NCBI Taxonomy: 2708828

Erythrina vogelii (ncbi_taxid: 2708828)

found 96 associated metabolites at species taxonomy rank level.

Ancestor: Erythrina

Child Taxonomies: none taxonomy data.

Irigenin

4H-1-Benzopyran-4-one,5,7-dihydroxy-3-(3-hydroxy-4,5-dimethoxyphenyl)-6-methoxy-

C18H16O8 (360.0845136)


Irigenin, also known as 5,7,3-trihydroxy-6,4,5-trimethoxyisoflavone, is a member of the class of compounds known as 3-hydroxy,4-methoxyisoflavonoids. 3-hydroxy,4-methoxyisoflavonoids are isoflavonoids carrying a methoxy group attached to the C4 atom, as well as a hydroxyl group at the C3-position of the isoflavonoid backbone. Thus, irigenin is considered to be a flavonoid lipid molecule. Irigenin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Irigenin can be synthesized from isoflavone. Irigenin can also be synthesized into iridin. Irigenin can be found in lima bean, which makes irigenin a potential biomarker for the consumption of this food product. Irigenin is an O-methylated isoflavone, a type of flavonoid. It can be isolated from the rhizomes of the leopard lily (Belamcanda chinensis), and Iris kemaonensis . Irigenin is a hydroxyisoflavone that is isoflavone substituted by hydroxy groups at positions 5, 7 and 3 and methoxy groups at positions 6, 4 and 5 respectively. It has a role as a plant metabolite. It is a hydroxyisoflavone and a member of 4-methoxyisoflavones. It is functionally related to an isoflavone. Irigenin is a natural product found in Iris milesii, Iris tectorum, and other organisms with data available. Irigenin is a is a lead compound, and mediates its anti-metastatic effect by specifically and selectively blocking α9β1 and α4β1 integrins binding sites on C-C loop of Extra Domain A (EDA). Irigenin shows anti-cancer properties. It sensitizes TRAIL-induced apoptosis via enhancing pro-apoptotic molecules in gastric cancer cells[1]. Irigenin is a is a lead compound, and mediates its anti-metastatic effect by specifically and selectively blocking α9β1 and α4β1 integrins binding sites on C-C loop of Extra Domain A (EDA). Irigenin shows anti-cancer properties. It sensitizes TRAIL-induced apoptosis via enhancing pro-apoptotic molecules in gastric cancer cells[1].

   

Lampranthin II

3-{[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C27H30O16 (610.153378)


Panasenoside, also known as lilyn, 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. Panasenoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Panasenoside can be found in tea, which makes panasenoside a potential biomarker for the consumption of this food product. Kaempferol 3-O-sophoroside, a derivative of Kaempferol, is isolated from the leaves of cultivated mountain ginseng (Panax ginseng) with anti-inflammatory effects[1]. Kaempferol 3-O-sophoroside, a derivative of Kaempferol, is isolated from the leaves of cultivated mountain ginseng (Panax ginseng) with anti-inflammatory effects[1].

   

3'-(gamma,gamma-Dimethylallyl)genistein

5,7-Dihydroxy-3-[4-hydroxy-3-(3-methyl-2-butenyl)phenyl]-4H-1-benzopyran-4-one, 9CI

C20H18O5 (338.1154178)


Isowighteone is a member of the class of 7-hydroxyisoflavones that is isoflavone substituted by hydroxy groups at positions 5, 7 and 4 and a prenyl group at position 3. It has been isolated from Ficus mucuso. It has a role as a plant metabolite. It is functionally related to an isoflavone. Isowighteone is a natural product found in Sophora tomentosa, Erythrina addisoniae, and other organisms with data available. A member of the class of 7-hydroxyisoflavones that is isoflavone substituted by hydroxy groups at positions 5, 7 and 4 and a prenyl group at position 3. It has been isolated from Ficus mucuso. 3-(gamma,gamma-Dimethylallyl)genistein is found in pigeon pea. 3-(gamma,gamma-Dimethylallyl)genistein is isolated from Cajanus cajan (pigeon pea). Isolated from Cajanus cajan (pigeon pea). 3-(gamma,gamma-Dimethylallyl)genistein is found in pigeon pea and pulses.

   

Cyanidin 3-rhamnoside

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-1λ⁴-chromen-1-ylium

C21H21O10+ (433.11346660000004)


Cyanidin 3-rhamnoside is found in blackcurrant. Cyanidin 3-rhamnoside is isolated from various plant species, e.g. Chamaecyparis sp. and Plumbago rosea [CCD]. Isolated from various plant subspecies, e.g. Chamaecyparis species and Plumbago rosea [CCD]. Cyanidin 3-rhamnoside is found in common pea and blackcurrant.

