PhytoHub: Showing entry for Swiss chard

Swiss chard

Group:: Vegetables, Leaf vegetables

Identification

Name: Swiss chard
ID: 273
Food group: Vegetables, Leaf vegetables

Synonyms

No Synonyms

External Links

ITIS: 524868

Compounds

Name	Structure	Monoisotopic mass	Formula	Family	Class
tyrosine-betaxanthin	OC(=O)[C@H](CC1=CC=C(O)C=C1)N\C=C\C1=CC(=N[C@@H](C1)C(O)=O)C(O)=O	374.111400928	C₁₈H₁₈N₂O₇	N-containing compounds	Alkaloids	Publications	Show
Serine-betaxantin	OC[C@H](\N=C/C=C1\C[C@H](NC(=C1)C(O)=O)C(O)=O)C(O)=O	298.080100799	C₁₂H₁₄N₂O₇	N-containing compounds	Alkaloids	Publications	Show
Histamine-betaxanthin	[H][C@]1(C\C(=C/C=N\CCC2=CN=CN2)C=C(N1)C(O)=O)C(O)=O	304.117155011	C₁₄H₁₆N₄O₄	N-containing compounds	Alkaloids	Publications	Show
Phenylalanine-betaxanthin	[H][C@]1(C\C(=C/C=N\[C@@H](CC2=CC=CC=C2)C(O)=O)C=C(N1)C(O)=O)C(O)=O	358.116486308	C₁₈H₁₈N₂O₆	N-containing compounds	Alkaloids	Publications	Show
γ-Aminobutyric acid-betaxanthin	OC(=O)CCC\N=C/C=C1\C[C@H](NC(=C1)C(O)=O)C(O)=O	296.100836243	C₁₃H₁₆N₂O₆	N-containing compounds	Alkaloids	Publications	Show
Valine-betaxanthin	CC(C)[C@H](\N=C/C=C1\C[C@H](NC(=C1)C(O)=O)C(O)=O)C(O)=O	310.116486308	C₁₄H₁₈N₂O₆	N-containing compounds	Alkaloids	Publications	Show
3-Methoxy-tyramine-betaxanthin	[H][C@]1(C\C(=C/C=N\CCC2=CC(OC)=C(O)C=C2)C=C(N1)C(O)=O)C(O)=O	360.132136372	C₁₈H₂₀N₂O₆	N-containing compounds	Alkaloids	Publications	Show
Isoleucine-betaxanthin	[H][C@]1(C\C(=C/C=NC(C(C)CC)C(O)=O)C=C(N1)C(O)=O)C(O)=O	324.132136372	C₁₅H₂₀N₂O₆	N-containing compounds	Alkaloids	Publications	Show
Tryptophan-betaxanthin	OC(=O)[C@H](CC1=CNC2=CC=CC=C12)\N=C/C=C1\C[C@H](NC(=C1)C(O)=O)C(O)=O	397.127385344	C₂₀H₁₉N₃O₆	N-containing compounds	Alkaloids	Publications	Show
Betanin	OC[C@H]1O[C@@H](OC2=CC3=C(C=C2O)\[N+](=C\C=C2/C[C@H](NC(=C2)C(O)=O)C(O)=O)[C@@H](C3)C([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O	550.143488905	C₂₄H₂₆N₂O₁₃	N-containing compounds	Alkaloids	Publications	Show
Isobetanin	OC[C@H]1O[C@@H](OC2=C(O)C=C3C(C[C@@H](C([O-])=O)\[N+]3=C/C=C3\C[C@@H](NC(=C3)C(O)=O)C(O)=O)=C2)[C@H](O)[C@@H](O)[C@@H]1O	550.143488905	C₂₄H₂₆N₂O₁₃	N-containing compounds	Alkaloids	Publications	Show
Betanidin	OC(=O)[C@H]1C\C(=C\C=[N+]2\[C@H](CC3=C2C=C(O)C(O)=C3)C([O-])=O)C=C(N1)C(O)=O	388.090665483	C₁₈H₁₆N₂O₈	N-containing compounds	Alkaloids	Publications	Show
