PhytoHub: Showing entry for Red raspberry

Red raspberry

Group:: Fruit, Berries

Identification

Name: Red raspberry
ID: 256
Food group: Fruit, Berries

Synonyms

No Synonyms

External Links

ITIS: 24947

Compounds

Name	Structure	Monoisotopic mass	Formula	Family	Class
Ellagic acid	OC1=CC2=C3C(OC(=O)C4=CC(O)=C(O)C(OC2=O)=C34)=C1O	302.006267153	C₁₄H₆O₈	Polyphenols	Phenolic acids	Publications	Show
Malvidin-3-O-glucoside	COC1=CC(=CC(OC)=C1O)C1=[O+]C2=CC(O)=CC(O)=C2C=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	493.134052665	C₂₃H₂₅O₁₂	Polyphenols	Flavonoids	Publications	Show
Delphinidin	OC1=CC(O)=C2C=C(O)C(=[O+]C2=C1)C1=CC(O)=C(O)C(O)=C1	303.049929114	C₁₅H₁₁O₇	Polyphenols	Flavonoids	Publications	Show
Ferulic acid	COC1=C(O)C=CC(\C=C\C(O)=O)=C1	194.057908802	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	1870.158111979	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	1568.151844826	C₆₈H₄₈O₄₄	Polyphenols	Ellagitannins	Publications	Show
Potentillin	OC1=CC(=CC(O)=C1O)C(=O)OC1OC2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=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	936.086881022	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
Cyanidin 3-O-sophoroside	OC[C@H]1O[C@@H](O[C@H]2[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC(O)=C(O)C=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	611.160661338	C₂₇H₃₁O₁₆	Polyphenols	Flavonoids	Publications	Show
Cyanidin 3-O-glucoside	OC[C@@H]1O[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC(O)=C(O)C=C2)[C@@H](O)[C@H](O)[C@H]1O	449.107837916	C₂₁H₂₁O₁₁	Polyphenols	Flavonoids	Publications	Show
Cyanidin 3-O-glucosyl-rutinoside	CC1OC(OCC2OC(OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)C(OC3OC(CO)C(O)C(O)C3O)C(O)C2O)C(O)C(O)C1O	757.21857014	C₃₃H₄₁O₂₀	Polyphenols	Flavonoids	Publications	Show

