PhytoHub: Showing entry for Banana

Banana

Group:: Fruit, Tropical fruits

Identification

Name: Banana
ID: 12
Food group: Fruit, Tropical fruits

Synonyms

No Synonyms

External Links

ITIS: 42390
FooDB (Foods): 208

Compounds

Name	Structure	Monoisotopic mass	Formula	Family	Class
α-carotene	C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=CCCC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)CCCC1(C)C	536.438201803	C₄₀H₅₆	Terpenoids	Carotenoids	Publications	Show
Lutein	C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=CC(O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C[C@@H](O)CC1(C)C	568.428031043	C₄₀H₅₆O₂	Terpenoids	Carotenoids	Publications	Show
Campesterol	[H][C@@]1(CC[C@@]2([H])[C@]3([H])CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CC[C@@H](C)C(C)C	400.370516166	C₂₈H₄₈O	Terpenoids	Phytosterols	Publications	Show
Sitosterol-beta	CC[C@H](CC[C@@H](C)C1CCC2C3CC=C4C[C@@H](O)CC[C@]4(C)C3CC[C@]12C)C(C)C	414.38616623	C₂₉H₅₀O	Terpenoids	Phytosterols	Publications	Show
Stigmasterol	CC[C@H](\C=C\[C@@H](C)C1CCC2C3CC=C4C[C@@H](O)CC[C@]4(C)C3CC[C@]12C)C(C)C	412.370516166	C₂₉H₄₈O	Terpenoids	Phytosterols	Publications	Show
(-)-Salsolinol	C[C@@H]1NCCC2=CC(O)=C(O)C=C12	179.094628663	C₁₀H₁₃NO₂	N-containing compounds	Miscellaneous N-containing compounds	Publications	Show
Dopamine	NCCC1=CC(O)=C(O)C=C1	153.078978598	C₈H₁₁NO₂	N-containing compounds	Amines	Publications	Show
Serotonin	NCCC1=CNC2=C1C=C(O)C=C2	176.094963014	C₁₀H₁₂N₂O	N-containing compounds	Amines	Publications	Show
Noradrenaline (L-)	NC[C@H](O)C1=CC(O)=C(O)C=C1	169.073893218	C₈H₁₁NO₃	N-containing compounds	Amines	Publications	Show
Quinic acid	OC1C[C@@](O)(C[C@@H](O)[C@H]1O)C(O)=O	192.063388106	C₇H₁₂O₆	Miscellaneous phytochemicals	Miscellaneous phytochemicals	Publications	Show
2-Pentanone	CCCC(C)=O	86.073164942	C₅H₁₀O	Miscellaneous phytochemicals	Not Available	Publications	Show
Hexanal	CCCCCC=O	100.088815006	C₆H₁₂O	Miscellaneous phytochemicals	Not Available	Publications	Show
Isoamyl acetate	CC(C)CCOC(C)=O	130.099379691	C₇H₁₄O₂	Miscellaneous phytochemicals	Not Available	Publications	Show
Isoamyl isobutyrate	CC(C)CCOC(=O)C(C)C	158.13067982	C₉H₁₈O₂	Miscellaneous phytochemicals	Not Available	Publications	Show
Butyl butyrate	CCCCOC(=O)CCC	144.115029755	C₈H₁₆O₂	Miscellaneous phytochemicals	Not Available	Publications	Show
Butyl acetate	CCCCOC(C)=O	116.083729626	C₆H₁₂O₂	Miscellaneous phytochemicals	Not Available	Publications	Show
(+)-Catechin	O[C@H]1CC2=C(O)C=C(O)C=C2O[C@@H]1C1=CC(O)=C(O)C=C1	290.079038171	C₁₅H₁₄O₆	Polyphenols	Flavonoids	Publications	Show
Tryptophan	NC(CC1=CNC2=C1C=CC=C2)C(O)=O	204.089877634	C₁₁H₁₂N₂O₂	N-containing compounds	Amino acids	Publications	Show
Elemicin	COC1=CC(CC=C)=CC(OC)=C1OC	208.109944375	C₁₂H₁₆O₃	Miscellaneous phytochemicals	Not Available	Publications	Show
Methoxyeugenol	COC1=CC(CC=C)=CC(OC)=C1O	194.094294311	C₁₁H₁₄O₃	Polyphenols	Phenolic acids	Publications	Show
Eugenol	COC1=CC(CC=C)=CC=C1O	164.083729626	C₁₀H₁₂O₂	Polyphenols	Miscellaneous polyphenols	Publications	Show
6-hydroxy-1-methyl-1,2,3,4-tetrahydro-beta-carboline	CC1NCCC2=C1NC1=CC=C(O)C=C21	202.110613079	C₁₂H₁₄N₂O	N-containing compounds	Miscellaneous N-containing compounds	Publications	Show
Trigonelline	C[N+]1=CC=CC(=C1)C([O-])=O	137.047678469	C₇H₇NO₂	N-containing compounds	Miscellaneous N-containing compounds	Publications	Show
Histamine	NCCC1=CNC=N1	111.079647302	C₅H₉N₃	N-containing compounds	Amines	Publications	Show
Phenethylamine	NCCC1=CC=CC=C1	121.089149358	C₈H₁₁N	N-containing compounds	Amines	Publications	Show
β-Carotene	C\C(\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)CCCC1(C)C	536.438201803	C₄₀H₅₆	Terpenoids	Carotenoids	Publications	Show

