NCBI Taxonomy: 1573921

Dichrocephala integrifolia (ncbi_taxid: 1573921)

found 22 associated metabolites at species taxonomy rank level.

Ancestor: Dichrocephala

Child Taxonomies: none taxonomy data.

Astragalin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C21H20O11 (448.1006)


Kaempferol 3-O-beta-D-glucoside is a kaempferol O-glucoside in which a glucosyl residue is attached at position 3 of kaempferol via a beta-glycosidic linkage. It has a role as a trypanocidal drug and a plant metabolite. It is a kaempferol O-glucoside, a monosaccharide derivative, a trihydroxyflavone and a beta-D-glucoside. It is a conjugate acid of a kaempferol 3-O-beta-D-glucoside(1-). Astragalin is a natural product found in Xylopia aromatica, Ficus virens, and other organisms with data available. See also: Moringa oleifera leaf (has part). Astragalin is found in alcoholic beverages. Astragalin is present in red wine. It is isolated from many plant species.Astragalin is a 3-O-glucoside of kaempferol. Astragalin is a chemical compound. It can be isolated from Phytolacca americana (the American pokeweed). A kaempferol O-glucoside in which a glucosyl residue is attached at position 3 of kaempferol via a beta-glycosidic linkage. Present in red wine. Isolated from many plant subspecies Acquisition and generation of the data is financially supported in part by CREST/JST. CONFIDENCE standard compound; INTERNAL_ID 173 Astragalin (Astragaline) a flavonoid with anti-inflammatory, antioxidant, anticancer, bacteriostatic activity. Astragalin inhibits cancer cells proliferation and migration, induces apoptosis. Astragalin is orally active and provides nerve and heart protection, and resistance against and osteoporosis[1]. Astragalin (Astragaline) a flavonoid with anti-inflammatory, antioxidant, anticancer, bacteriostatic activity. Astragalin inhibits cancer cells proliferation and migration, induces apoptosis. Astragalin is orally active and provides nerve and heart protection, and resistance against and osteoporosis[1].

   

Tomentin

2- (3,4-Dihydroxyphenyl) -5,6-dihydroxy-3,7-dimethoxy-4H-1-benzopyran-4-one

C17H14O8 (346.0689)


   

Parthenin

(3aS,6S,6aS,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylidene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione

C15H18O4 (262.1205)


Parthenin is a sesquiterpene lactone.

   

Trifolin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one

C21H20O11 (448.1006)


Kaempferol 3-o-beta-d-galactopyranoside, also known as trifolin or trifolioside, is a member of the class of compounds known as flavonoid-3-o-glycosides. Flavonoid-3-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Kaempferol 3-o-beta-d-galactopyranoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Kaempferol 3-o-beta-d-galactopyranoside can be found in horseradish, which makes kaempferol 3-o-beta-d-galactopyranoside a potential biomarker for the consumption of this food product. Kaempferol 3-O-beta-D-galactoside is a beta-D-galactoside compound with a 4,5,7-trihydroxychromen-3-yl group at the anomeric position. It has a role as a plant metabolite and an antifungal agent. It is a beta-D-galactoside, a monosaccharide derivative, a glycosyloxyflavone and a trihydroxyflavone. It is functionally related to a kaempferol. It is a conjugate acid of a kaempferol 3-O-beta-D-galactoside(1-). Trifolin is a natural product found in Lotus ucrainicus, Saxifraga tricuspidata, and other organisms with data available. Isoastragalin is found in fats and oils. Isoastragalin is isolated from Gossypium hirsutum (cotton) and other plant species. A beta-D-galactoside compound with a 4,5,7-trihydroxychromen-3-yl group at the anomeric position.

   

Hymenin

6a-hydroxy-6,9a-dimethyl-3-methylidene-2H,3H,3aH,4H,5H,6H,6aH,9H,9aH,9bH-azuleno[4,5-b]furan-2,9-dione

C15H18O4 (262.1205)


   

6-Hydroxykaempferol 3,6-dimethylether

5,7-dihydroxy-2-(4-hydroxyphenyl)-3,6-dimethoxy-4H-chromen-4-one

C17H14O7 (330.0739)


6-hydroxykaempferol 3,6-dimethylether, also known as 4,5,7-trihydroxy-3,6-dimethoxyflavone, is a member of the class of compounds known as 6-o-methylated flavonoids. 6-o-methylated flavonoids are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone. Thus, 6-hydroxykaempferol 3,6-dimethylether is considered to be a flavonoid lipid molecule. 6-hydroxykaempferol 3,6-dimethylether is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 6-hydroxykaempferol 3,6-dimethylether can be found in sweet cherry, which makes 6-hydroxykaempferol 3,6-dimethylether a potential biomarker for the consumption of this food product.

   

Astragalin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone

C21H20O11 (448.1006)


Astragalin (Astragaline) a flavonoid with anti-inflammatory, antioxidant, anticancer, bacteriostatic activity. Astragalin inhibits cancer cells proliferation and migration, induces apoptosis. Astragalin is orally active and provides nerve and heart protection, and resistance against and osteoporosis[1]. Astragalin (Astragaline) a flavonoid with anti-inflammatory, antioxidant, anticancer, bacteriostatic activity. Astragalin inhibits cancer cells proliferation and migration, induces apoptosis. Astragalin is orally active and provides nerve and heart protection, and resistance against and osteoporosis[1].