Related Metabolites

Name	Structure	Monoisotopic mass	Formula	Family	Class
4-(1-Carboxy-3-hydroxyphenyl)beta-D-glucuronic acid	O[C@@H]1[C@@H](O)[C@@H](OC2=C(O)C=C(C=C2)C(O)=O)OC([C@H]1O)C(O)=O	330.058696651	C₁₃H₁₄O₁₀	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Cyanidin glucuronide		477.4019678	C₂₂H₂₁O₁₂	(Poly)phenol metabolites	Flavonoid metabolites	Show
Cyanidin 3-glucoside glucuronide		639.5444741	C₂₈H₃₁O₁₇	(Poly)phenol metabolites	Flavonoid metabolites	Show
4-Methoxybenzaldehyde	COC1=CC=C(C=O)C=C1	136.052429498	C₈H₈O₂	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Protocatechualdehyde	OC1=CC=C(C=O)C=C1O	138.031694053	C₇H₆O₃	(Poly)phenol metabolites	Phenolic acid metabolites	Show
2-Hydroxy-4-methoxybenzoic acid	COC1=CC(O)=C(C=C1)C(O)=O	168.042258738	C₈H₈O₄	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Peonidin 3-glucoside	COC1=C(O)C=CC(=C1)C1=[O+]C2=CC(O)=CC(O)=C2C=C1O[C@H]1O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1O	463.123487981	C₂₂H₂₃O₁₁	Polyphenols	Flavonoids	Show
4-(1-Carboxyphenyl)beta-D-glucuronic acid	O[C@@H]1[C@@H](O)[C@@H](OC2=CC=C(C=C2)C(O)=O)OC([C@H]1O)C(O)=O	314.063782031	C₁₃H₁₄O₉	(Poly)phenol metabolites	Phenolic acid metabolites	Show
p-Hydroxybenzoic acid	OC(=O)C1=CC=C(O)C=C1	138.031694053	C₇H₆O₃	Polyphenols	Phenolic acids	Show
Protocatechuic acid	OC(=O)C1=CC(O)=C(O)C=C1	154.026608673	C₇H₆O₄	Polyphenols	Phenolic acids	Show
Isopeonidin 3-glucoside	COC1=C(O)C=C(C=C1)C1=[O+]C2=CC(O)=CC(O)=C2C=C1O[C@H]1O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1O	463.123487981	C₂₂H₂₃O₁₁	(Poly)phenol metabolites	Flavonoid metabolites	Show
3-(1-Carboxy-4-hydroxyphenyl)beta-D-glucuronic acid	O[C@@H]1[C@@H](O)[C@@H](OC2=C(O)C=CC(=C2)C(O)=O)OC([C@H]1O)C(O)=O	330.058696651	C₁₃H₁₄O₁₀	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Hippuric acid	OC(=O)CNC(=O)C1=CC=CC=C1	179.058243154	C₉H₉NO₃	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Ferulic acid	COC1=C(O)C=CC(\C=C\C(O)=O)=C1	194.057908802	C₁₀H₁₀O₄	Polyphenols	Phenolic acids	Show
Caffeic acid	OC(=O)\C=C\C1=CC(O)=C(O)C=C1	180.042258738	C₉H₈O₄	Polyphenols	Phenolic acids	Show
4'-Hydroxyphenylacetic acid	OC(=O)CC1=CC=C(O)C=C1	152.047344118	C₈H₈O₃	Polyphenols	Phenolic acids	Show
p-Hydroxybenzaldehyde	OC1=CC=C(C=O)C=C1	122.036779433	C₇H₆O₂	Polyphenols	Phenolic acids	Show
3',4'-Dihydroxyphenylacetic acid	OC(=O)CC1=CC(O)=C(O)C=C1	168.042258738	C₈H₈O₄	Polyphenols	Phenolic acids	Show
Cyanidin 3-O-glucoside	OC[C@@H]1O[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC(O)=C(O)C=C2)[C@@H](O)[C@H](O)[C@H]1O	449.107837916	C₂₁H₂₁O₁₁	Polyphenols	Flavonoids	Show
Vanillic acid	COC1=CC(=CC=C1O)C(O)=O	168.042258738	C₈H₈O₄	Polyphenols	Phenolic acids	Show
Peonidin 3-glucoside glucuronide		653.5714628	C₂₉H₃₃O₁₇	(Poly)phenol metabolites	Flavonoid metabolites	Show
3-Hydroxybenzoic acid	OC(=O)C1=CC(O)=CC=C1	138.031694053	C₇H₆O₃	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Vanillic acid-4-O-sulfate	COC1=C(OS(O)(=O)=O)C=CC(=C1)C(O)=O	247.999073772	C₈H₈O₇S	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Vanillic acid 4-O-glucuronide	COC1=CC=C(C=C1OC1OC(C(O)C(O)C1O)C(O)=O)C(O)=O	344.074346715	C₁₄H₁₆O₁₀	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Protocatechuic acid-4-O-sulfate	OC(=O)C1=CC(O)=C(OS(O)(=O)=O)C=C1	233.983423707	C₇H₆O₇S	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Protocatechuic acid-4-O-glucuronide	OC1C(O)C(OC2=C(O)C=C(C=C2)C(O)=O)OC(C1O)C(O)=O	330.058696651	C₁₃H₁₄O₁₀	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Protocatechuic acid-3-O-sulfate	OC(=O)C1=CC(OS(O)(=O)=O)=C(O)C=C1	233.983423707	C₇H₆O₇S	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Protocatechuic acid-3-O-glucuronide	OC1C(O)C(OC2=C(O)C=CC(=C2)C(O)=O)OC(C1O)C(O)=O	330.058696651	C₁₃H₁₄O₁₀	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Phloroglucinaldehyde	OC1=CC(O)=C(C=O)C(O)=C1	154.026608673	C₇H₆O₄	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Peonidin glucuronide		491.4289566	C₂₃H₂₃O₁₂	(Poly)phenol metabolites	Flavonoid metabolites	Show