   

Atalantoflavone

5-Hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b]dipyran-4-one, 9ci

C20H16O5 (336.0997686)


Atalantoflavone is found in citrus. Atalantoflavone is isolated from rootbark of lemon tree

   

Isolupalbigenin

5,7-dihydroxy-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

C25H26O5 (406.17801460000004)


   

Sophoraflavonoloside

3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C27H30O16 (610.153378)


Kaempferol 3-O-beta-D-glucosyl-(1->2)-beta-D-glucoside is a sophoroside that is kaempferol attached to a beta-D-sophorosyl residue at position 3 via a glycosidic linkage. It has a role as a plant metabolite. It is a trihydroxyflavone and a sophoroside. Sophoraflavonoloside is a natural product found in Equisetum palustre, Vigna subterranea, and other organisms with data available. Kaempferol 3-O-sophoroside, a derivative of Kaempferol, is isolated from the leaves of cultivated mountain ginseng (Panax ginseng) with anti-inflammatory effects[1]. Kaempferol 3-O-sophoroside, a derivative of Kaempferol, is isolated from the leaves of cultivated mountain ginseng (Panax ginseng) with anti-inflammatory effects[1].

   

VOGELIN G

4,5-Dihydro-5,7-dihydroxy-3-prenyl-6,6-dimethylpyrano[2,3:4,5]isoflavone

C25H26O6 (422.17292960000003)


   

VOGELIN F

5,7,4-Trihydroxy-2-methoxy-5-prenylisoflavone

C21H20O6 (368.125982)


   

Vogelin C

5,7,2,4-Tetrahydroxy-8,5-diprenylisoflavone

C25H26O6 (422.17292960000003)


   
   

6-Prenylapigenin

5,7-Dihydroxy-2- (4-hydroxyphenyl) -6- (3-methyl-2-butenyl) -4H-1-benzopyran-4-one

C20H18O5 (338.1154178)


6-Prenylapigenin is a natural product found in Ficus glumosa, Maclura cochinchinensis, and other organisms with data available.

   

Carpachromene

5-Hydroxy-8- (4-hydroxyphenyl) -2,2-dimethyl-2H,6H-benzo [ 1,2-b:5,4-b ] dipyran-6-one

C20H16O5 (336.0997686)


   

isoderrone

5,7-Dihydroxy-6",6"-dimethylpyrano [ 2",3":4,3 ] isoflavone

C20H16O5 (336.0997686)


A hydroxyisoflavone that is isoflavone substituted by hydroxy groups at positions 5 and 7 and a 6,6-dimethyl-3,6-dihydro-2H-pyran across positions 3 and 4 respectively. It has been isolated from Ficus mucuso.

   

Isochandalone

5,7-Dihydroxy-6-prenyl-6",6"-dimethylpyrano [ 2",3":4,3 ] isoflavone

C25H24O5 (404.1623654)


   

ulexone A

5,7-Dihydroxy-8-prenyl-6,6-dimethylpyrano[2,3:4,3]isoflavone

C25H24O5 (404.1623654)


   

6,8-diprenylgenistein

3- (4-Hydroxyphenyl) -5,7-dihydroxy-6,8-bis (3-methyl-2-butenyl) -4H-1-benzopyran-4-one

C25H26O5 (406.17801460000004)


   

8-prenylluteone

5,7,2,4-Tetrahydroxy-6,8-diprenylisoflavone

C25H26O6 (422.17292960000003)


   

Isowighteone

5,7,4-Trihydroxy-3-prenylisoflavone

C20H18O5 (338.1154178)


   

Irigenin

4H-1-Benzopyran-4-one,5,7-dihydroxy-3-(3-hydroxy-4,5-dimethoxyphenyl)-6-methoxy-

C18H16O8 (360.0845136)


Irigenin is a hydroxyisoflavone that is isoflavone substituted by hydroxy groups at positions 5, 7 and 3 and methoxy groups at positions 6, 4 and 5 respectively. It has a role as a plant metabolite. It is a hydroxyisoflavone and a member of 4-methoxyisoflavones. It is functionally related to an isoflavone. Irigenin is a natural product found in Iris milesii, Iris tectorum, and other organisms with data available. A hydroxyisoflavone that is isoflavone substituted by hydroxy groups at positions 5, 7 and 3 and methoxy groups at positions 6, 4 and 5 respectively. Irigenin is a is a lead compound, and mediates its anti-metastatic effect by specifically and selectively blocking α9β1 and α4β1 integrins binding sites on C-C loop of Extra Domain A (EDA). Irigenin shows anti-cancer properties. It sensitizes TRAIL-induced apoptosis via enhancing pro-apoptotic molecules in gastric cancer cells[1]. Irigenin is a is a lead compound, and mediates its anti-metastatic effect by specifically and selectively blocking α9β1 and α4β1 integrins binding sites on C-C loop of Extra Domain A (EDA). Irigenin shows anti-cancer properties. It sensitizes TRAIL-induced apoptosis via enhancing pro-apoptotic molecules in gastric cancer cells[1].

