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
Carotene-beta	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)[[email protected]@H](C)\C=C\[[email protected]@H](C)C1CCC2C3CC=C4C[[email protected]@H](O)CC[[email protected]]4(C)C3CC[[email protected]]12C	398.354866101	C₂₈H₄₆O	Terpenoids	Phytosterols	Publications	Show
Campesterol	[H][[email protected]@]1(CC[[email protected]@]2([H])[[email protected]]3([H])CC=C4C[[email protected]@H](O)CC[[email protected]]4(C)[[email protected]@]3([H])CC[[email protected]]12C)[[email protected]](C)CC[[email protected]@H](C)C(C)C	400.370516166	C₂₈H₄₈O	Terpenoids	Phytosterols	Publications	Show
Sitostanol-beta	CC[[email protected]](CC[[email protected]@H](C)C1CCC2C3CCC4C[[email protected]@H](O)CC[[email protected]]4(C)C3CC[[email protected]]12C)C(C)C	416.401816294	C₂₉H₅₂O	Terpenoids	Phytosterols	Publications	Show
Sitosterol-beta	CC[[email protected]](CC[[email protected]@H](C)C1CCC2C3CC=C4C[[email protected]@H](O)CC[[email protected]]4(C)C3CC[[email protected]]12C)C(C)C	414.38616623	C₂₉H₅₀O	Terpenoids	Phytosterols	Publications	Show
Stigmasterol	CC[[email protected]](\C=C\[[email protected]@H](C)C1CCC2C3CC=C4C[[email protected]@H](O)CC[[email protected]]4(C)C3CC[[email protected]]12C)C(C)C	412.370516166	C₂₉H₄₈O	Terpenoids	Phytosterols	Publications	Show
(+)-Pinoresinol	[H][[email protected]@]12CO[[email protected]@H](C3=CC=C(O)C(OC)=C3)[[email protected]]1([H])CO[[email protected]]2C1=CC(OC)=C(O)C=C1	358.141638428	C₂₀H₂₂O₆	Polyphenols	Lignans	Publications	Show
(+)-Lariciresinol	COC1=C(O)C=CC(C[[email protected]]2CO[[email protected]@H]([[email protected]]2CO)C2=CC(OC)=C(O)C=C2)=C1	360.157288493	C₂₀H₂₄O₆	Polyphenols	Lignans	Publications	Show
Neoglucobrassicin	CON1C=C(C\C(S[[email protected]@H]2OC(CO)[[email protected]@H](O)[[email protected]](O)C2O)=N/OS([O-])(=O)=O)C2=C1C=CC=C2	477.064310812	C₁₇H₂₁N₂O₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show
Progoitrin	[H][[email protected]@](O)(C\C(S[[email protected]@H]1OC(CO)[[email protected]@H](O)[[email protected]](O)C1O)=N/OS([O-])(=O)=O)C=C	388.037761712	C₁₁H₁₈NO₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show
Gluconasturtiin	OCC1O[[email protected]@H](S\C(CCC2=CC=CC=C2)=N\OS([O-])(=O)=O)C(O)[[email protected]@H](O)[[email protected]@H]1O	422.058497156	C₁₅H₂₀NO₉S₂	N-containing compounds	Glucosinolates	Publications	Show
Sinigrin	OCC1O[[email protected]@H](S\C(CC=C)=N\OS([O-])(=O)=O)C(O)[[email protected]@H](O)[[email protected]@H]1O	358.027197027	C₁₀H₁₆NO₉S₂	N-containing compounds	Glucosinolates	Publications	Show
Glucoiberin	CS(=O)CCC\C(S[[email protected]@H]1OC(CO)[[email protected]@H](O)[[email protected]](O)C1O)=N/OS([O-])(=O)=O	422.02548295	C₁₁H₂₀NO₁₀S₃	N-containing compounds	Glucosinolates	Publications	Show
4-Hydroxyglucobrassicin	OCC1O[[email protected]@H](S\C(CC2=CNC3=C2C(O)=CC=C3)=N\OS([O-])(=O)=O)C(O)[[email protected]@H](O)[[email protected]@H]1O	463.048660748	C₁₆H₁₉N₂O₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show
4-Methoxyglucobrassicin	COC1=CC=CC2=C1C(C\C(S[[email protected]@H]1OC(CO)[[email protected]@H](O)[[email protected]](O)C1O)=N/OS([O-])(=O)=O)=CN2	477.064310812	C₁₇H₂₁N₂O₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show
Glucoraphanin	CS(=O)CCCC\C(S[[email protected]@H]1OC(CO)[[email protected]@H](O)[[email protected]](O)C1O)=N/OS([O-])(=O)=O	436.041133014	C₁₂H₂₂NO₁₀S₃	N-containing compounds	Glucosinolates	Publications	Show
Gluconapin	OCC1O[[email protected]@H](S\C(CCC=C)=N\OS([O-])(=O)=O)C(O)[[email protected]@H](O)[[email protected]@H]1O	372.042847092	C₁₁H₁₈NO₉S₂	N-containing compounds	Glucosinolates	Publications	Show
Glucobrassicin	OCC1O[[email protected]@H](S\C(CC2=CNC3=C2C=CC=C3)=N\OS([O-])(=O)=O)C(O)[[email protected]@H](O)[[email protected]@H]1O	447.053746128	C₁₆H₁₉N₂O₉S₂	N-containing compounds	Glucosinolates	Publications	Show
Secoisolariciresinol	COC1=C(O)C=CC(C[[email protected]@H](CO)[[email protected]](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	Alkaloids	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

Related Metabolites

Name	Structure	Monoisotopic mass	Formula	Family	Class
Retinal	C\C(\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C)=C/C=O	284.214015522	C₂₀H₂₈O	Terpenoids	Carotenoids	Show
Enterodiol	OC[[email protected]](CC1=CC(O)=CC=C1)[[email protected]](CO)CC1=CC(O)=CC=C1	302.151809188	C₁₈H₂₂O₄	Polyphenols	Lignans	Show
Enterolactone	OC1=CC=CC(C[[email protected]@H]2COC(=O)[[email protected]]2CC2=CC(O)=CC=C2)=C1	298.12050906	C₁₈H₁₈O₄	Polyphenols	Lignans	Show
Trigonelline	C[N+]1=CC=CC(=C1)C([O-])=O	137.047678469	C₇H₇NO₂	N-containing compounds	Alkaloids	Show

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