Methylvanillate	COC(=O)C1=CC(OC)=C(O)C=C1	182.057908802	C₉H₁₀O₄	(Poly)phenol metabolites	Miscellaneous polyphenol metabolites	Show
Methylcyanidin glucuronide		491.4289566	C₂₃H₂₃O₁₂	(Poly)phenol metabolites	Flavonoid metabolites	Show
Methylcyanidin 3-glucoside-glucuronide		653.5714628	C₂₉H₃₃O₁₇	(Poly)phenol metabolites	Flavonoid metabolites	Show
Methyl-3,4-dihydroxybenzoate	COC(=O)C1=CC=C(O)C(O)=C1	168.042258738	C₈H₈O₄	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Isovanillic acid-3-O-sulfate	COC1=C(OS(O)(=O)=O)C=C(C=C1)C(O)=O	247.999073772	C₈H₈O₇S	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Isovanillic acid-3-O-glucuronide	COC1=C(OC2OC(C(O)C(O)C2O)C(O)=O)C=C(C=C1)C(O)=O	344.074346715	C₁₄H₁₆O₁₀	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Isovanillic acid	COC1=CC=C(C=C1O)C(O)=O	168.042258738	C₈H₈O₄	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Isopeonidin glucuronide		491.4289566	C₂₃H₂₃O₁₂	(Poly)phenol metabolites	Flavonoid metabolites	Show
Cyanidin 3-O-glucosyl-rutinoside	CC1OC(OCC2OC(OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)C(OC3OC(CO)C(O)C(O)C3O)C(O)C2O)C(O)C(O)C1O	757.21857014	C₃₃H₄₁O₂₀	Polyphenols	Flavonoids	Show
Cyanidin 3-O-sophoroside	OC[C@H]1O[C@@H](O[C@H]2[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC(O)=C(O)C=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	611.160661338	C₂₇H₃₁O₁₆	Polyphenols	Flavonoids	Show
Delphinidin glucuronide			C₂₁H₁₉O₁₃	(Poly)phenol metabolites	Flavonoid metabolites	Show
Delphinidin	OC1=CC(O)=C2C=C(O)C(=[O+]C2=C1)C1=CC(O)=C(O)C(O)=C1	303.049929114	C₁₅H₁₁O₇	Polyphenols	Flavonoids	Show
Urolithin A	OC1=CC2=C(C=C1)C1=C(C=C(O)C=C1)C(=O)O2	228.042258738	C₁₃H₈O₄	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Ellagic acid	OC1=CC2=C3C(OC(=O)C4=CC(O)=C(O)C(OC2=O)=C34)=C1O	302.006267153	C₁₄H₆O₈	Polyphenols	Phenolic acids	Show
Isourolithin A-9-glucuronide			C₁₉H₁₆O₁₀	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin B-sulfate				(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin A-3-sulfate	OC1=CC2=C(C=C1)C1=C(OC2=O)C=C(OS(O)(=O)=O)C=C1	307.999073772	C₁₃H₈O₇S	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin M5	OC1=CC2=C(C(O)=C1O)C1=C(OC2=O)C(O)=C(O)C=C1	276.027002598	C₁₃H₈O₇	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin AR	OC1=CC2=C(C=C1)C1=C(OC2=O)C(O)=CC=C1	228.042258738	C₁₃H₈O₄	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin M7R	OC1=CC2=C(C(O)=C1)C1=C(OC2=O)C(O)=CC=C1	244.037173358	C₁₃H₈O₅	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin CR	OC1=CC2=C(C=C1O)C1=C(OC2=O)C(O)=CC=C1	244.037173358	C₁₃H₈O₅	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin M7	OC1=CC2=C(C=C1)C1=C(C=C(O)C=C1O)C(=O)O2	244.037173358	C₁₃H₈O₅	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin M6R	OC1=CC=CC2=C1OC(=O)C1=C2C(O)=C(O)C(O)=C1	260.032087978	C₁₃H₈O₆	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin M6	OC1=CC2=C(C=C1)C1=C(C=C(O)C(O)=C1O)C(=O)O2	260.032087978	C₁₃H₈O₆	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Isourolithin A-3-glucuronide	OC1C(O)C(OC2=CC3=C(C=C2)C2=C(C=CC(O)=C2)C(=O)O3)OC(C1O)C(O)=O	404.074346715	C₁₉H₁₆O₁₀	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Isourolithin A	OC1=CC2=C(C=C1)C1=C(C=CC(O)=C1)C(=O)O2	228.042258738	C₁₃H₈O₄	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin D glucuronide				(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin D	OC1=CC2=C(C=C1O)C1=CC=C(O)C(O)=C1OC2=O	260.032087978	C₁₃H₈O₆	(Poly)phenol metabolites	Ellagitannin 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	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin C	OC1=CC2=C(C=C1)C1=C(C=C(O)C(O)=C1)C(=O)O2	244.037173358	C₁₃H₈O₅	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin B-3-glucuronide	O[C@@H]1[C@@H](O)[C@H](OC2=CC3=C(C=C2)C2=CC=CC=C2C(=O)O3)O[C@@H]([C@H]1O)C(O)=O	388.079432095	C₁₉H₁₆O₉	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin B	OC1=CC2=C(C=C1)C1=C(C=CC=C1)C(=O)O2	212.047344118	C₁₃H₈O₃	(Poly)phenol metabolites	Ellagitannin 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	404.074346715	C₁₉H₁₆O₁₀	(Poly)phenol metabolites	Ellagitannin 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	404.074346715	C₁₉H₁₆O₁₀	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Hippuric acid	OC(=O)CNC(=O)C1=CC=CC=C1	179.058243154	C₉H₉NO₃	(Poly)phenol metabolites	Phenolic acid metabolites	Show
