PhytoHub: Showing entry for Rapeseed

Rapeseed

Group:: Oilseed crops

Identification

Name: Rapeseed
Food group: Oilseed crops

External Links

ITIS: 509696

Compounds

	Name	Structure	Monoisotopic mass	Formula	Family	Class
	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	CC(C)[C@H](C)CC[C@@H](C)C1CCC2C3CC=C4C[C@@H](O)CC[C@]4(C)C3CC[C@]12C	400.370516158	C₂₈H₄₈O	Terpenoids	Phytosterols	Publications	Show
	Sinapic acid	COC1=CC(\C=C\C(O)=O)=CC(OC)=C1O	224.068473494	C₁₁H₁₂O₅	Polyphenols	Phenolic acids	Publications	Show
	Ferulic acid	COC1=C(O)C=CC(\C=C\C(O)=O)=C1	194.057908808	C₁₀H₁₀O₄	Polyphenols	Phenolic acids	Publications	Show
	Sinapine	COC1=CC(\C=C/C(=O)OCC[N+](C)(C)C)=CC(OC)=C1O	310.165447883	C₁₆H₂₄NO₅	Polyphenols	Phenolic acids	Publications	Show
	Hesperalin	COC1=C(OC)C=C(C=C1)C(=O)OCC[N+](C)(C)C	268.154883197	C₁₄H₂₂NO₄	Miscellaneous phytochemicals	Not Available	Publications	Show
	4-Hydroxybenzoylcholine	C[N+](C)(C)CCOC(O)=C1C=CC(=O)C=C1	224.128668447	C₁₂H₁₈NO₃	Miscellaneous phytochemicals	Not Available	Publications	Show

Related Metabolites

	Name	Structure	Monoisotopic mass	Formula	Family	Class
	3-(3'-Hydroxyphenyl)propionic acid	OC(=O)CCC1=CC=CC(O)=C1	166.062994186	C₉H₁₀O₃	Polyphenols	Phenolic acids		Show
	3-Hydroxybenzoic acid	OC(=O)C1=CC(O)=CC=C1	138.031694053	C₇H₆O₃	Polyphenols	Phenolic acids		Show
	3-Phenylpropionic acid	OC(=O)CCC1=CC=CC=C1	150.068079564	C₉H₁₀O₂	Polyphenols	Phenolic acids		Show
	3,4-Dimethoxybenzoic acid	COC1=C(OC)C=C(C=C1)C(O)=O	182.057908808	C₉H₁₀O₄	Polyphenols	Phenolic acids		Show
	3',4'-Dihydroxyphenylacetic acid	OC(=O)CC1=CC(O)=C(O)C=C1	168.042258744	C₈H₈O₄	Polyphenols	Phenolic acids		Show
	4-Hydroxybenzoic acid	OC(=O)C1=CC=C(O)C=C1	138.031694053	C₇H₆O₃	Polyphenols	Phenolic acids		Show
	Dihydro-p-coumaric acid	OC(=O)CCC1=CC=C(O)C=C1	166.062994186	C₉H₁₀O₃	Polyphenols	Phenolic acids		Show
	Dihydrocaffeic acid	OC(=O)CCC1=CC=C(O)C(O)=C1	182.057908808	C₉H₁₀O₄	Polyphenols	Phenolic acids		Show
	Dihydroferulic acid	COC1=C(O)C=CC(CCC(O)=O)=C1	196.073558872	C₁₀H₁₂O₄	Polyphenols	Phenolic acids		Show
	Ferulic acid sulfoglucuronide		450.375513	C₁₆H₁₈O₁₃S	Polyphenols	Phenolic acids		Show
	Ferulic acid-4'-O-glucuronide	[H]\C(=C(\[H])C1=CC(OC)=C(O[C@H]2O[C@H]([C@H](O)[C@H](O)[C@@H]2O)C(O)=O)C=C1)C(O)=O	370.08999678	C₁₆H₁₈O₁₀	Polyphenols	Phenolic acids		Show
	Ferulic acid-4'-sulfate	[H]\C(=C(\[H])C1=CC(OC)=C(OS(O)(=O)=O)C=C1)C(O)=O	274.014723364	C₁₀H₁₀O₇S	Polyphenols	Phenolic acids		Show
	Feruloylglycine	COC1=CC(\C=C\C(=O)NCC(O)=O)=CC=C1O	251.079372531	C₁₂H₁₃NO₅	Polyphenols	Phenolic acids		Show
	Hippuric acid	OC(=O)CNC(=O)C1=CC=CC=C1	179.058243159	C₉H₉NO₃	Polyphenols	Polyphenol metabolites		Show
	Protocatechuic acid	OC(=O)C1=CC(O)=C(O)C=C1	154.026608673	C₇H₆O₄	Polyphenols	Phenolic acids		Show
	Sinapic acid O-glucuronide	COC1=CC(\C=C\C(=O)O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=CC(OC)=C1O	400.100561482	C₁₇H₂₀O₁₁	Polyphenols	Phenolic acids		Show
	Sinapic acid-O-sulfate	COC1=CC(\C=C\C(=O)OS(O)(=O)=O)=CC(OC)=C1O	304.02528805	C₁₁H₁₂O₈S	Polyphenols	Phenolic acids		Show
	Vanillic acid	COC1=C(O)C=CC(=C1)C(O)=O	168.042258738	C₈H₈O₄	Polyphenols	Phenolic acids		Show
	Vanilloylglycine	COC1=C(O)C=CC(=C1)C(O)=NCC(O)=O	225.063722467	C₁₀H₁₁NO₅	Polyphenols	Phenolic acids		Show