   

Veronicafolin

3,5,4-Trihydroxy-6,7,3-trimeoxyflavone

C18H16O8 (360.0845)


   

Trifolin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone

C21H20O11 (448.1006)


Isolated from Gossypium hirsutum (cotton) and other plant subspecies Isoastragalin is found in fats and oils. Isolated from liquorice (Glycyrrhiza glabra). Acetylastragalin is found in herbs and spices. Widespread occurrence in plant world, e.g. Pinus sylvestris (Scotch pine) and fruits of Scolymus hispanicus (Spanish salsify). Kaempferol 3-galactoside is found in many foods, some of which are horseradish, almond, peach, and tea.

   

Ethyl 3,4-dicaffeoylquinate

ethyl (1S,3R,4R,5R)-3,4-bis[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]-1,5-dihydroxycyclohexane-1-carboxylate

C27H28O12 (544.1581)


Ethyl 3,4-dicaffeoylquinate is a natural product found in Dichrocephala integrifolia with data available.

   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3,6-dimethoxy-4H-chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3,6-dimethoxy-4H-chromen-4-one

C17H14O7 (330.0739)


   

3,4,5,6-Tetrahydroxy-3,7-dimethoxyflavone

3,4,5,6-Tetrahydroxy-3,7-dimethoxyflavone

C17H14O8 (346.0689)


   

(6s,6ar,9as,9br)-6a-hydroxy-3-(hydroxymethyl)-6,9a-dimethyl-4h,5h,6h,7h,8h,9bh-azuleno[4,5-b]furan-2,9-dione

(6s,6ar,9as,9br)-6a-hydroxy-3-(hydroxymethyl)-6,9a-dimethyl-4h,5h,6h,7h,8h,9bh-azuleno[4,5-b]furan-2,9-dione

C15H20O5 (280.1311)


   

3-(2-{6a-hydroxy-6,9a-dimethyl-2,9-dioxo-4h,5h,6h,9bh-azuleno[4,5-b]furan-3-yl}ethyl)-3,6a-dihydroxy-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

3-(2-{6a-hydroxy-6,9a-dimethyl-2,9-dioxo-4h,5h,6h,9bh-azuleno[4,5-b]furan-3-yl}ethyl)-3,6a-dihydroxy-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

C30H36O9 (540.2359)


   

(3s,3ar,6s,6as,9as,9br)-3,6a-dihydroxy-3-(hydroxymethyl)-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

(3s,3ar,6s,6as,9as,9br)-3,6a-dihydroxy-3-(hydroxymethyl)-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

C15H20O6 (296.126)


   

(3s,3ar,6s,6as,9as,9br)-3-{2-[(6s,6as,9as,9br)-6a-hydroxy-6,9a-dimethyl-2,9-dioxo-4h,5h,6h,9bh-azuleno[4,5-b]furan-3-yl]ethyl}-3,6a-dihydroxy-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

(3s,3ar,6s,6as,9as,9br)-3-{2-[(6s,6as,9as,9br)-6a-hydroxy-6,9a-dimethyl-2,9-dioxo-4h,5h,6h,9bh-azuleno[4,5-b]furan-3-yl]ethyl}-3,6a-dihydroxy-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

C30H36O9 (540.2359)


   

(3r,3ar,6s,6as,9as,9br)-3,6a-dihydroxy-3-(hydroxymethyl)-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

(3r,3ar,6s,6as,9as,9br)-3,6a-dihydroxy-3-(hydroxymethyl)-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

C15H20O6 (296.126)


   

(6s,6as,9as,9br)-6a-hydroxy-3-(hydroxymethyl)-6,9a-dimethyl-4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

(6s,6as,9as,9br)-6a-hydroxy-3-(hydroxymethyl)-6,9a-dimethyl-4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

C15H18O5 (278.1154)


   

(3r,3ar,6s,6as,9as,9br)-3-{2-[(6s,6as,9as,9br)-6a-hydroxy-6,9a-dimethyl-2,9-dioxo-4h,5h,6h,9bh-azuleno[4,5-b]furan-3-yl]ethyl}-3,6a-dihydroxy-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

(3r,3ar,6s,6as,9as,9br)-3-{2-[(6s,6as,9as,9br)-6a-hydroxy-6,9a-dimethyl-2,9-dioxo-4h,5h,6h,9bh-azuleno[4,5-b]furan-3-yl]ethyl}-3,6a-dihydroxy-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

C30H36O9 (540.2359)


   

6a-hydroxy-3-(hydroxymethyl)-6,9a-dimethyl-4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

6a-hydroxy-3-(hydroxymethyl)-6,9a-dimethyl-4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

C15H18O5 (278.1154)


   

3,6a-dihydroxy-3-(hydroxymethyl)-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

3,6a-dihydroxy-3-(hydroxymethyl)-6,9a-dimethyl-3ah,4h,5h,6h,9bh-azuleno[4,5-b]furan-2,9-dione

C15H20O6 (296.126)


   

6a-hydroxy-3-(hydroxymethyl)-6,9a-dimethyl-4h,5h,6h,7h,8h,9bh-azuleno[4,5-b]furan-2,9-dione

6a-hydroxy-3-(hydroxymethyl)-6,9a-dimethyl-4h,5h,6h,7h,8h,9bh-azuleno[4,5-b]furan-2,9-dione

C15H20O5 (280.1311)