Isobetanidin	[H]N1C(=C\C(C[C@@]1([H])C(O)=O)=C(/[H])\C=[N+]1/[C@@H](CC2=CC(O)=C(O)C=C12)C(O)=O)C(O)=O	389.097941936	C₁₈H₁₇N₂O₈	N-containing compounds	Alkaloids	Publications	Show
Phyllocactin	O[C@H]1[C@H](O)[C@@H](OC(=O)CCCC(O)=O)OC(OC2=C(O)C=C3C(C[C@@H](C([O-])=O)\[N+]3=C/C=C3/CC(NC(=C3)C(O)=O)C(O)=O)=C2)[C@@H]1O	650.159532894	C₂₈H₃₀N₂O₁₆	N-containing compounds	Alkaloids	Publications	Show
Lampranthin II	COC1=C([O-])C=CC(C=CC(=O)OC[C@H]2O[C@@H](OC3=C(O)C=C4C(C[C@@H](C(O)=O)[N+]4=CC=C4C[C@H](NC(=C4)C(O)=O)C(O)=O)=C3)[C@H](O)[C@@H](O)[C@@H]2O)=C1	726.190833023	C₃₄H₃₄N₂O₁₆	N-containing compounds	Alkaloids	Publications	Show
Isolampranthin II	[H]N1[C@H](C\C(C=C1C(O)=O)=C(\[H])/C=[N+]1\[C@@H](CC2=CC(OC3O[C@H](COC(=O)\C=C\C4=CC=C(O)C(OC)=C4)[C@@H](O)[C@H](O)[C@H]3O)=C(O)C=C12)C([O-])=O)C(O)=O	726.190833023	C₃₄H₃₄N₂O₁₆	N-containing compounds	Alkaloids	Publications	Show
Histidine-betaxanthin	[H][C@]1(C\C(=C/C=N\C(CC2=CNC=N2)C(O)=O)C=C(N1)C(O)=O)C(O)=O	348.106984251	C₁₅H₁₆N₄O₆	N-containing compounds	Alkaloids	Publications	Show
Asparagine-betaxanthin	[H][C@]1(C\C(=C/C=N[C@@H](CC(N)=O)C(O)=O)C=C(N1)C(O)=O)C(O)=O	325.090999835	C₁₃H₁₅N₃O₇	N-containing compounds	Alkaloids	Publications	Show
glutamine-betaxanthin	NC(=O)CC[C@H](\N=C/C=C1\C[C@H](NC(=C1)C(O)=O)C(O)=O)C(O)=O	339.106649899	C₁₄H₁₇N₃O₇	N-containing compounds	Alkaloids	Publications	Show
Glycine-betaxanthin	OC(=O)C\N=C/C=C1\C[C@H](NC(=C1)C(O)=O)C(O)=O	268.069536114	C₁₁H₁₂N₂O₆	N-containing compounds	Alkaloids	Publications	Show
Glutamic acid-betaxanthin	OC(=O)CC[C@H](N\C=C\C1=CC(=N[C@@H](C1)C(O)=O)C(O)=O)C(O)=O	340.090665483	C₁₄H₁₆N₂O₈	N-containing compounds	Alkaloids	Publications	Show
Proline-betaxanthin	OC(=O)[C@@H]1CCC[N+]1=CC=C1C[C@H](NC(=C1)C([O-])=O)C(O)=O	308.100836243	C₁₄H₁₆N₂O₆	N-containing compounds	Alkaloids	Publications	Show
Dopamine-betaxanthin	OC(=O)C1C\C(=C/C=N\CCC2=CC=C(O)C(O)=C2)C=C(N1)C(O)=O	346.116486308	C₁₇H₁₈N₂O₆	N-containing compounds	Alkaloids	Publications	Show
Tyramine-betaxanthin	OC(=O)C1C\C(=C/C=N\CCC2=CC=C(O)C=C2)C=C(N1)C(O)=O	330.121571688	C₁₇H₁₈N₂O₅	N-containing compounds	Alkaloids	Publications	Show
Leucine-betaxanthin	[H][C@]1(C\C(=C/C=N/C(CC(C)C)C(O)=O)C=C(N1)C(O)=O)C(O)=O	324.132136372	C₁₅H₂₀N₂O₆	N-containing compounds	Alkaloids	Publications	Show
Alanine-betaxanthin	CC(\N=C/C=C1\C[C@H](NC(=C1)C(O)=O)C(O)=O)C(O)=O	282.085186179	C₁₂H₁₄N₂O₆	N-containing compounds	Alkaloids	Publications	Show

