NCBI Taxonomy: 1764340

Boronia lanceolata (ncbi_taxid: 1764340)

found 28 associated metabolites at species taxonomy rank level.

Ancestor: Boronia

Child Taxonomies: none taxonomy data.

demethylsuberosin

2H-1-Benzopyran-2-one, 7-hydroxy-6-(3-methyl-2-buten-1-yl)-

C14H14O3 (230.0943)


Demethylsuberosin, also known as 7-hydroxy-6-prenylcoumarin or 7-hydroxy-6-prenyl-1-benzopyran-2-one, is a member of the class of compounds known as 7-hydroxycoumarins. 7-hydroxycoumarins are coumarins that contain one or more hydroxyl groups attached to the C7 position the coumarin skeleton. Demethylsuberosin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Demethylsuberosin can be found in a number of food items such as rice, apple, black radish, and cloudberry, which makes demethylsuberosin a potential biomarker for the consumption of these food products. 7-demethylsuberosin is a hydroxycoumarin that is 7-hydroxycoumarin which is substituted at position 6 by a 3-methylbut-2-en-1-yl group. A natural product found in Citropsis articulata. It has a role as a plant metabolite. Demethylsuberosin is a natural product found in Prangos tschimganica, Limonia acidissima, and other organisms with data available. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Demethylsuberosin (7-Demethylsuberosin) is a coumarin compound isolated from Angelica gigas Nakai, and has anti-inflammatory activity[1]. Demethylsuberosin (7-Demethylsuberosin) is a coumarin compound isolated from Angelica gigas Nakai, and has anti-inflammatory activity[1].

   

Xanthyletin

8,8-dimethyl-2H,8H-pyrano[3,2-g]chromen-2-one

C14H12O3 (228.0786)


Xanthyletin is a member of the class of compounds known as linear pyranocoumarins. Linear pyranocoumarins are organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety. Xanthyletin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Xanthyletin can be found in lemon, lime, mandarin orange (clementine, tangerine), and sweet orange, which makes xanthyletin a potential biomarker for the consumption of these food products.

   

1,3-dihydroxy-N-methylacridone

1,3-dihydroxy-10-methyl-9,10-dihydroacridin-9-one

C14H11NO3 (241.0739)


1,3-dihydroxy-n-methylacridone is a member of the class of compounds known as acridones. Acridones are acridines containing a ketone group attached to the C9 carbon atom of the acridine moiety. 1,3-dihydroxy-n-methylacridone is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 1,3-dihydroxy-n-methylacridone can be found in a number of food items such as canada blueberry, italian oregano, cashew nut, and pepper (c. annuum), which makes 1,3-dihydroxy-n-methylacridone a potential biomarker for the consumption of these food products.

   

8-Geranylumbelliferone

8-Geranyl-7-hydroxycoumarin

C19H22O3 (298.1569)


A member of the class of hydroxycoumarins that is umbelliferone in which the ring hydrogen at position 8 has been replaced by a geranyl group.

   

1-Hydroxy-10-methylacridone

InChI=1/C14H11NO2/c1-15-10-6-3-2-5-9(10)14(17)13-11(15)7-4-8-12(13)16/h2-8,16H,1H

C14H11NO2 (225.079)


1-Hydroxy-10-methylacridone is found in herbs and spices. 1-Hydroxy-10-methylacridone is an alkaloid from the roots of Ruta graveolens (rue). Also isolated from the callus cultures obtained from the meristematic cells of Ruta graveolens. 1-Hydroxy-10-methylacridone is a member of acridines. It is functionally related to an acridone. 1-Hydroxy-10-methylacridone is a natural product found in Boronia lanceolata, Ruta graveolens, and other organisms with data available. Alkaloid from the roots of Ruta graveolens (rue)and is also isolated from the callus cultures obtained from the meristematic cells of Ruta graveolens. 1-Hydroxy-10-methylacridone is found in herbs and spices.

   

1,3,8-Trihydroxy-10-methylacridin-9(10H)-one

1,3,8-Trihydroxy-10-methylacridin-9(10H)-one

C14H11NO4 (257.0688)


   

1-hydroxyacridone

1-hydroxyacridone

C13H9NO2 (211.0633)


   

1,7-Dihydroxyacridone

1,7-dihydroxy-9,10-dihydroacridin-9-one

C13H9NO3 (227.0582)


1,7-Dihydroxyacridone is a natural product found in Boronia lanceolata with data available.

