NCBI Taxonomy: 13563

Heterobasidion annosum (ncbi_taxid: 13563)

found 39 associated metabolites at species taxonomy rank level.

Ancestor: Heterobasidion annosum species complex

Child Taxonomies: Heterobasidion annosum 03012

D-Pinitol

(1R,2S,3R,4S,5S,6S)-6-methoxycyclohexane-1,2,3,4,5-pentol

C7H14O6 (194.079)


Widely distributed in plants. Pinitol is a cyclitol, a cyclic polyol. It is a known anti-diabetic agent isolated from Sutherlandia frutescens leaves. D-Pinitol is a biomarker for the consumption of soy beans and other soy products. D-Pinitol is found in many foods, some of which are ginkgo nuts, carob, soy bean, and common pea. D-Pinitol is found in carob. D-Pinitol is widely distributed in plants.Pinitol is a cyclitol, a cyclic polyol. It is a known anti-diabetic agent isolated from Sutherlandia frutescens leaves. (Wikipedia). D-Pinitol is a biomarker for the consumption of soy beans and other soy products. D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3]. D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3].

   

24,25-Dihydrolanosterol

(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

C30H52O (428.4018)


24,25-dihydrolanosterol is a 3beta-sterol formed from lanosterol by reduction across the C-24-C-25 double bond. It has a role as a human metabolite and a mouse metabolite. It is a 3beta-sterol and a tetracyclic triterpenoid. It is functionally related to a lanosterol. 24,25-Dihydrolanosterol is a natural product found in Euphorbia sapinii, Heterobasidion annosum, and other organisms with data available. 24,25-dihydrolanosterol is a metabolite found in or produced by Saccharomyces cerevisiae. 24,25-Dihydrolanosterol is involved in the biosynthesis of steriods. 24,25-Dihydrolanosterol is reversibly converted to lanosterol by delta24-sterol reductase [EC:1.3.1.72]. A 3beta-sterol formed from lanosterol by reduction across the C-24-C-25 double bond. 24,25-Dihydrolanosterol (Lanostenol) is a component of the seeds of red pepper (Capsicum annuum)[1].

   

Patulin

(2,4-Dihydroxy-2H-pyran-3(6H)-ylidene)acetic acid, 3,4-lactone

C7H6O4 (154.0266)


Patulin is found in pomes. Mycotoxin, found as a contaminant of foods, e.g. apple juice. Sometimes detd. in apple juice Patulin is a mycotoxin produced by a variety of molds, particularly Aspergillus and Penicillium. It is commonly found in rotting apples, and the amount of patulin in apple products is generally viewed as a measure of the quality of the apples used in production. It is not a particularly potent toxin, but a number of studies have shown that it is genotoxic, which has led to some theories that it may be a carcinogen, though animal studies have remained inconclusive. Patulin is also an antibiotic. Several countries have instituted patulin restrictions in apple products. The World Health Organization recommends a maximum concentration of 50 µg/L in apple juice Mycotoxin, found as a contaminant of foods, e.g. apple juice. Sometimes detd. in apple juice D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D009153 - Mutagens Patulin (Terinin) is a mycotoxin produced by fungi including the Aspergillus, Penicillium, and Byssochlamys species, is suspected to be clastogenic, mutagenic, teratogenic and cytotoxic. Patulin induces autophagy-dependent apoptosis through lysosomal-mitochondrial axis, and causes DNA damage[1][2][3][4].

   

Pinitol

(1R,2S,3R,4S,5S,6S)-6-methoxycyclohexane-1,2,3,4,5-pentaol

C7H14O6 (194.079)


D-pinitol is the D-enantiomer of pinitol. It has a role as a geroprotector and a member of compatible osmolytes. It is functionally related to a 1D-chiro-inositol. It is an enantiomer of a L-pinitol. Methylinositol has been used in trials studying the treatment of Dementia and Alzheimers Disease. D-Pinitol is a natural product found in Aegialitis annulata, Senna macranthera var. micans, and other organisms with data available. A member of the class of methyl myo-inositols that is cyclohexane-1,2,3,4,5-pentol substituted by a methoxy group at position 6 (the 1R,2S,3S,4S,5S,6S-isomer). D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3]. D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3].

