PhytoHub: Showing entry for Cranberry

Cranberry

Group:: Fruit, Berries

Identification

Name: Cranberry
ID: 318
Food group: Fruit, Berries

Synonyms

No Synonyms

External Links

No external links

Compounds

Name	Structure	Monoisotopic mass	Formula	Family	Class
Resveratrol (trans-)	OC1=CC=C(\C=C\C2=CC(O)=CC(O)=C2)C=C1	228.078644246	C₁₄H₁₂O₃	Polyphenols	Stilbenes	Publications	Show
Resveratrol (cis-)	[H]\C(=C(/[H])C1=CC(O)=CC(O)=C1)C1=CC=C(O)C=C1	228.078644246	C₁₄H₁₂O₃	Polyphenols	Stilbenes	Publications	Show
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
Sinapic acid	COC1=CC(\C=C\C(O)=O)=CC(OC)=C1O	224.068473486	C₁₁H₁₂O₅	Polyphenols	Phenolic acids	Publications	Show
Cyanidin-3-O-galactoside	O1C(C(O)C(O)C(O)C1OC=2C(=[O+]C=3C(C2)=C(O)C=C(O)C3)C4=CC(O)=C(O)C=C4)CO	449.107837916	C₂₁H₂₁O₁₁	Polyphenols	Flavonoids	Publications	Show
Cyanidin 3-O-arabinoside	O[C@H]1CO[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC(O)=C(O)C=C2)[C@H](O)[C@H]1O	419.097273232	C₂₀H₁₉O₁₀	Polyphenols	Flavonoids	Publications	Show
Peonidin 3-O-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	Publications	Show
Peonidin 3-O-arabinoside	COC1=CC(=CC(O)=C1O)C1=[O+]C2=CC(O)=CC(O)=C2C=C1O[C@H]1OC[C@@H](O)[C@H](O)[C@H]1O	449.107837916	C₂₁H₂₁O₁₁	Polyphenols	Flavonoids	Publications	Show

