PhytoHub: Showing entry for Red raspberry

Red raspberry

Group:: Fruit, Berries

Identification

Name: Red raspberry
Food group: Fruit, Berries

External Links

ITIS: 24947

Compounds

Name	Structure	Monoisotopic mass	Formula	Family	Class
Ellagic acid	OC1=C(O)C2=C3C(=C1)C(=O)OC1=C3C(=CC(O)=C1O)C(=O)O2	302.006267153	C₁₄H₆O₈	Polyphenols	Phenolic acids	Publications	Show
Malvidin-3-O-glucoside	COC1=CC(=CC(OC)=C1O)C1=[O+]C2=C(C=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(O)=CC(O)=C2	493.134601264	C₂₃H₂₅O₁₂	Polyphenols	Flavonoids	Publications	Show
Delphinidin	OC1=CC(O)=C2C=C(O)C(=[O+]C2=C1)C1=CC(O)=C(O)C(O)=C1	303.050477706	C₁₅H₁₁O₇	Polyphenols	Flavonoids	Publications	Show
Ferulic acid	COC1=C(O)C=CC(\C=C\C(O)=O)=C1	194.057908808	C₁₀H₁₀O₄	Polyphenols	Phenolic acids	Publications	Show
4-Hydroxybenzoic acid 4-O-glucoside	OCC1OC(OC2=CC=C(C=C2)C(O)=O)C(O)C(O)C1O	300.084517475	C₁₃H₁₆O₈	Polyphenols	Phenolic acids	Publications	Show
Sanguiin H-6	OC1=CC(=CC(O)=C1O)C(=O)OC1OC2COC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(C(OC4=CC(=CC(O)=C4O)C(=O)OC4OC5COC(=O)C6=C(C(O)=C(O)C(O)=C6)C6=C(C=C(O)C(O)=C6O)C(=O)OC5C5OC(=O)C6=CC(O)=C(O)C(O)=C6C6=C(O)C(O)=C(O)C=C6C(=O)OC45)=C(O)C(O)=C3O)C(=O)OC2C2OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC12	1870.158112072	C₈₂H₅₄O₅₂	Polyphenols	Ellagitannins	Publications	Show
Lambertianin C	OC1=CC(=CC(O)=C1O)C(=O)OC1OC2COC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(O)C(O)=C(O)C(OC4=CC(=CC(O)=C4O)C(=O)OC4OC5COC(=O)C6=C(C(O)=C(O)C(O)=C6)C6=C(O)C(O)=C(O)C(OC7=CC(=CC(O)=C7O)C(=O)OC7OC8COC(=O)C9=C(C(O)=C(O)C(O)=C9)C9=C(O)C(O)=C(O)C=C9C(=O)OC8C8OC(=O)C9=CC(O)=C(O)C(O)=C9C9=C(O)C(O)=C(O)C=C9C(=O)OC78)=C6C(=O)OC5C5OC(=O)C6=CC(O)=C(O)C(O)=C6C6=C(O)C(O)=C(O)C=C6C(=O)OC45)=C3C(=O)OC2C2OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC12	2804.229342936	C₁₂₃H₈₀O₇₈	Polyphenols	Ellagitannins	Publications	Show
Sanguiin H-10	OC1C(O)C2OC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(C=C(O)C(O)=C3O)C(=O)OCC2OC1OC(=O)C1=CC(OC2=C(O)C(O)=C(O)C3=C2C(=O)OC2C(COC(=O)C4=C3C(O)=C(O)C(O)=C4)OC(OC(=O)C3=CC(O)=C(O)C(O)=C3)C3OC(=O)C4=C(C(O)=C(O)C(O)=C4)C4=C(O)C(O)=C(O)C=C4C(=O)OC23)=C(O)C(O)=C1	1568.151844904	C₆₈H₄₈O₄₄	Polyphenols	Ellagitannins	Publications	Show
Potentillin	OC1=CC(=CC(O)=C1O)C(=O)OC1OC2COC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(O)C(O)=C(O)C=C3C(=O)OC2C2OC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(O)C(O)=C(O)C=C3C(=O)OC12	936.086881068	C₄₁H₂₈O₂₆	Polyphenols	Ellagitannins	Publications	Show
Pedunculagin	CC1OC2COC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(O)C(O)=C(O)C=C3C(=O)OC2C2OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC12	782.096657857	C₃₅H₂₆O₂₁	Polyphenols	Ellagitannins	Publications	Show