   

Fomajorin D

Fomajorin D

C15H16O3 (244.1099)


   

2-(2-hydroxypropan-2-yl)benzofuran-5-carbaldehyde

2-(2-hydroxypropan-2-yl)benzofuran-5-carbaldehyde

C12H12O3 (204.0786)


   

patulin

patulin

C7H6O4 (154.0266)


D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins CONFIDENCE standard compound; INTERNAL_ID 5971 D009676 - Noxae > D009153 - Mutagens CONFIDENCE Reference Standard (Level 1) Patulin (Terinin) is a mycotoxin produced by fungi including the Aspergillus, Penicillium, and Byssochlamys species, is suspected to be clastogenic, mutagenic, teratogenic and cytotoxic. Patulin induces autophagy-dependent apoptosis through lysosomal-mitochondrial axis, and causes DNA damage[1][2][3][4].

   

pinitol

(1R,2S,3R,4S,5S,6S)-6-methoxycyclohexane-1,2,3,4,5-pentol

C7H14O6 (194.079)


D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3]. D-pinitol (3-O-Methyl-D-chiro-inositol) is a natural compound presented in several plants, like Pinaceae and Leguminosae plants. D-pinitol exerts hypoglycemic activity and protective effects in the cardiovascular system[1][2]. D-pinitol has antiviral and larvicidal activities[3].

   

CHEBI:28113

(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

C30H52O (428.4018)


   

Mycoin

4-Hydroxy-4H-furo[3,2-c]pyran-2(6H)-one

C7H6O4 (154.0266)


A furopyran and lactone that is (2H-pyran-3(6H)-ylidene)acetic acid which is substituted by hydroxy groups at positions 2 and 4 and in which the hydroxy group at position 4 has condensed with the carboxy group to give the corresponding bicyclic lactone. A mycotoxin produced by several species of Aspergillus and Penicillium, it has antibiotic properties but has been shown to be carcinogenic and mutagenic. D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D009153 - Mutagens Patulin (Terinin) is a mycotoxin produced by fungi including the Aspergillus, Penicillium, and Byssochlamys species, is suspected to be clastogenic, mutagenic, teratogenic and cytotoxic. Patulin induces autophagy-dependent apoptosis through lysosomal-mitochondrial axis, and causes DNA damage[1][2][3][4].

   

1-(hydroxymethyl)-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalene-2,3-diol

1-(hydroxymethyl)-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalene-2,3-diol

C15H28O3 (256.2038)


   

(2s)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

(2s)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H14O3 (206.0943)


   

(1r)-1-[(1r)-4,4-dimethyl-2-oxocyclopentyl]-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

(1r)-1-[(1r)-4,4-dimethyl-2-oxocyclopentyl]-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

C15H18O4 (262.1205)


   

(1s,2r,3r,4as,8as)-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalene-2,3-diol

(1s,2r,3r,4as,8as)-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalene-2,3-diol

C15H28O3 (256.2038)


   

1-(5,6-dimethylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

1-(5,6-dimethylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

C28H44O (396.3392)


   

2-(1,3-dihydroxypropan-2-yl)-3-hydroxy-2,3-dihydro-1-benzofuran-5-carbaldehyde

2-(1,3-dihydroxypropan-2-yl)-3-hydroxy-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H14O5 (238.0841)


   

3-hydroxy-2-(1,2,3-trihydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

3-hydroxy-2-(1,2,3-trihydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H14O6 (254.079)


   

(2s)-2-[(2r)-1,2-dihydroxypropan-2-yl]-2,3-dihydro-1-benzofuran-5-carbaldehyde

(2s)-2-[(2r)-1,2-dihydroxypropan-2-yl]-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H14O4 (222.0892)


   

1-(4,4-dimethyl-2-oxocyclopentyl)-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