Related Metabolites

Name	Structure	Monoisotopic mass	Formula	Family	Class
Cyanidin 3-O-arabinoside	O[C@H]1CO[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC(O)=C(O)C=C2)[C@H](O)[C@H]1O	419.097273232	C₂₀H₁₉O₁₀	Polyphenols	Flavonoids	Show
Cyanidin-3-O-galactoside	O1C(C(O)C(O)C(O)C1OC=2C(=[O+]C=3C(C2)=C(O)C=C(O)C3)C4=CC(O)=C(O)C=C4)CO	449.107837916	C₂₁H₂₁O₁₁	Polyphenols	Flavonoids	Show
Cyanidin 3-O-galactoside	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
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 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
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
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 B	OC1=CC2=C(C=C1)C1=C(C=CC=C1)C(=O)O2	212.047344118	C₁₃H₈O₃	(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 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 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 D	OC1=CC2=C(C=C1O)C1=CC=C(O)C(O)=C1OC2=O	260.032087978	C₁₃H₈O₆	(Poly)phenol metabolites	Ellagitannin metabolites	Show
Urolithin D glucuronide				(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
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
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
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 CR	OC1=CC2=C(C=C1O)C1=C(OC2=O)C(O)=CC=C1	244.037173358	C₁₃H₈O₅	(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 AR	OC1=CC2=C(C=C1)C1=C(OC2=O)C(O)=CC=C1	228.042258738	C₁₃H₈O₄	(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 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 B-sulfate				(Poly)phenol metabolites	Ellagitannin metabolites	Show
Isourolithin A-9-glucuronide			C₁₉H₁₆O₁₀	(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
Peonidin 3-O-arabinoside	COC1=CC(=CC(O)=C1O)C1=[O+]C2=CC(O)=CC(O)=C2C=C1O[C@H]1OC[C@@H](O)[C@H](O)[C@H]1O	449.107837916	C₂₁H₂₁O₁₁	Polyphenols	Flavonoids	Show
cis-Resveratrol-4'-O-glucuronide	OC1C(OC2=CC=C(\C=C/C3=CC(O)=CC(O)=C3)C=C2)OC(C(O)C1O)C(O)=O	404.110732224	C₂₀H₂₀O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
cis-Resveratrol-3-O-glucuronide	OC1C(OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)OC(C(O)C1O)C(O)=O	404.110732224	C₂₀H₂₀O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
cis-Resveratrol-4'-sulfate	OC1=CC(\C=C/C2=CC=C(OS(O)(=O)=O)C=C2)=CC(O)=C1	308.03545928	C₁₄H₁₂O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
cis-Resveratrol-3-sulfate	OC1=CC=C(\C=C/C2=CC(OS(O)(=O)=O)=CC(O)=C2)C=C1	308.03545928	C₁₄H₁₂O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
Resveratrol (cis-)	[H]\C(=C(/[H])C1=CC(O)=CC(O)=C1)C1=CC=C(O)C=C1	228.078644246	C₁₄H₁₂O₃	Polyphenols	Stilbenes	Show
Piceid (cis-)	[H]\C(=C(/[H])C1=CC(O[C@@H]2OC(CO)[C@@H](O)[C@H](O)C2O)=CC(O)=C1)C1=CC=C(O)C=C1	390.131467668	C₂₀H₂₂O₈	Polyphenols	Stilbenes	Show
Resveratrol disulfate		387.992	C₁₄H₁₂O₉S₂	(Poly)phenol metabolites	Stilbene metabolites	Show
resveratrol sulfate		308.035	C₁₄H₁₂O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
resveratrol glucuronide		404.111	C₂₀H₂₀O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
Piceatannol	OC1=CC(\C=C\C2=CC=C(O)C(O)=C2)=CC(O)=C1	244.073558866	C₁₄H₁₂O₄	Polyphenols	Stilbenes	Show
trans-resveratrol-5-O-glucuronide	OC1C(OC2=CC(\C=C\C3=CC=C(O)C=C3)=CC(O)=C2)OC(C(O)C1O)C(O)=O	404.110732224	C₂₀H₂₀O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
trans-resveratrol-4'-O-β-sulfate	OC1=CC(\C=C\C2=CC=C(OS(O)(=O)=O)C=C2)=CC(O)=C1	308.03545928	C₁₄H₁₂O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol-trisulfate		469.965	C₁₄H₁₄O₁₂S₃	(Poly)phenol metabolites	Stilbene metabolites	Show
trans-Resveratrol-3,4′,5-trisulfate	OS(=O)(=O)OC1=CC=C(\C=C\C2=CC(OS(O)(=O)=O)=CC(OS(O)(=O)=O)=C2)C=C1	467.949089348	C₁₄H₁₂O₁₂S₃	(Poly)phenol metabolites	Stilbene metabolites	Show
trans-Resveratrol-3,4′-disulfate	OC1=CC(OS(O)(=O)=O)=CC(\C=C\C2=CC=C(OS(O)(=O)=O)C=C2)=C1	387.992274314	C₁₄H₁₂O₉S₂	(Poly)phenol metabolites	Stilbene metabolites	Show
trans-Resveratrol-3,5-disulfate	OC1=CC=C(\C=C\C2=CC(OS(O)(=O)=O)=CC(OS(O)(=O)=O)=C2)C=C1	387.992274314	C₁₄H₁₂O₉S₂	(Poly)phenol metabolites	Stilbene metabolites	Show
resveratrol sulfoglucuronide		484.068	C₂₀H₂₀O₁₂S	(Poly)phenol metabolites	Stilbene metabolites	Show
resveratrol-4′-O-sulfate	OC1=CC(\C=C\C2=CC=C(OS(O)(=O)=O)C=C2)=CC(O)=C1	308.03545928	C₁₄H₁₂O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
