Chemical Formula: C26H30O5
Chemical Formula C26H30O5
Found 68 metabolite its formula value is C26H30O5
Kanzonol J
Kanzonol J is found in herbs and spices. Kanzonol J is a constituent of Glycyrrhiza uralensis (Chinese licorice). Constituent of Glycyrrhiza uralensis (Chinese licorice). Kanzonol J is found in herbs and spices.
2',4,4'-Trihydroxy-6'-methoxy-3',5'-diprenylchalcone
2,4,4-Trihydroxy-6-methoxy-3,5-diprenylchalcone is found in alcoholic beverages. 2,4,4-Trihydroxy-6-methoxy-3,5-diprenylchalcone is a constituent of Humulus lupulus (hops) Constituent of Humulus lupulus (hops). 2,4,4-Trihydroxy-6-methoxy-3,5-diprenylchalcone is found in alcoholic beverages.
1-Methoxyficifolinol
1-Methoxyficifolinol is found in root vegetables. 1-Methoxyficifolinol is isolated from licorice (Glycyrrhiza sp.). Isolated from licorice (Glycyrrhiza species). 1-Methoxyficifolinol is found in root vegetables.
Xanthoangelol G
Xanthoangelol g is a member of the class of compounds known as 3-prenylated chalcones. 3-prenylated chalcones are chalcones featuring a C5-isoprenoid unit at the 3-position. Thus, xanthoangelol g is considered to be a flavonoid lipid molecule. Xanthoangelol g is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Xanthoangelol g can be found in angelica, which makes xanthoangelol g a potential biomarker for the consumption of this food product.
Nitidulin
5-Deoxyhomoflemingin
1-Methoxyficifolinol
A member of the class of pterocarpans that is (6aR,11aR)-pterocarpan substituted by hydroxy groups at positions 3 and 9, a methoxy group at position 1 and a prenyl groups at positions 2 and 8. It has been isolated from Glycyrrhiza uralensis.
1-[2-Methoxy-3-(3-methyl-2-butenyl)-4-hydroxyphenyl]-3-[3-(3-methyl-2-butenyl)-4-hydroxyphenyl]-1,3-propanedione
14,15beta;21,23-Diepoxy-4,4,8-trimethyl-24-nor-5xi,13alpha,14beta,17betaH-chola-1,20,22-trien-3,6,7-trion|14,15beta;21,23-diepoxy-4,4,8-trimethyl-24-nor-5xi,13alpha,14beta,17betaH-chola-1,20,22-triene-3,6,7-trione
lespeflorin D1
A hydroxyisoflavanone that is isoflavanone substituted by hydroxy groups at positions 7 and 4, a methoxy group at position 2 and prenyl groups at positions 8 and 3. Isolated from the roots of Lespedeza floribunda, it acts as a melanin synthesis inhibitor.
OC1=C(C=C2C(C(COC2=C1)C1=C(C=C(C=C1)O)OC)=O)CC=C(/C)CCC=C(C)C
2,4,4-trihydroxy-3-[(2E)-5-methoxy-3,7-dimethylocta-2,6-dienyl]chalcone
1,1-bis-<2-senecionyl-4-(1-ethyl)-phenoxy>ether|1,1-bis-[2-senecionyl-4-(1-ethyl)-phenoxy]ether|meso-1,1-bis-<2-senecionyl-4-(1-ethyl)-phenoxy>ether
5,7-dihydroxy-4-methoxy-8,3-bis(3-methylbut-2-enyl)-flavan-4-one|nimbaflavone
2,2-Dimethyl-5-(4-hydroxyphenethyl)-7-hydroxy-8-(3-methyl-2-butenyl)-2H-1-benzopyran-6-carboxylic acid methyl ester
(6aR,11aR)-3,9-dihydroxy-4-geranyl-1-methoxypterocarpan|bicolosin C
withahisolide E|[(20S,22R,24R)-6alpha,7alpha-epoxy-5alpha-hydroxy-27,28-dinor-17(13?18)-abeo-1-oxo-5alpha-ergost-2,13,15,17-tetraen-22,25-olide]
2,3-Dihydro-3-(2-methoxy-4-hydroxyphenyl)-6,8-di(3-methyl-2-butenyl)-7-hydroxychromone
lespeflorin G2
A member of the class of pterocarpans that is (6aR,11aR)-pterocarpan substituted by hydroxy groups at positions 3 and 8, a methoxy group at position 9 and prenyl groups at positions 2 and 10. Isolated from the roots of Lespedeza floribunda, it acts as a melanin synthesis inhibitor.