Related Metabolites

Name	Structure	Monoisotopic mass	Formula	Family	Class
2-decarboxy-betanidin				N-containing compound metabolites	Alkaloid metabolites	Show
17-decarboxy-isobetanidin				N-containing compound metabolites	Alkaloid metabolites	Show
17-decarboxy-betanidin				N-containing compound metabolites	Alkaloid metabolites	Show
2,15,17-tridecarboxy-betanin	[H]N1CC\C(C=C1)=C(\[H])/C=[N+]1\CCC2=CC(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C(O)C=C12	419.181277638	C₂₁H₂₇N₂O₇	N-containing compounds	Alkaloids	Show
2,17-didecarboxy-betanin	[H]N1C=C\C(C[C@]1([H])C(O)=O)=C\C=[N+]1/CCC2=CC(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C(O)C=C12	463.171106878	C₂₂H₂₇N₂O₉	N-containing compounds	Alkaloids	Show
15-decarboxy-betanin	[H]N1CC\C(C=C1C(O)=O)=C(\[H])/C=[N+]1/C2=CC(O)=C(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2C[C@]1([H])C(O)=O	507.160936118	C₂₃H₂₇N₂O₁₁	N-containing compounds	Alkaloids	Show
17-decarboxy-betanin	[H]N1C=C\C(C[C@]1([H])C(O)=O)=C(/[H])\C=[N+]1\C2=CC(O)=C(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2C[C@]1([H])C(O)=O	507.160936118	C₂₃H₂₇N₂O₁₁	N-containing compounds	Alkaloids	Show
2-decarboxy-betanin	[H]N1C(=C\C(C[C@]1([H])C(O)=O)=C(/[H])\C=[N+]1/CCC2=CC(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C(O)C=C12)C(O)=O	507.160936118	C₂₃H₂₇N₂O₁₁	N-containing compounds	Alkaloids	Show
Betanidin	OC(=O)[C@H]1C\C(=C\C=[N+]2\[C@H](CC3=C2C=C(O)C(O)=C3)C([O-])=O)C=C(N1)C(O)=O	388.090665483	C₁₈H₁₆N₂O₈	N-containing compounds	Alkaloids	Show
Betanidin	OC(=O)[C@H]1C\C(=C\C=[N+]2\[C@H](CC3=C2C=C(O)C(O)=C3)C([O-])=O)C=C(N1)C(O)=O	388.090665483	C₁₈H₁₆N₂O₈	N-containing compounds	Alkaloids	Show
2,15,17-tridecarboxy-2,3-dehydro-neobetanin				N-containing compound metabolites	Alkaloid metabolites	Show
2,15,17-tridecarboxy-betanin	[H]N1CC\C(C=C1)=C(\[H])/C=[N+]1\CCC2=CC(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C(O)C=C12	419.181277638	C₂₁H₂₇N₂O₇	N-containing compounds	Alkaloids	Show
2,17-didecarboxy-betanin	[H]N1C=C\C(C[C@]1([H])C(O)=O)=C\C=[N+]1/CCC2=CC(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C(O)C=C12	463.171106878	C₂₂H₂₇N₂O₉	N-containing compounds	Alkaloids	Show
15-decarboxy-betanin	[H]N1CC\C(C=C1C(O)=O)=C(\[H])/C=[N+]1/C2=CC(O)=C(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2C[C@]1([H])C(O)=O	507.160936118	C₂₃H₂₇N₂O₁₁	N-containing compounds	Alkaloids	Show
2-decarboxy-betanin	[H]N1C(=C\C(C[C@]1([H])C(O)=O)=C(/[H])\C=[N+]1/CCC2=CC(OC3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C(O)C=C12)C(O)=O	507.160936118	C₂₃H₂₇N₂O₁₁	N-containing compounds	Alkaloids	Show
Betanin	OC[C@H]1O[C@@H](OC2=CC3=C(C=C2O)\[N+](=C\C=C2/C[C@H](NC(=C2)C(O)=O)C(O)=O)[C@@H](C3)C([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O	550.143488905	C₂₄H₂₆N₂O₁₃	N-containing compounds	Alkaloids	Show
Isobetanidin	[H]N1C(=C\C(C[C@@]1([H])C(O)=O)=C(/[H])\C=[N+]1/[C@@H](CC2=CC(O)=C(O)C=C12)C(O)=O)C(O)=O	389.097941936	C₁₈H₁₇N₂O₈	N-containing compounds	Alkaloids	Show
Isobetanin	OC[C@H]1O[C@@H](OC2=C(O)C=C3C(C[C@@H](C([O-])=O)\[N+]3=C/C=C3\C[C@@H](NC(=C3)C(O)=O)C(O)=O)=C2)[C@H](O)[C@@H](O)[C@@H]1O	550.143488905	C₂₄H₂₆N₂O₁₃	N-containing compounds	Alkaloids	Show
Proline-betaxanthin	OC(=O)[C@@H]1CCC[N+]1=CC=C1C[C@H](NC(=C1)C([O-])=O)C(O)=O	308.100836243	C₁₄H₁₆N₂O₆	N-containing compounds	Alkaloids	Show

Biomarkers of intake

No Biomarkers of intake found

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