PhytoHub: Showing entry for Mustard

Mustard

Group:: Condiments and seasonings

Identification

Name: Mustard
ID: 97
Food group: Condiments and seasonings

Synonyms

No Synonyms

External Links

FooDB (Foods): 673

Compounds

	Name	Structure	Monoisotopic mass	Formula	Family	Class
	Ursolic acid	[H][C@@]12[C@@H](C)[C@H](C)CC[C@@]1(CC[C@]1(C)C2=CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(O)=O	456.360345406	C₃₀H₄₈O₃	Terpenoids	Triterpenoids	Publications	Show
	Melatonin	COC1=CC2=C(NC=C2CCNC(C)=O)C=C1	232.121177763	C₁₃H₁₆N₂O₂	Miscellaneous phytochemicals	Not Available	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
	Allyl isothiocyanate	C=CCN=C=S	99.014270339	C₄H₅NS	N-containing compounds	Isothiocyanates	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
	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
	Glucobrassicanapin	OCC1O[C@@H](S\C(CCCC=C)=N\OS([O-])(=O)=O)C(O)[C@@H](O)[C@@H]1O	386.058497156	C₁₂H₂₀NO₉S₂	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
	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
	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
	Sinalbin	OCC1O[C@@H](S\C(CC2=CC=C(O)C=C2)=N\OS(O)(=O)=O)C(O)[C@@H](O)[C@@H]1O	425.045038164	C₁₄H₁₉NO₁₀S₂	N-containing compounds	Glucosinolates	Publications	Show

Related Metabolites

	Name	Structure	Monoisotopic mass	Formula	Family	Class
	Allyl isothiocyanate-N-acetyl-L-cysteine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Allyl isothiocyanate-glutathione				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Allyl isothiocyanate-cysteine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	Allyl isothiocyanate-cysteine-glycine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	1-Cyano-4,5-epithiopentane	N#CCCCC1CS1	127.045570468	C₆H₉NS	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
	Indole-3-carbinol	OCC1=CNC2=CC=CC=C12	147.068413914	C₉H₉NO	N-containing compounds	Miscellaneous N-containing compounds		Show
	Indole-3-acetonitrile	N#CCC1=CNC2=C1C=CC=C2	156.068748266	C₁₀H₈N₂	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	1-Cyano-3,4-epithiobutane	N#CCCC1CS1	113.029920403	C₅H₇NS	N-containing compound metabolites	Miscellaneous N-containing compound metabolites		Show
	6-Sulfatoxymelatonin	[H]N(CCC1=CN([H])C2=CC(OS(O)(=O)=O)=C(OC)C=C12)C(C)=O	328.072907417	C₁₃H₁₆N₂O₆S	Miscellaneous phytochemical metabolites	Miscellaneous phytochemical metabolites		Show
	Allyl isothiocyanate	C=CCN=C=S	99.014270339	C₄H₅NS	N-containing compounds	Isothiocyanates		Show
	1-cyano-2,3-epithiopropane	N#CCC1CS1	99.014270339	C₄H₅NS	N-containing compounds	Miscellaneous N-containing compounds		Show
	Allyl isothiocyanate-N-acetyl-L-cysteine				N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show
	3-butenenitrile	C=CCC#N	67.042199165	C₄H₅N	N-containing compound metabolites	Glucosinolate and isothiocyanate metabolites		Show

Biomarkers of intake

No Biomarkers of intake found