks. High level inclusion of raw kernels had toxic effects, as evidenced by increased mortality. In experiment 2, soaking and boiling treatments improved ( P< 0·05) feed intake of chicks fed on diets containing 100 g kg⁻¹ kernels and reduced mortality. Feed/gain was unaffected by processing. Soaking had no effect, whereas boiling of kernels improved the weight gains. However, weight gains of chicks receiving diets containing 100 g kg⁻¹ boiled kernels were numerically, though non-significantly, lower than those of the maize-control group. It is concluded that raw mango seed kernels are unsuitable as a feed ingredient in chick diets and, that soaking and boiling do not completely overcome the anti-nutritive effects of raw kernels.