NCBI Taxonomy: 1130104
Graphideae (ncbi_taxid: 1130104)
found 78 associated metabolites at tribe taxonomy rank level.
Ancestor: Graphidoideae
Child Taxonomies: Glyphis, Graphis, Diorygma, Thecaria, Graphina, Leiorreuma, Allographa, Halegrapha, Pycnotrema, Thalloloma, Hemithecium, Sarcographa, Platygramme, Myriochapsa, Phaeographis, Platythecium, Pallidogramme
2,6-Dihydroxybenzoic acid
2,6-dihydroxybenzoic acid, also known as gamma-resorcylic acid or 6-hydroxysalicylic acid, is a member of the class of compounds known as salicylic acids. Salicylic acids are ortho-hydroxylated benzoic acids. 2,6-dihydroxybenzoic acid is slightly soluble (in water) and a moderately acidic compound (based on its pKa). 2,6-dihydroxybenzoic acid can be found in beer and olive, which makes 2,6-dihydroxybenzoic acid a potential biomarker for the consumption of these food products. 2,6-dihydroxybenzoic acid can be found primarily in blood and urine. 2,6-Dihydroxybenzoic acid (γ-resorcylic acid) is a dihydroxybenzoic acid. It is a very strong acid due to its intramolecular hydrogen bonding . 2,6-dihydroxybenzoic acid is a secondary metabolite of salicylic acid which has been hydrolyzed by liver enzymes during phase I metabolism. 2,6-Dihydroxybenzoic acid is a secondary metabolite of salicylic acid which has been hydrolyzed by liver enzymes during phase I metabolism. 2,6-Dihydroxybenzoic acid is a secondary metabolite of salicylic acid which has been hydrolyzed by liver enzymes during phase I metabolism.
6-Methoxymellein
Isolated from Aspergillus caespitosus, Aspergillus variecolor and Sporormia bipartis. Reaches fungitoxic levels in stored infected carrot. Shows broad antimicrobial action. 6-Methoxymellein is found in wild carrot, root vegetables, and carrot. 6-Methoxymellein is found in carrot. 6-Methoxymellein is isolated from Aspergillus caespitosus, Aspergillus variecolor and Sporormia bipartis. Reaches fungitoxic levels in stored infected carrot. Shows broad antimicrobial action.
Alternariol
Alternariol is found in mushrooms. Alternariol occurs in mycelium of Alternaria tenuis responsible for alternaria cone disorder in hops and fruit spot on papaya (Carica papaya) and Passiflora species.Alternariol is a toxic metabolite of Alternaria fungi. It is an important contaminant in cereals and fruits D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors D004791 - Enzyme Inhibitors
violaceol II
An aromatic ether in which the ether functionality links a 2,3-dihydroxy-5-methylphenyl group with a 2,6-dihydroxy-4-methylphenyl group. Fungal metabolite isolated inter alia from Aspergillus spp.
violaceol i
An aromatic ether in which the ether functionality links two 2,3-dihydroxy-5-methylphenyl groups. Fungal metabolite isolated inter alia from Aspergillus spp.
Diorcinol
An aromatic ether that is diphenyl ether in which both phenyl groups are substituted at position 3 by a hydroxy group and at position 5 by a methyl group.
Alternariol
A benzochromenone that is 6H-benzo[c]chromen-6-one which is substituted by a methyl group at position 1 and by hydroxy groups at positions 3, 7, and 9. It is the most important mycotoxin produced by the black mould Alternaria species, which are the most common mycoflora infecting small grain cereals worldwide. D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors D004791 - Enzyme Inhibitors CONFIDENCE Reference Standard (Level 1)
2,6-DIHYDROXYBENZOIC ACID
A dihydroxybenzoic acid having the two hydroxy groups at the C-2 and C-6 positions. 2,6-Dihydroxybenzoic acid is a secondary metabolite of salicylic acid which has been hydrolyzed by liver enzymes during phase I metabolism. 2,6-Dihydroxybenzoic acid is a secondary metabolite of salicylic acid which has been hydrolyzed by liver enzymes during phase I metabolism.