Related Metabolites

Name	Structure	Monoisotopic mass	Formula	Family	Class
Salsolinol-sulfate	C[C@@H]1NCCC2=C1C=C(O)C(OS(O)(=O)=O)=C2	259.051443697	C₁₀H₁₃NO₅S	N-containing compound metabolites	Miscellaneous N-containing compound metabolites	Show
3'-Methoxy-(+)-catechin	COC1=CC(=CC=C1O)[C@H]1OC2=C(C[C@@H]1O)C(O)=CC(O)=C2	304.094688235	C₁₆H₁₆O₆	(Poly)phenol metabolites	Flavonoid metabolites	Show
Methoxy-(epi)catechin-glucuronide				(Poly)phenol metabolites	Flavonoid metabolites	Show
Methoxy-(epi)catechin-sulfate				(Poly)phenol metabolites	Flavonoid metabolites	Show
(+)-Catechin	O[C@H]1CC2=C(O)C=C(O)C=C2O[C@@H]1C1=CC(O)=C(O)C=C1	290.079038171	C₁₅H₁₄O₆	Polyphenols	Flavonoids	Show
4'-Hydroxyphenylacetic acid	OC(=O)CC1=CC=C(O)C=C1	152.047344118	C₈H₈O₃	Polyphenols	Phenolic acids	Show
(Epi)catechin O-glucuronide		466.3989068	C₂₁H₂₂O₁₂	(Poly)phenol metabolites	Flavonoid metabolites	Show
(Epi)catechin O-sulfate		370.335352	C₁₅H₁₄O₉S	(Poly)phenol metabolites	Flavonoid metabolites	Show
5-(3',4'-dihydroxyphenyl)-gamma-valerolactone	OC1=C(O)C=C(CC2CCC(=O)O2)C=C1	208.073558866	C₁₁H₁₂O₄	(Poly)phenol metabolites	Flavonoid metabolites	Show
5-(3',4'-dihydroxyphenyl)valeric acid	OC(=O)CCCCC1=CC(O)=C(O)C=C1	210.089208931	C₁₁H₁₄O₄	(Poly)phenol metabolites	Flavonoid metabolites	Show
5-(4’-hydroxyphenyl)-gamma-valerolactone	OC1=CC=C(CC2CCC(=O)O2)C=C1	192.078644246	C₁₁H₁₂O₃	(Poly)phenol metabolites	Flavonoid metabolites	Show
6-hydroxy-1-methyl-1,2,3,4-tetrahydro-beta-carboline sulfate	CC1NCCC2=C1NC1=CC=C(OS(O)(=O)=O)C=C21	282.067428113	C₁₂H₁₄N₂O₄S	N-containing compound metabolites	Miscellaneous N-containing compound metabolites	Show
Dopamine 3-O-sulfate	NCCC1=CC(OS(O)(=O)=O)=C(O)C=C1	233.035793632	C₈H₁₁NO₅S	N-containing compound metabolites	Amine metabolites	Show
3-Methoxytyramine sulfate	COC1=CC(CCN)=CC=C1OS(O)(=O)=O	247.051443697	C₉H₁₃NO₅S	Miscellaneous phytochemical metabolites	Miscellaneous phytochemical metabolites	Show
Dopamine 4-O-sulfate	NCCC1=CC=C(OS(O)(=O)=O)C(O)=C1	233.035793632	C₈H₁₁NO₅S	N-containing compound metabolites	Amine metabolites	Show
Methoxyeugenol	COC1=CC(CC=C)=CC(OC)=C1O	194.094294311	C₁₁H₁₄O₃	Polyphenols	Phenolic acids	Show
Methoxyeugenol glucuronide	COC1=CC(CC=C)=CC(OC)=C1OC1O[C@@H](C(O)[C@H](O)C1O)C(O)=O	370.126382288	C₁₇H₂₂O₉	Miscellaneous phytochemical metabolites	Miscellaneous phytochemical metabolites	Show
Hippuric acid	OC(=O)CNC(=O)C1=CC=CC=C1	179.058243154	C₉H₉NO₃	(Poly)phenol metabolites	Phenolic acid metabolites	Show
5-Hydroxyindole acetic acid	OC(=O)CC1=CNC2=C1C=C(O)C=C2	191.058243154	C₁₀H₉NO₃	N-containing compound metabolites	Amine metabolites	Show
Trigonelline	C[N+]1=CC=CC(=C1)C([O-])=O	137.047678469	C₇H₇NO₂	N-containing compounds	Miscellaneous N-containing compounds	Show
Xanthurenic acid	OC(=O)C1=CC(O)=C2C=CC=C(O)C2=N1	205.037507709	C₁₀H₇NO₄	Miscellaneous phytochemicals	Miscellaneous phytochemicals	Show
Indole-3-aldehyde	OC(=O)CC1=CNC2=CC=CC=C12	175.063328534	C₁₀H₉NO₂	N-containing compound metabolites	Amino acid metabolites	Show
Indole-3-lactic acid	OC(=O)CC1=CNC2=CC=CC=C12	175.063328534	C₁₀H₉NO₂	N-containing compound metabolites	Amino acid metabolites	Show
β-Carotene	C\C(\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)CCCC1(C)C	536.438201803	C₄₀H₅₆	Terpenoids	Carotenoids	Show
Retinal	C\C(\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C)=C/C=O	284.214015522	C₂₀H₂₈O	Terpenoid metabolites	Carotenoid metabolites	Show
13-apo-β-carotenone	CC(=O)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C	258.198365457	C₁₈H₂₆O	Terpenoid metabolites	Carotenoid metabolites	Show

Biomarkers of intake

	Compound Name	Food Name	Specificity
	Dopamine 3-O-sulfate	Banana	High	Publications

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