1-(4,4-dimethyl-2-oxocyclopentyl)-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

C15H18O4 (262.1205)


   

(1r,3ar,5ar,9as,9br,11ar)-1-[(2r,3e,5s)-5,6-dimethylhept-3-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

(1r,3ar,5ar,9as,9br,11ar)-1-[(2r,3e,5s)-5,6-dimethylhept-3-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,5h,5ah,6h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

C28H44O (396.3392)


   

(2s,3r)-3-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

(2s,3r)-3-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H12O3 (204.0786)


   

9-hydroxy-5,7-dimethyl-1-oxo-6h,8h-cyclopenta[g]isochromene-7-carboxylic acid

9-hydroxy-5,7-dimethyl-1-oxo-6h,8h-cyclopenta[g]isochromene-7-carboxylic acid

C15H14O5 (274.0841)


   

(7s)-9-hydroxy-5,7-dimethyl-1-oxo-6h,8h-cyclopenta[g]isochromene-7-carboxylic acid

(7s)-9-hydroxy-5,7-dimethyl-1-oxo-6h,8h-cyclopenta[g]isochromene-7-carboxylic acid

C15H14O5 (274.0841)


   

3-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

3-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H12O3 (204.0786)


   

1-(2,3-dimethyl-5-oxocyclopentyl)-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

1-(2,3-dimethyl-5-oxocyclopentyl)-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

C15H18O4 (262.1205)


   

(2s,3s)-3-hydroxy-2-(1,2,3-trihydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

(2s,3s)-3-hydroxy-2-(1,2,3-trihydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H14O6 (254.079)


   

2,2,7-trimethylbenzo[g]chromene-5,10-dione

2,2,7-trimethylbenzo[g]chromene-5,10-dione

C16H14O3 (254.0943)


   

(1r,2s)-1-[(2s)-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]propane-1,2-diol

(1r,2s)-1-[(2s)-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]propane-1,2-diol

C14H18O3 (234.1256)


   

3-hydroxy-2,3-dihydro-1-benzofuran-5-carboxylic acid

3-hydroxy-2,3-dihydro-1-benzofuran-5-carboxylic acid

C9H8O4 (180.0423)


   

(1r,5ar,7s,9as,11ar)-3a,6,6,9a,11a-pentamethyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol

(1r,5ar,7s,9as,11ar)-3a,6,6,9a,11a-pentamethyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol

C30H52O (428.4018)


   

(1s)-1-[(1r,2s,3r)-2,3-dimethyl-5-oxocyclopentyl]-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

(1s)-1-[(1r,2s,3r)-2,3-dimethyl-5-oxocyclopentyl]-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

C15H18O4 (262.1205)


   

(2r,3s)-2-(1,3-dihydroxypropan-2-yl)-3-hydroxy-2,3-dihydro-1-benzofuran-5-carbaldehyde

(2r,3s)-2-(1,3-dihydroxypropan-2-yl)-3-hydroxy-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H14O5 (238.0841)


   

2-(2-hydroxypropan-2-yl)-1-benzofuran-5-carbaldehyde

2-(2-hydroxypropan-2-yl)-1-benzofuran-5-carbaldehyde

C12H12O3 (204.0786)


   

2-(1,2-dihydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

2-(1,2-dihydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H14O4 (222.0892)


   

1-[2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]propane-1,2-diol

1-[2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]propane-1,2-diol

C14H18O3 (234.1256)


   

(1s)-1-[(1r)-4,4-dimethyl-2-oxocyclopentyl]-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

(1s)-1-[(1r)-4,4-dimethyl-2-oxocyclopentyl]-5-(hydroxymethyl)-3-oxabicyclo[4.2.0]octa-5,7-dien-4-one

C15H18O4 (262.1205)


   

2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H14O3 (206.0943)


   

(2s)-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

(2s)-2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H12O2 (188.0837)


   

2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

2-(prop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-carbaldehyde

C12H12O2 (188.0837)