NCBI Taxonomy: 56519

Anvillea garcinii (ncbi_taxid: 56519)

found 26 associated metabolites at species taxonomy rank level.

Ancestor: Anvillea

Child Taxonomies: Anvillea garcinii subsp. radiata

Spinacetin

3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-4H-1-benzopyran-4-one, 9ci

C17H14O8 (346.0689)


Isolated from spinach (Spinacia oleracea). Spinacetin is found in german camomile, green vegetables, and spinach. Spinacetin is found in german camomile. Spinacetin is isolated from spinach (Spinacia oleracea

   

Hispidulin

4H-1-Benzopyran-4-one, 5, 7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-

C16H12O6 (300.0634)


Hispidulin is a monomethoxyflavone that is scutellarein methylated at position 6. It has a role as an apoptosis inducer, an anti-inflammatory agent, an antioxidant, an anticonvulsant, an antineoplastic agent and a plant metabolite. It is a trihydroxyflavone and a monomethoxyflavone. It is functionally related to a scutellarein. Hispidulin (4,5,7-trihydroxy-6-methoxyflavone) is a potent benzodiazepine (BZD) receptor ligand with positive allosteric properties. Hispidulin is a natural product found in Eupatorium cannabinum, Eupatorium perfoliatum, and other organisms with data available. See also: Arnica montana Flower (part of). A monomethoxyflavone that is scutellarein methylated at position 6. 6-methylscutellarein, also known as 4,5,7-trihydroxy-6-methoxyflavone or dinatin, 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-methylscutellarein is considered to be a flavonoid lipid molecule. 6-methylscutellarein is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 6-methylscutellarein can be found in a number of food items such as italian oregano, common sage, sunflower, and common thyme, which makes 6-methylscutellarein a potential biomarker for the consumption of these food products. Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM. Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM.

   

nepetin

4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy- (9CI)

C16H12O7 (316.0583)


Eupafolin, also known as 6-methoxy 5 or 734-tetrahydroxyflavone, 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, eupafolin is considered to be a flavonoid lipid molecule. Eupafolin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Eupafolin can be found in common sage, lemon verbena, rosemary, and sesame, which makes eupafolin a potential biomarker for the consumption of these food products. 6-Methoxyluteolin is a natural product found in Eupatorium album, Eupatorium altissimum, and other organisms with data available. See also: Arnica montana Flower (has part). Nepetin (6-Methoxyluteolin) is a natural flavonoid isolated from Eupatorium ballotaefolium HBK with potent anti-inflammatory activities. Nepetin inhibits IL-6, IL-8 and MCP-1 secretion with IC50 values of 4.43 μM, 3.42 μM and 4.17 μM, respectively in ARPE-19 cells[1][2]. Nepetin (6-Methoxyluteolin) is a natural flavonoid isolated from Eupatorium ballotaefolium HBK with potent anti-inflammatory activities. Nepetin inhibits IL-6, IL-8 and MCP-1 secretion with IC50 values of 4.43 μM, 3.42 μM and 4.17 μM, respectively in ARPE-19 cells[1][2].

   

Spinacetin 7-glucoside

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

C23H24O13 (508.1217)


   

Jaceosidin

4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-

C17H14O7 (330.0739)


Jaceosidin, 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, jaceosidin is considered to be a flavonoid lipid molecule. Jaceosidin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Jaceosidin can be found in lemon verbena, which makes jaceosidin a potential biomarker for the consumption of this food product. Jaceosidin is a flavonoid isolated from Artemisia vestita, induces apoptosis in cancer cells, activates Bax and down-regulates Mcl-1 and c-FLIP expression[1]. Jaceosidin exhibits anti-cancer[2], anti-inflammatory activities, decreases leves of inflammatory markers, and suppresses COX-2 expression and NF-κB activation[3]. Jaceosidin is a flavonoid isolated from Artemisia vestita, induces apoptosis in cancer cells, activates Bax and down-regulates Mcl-1 and c-FLIP expression[1]. Jaceosidin exhibits anti-cancer[2], anti-inflammatory activities, decreases leves of inflammatory markers, and suppresses COX-2 expression and NF-κB activation[3].