4,6,8-trihydroxy-3-methylidene-4h-2-benzopyran-1-one
4-hydroxy-3,7,9-trimethoxy-1-methylbenzo[c]chromen-6-one
4,5-dihydroxy-6-[2-(5-hydroxy-7,8-dimethoxy-4-oxochromen-2-yl)phenoxy]-2-(hydroxymethyl)oxan-3-yl 3-phenylprop-2-enoate
methyl 2-(2,6-dihydroxy-4-methylbenzoyl)-3,6-dihydroxybenzoate
(2s)-2,4-dimethyl-5-oxo-2h-furan-3-carboxylic acid
(3s,4ar,5r,6s)-6-hydroxy-4a,5-dimethyl-3-(prop-1-en-2-yl)-3,4,5,6,7,8-hexahydronaphthalen-2-one
6-hydroxy-3-(hydroxymethyl)-8-methoxyisochromen-1-one
4,7-dihydroxy-1-(hydroxymethyl)-3,9-dimethoxybenzo[c]chromen-6-one
methyl 13-hydroxy-2,6-dimethoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate
(2r)-2,4-dimethyl-5-oxo-2h-furan-3-carboxylic acid
3-methyl-4-[(1e,3e,5e)-6-methyl-7-oxoocta-1,3,5-trien-1-yl]furan-2,5-dione
5,13,17-trihydroxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3(8),4,6,11,13-hexaene-4-carboxylic acid
methyl 2-{3-acetyl-5-[2,3-dihydroxy-4-methoxy-6-(methoxycarbonyl)benzoyl]-4-hydroxybenzoyl}-3,4-dihydroxy-5-methoxybenzoate
(3r,4s)-4,6,8-trihydroxy-3-methyl-3,4-dihydro-2-benzopyran-1-one
(2r)-2,4,12,15-tetrahydroxy-6-methyl-9-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaen-10-one
methyl 13-hydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate
5-hydroxy-2-(hydroxymethyl)-7-methoxy-3-methylchromen-4-one
2,4,12,15-tetrahydroxy-6-methyl-9-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaen-10-one
(2r,3s,4s)-2,4-dimethyl-5-oxooxolane-3-carboxylic acid
methyl 2-[2,6-dihydroxy-4-(hydroxymethyl)benzoyl]-3,6-dihydroxybenzoate
5-hydroxy-7,8-dimethoxy-2-(2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one
C23H24O11 (476.13185539999995)
methyl (2r)-13-hydroxy-2,6-dimethoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate
3,12,20-trimethyl-8,15-dioxatetracyclo[14.4.0.0²,⁷.0⁹,¹⁴]icosa-1(16),2(7),3,5,9,11,13,17,19-nonaene-5,6,10,17,18-pentol
(2s)-8-methoxy-2-methyl-4-oxo-2h,3h,5h-pyrano[3,2-c]chromene-10-carboxylic acid
(3s,3ar,4ar,5r,6r,9as)-3,4a,5-trimethyl-2h,3ah,4h,5h,6h,7h,8h,9ah-naphtho[2,3-b]furan-3,6-diol
4,7,9-tris(acetyloxy)-3-methoxy-6-oxobenzo[c]chromen-1-yl acetate
8-methoxy-2-methyl-4-oxo-2h,3h,5h-pyrano[3,2-c]chromene-10-carboxylic acid
3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione
(2s,6e,9z)-11-hydroxy-14-oxo-1-oxacyclotetradeca-6,9,12-triene-2-carboxylic acid
3,4a,5-trimethyl-2h,3ah,4h,5h,6h,7h,8h,9ah-naphtho[2,3-b]furan-3,6-diol
(2r,3s,4r,5r,6s)-4,5-dihydroxy-6-[2-(5-hydroxy-7,8-dimethoxy-4-oxochromen-2-yl)phenoxy]-2-(hydroxymethyl)oxan-3-yl (2e)-3-phenylprop-2-enoate
14,15-dihydroxy-4,6,13-trimethoxy-9-oxatricyclo[9.4.0.0²,⁷]pentadeca-1(11),2,4,6,12,14-hexaen-8-one
5,13-dihydroxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3(8),4,6,11,13-hexaene-4-carboxylic acid
5-hydroxy-3-(hydroxymethyl)-7-methoxy-2-methylchromen-4-one
2-(2,6-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one
(4s)-4,6,8-trihydroxy-3-methylidene-4h-2-benzopyran-1-one
4,7-dihydroxy-3,9-dimethoxy-1-methylbenzo[c]chromen-6-one
methyl 2,13-dihydroxy-6-methoxy-11-methyl-4-oxo-3,10-dioxatricyclo[7.4.1.0⁵,¹⁴]tetradeca-1(13),5,7,9(14),11-pentaene-8-carboxylate
5-hydroxy-7,8-dimethoxy-2-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one
C23H24O11 (476.13185539999995)