2006•ACS symposium seriesRequires access

Citrus sp.: A Source of Flavonoids of Pharmaceutical Interest

Ana M. Ortuño, Pedro Gómez, Ana González Báidez, Victor Frías, José Antonio del Rı́o

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Abstract

Flavonoids in Citrus sp. are a widely distributed group of polyphenolic compounds characterized by a common benzo-γ-pyrone structure. Flavonoids are present in a large variety of edible plants, especially in Citrus species. All flavonoids described in Citrus sp. to date can be classified into four clearly differentiated groups: flavones, flavonols, flavanones and their corresponding glycosides with these two possible types of of glycoside substitution: β-neohesperidosides (2-O-α-L-rhamnopyranosyl-β-D-glucopyranose) or β-rutinoside (6-O-α-L-rhatrmopyranosyl-β-D-glucopyranose) ( 1 ). Depending on the particular citrus species, the biosynthetic pathways result in the synthesis of: naringin, the 7-β-neohesperidoside of naringenin (4′,5,7-trihydroxyflavone), which is the major flavonoid in Citrus paradisi; neohesperidin, the 7-β-neohesperidoside of hesperetin (3′,5,7-trihydroxy-4′-methoxy flavanone), which is the principal flavonoid in Citrus aurantium; or hesperidin, the 7-β-rutinoside of hesperetin, which is the principal flavonoid in Citrus sinensis and Citrus limon (Figure 1). The flavanone glycosides are accumulated in the greatest quantity, although the concentration of these

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Flavonoids in Citrus sp. are a widely distributed group of polyphenolic compounds characterized by a common benzo-γ-pyrone structure. Flavonoids are present in a large variety of edible plants, especially in Citrus species. All flavonoids described in Citrus sp. to date can be classified into four clearly differentiated groups: flavones, flavonols, flavanones and their corresponding glycosides with these two possible types of of glycoside substitution: β-neohesperidosides (2-O-α-L-rhamnopyranosyl-β-D-glucopyranose) or β-rutinoside (6-O-α-L-rhatrmopyranosyl-β-D-glucopyranose) ( 1 ). Depending on the particular citrus species, the biosynthetic pathways result in the synthesis of: naringin, the 7-β-neohesperidoside of naringenin (4′,5,7-trihydroxyflavone), which is the major flavonoid in Citrus paradisi; neohesperidin, the 7-β-neohesperidoside of hesperetin (3′,5,7-trihydroxy-4′-methoxy flavanone), which is the principal flavonoid in Citrus aurantium; or hesperidin, the 7-β-rutinoside of hesperetin, which is the principal flavonoid in Citrus sinensis and Citrus limon (Figure 1). The flavanone glycosides are accumulated in the greatest quantity, although the concentration of these

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Available abstract

Flavonoids in Citrus sp. are a widely distributed group of polyphenolic compounds characterized by a common benzo-γ-pyrone structure. Flavonoids are present in a large variety of edible plants, especially in Citrus species. All flavonoids described in Citrus sp. to date can be classified into four clearly differentiated groups: flavones, flavonols, flavanones and their corresponding glycosides with these two possible types of of glycoside substitution: β-neohesperidosides (2-O-α-L-rhamnopyranosyl-β-D-glucopyranose) or β-rutinoside (6-O-α-L-rhatrmopyranosyl-β-D-glucopyranose) ( 1 ). Depending on the particular citrus species, the biosynthetic pathways result in the synthesis of: naringin, the 7-β-neohesperidoside of naringenin (4′,5,7-trihydroxyflavone), which is the major flavonoid in Citrus paradisi; neohesperidin, the 7-β-neohesperidoside of hesperetin (3′,5,7-trihydroxy-4′-methoxy flavanone), which is the principal flavonoid in Citrus aurantium; or hesperidin, the 7-β-rutinoside of hesperetin, which is the principal flavonoid in Citrus sinensis and Citrus limon (Figure 1). The flavanone glycosides are accumulated in the greatest quantity, although the concentration of these

Key concepts: Flavanone, Naringin, Hesperetin, Hesperidin, Naringenin, Chemistry, Flavonoid, Citrus paradisi

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