   
   

kaempferol 3-O-sophoroside

kaempferol 3-O-sophoroside

C27H30O16 (610.153378)


Annotation level-1

   
   

30373-88-7

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

C27H30O16 (610.153378)


Kaempferol 3-O-sophoroside, a derivative of Kaempferol, is isolated from the leaves of cultivated mountain ginseng (Panax ginseng) with anti-inflammatory effects[1]. Kaempferol 3-O-sophoroside, a derivative of Kaempferol, is isolated from the leaves of cultivated mountain ginseng (Panax ginseng) with anti-inflammatory effects[1].

   
   

(3s)-5,7-dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-2,3-dihydro-1-benzopyran-4-one

(3s)-5,7-dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-2,3-dihydro-1-benzopyran-4-one

C21H22O6 (370.1416312)


   

5,7-dihydroxy-3-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

5,7-dihydroxy-3-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C26H30O5 (422.209313)


   

5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethylpyrano[2,3-h]chromen-10-one

5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethylpyrano[2,3-h]chromen-10-one

C20H16O5 (336.0997686)


   

(2s)-4-hydroxy-8-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2h,3h-furo[2,3-f]chromen-9-one

(2s)-4-hydroxy-8-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2h,3h-furo[2,3-f]chromen-9-one

C25H26O6 (422.17292960000003)


   

5,7-dihydroxy-3-{4-hydroxy-3-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]phenyl}chromen-4-one

5,7-dihydroxy-3-{4-hydroxy-3-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]phenyl}chromen-4-one

C20H18O6 (354.1103328)


   

6-[(2r)-2,3-dihydroxy-3-methylbutyl]-5-hydroxy-9-(4-hydroxyphenyl)-2,2-dimethylpyrano[2,3-h]chromen-10-one

6-[(2r)-2,3-dihydroxy-3-methylbutyl]-5-hydroxy-9-(4-hydroxyphenyl)-2,2-dimethylpyrano[2,3-h]chromen-10-one

C25H26O7 (438.1678446)


   

5,7-dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-2,3-dihydro-1-benzopyran-4-one

5,7-dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-2,3-dihydro-1-benzopyran-4-one

C21H22O6 (370.1416312)


   

3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)chromen-4-one

3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)chromen-4-one

C25H26O6 (422.17292960000003)


   

5,7-dihydroxy-3-[(3r)-3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-6-yl]chromen-4-one

5,7-dihydroxy-3-[(3r)-3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-6-yl]chromen-4-one

C25H26O6 (422.17292960000003)


   

6-(2,3-dihydroxy-3-methylbutyl)-5-hydroxy-9-(4-hydroxyphenyl)-2,2-dimethylpyrano[2,3-h]chromen-10-one

6-(2,3-dihydroxy-3-methylbutyl)-5-hydroxy-9-(4-hydroxyphenyl)-2,2-dimethylpyrano[2,3-h]chromen-10-one

C25H26O7 (438.1678446)


   

3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-6h,7h-pyrano[3,2-g]chromen-4-one

3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-6h,7h-pyrano[3,2-g]chromen-4-one

C25H26O6 (422.17292960000003)


   

5,7-dihydroxy-3-[4-hydroxy-2-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one

5,7-dihydroxy-3-[4-hydroxy-2-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one

C21H20O6 (368.125982)


   

5,7-dihydroxy-3-[(3s)-3-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]chromen-4-one

5,7-dihydroxy-3-[(3s)-3-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]chromen-4-one

C20H18O6 (354.1103328)


   

(3s)-5,7-dihydroxy-3-[4-hydroxy-2-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-2,3-dihydro-1-benzopyran-4-one

(3s)-5,7-dihydroxy-3-[4-hydroxy-2-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-2,3-dihydro-1-benzopyran-4-one

C21H22O6 (370.1416312)


   

5,7-dihydroxy-3-[4-hydroxy-3-(4-hydroxy-3-methylbut-2-en-1-yl)phenyl]chromen-4-one

5,7-dihydroxy-3-[4-hydroxy-3-(4-hydroxy-3-methylbut-2-en-1-yl)phenyl]chromen-4-one

C20H18O6 (354.1103328)


   

(3r)-5,7-dihydroxy-3-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

(3r)-5,7-dihydroxy-3-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C26H30O5 (422.209313)


   

4-hydroxy-8-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2h,3h-furo[2,3-f]chromen-9-one

4-hydroxy-8-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2h,3h-furo[2,3-f]chromen-9-one

C25H26O6 (422.17292960000003)


   

(1s,10s)-3-methoxy-15-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,14-diol

(1s,10s)-3-methoxy-15-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,14-diol

C21H22O5 (354.1467162)


   

5,7-dihydroxy-3-[3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-6-yl]chromen-4-one

5,7-dihydroxy-3-[3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-6-yl]chromen-4-one

C25H26O6 (422.17292960000003)