   

Xanthyletin

Xanthyletin

C14H12O3 (228.0786)


   

1-Hydroxy-N-methylacridone

1-HYDROXY-10-METHYL-9,10-DIHYDROACRIDIN-9-ONE

C14H11NO2 (225.079)


   

Demethylsuberosin

2H-1-Benzopyran-2-one, 7-hydroxy-6-(3-methyl-2-buten-1-yl)-

C14H14O3 (230.0943)


7-demethylsuberosin is a hydroxycoumarin that is 7-hydroxycoumarin which is substituted at position 6 by a 3-methylbut-2-en-1-yl group. A natural product found in Citropsis articulata. It has a role as a plant metabolite. Demethylsuberosin is a natural product found in Prangos tschimganica, Limonia acidissima, and other organisms with data available. A hydroxycoumarin that is 7-hydroxycoumarin which is substituted at position 6 by a 3-methylbut-2-en-1-yl group. A natural product found in Citropsis articulata. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Demethylsuberosin (7-Demethylsuberosin) is a coumarin compound isolated from Angelica gigas Nakai, and has anti-inflammatory activity[1]. Demethylsuberosin (7-Demethylsuberosin) is a coumarin compound isolated from Angelica gigas Nakai, and has anti-inflammatory activity[1].

   

1,3-dihydroxy-N-methylacridone

1,3-dihydroxy-N-methylacridone

C14H11NO3 (241.0739)


   

(8r)-8-[(3s)-3-hydroperoxy-4-methylpent-4-en-1-yl]-8-methylpyrano[2,3-f]chromen-2-one

(8r)-8-[(3s)-3-hydroperoxy-4-methylpent-4-en-1-yl]-8-methylpyrano[2,3-f]chromen-2-one

C19H20O5 (328.1311)


   

(2,3-dimethyl-4-oxoquinolin-1-yl)methyl acetate

(2,3-dimethyl-4-oxoquinolin-1-yl)methyl acetate

C14H15NO3 (245.1052)


   

(8s)-8-[(2e)-4-hydroperoxy-4-methylpent-2-en-1-yl]-8-methylpyrano[2,3-f]chromen-2-one

(8s)-8-[(2e)-4-hydroperoxy-4-methylpent-2-en-1-yl]-8-methylpyrano[2,3-f]chromen-2-one

C19H20O5 (328.1311)


   

1,8-dihydroxy-10h-acridin-9-one

1,8-dihydroxy-10h-acridin-9-one

C13H9NO3 (227.0582)


   

7-hydroxy-6-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

7-hydroxy-6-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

C14H14O4 (246.0892)


   

1-hydroxy-10h-acridin-9-one

1-hydroxy-10h-acridin-9-one

C13H9NO2 (211.0633)


   

8-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxychromen-2-one

8-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxychromen-2-one

C19H22O3 (298.1569)


   

(2-methyl-4-oxoquinolin-1-yl)methyl acetate

(2-methyl-4-oxoquinolin-1-yl)methyl acetate

C13H13NO3 (231.0895)


   

1,8-dihydroxy-10-methylacridin-9-one

1,8-dihydroxy-10-methylacridin-9-one

C14H11NO3 (241.0739)


   

1,3,8-trihydroxy-10-methylacridin-9-one

1,3,8-trihydroxy-10-methylacridin-9-one

C14H11NO4 (257.0688)


   

2,3-dimethyl-1h-quinolin-4-one

2,3-dimethyl-1h-quinolin-4-one

C11H11NO (173.0841)


   

7-hydroxy-6-(2-hydroxy-3-methylbut-3-en-1-yl)chromen-2-one

7-hydroxy-6-(2-hydroxy-3-methylbut-3-en-1-yl)chromen-2-one

C14H14O4 (246.0892)


   

2,3-dimethyl-4-oxoquinolin-1-yl acetate

2,3-dimethyl-4-oxoquinolin-1-yl acetate

C13H13NO3 (231.0895)


   

(8s)-8-methyl-8-(4-methylpent-3-en-1-yl)pyrano[2,3-f]chromen-2-one

(8s)-8-methyl-8-(4-methylpent-3-en-1-yl)pyrano[2,3-f]chromen-2-one

C19H20O3 (296.1412)


   

8-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-7-hydroxychromen-2-one

8-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-7-hydroxychromen-2-one

C19H22O3 (298.1569)


   

7-hydroxy-6-[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

7-hydroxy-6-[(2s)-2-hydroxy-3-methylbut-3-en-1-yl]chromen-2-one

C14H14O4 (246.0892)