PhytoHub: Showing entry for Brussel sprouts

Brussel sprouts

Group:: Vegetables, Cabbages

Identification

Name: Brussel sprouts
ID: 20
Food group: Vegetables, Cabbages

Synonyms

No Synonyms

External Links

ITIS: 530959
FooDB (Foods): 32

Compounds

Name	Structure	Monoisotopic mass	Formula	Family	Class
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
Brassicasterol	CC(C)[C@@H](C)\C=C\[C@@H](C)C1CCC2C3CC=C4C[C@@H](O)CC[C@]4(C)C3CC[C@]12C	398.354866101	C₂₈H₄₆O	Terpenoids	Phytosterols	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
Sitostanol-beta	CC[C@H](CC[C@@H](C)C1CCC2C3CCC4C[C@@H](O)CC[C@]4(C)C3CC[C@]12C)C(C)C	416.401816294	C₂₉H₅₂O	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
(+)-Pinoresinol	[H][C@@]12CO[C@@H](C3=CC=C(O)C(OC)=C3)[C@]1([H])CO[C@H]2C1=CC(OC)=C(O)C=C1	358.141638428	C₂₀H₂₂O₆	Polyphenols	Lignans	Publications	Show
(+)-Lariciresinol	COC1=C(O)C=CC(C[C@H]2CO[C@@H]([C@H]2CO)C2=CC(OC)=C(O)C=C2)=C1	360.157288493	C₂₀H₂₄O₆	Polyphenols	Lignans	Publications	Show
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
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
Secoisolariciresinol	COC1=C(O)C=CC(C[C@@H](CO)[C@H](CO)CC2=CC(OC)=C(O)C=C2)=C1	362.172938557	C₂₀H₂₆O₆	Polyphenols	Lignans	Publications	Show
Trigonelline	C[N+]1=CC=CC(=C1)C([O-])=O	137.047678469	C₇H₇NO₂	N-containing compounds	Miscellaneous N-containing compounds	Publications	Show
3-O-Caffeoylquinic acid	[H]\C(=C(\[H])C1=CC(O)=C(O)C=C1)C(=O)OC1CC(O)(CC(O)C1O)C(O)=O	354.09508216	C₁₆H₁₈O₉	Polyphenols	Phenolic acids	Publications	Show
3-p-Coumaroylquinic acid	OC1CC(O)(CC(OC(=O)\C=C\C2=CC=C(O)C=C2)C1O)C(O)=O	338.10016754	C₁₆H₁₈O₈	Polyphenols	Phenolic acids	Publications	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	Publications	Show

Related Metabolites

Name	Structure	Monoisotopic mass	Formula	Family	Class
3-O-Caffeoylquinic acid	[H]\C(=C(\[H])C1=CC(O)=C(O)C=C1)C(=O)OC1CC(O)(CC(O)C1O)C(O)=O	354.09508216	C₁₆H₁₈O₉	Polyphenols	Phenolic acids	Show
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
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
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-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
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-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	436.041133014	C₁₂H₂₂NO₁₀S₃	N-containing compounds	Glucosinolates	Show
Secoisolariciresinol	COC1=C(O)C=CC(C[C@@H](CO)[C@H](CO)CC2=CC(OC)=C(O)C=C2)=C1	362.172938557	C₂₀H₂₆O₆	Polyphenols	Lignans	Show
Enterodiol	OC[C@H](CC1=CC(O)=CC=C1)[C@H](CO)CC1=CC(O)=CC=C1	302.151809188	C₁₈H₂₂O₄	(Poly)phenol metabolites	Lignan metabolites	Show
Enterolactone	OC1=CC=CC(C[C@@H]2COC(=O)[C@H]2CC2=CC(O)=CC=C2)=C1	298.12050906	C₁₈H₁₈O₄	(Poly)phenol metabolites	Lignan metabolites	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
Allyl isothiocyanate	C=CCN=C=S	99.014270339	C₄H₅NS	N-containing compounds	Isothiocyanates	Show
Trigonelline	C[N+]1=CC=CC(=C1)C([O-])=O	137.047678469	C₇H₇NO₂	N-containing compounds	Miscellaneous N-containing compounds	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
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
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

Biomarkers of intake

No Biomarkers of intake found

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