Related Metabolites

Name	Structure	Monoisotopic mass	Formula	Family	Class
3-(3'-Hydroxyphenyl)propionic acid	OC(=O)CCC1=CC=CC(O)=C1	166.062994186	C₉H₁₀O₃	Polyphenols	Phenolic acids	Show
3-Hydroxybenzoic acid	OC(=O)C1=CC(O)=CC=C1	138.031694053	C₇H₆O₃	Polyphenols	Phenolic acids	Show
3-Phenylpropionic acid	OC(=O)CCC1=CC=CC=C1	150.068079564	C₉H₁₀O₂	Polyphenols	Phenolic acids	Show
3,4-Dimethoxybenzoic acid	COC1=C(OC)C=C(C=C1)C(O)=O	182.057908808	C₉H₁₀O₄	Polyphenols	Phenolic acids	Show
3',4'-Dihydroxyphenylacetic acid	OC(=O)CC1=CC(O)=C(O)C=C1	168.042258744	C₈H₈O₄	Polyphenols	Phenolic acids	Show
4-Hydroxybenzoic acid	OC(=O)C1=CC=C(O)C=C1	138.031694053	C₇H₆O₃	Polyphenols	Phenolic acids	Show
Dihydro-p-coumaric acid	OC(=O)CCC1=CC=C(O)C=C1	166.062994186	C₉H₁₀O₃	Polyphenols	Phenolic acids	Show
Dihydrocaffeic acid	OC(=O)CCC1=CC=C(O)C(O)=C1	182.057908808	C₉H₁₀O₄	Polyphenols	Phenolic acids	Show
Dihydroferulic acid	COC1=C(O)C=CC(CCC(O)=O)=C1	196.073558872	C₁₀H₁₂O₄	Polyphenols	Phenolic acids	Show
Ellagic acid	OC1=C(O)C2=C3C(=C1)C(=O)OC1=C3C(=CC(O)=C1O)C(=O)O2	302.006267153	C₁₄H₆O₈	Polyphenols	Phenolic acids	Show
Ellagic acid	OC1=C(O)C2=C3C(=C1)C(=O)OC1=C3C(=CC(O)=C1O)C(=O)O2	302.006267153	C₁₄H₆O₈	Polyphenols	Phenolic acids	Show
Ferulic acid sulfoglucuronide		450.375513	C₁₆H₁₈O₁₃S	Polyphenols	Phenolic acids	Show
Ferulic acid-4'-O-glucuronide	[H]\C(=C(\[H])C1=CC(OC)=C(O[C@H]2O[C@H]([C@H](O)[C@H](O)[C@@H]2O)C(O)=O)C=C1)C(O)=O	370.08999678	C₁₆H₁₈O₁₀	Polyphenols	Phenolic acids	Show
Ferulic acid-4'-sulfate	[H]\C(=C(\[H])C1=CC(OC)=C(OS(O)(=O)=O)C=C1)C(O)=O	274.014723364	C₁₀H₁₀O₇S	Polyphenols	Phenolic acids	Show
Feruloylglycine	COC1=CC(\C=C\C(=O)NCC(O)=O)=CC=C1O	251.079372531	C₁₂H₁₃NO₅	Polyphenols	Phenolic acids	Show
Hippuric acid	OC(=O)CNC(=O)C1=CC=CC=C1	179.058243159	C₉H₉NO₃	Polyphenols	Polyphenol metabolites	Show
Malvidin	COC1=CC(=CC(OC)=C1O)C1=[O+]C2=C(C=C1O)C(O)=CC(O)=C2	331.081777834	C₁₇H₁₅O₇	Polyphenols	Flavonoids	Show
Protocatechuic acid	OC(=O)C1=CC(O)=C(O)C=C1	154.026608673	C₇H₆O₄	Polyphenols	Phenolic acids	Show
Syringic acid	COC1=CC(=CC(OC)=C1O)C(O)=O	198.052823422	C₉H₁₀O₅	Polyphenols	Phenolic acids	Show
Syringic acid-4-O-glucuronide	COC1=CC(=CC(OC)=C1O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C(O)=O	374.0849114	C₁₅H₁₈O₁₁	Polyphenols	Phenolic acids	Show
Urolithin A	OC1=CC2=C(C=C1)C1=C(C=C(O)C=C1)C(=O)O2	228.042258744	C₁₃H₈O₄	Polyphenols	Polyphenol metabolites	Show
Urolithin A-3-glucuronide	OC1C(O)C(OC2=CC=C3C(OC(=O)C4=CC(O)=CC=C34)=C2)OC(C1O)C(O)=O	404.074346732	C₁₉H₁₆O₁₀	Polyphenols	Polyphenol metabolites	Show
Urolithin A-8-O-glucuronide	O[C@H]1[C@H](O)[C@@H](OC2=CC=C3C(OC(=O)C4=C3C=CC(O)=C4)=C2)O[C@H]([C@@H]1O)C(O)=O	404.074346732	C₁₉H₁₆O₁₀	Polyphenols	Polyphenol metabolites	Show
Urolithin B	OC1=CC2=C(C=C1)C1=C(C=CC=C1)C(=O)O2	212.047344122	C₁₃H₈O₃	Polyphenols	Polyphenol metabolites	Show
Urolithin B-3-glucuronide	O[C@@H]1[C@@H](O)[C@H](OC2=CC3=C(C=C2)C2=C(C=CC=C2)C(=O)O3)O[C@@H]([C@H]1O)C(O)=O	388.07943211	C₁₉H₁₆O₉	Polyphenols	Polyphenol metabolites	Show
Urolithin C	OC1=CC2=C(C=C1)C1=C(C=C(O)C(O)=C1)C(=O)O2	244.037173366	C₁₃H₈O₅	Polyphenols	Polyphenol metabolites	Show
Urolithin C-3-glucuronide	OC1C(O)C(OC2=CC3=C(C=C2)C2=CC(O)=C(O)C=C2C(=O)O3)OC(C1O)C(O)=O	420.069261335	C₁₉H₁₆O₁₁	Polyphenols	Polyphenol metabolites	Show
Urolithin D	OC1=CC2=C(C=C1O)C1=CC=C(O)C(O)=C1OC2=O	260.032087988	C₁₃H₈O₆	Polyphenols	Polyphenol metabolites	Show
Vanillic acid	COC1=C(O)C=CC(=C1)C(O)=O	168.042258738	C₈H₈O₄	Polyphenols	Phenolic acids	Show
Vanilloylglycine	COC1=C(O)C=CC(=C1)C(O)=NCC(O)=O	225.063722467	C₁₀H₁₁NO₅	Polyphenols	Phenolic acids	Show

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