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	389.045038164	C₁₁H₁₉NO₁₀S₂	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	423.032759402	C₁₁H₂₁NO₁₀S₃	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	435.032759402	C₁₂H₂₁NO₁₀S₃	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	437.048409467	C₁₂H₂₃NO₁₀S₃	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
Indole-3-acetonitrile	N#CCC1=CNC2=C1C=CC=C2	156.068748266	C₁₀H₈N₂	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	Show
Indole-3-carbinol	OCC1=CNC2=CC=CC=C12	147.068413914	C₉H₉NO	N-containing compounds	Miscellaneous N-containing compounds	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
Iberin	CS(=O)CCCN=C=S	163.012556262	C₅H₉NOS₂	N-containing compounds	Isothiocyanates	Show
1-Cyano-3,4-epithiobutane	N#CCCC1CS1	113.029920403	C₅H₇NS	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
Erucin	CSCCCCN=C=S	161.033291706	C₆H₁₁NS₂	N-containing compounds	Isothiocyanates	Show
Erucin-N-acetyl-cysteine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	Show
Erucin-cysteine-glycine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	Show
Erucin-cysteine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	Show
Erucin-glutathione				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	Show
Sulforaphane-glutathione	[H]OC(=O)CN([H])C(=O)[C@H](CSC(=S)N([H])CCCCS(C)=O)N([H])C(=O)CC[C@H](N([H])[H])C(=O)O[H]	484.11201278	C₁₆H₂₈N₄O₇S₃	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-cysteine	[H]OC(=O)C(CSC(=S)N([H])CCCCS(C)=O)N([H])[H]	298.04795597	C₉H₁₈N₂O₃S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	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	CS(=O)CCCCN=C=S	177.028206326	C₆H₁₁NOS₂	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	437.048409467	C₁₂H₂₃NO₁₀S₃	N-containing compounds	Glucosinolates	Show
Sulforaphane-glutathione	[H]OC(=O)CN([H])C(=O)[C@H](CSC(=S)N([H])CCCCS(C)=O)N([H])C(=O)CC[C@H](N([H])[H])C(=O)O[H]	484.11201278	C₁₆H₂₈N₄O₇S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	Show
Sulforaphane-cysteine	[H]OC(=O)C(CSC(=S)N([H])CCCCS(C)=O)N([H])[H]	298.04795597	C₉H₁₈N₂O₃S₃	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	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
Sulforaphene	CS(=O)\C=C\CCN=C=S	175.012556262	C₆H₉NOS₂	N-containing compounds	Isothiocyanates	Show
Sulforaphane	CS(=O)CCCCN=C=S	177.028206326	C₆H₁₁NOS₂	N-containing compounds	Isothiocyanates	Show
Allyl isothiocyanate	C=CCN=C=S	99.014270339	C₄H₅NS	N-containing compounds	Isothiocyanates	Show
3-butenenitrile	C=CCC#N	67.042199165	C₄H₅N	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	Show
Allyl isothiocyanate-N-acetyl-L-cysteine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites	Show
1-cyano-2,3-epithiopropane	N#CCC1CS1	99.014270339	C₄H₅NS	N-containing compounds	Miscellaneous N-containing compounds	Show

Biomarkers of intake

No Biomarkers of intake found

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