trans-Resveratrol-4'-O-glucuronide	[H]\C(=C(\[H])C1=CC(O)=CC(O)=C1)C1=CC=C(OC2OC(C(O)C(O)C2O)C(O)=O)C=C1	404.110732224	C₂₀H₂₀O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
Resveratrol ribosyl sulfate		440.078	C₁₉H₂₀O₁₀S	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol-3-O-sulfate	OC1=CC=C(CCC2=CC(O)=CC(OS(O)(=O)=O)=C2)C=C1	310.051109345	C₁₄H₁₄O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol-3-O-glucuronide	OC1C(O)C(OC2=CC(CCC3=CC=C(O)C=C3)=CC(O)=C2)OC(C1O)C(O)=O	406.126382288	C₂₀H₂₂O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
trans-Resveratrol 3-O-sulfate	OC1=CC=C(\C=C\C2=CC(O)=CC(OS(O)(=O)=O)=C2)C=C1	308.03545928	C₁₄H₁₂O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
trans-Resveratrol 3-O-glucuronide	O[C@H]1[C@H](OC2=CC(\C=C\C3=CC=C(O)C=C3)=CC(O)=C2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O	404.110732224	C₂₀H₂₀O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol	OC1=CC=C(CCC2=CC(O)=CC(O)=C2)C=C1	230.094294311	C₁₄H₁₄O₃	Polyphenols	Stilbenes	Show
Resveratrol (cis-)	[H]\C(=C(/[H])C1=CC(O)=CC(O)=C1)C1=CC=C(O)C=C1	228.078644246	C₁₄H₁₂O₃	Polyphenols	Stilbenes	Show
Piceid (trans-)	OC[C@H]1O[C@@H](OC2=CC(\C=C\C3=CC=C(O)C=C3)=CC(O)=C2)[C@H](O)[C@@H](O)[C@@H]1O	390.131467668	C₂₀H₂₂O₈	Polyphenols	Stilbenes	Show
Resveratrol (trans-)	OC1=CC=C(\C=C\C2=CC(O)=CC(O)=C2)C=C1	228.078644246	C₁₄H₁₂O₃	Polyphenols	Stilbenes	Show
3,4'-dihydroxy-trans-stilbene	OC1=CC=C(\C=C\C2=CC=CC(O)=C2)C=C1	212.083729626	C₁₄H₁₂O₂	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol-glucuronide		406.1264	C₂₀H₂₂O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol sulfate		310.0511	C₁₄H₁₄O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
Resveratroloside	OCC1OC(OC2=CC=C(\C=C\C3=CC(O)=CC(O)=C3)C=C2)C(O)C(O)C1O	390.131467668	C₂₀H₂₂O₈	(Poly)phenol metabolites	Stilbene metabolites	Show
cis-Resveratrol-4'-O-glucuronide	OC1C(OC2=CC=C(\C=C/C3=CC(O)=CC(O)=C3)C=C2)OC(C(O)C1O)C(O)=O	404.110732224	C₂₀H₂₀O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
cis-Resveratrol-3-O-glucuronide	OC1C(OC2=CC(\C=C/C3=CC=C(O)C=C3)=CC(O)=C2)OC(C(O)C1O)C(O)=O	404.110732224	C₂₀H₂₀O₉	(Poly)phenol metabolites	Stilbene metabolites	Show
cis-Resveratrol-4'-sulfate	OC1=CC(\C=C/C2=CC=C(OS(O)(=O)=O)C=C2)=CC(O)=C1	308.03545928	C₁₄H₁₂O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
cis-Resveratrol-3-sulfate	OC1=CC=C(\C=C/C2=CC(OS(O)(=O)=O)=CC(O)=C2)C=C1	308.03545928	C₁₄H₁₂O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol-3,5-diglucuronide	OC1C(O)C(OC2=CC(OC3OC(C(O)C(O)C3O)C(O)=O)=CC(CCC3=CC=C(O)C=C3)=C2)OC(C1O)C(O)=O	582.158470266	C₂₆H₃₀O₁₅	(Poly)phenol metabolites	Stilbene metabolites	Show
Lunularin	OC1=CC=C(CCC2=CC=CC(O)=C2)C=C1	214.099379691	C₁₄H₁₄O₂	(Poly)phenol metabolites	Stilbene metabolites	Show
resveratrol-glucoside-phosphate	OC1C(COP(O)(O)=O)OC(OC2=CC=C(\C=C\C3=CC(O)=CC(O)=C3)C=C2)C(O)C1O	470.097798559	C₂₀H₂₃O₁₁P	(Poly)phenol metabolites	Stilbene metabolites	Show
Piceid-sulfate		470.088	C₂₀H₂₂O₁₁S	(Poly)phenol metabolites	Stilbene metabolites	Show
Piceid-glucuronide		566.164	C₂₆H₃₀O₁₄	(Poly)phenol metabolites	Stilbene metabolites	Show
Resveratrol-glucoside-phosphate-glycerol	[H]C(O)(CO)COP(O)(=O)OC[C@@]1([H])OC(OC2=CC=C(\C=C\C3=CC(O)=CC(O)=C3)C=C2)[C@H](O)[C@@H](O)[C@@H]1O	544.134577992	C₂₃H₂₉O₁₃P	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol-disulfate	OC1=CC=C(CCC2=CC(OS(O)(=O)=O)=CC(OS(O)(=O)=O)=C2)C=C1	390.007924379	C₁₄H₁₄O₉S₂	(Poly)phenol metabolites	Stilbene metabolites	Show
5-methoxyresveratrol-3-O-sulfate	COC1=CC(OS(O)(=O)=O)=CC(\C=C\C2=CC=C(O)C=C2)=C1	322.051109345	C₁₅H₁₄O₆S	(Poly)phenol metabolites	Stilbene metabolites	Show
5-methoxyresveratrol-3-O-β-glucoside	COC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC(\C=C\C2=CC=C(O)C=C2)=C1	404.147117733	C₂₁H₂₄O₈	(Poly)phenol metabolites	Stilbene metabolites	Show
Dihydro-resveratrol-sulfoglucuronide		486.083	C₂₀H₂₂O₁₂S	(Poly)phenol metabolites	Stilbene metabolites	Show
Sinapic acid O-glucuronide	COC1=CC(\C=C\C(=O)O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=CC(OC)=C1O	400.100561464	C₁₇H₂₀O₁₁	(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

Biomarkers of intake

No Biomarkers of intake found

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