PhytoHub: Showing entry for Cabbage, red

Cabbage, red

Group:: Vegetables, Cabbages

Identification

Name: Cabbage, red
ID: 349
Food group: Vegetables, Cabbages

Synonyms

No Synonyms

External Links

No external links

Compounds

	Name	Structure	Monoisotopic mass	Formula	Family	Class
	Neoglucobrassicin	CON1C=C(C\C(S[C@@H]2OC(CO)[C@@H](O)[C@H](O)C2O)=N/OS(O)(=O)=O)C2=C1C=CC=C2	478.071587264	C₁₇H₂₂N₂O₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show
	Progoitrin	[H][C@@](O)(C\C(S[C@@H]1OC(CO)[C@@H](O)[C@H](O)C1O)=N/OS([O-])(=O)=O)C=C	388.037761712	C₁₁H₁₈NO₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show
	Gluconasturtiin	OCC1O[C@@H](S\C(CCC2=CC=CC=C2)=N\OS(O)(=O)=O)C(O)[C@@H](O)[C@@H]1O	423.065773608	C₁₅H₂₁NO₉S₂	N-containing compounds	Glucosinolates	Publications	Show
	Sinigrin	OCC1O[C@@H](S\C(CC=C)=N\OS(O)(=O)=O)C(O)[C@@H](O)[C@@H]1O	359.034473479	C₁₀H₁₇NO₉S₂	N-containing compounds	Glucosinolates	Publications	Show
	Glucoiberin	CS(=O)CCC\C(S[C@@H]1OC(CO)[C@@H](O)[C@H](O)C1O)=N/OS([O-])(=O)=O	422.02548295	C₁₁H₂₀NO₁₀S₃	N-containing compounds	Glucosinolates	Publications	Show
	4-Hydroxyglucobrassicin	OCC1O[C@@H](S\C(CC2=CNC3=C2C(O)=CC=C3)=N\OS(O)(=O)=O)C(O)[C@@H](O)[C@@H]1O	464.0559372	C₁₆H₂₀N₂O₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show
	4-Methoxyglucobrassicin	COC1=CC=CC2=C1C(C\C(S[C@@H]1OC(CO)[C@@H](O)[C@H](O)C1O)=N/OS(O)(=O)=O)=CN2	478.071587264	C₁₇H₂₂N₂O₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show
	Glucoraphenin	CS(=O)\C=C\CC\C(S[C@@H]1OC(CO)[C@@H](O)[C@H](O)C1O)=N/OS([O-])(=O)=O	434.02548295	C₁₂H₂₀NO₁₀S₃	N-containing compounds	Glucosinolates	Publications	Show
	Glucoraphanin	CS(=O)CCCC\C(S[C@@H]1OC(CO)[C@@H](O)[C@H](O)C1O)=N/OS([O-])(=O)=O	436.041133014	C₁₂H₂₂NO₁₀S₃	N-containing compounds	Glucosinolates	Publications	Show
	Gluconapin	OCC1O[C@@H](S\C(CCC=C)=N\OS(O)(=O)=O)C(O)[C@@H](O)[C@@H]1O	373.050123544	C₁₁H₁₉NO₉S₂	N-containing compounds	Glucosinolates	Publications	Show
	Glucobrassicin	OCC1O[C@@H](S\C(CC2=CNC3=C2C=CC=C3)=N\OS(O)(=O)=O)C(O)[C@@H](O)[C@@H]1O	448.06102258	C₁₆H₂₀N₂O₉S₂	N-containing compounds	Glucosinolates	Publications	Show
	Iberin N-acetyl-cysteine	[H][C@@](CSC(S)=NCCCS(C)=O)(N=C(C)O)C(O)=O	326.04287059	C₁₀H₁₈N₂O₄S₃	N-containing compounds	Isothiocyanates	Publications	Show

Related Metabolites

	Name	Structure	Monoisotopic mass	Formula	Family	Class
	Iberin	CS(=O)CCCN=C=S	163.012556262	C₅H₉NOS₂	N-containing compounds	Isothiocyanates		Show
	Glucoraphanin	CS(=O)CCCC\C(S[C@@H]1OC(CO)[C@@H](O)[C@H](O)C1O)=N/OS([O-])(=O)=O	436.041133014	C₁₂H₂₂NO₁₀S₃	N-containing compounds	Glucosinolates		Show
	Sulforaphane	CS(=O)CCCCN=C=S	177.028206326	C₆H₁₁NOS₂	N-containing compounds	Isothiocyanates		Show
	Sulforaphane-N-acetyl-L-cysteine	CC(=O)NC(CSC(=S)NCCCCS(C)=O)C(O)=O	340.058520654	C₁₁H₂₀N₂O₄S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	3,3′-Diindolylmethane	C(C1=CNC2=C1C=CC=C2)C1=CNC2=C1C=CC=C2	246.115698459	C₁₇H₁₄N₂	N-containing compound metabolites	Miscellaneous N-containing compound metabolites		Show
	2-thiothiazolidine-4-carboxylic acid	[H][C@]1(CSC(S)=N1)C(O)=O	162.976170753	C₄H₅NO₂S₂	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Sulforaphane-cysteine	[H]OC(=O)C([H])(N([H])[H])C([H])([H])SC(=S)N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])S(=O)C([H])([H])[H]	298.04795597	C₉H₁₈N₂O₃S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Sulforaphane-cysteine-glycine	[H]OC(=O)C([H])([H])N([H])C(=O)[C@@]([H])(N([H])[H])C([H])([H])SC(=S)N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[S@](=O)C([H])([H])[H]	355.06941969	C₁₁H₂₁N₃O₄S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Sulforaphane-glutathione	[H]OC(=O)C([H])([H])N([H])C(=O)C([H])(N([H])C(=O)C([H])([H])C([H])([H])C([H])(N([H])[H])C(=O)O[H])C([H])([H])SC(=S)N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])S(=O)C([H])([H])[H]	484.11201278	C₁₆H₂₈N₄O₇S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Erucin-glutathione				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Sulforaphane	CS(=O)CCCCN=C=S	177.028206326	C₆H₁₁NOS₂	N-containing compounds	Isothiocyanates		Show
	Sulforaphene	CS(=O)\C=C\CCN=C=S	175.012556262	C₆H₉NOS₂	N-containing compounds	Isothiocyanates		Show
	Sulforaphane-N-acetyl-L-cysteine	CC(=O)NC(CSC(=S)NCCCCS(C)=O)C(O)=O	340.058520654	C₁₁H₂₀N₂O₄S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Sulforaphane-cysteine	[H]OC(=O)C([H])(N([H])[H])C([H])([H])SC(=S)N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])S(=O)C([H])([H])[H]	298.04795597	C₉H₁₈N₂O₃S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Sulforaphane-glutathione	[H]OC(=O)C([H])([H])N([H])C(=O)C([H])(N([H])C(=O)C([H])([H])C([H])([H])C([H])(N([H])[H])C(=O)O[H])C([H])([H])SC(=S)N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])S(=O)C([H])([H])[H]	484.11201278	C₁₆H₂₈N₄O₇S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Allyl isothiocyanate-N-acetyl-L-cysteine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show

Biomarkers of intake

No Biomarkers of intake found