   

Spinacetin

3,5,7-Trihydroxy-2- (4-hydroxy-3-methoxyphenyl) -6-methoxy-4H-1-benzopyran-4-one

C17H14O8 (346.0689)


   

(2r,4s,5e,9r,12s)-5,9-dimethyl-15-methylidene-3,10,13-trioxatetracyclo[10.3.0.0²,⁴.0⁹,¹¹]pentadec-5-en-14-one

(2r,4s,5e,9r,12s)-5,9-dimethyl-15-methylidene-3,10,13-trioxatetracyclo[10.3.0.0²,⁴.0⁹,¹¹]pentadec-5-en-14-one

C15H18O4 (262.1205)


   

4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

C15H18O4 (262.1205)


   

5,9-dimethyl-15-methylidene-3,10,13-trioxatetracyclo[10.3.0.0²,⁴.0⁹,¹¹]pentadec-5-en-14-one

5,9-dimethyl-15-methylidene-3,10,13-trioxatetracyclo[10.3.0.0²,⁴.0⁹,¹¹]pentadec-5-en-14-one

C15H18O4 (262.1205)


   

(2s,4r,7z,11s)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

(2s,4r,7z,11s)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

C15H18O4 (262.1205)


   

2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-3-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-3-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

C29H34O16 (638.1847)


   

(1r,2r,4s,5e,9r,11s,12s)-5,9-dimethyl-15-methylidene-3,10,13-trioxatetracyclo[10.3.0.0²,⁴.0⁹,¹¹]pentadec-5-en-14-one

(1r,2r,4s,5e,9r,11s,12s)-5,9-dimethyl-15-methylidene-3,10,13-trioxatetracyclo[10.3.0.0²,⁴.0⁹,¹¹]pentadec-5-en-14-one

C15H18O4 (262.1205)


   

9-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-13-one

9-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-13-one

C15H20O4 (264.1362)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-3-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-3-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C22H22O12 (478.1111)


   

(1s,2r,4r,7z,11s)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

(1s,2r,4r,7z,11s)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

C15H18O4 (262.1205)


   

5-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C24H26O12 (506.1424)


   

(1s,2s,4r,7e,11s)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

(1s,2s,4r,7e,11s)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

C15H18O4 (262.1205)


   

(1s,2s,4r,7z,11s)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

(1s,2s,4r,7z,11s)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-9,13-dione

C15H18O4 (262.1205)


   

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(1r,2s,3r,4r)-1,2,3,4-tetrahydroxypentyl]oxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(1r,2s,3r,4r)-1,2,3,4-tetrahydroxypentyl]oxan-2-yl]oxy}chromen-4-one

C25H28O15 (568.1428)


   

3-{[(2s,5r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one

3-{[(2s,5r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one

C28H32O17 (640.1639)


   

2-(3,4-dihydroxyphenyl)-3,7-bis({[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]peroxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-3,7-bis({[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-5-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]peroxy}chromen-4-one

C33H40O23 (804.196)


   

5-hydroxy-2-(4-hydroxyphenyl)-6,7-dimethoxy-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(4-hydroxyphenyl)-6,7-dimethoxy-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C23H24O12 (492.1268)


   

3-{[(2s,5r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-4-one

3-{[(2s,5r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-4-one

C29H34O18 (670.1745)


   

7-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-3,5,6-trihydroxychromen-4-one

7-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-3,5,6-trihydroxychromen-4-one

C27H30O18 (642.1432)


   

(1s,2s,4r,7e,9r,11s)-9-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-13-one

(1s,2s,4r,7e,9r,11s)-9-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-13-one

C15H20O4 (264.1362)


   

(1s,2s,4r,7e,9s,11s)-9-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-13-one

(1s,2s,4r,7e,9s,11s)-9-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-13-one

C15H20O4 (264.1362)