3-Hydroxybenzoic acid	OC(=O)C1=CC(O)=CC=C1	138.031694053	C₇H₆O₃	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Dihydroferulic acid	COC1=CC(CCC(O)=O)=CC=C1O	196.073558866	C₁₀H₁₂O₄	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Feruloylglycine	COC1=CC(\C=C\C(=O)NCC(O)=O)=CC=C1O	251.079372523	C₁₂H₁₃NO₅	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Vanilloyl-glycine	COC1=C(O)C=CC(=C1)C(O)=NCC(O)=O	225.063722458	C₁₀H₁₁NO₅	(Poly)phenol metabolites	Phenolic acid metabolites	Show
veratric acid	COC1=C(OC)C=C(C=C1)C(O)=O	182.057908802	C₉H₁₀O₄	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Sinapic acid-O-sulfate	COC1=CC(\C=C\C(=O)OS(O)(=O)=O)=CC(OC)=C1O	304.02528852	C₁₁H₁₂O₈S	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Dihydroferulic acid-4'-O-glucuronide	COC1=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=CC(CCC(O)=O)=C1	372.105646844	C₁₆H₂₀O₁₀	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Dihydroferulic acid-4'-sulfate	COC1=C(OS(O)(=O)=O)C=CC(CCC(O)=O)=C1	276.0303739	C₁₀H₁₂O₇S	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Dihydrocaffeic acid-3-sulfate	OC(=O)CCC1=CC(OS(O)(=O)=O)=C(O)C=C1	262.014723836	C₉H₁₀O₇S	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Ferulic acid glucuronide				(Poly)phenol metabolites	Phenolic acid metabolites	Show
Ferulic acid sulfoglucuronide		450.375513	C₁₆H₁₈O₁₃S	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Ferulic acid-4'-sulfate	COC1=C(OS(O)(=O)=O)C=CC(\C=C\C(O)=O)=C1	274.014723836	C₁₀H₁₀O₇S	(Poly)phenol metabolites	Phenolic acid metabolites	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	(Poly)phenol metabolites	Phenolic acid metabolites	Show
p-Hydroxybenzoic acid	OC(=O)C1=CC=C(O)C=C1	138.031694053	C₇H₆O₃	Polyphenols	Phenolic acids	Show
3-Phenylpropionic acid	OC(=O)CCC1=CC=CC=C1	150.068079562	C₉H₁₀O₂	(Poly)phenol metabolites	Phenolic acid metabolites	Show
3-(3'-Hydroxyphenyl)propionic acid	OC(=O)CCC1=CC(O)=CC=C1	166.062994182	C₉H₁₀O₃	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Ferulic acid	COC1=C(O)C=CC(\C=C\C(O)=O)=C1	194.057908802	C₁₀H₁₀O₄	Polyphenols	Phenolic acids	Show
Phloretic acid	OC(=O)CCC1=CC=C(O)C=C1	166.062994182	C₉H₁₀O₃	Polyphenols	Phenolic acids	Show
Dihydrocaffeic acid	OC(=O)CCC1=CC(O)=C(O)C=C1	182.057908802	C₉H₁₀O₄	Polyphenols	Phenolic acids	Show
3',4'-Dihydroxyphenylacetic acid	OC(=O)CC1=CC(O)=C(O)C=C1	168.042258738	C₈H₈O₄	Polyphenols	Phenolic acids	Show
Vanillic acid	COC1=CC(=CC=C1O)C(O)=O	168.042258738	C₈H₈O₄	Polyphenols	Phenolic acids	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
Malvidin-3-O-glucoside	COC1=CC(=CC(OC)=C1O)C1=[O+]C2=CC(O)=CC(O)=C2C=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	493.134052665	C₂₃H₂₅O₁₂	Polyphenols	Flavonoids	Show
Syringic acid-4-O-glucuronide	[H][C@@]1(OC2=C(OC)C=C(C=C2OC)C(O)=O)O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O	374.0849114	C₁₅H₁₈O₁₁	(Poly)phenol metabolites	Phenolic acid metabolites	Show
Malvidin	COC1=CC(=CC(OC)=C1O)C1=[O+]C2=CC(O)=CC(O)=C2C=C1O	331.081229243	C₁₇H₁₅O₇	Polyphenols	Flavonoids	Show
Malvidin 3-O-glucoside	COC1=CC(=CC(OC)=C1O)C1=[O+]C2=CC(O)=CC(O)=C2C=C1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	493.134052665	C₂₃H₂₅O₁₂	Polyphenols	Flavonoids	Show
Ellagic acid	OC1=CC2=C3C(OC(=O)C4=CC(O)=C(O)C(OC2=O)=C34)=C1O	302.006267153	C₁₄H₆O₈	Polyphenols	Phenolic acids	Show
Ellagic acid	OC1=CC2=C3C(OC(=O)C4=CC(O)=C(O)C(OC2=O)=C34)=C1O	302.006267153	C₁₄H₆O₈	Polyphenols	Phenolic acids	Show

Biomarkers of intake

No Biomarkers of intake found

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