NCBI Taxonomy: 5227

Auriculariaceae (ncbi_taxid: 5227)

found 92 associated metabolites at family taxonomy rank level.

Child Taxonomies: Auricularia, Grammatus, Protodaedalea, Heteroradulum, Alloexidiopsis, Tremellochaete, Heterocorticium, environmental samples, unclassified Auriculariaceae

Tryptophol

3-(2-Hydroxyethyl)-1H-indole

C10H11NO (161.0841)

Tryptophol, also known as indole-3-ethanol, is an indolyl alcohol that is ethanol substituted by a 1H-indol-3-yl group at position 2. It has a role as a Saccharomyces cerevisiae metabolite, an auxin and a plant metabolite. Tryptophol is a catabolite of tryptophan converted by the gut microbiota. After absorption through the intestinal epithelium, tryptophan catabolites enter the bloodstream and are later excreted in the urine (PMID:30120222). Tryptophol production was negatively associated with interferon-gamma production (IFNγ) which suggests that tryptophol has anti-inflammatory properties (PMID:27814509). Tryptophol has also been identified as the hypnotic agent in trypanosomal sleeping sickness, and because it is formed in vivo after ethanol or disulfiram treatment, it is also associated with the study of alcoholism (PMID:7241135). Indole-3-ethanol is a dietary indole present in cruciferous vegetables that has been shown to influence estradiol metabolism in humans and may provide a new chemopreventive approach to estrogen-dependent diseases. (PMID 2342128) Tryptophol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=526-55-6 (retrieved 2024-06-29) (CAS RN: 526-55-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Tryptophol (Indole-3-ethanol) is an endogenous metabolite. Tryptophol (Indole-3-ethanol) is an endogenous metabolite.

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].

Helminthosporol

C15H24O2 (236.1776)

Aporpinone A

C11H12O4 (208.0736)

Tryptophol

5-21-03-00061 (Beilstein Handbook Reference)

C10H11NO (161.0841)

An indolyl alcohol that is ethanol substituted by a 1H-indol-3-yl group at position 2. Tryptophol (Indole-3-ethanol) is an endogenous metabolite. Tryptophol (Indole-3-ethanol) is an endogenous metabolite.

ethyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

NCGC00386069-01!ethyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

C12H14O5 (238.0841)

ethyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

C12H14O5 (238.0841)

patulin

4-hydroxy-4,6-dihydrofuro[3,2-c]pyran-2-one

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].

(1'r,2s,3s,3'r,5r,7'r,10'e)-5-[(1e)-3-hydroxy-2-methylprop-1-en-1-yl]-10'-(hydroxymethyl)-3,3',14'-trimethylspiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecane]-10',13'-diene-9',12'-dione

C25H34O5 (414.2406)

(1s,5s,9r,11r)-14-[(2s)-7-hydroxy-6-methylhept-5-en-2-yl]-4-(hydroxymethyl)-8,11-dimethyltetracyclo[9.3.0.0¹,⁵.0⁵,⁹]tetradeca-3,7,13-trien-6-one

C25H34O3 (382.2508)

n-(1,3-dihydroxy-3-methyl-4-oxopentan-2-yl)-6,8-dimethyldeca-2,4,6-trienamide

C18H29NO4 (323.2096)

(1'r,2s,3s,3'r,5r,7'r,10'z)-5-[(1e)-3-hydroxy-2-methylprop-1-en-1-yl]-10'-(hydroxymethyl)-3,3',14'-trimethylspiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecane]-10',13'-dien-12'-one

C25H36O4 (400.2613)

[(1r,4r,6r,8r)-8-(hydroxymethyl)-4-isopropyl-1-methyl-7-methylidenebicyclo[3.2.1]octan-6-yl]methanol

C15H26O2 (238.1933)

(2s,3r,4r)-2-[(2r,4ar,4br,10ar,12ar)-6,9-dihydroxy-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-5-oxo-3,4,4b,11,12,12a-hexahydro-2h-1,10-dioxatetraphen-8-yl]-4-methylhexan-3-yl acetate

C30H44O8 (532.3036)

(1'r,2s,3s,3'r,5r,7'r,9'e,11's,12'r,14'r)-10'-(hydroxymethyl)-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)spiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecan]-9'-ene-1',12'-diol

C25H40O4 (404.2926)

(3r,4r,5s,6r,10z)-3,4,6-trihydroxy-2-methoxy-3-methyl-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

C14H19NO6 (297.1212)

(1's,2s,3s,3'r,5r,7'r,11'r)-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)-12'-oxospiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecane]-9',13'-diene-10'-carboxylic acid

C25H34O4 (398.2457)

(1r,4r,5s)-6-formyl-4-isopropyl-1,7-dimethylbicyclo[3.2.1]oct-6-ene-8-carboxylic acid

C15H22O3 (250.1569)

6-formyl-4-isopropyl-1,7-dimethylbicyclo[3.2.1]oct-6-ene-8-carboxylic acid

C15H22O3 (250.1569)

(1's,2s,3s,3'r,5r,7's,8's,9'e,11'r)-8'-hydroxy-10'-(hydroxymethyl)-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)spiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecane]-9',13'-dien-12'-one

C25H36O4 (400.2613)

methyl 7-[(4-hydroxyphenyl)carbamoyl]heptanoate

C15H21NO4 (279.1471)

(4s,7e,10s,13e,16s)-4,10,16-trimethyl-1,5,11-trioxacyclohexadeca-7,13-diene-2,6,12-trione

C16H22O6 (310.1416)

10'-(hydroxymethyl)-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)spiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecan]-9'-en-14'-ol

C25H40O3 (388.2977)

9'-hydroxy-3,3',14'-trimethyl-5-(2-methylprop-1-en-1-yl)-12'-oxospiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecane]-10',13'-diene-10'-carboxylic acid

C25H34O5 (414.2406)

9'-hydroxy-5-(3-hydroxy-2-methylprop-1-en-1-yl)-10'-(hydroxymethyl)-3,3',14'-trimethylspiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecane]-10',13'-dien-12'-one

C25H36O5 (416.2563)

(1'r,2s,3s,4's,5r,5'r,7'r,11'r,14'r)-4'-hydroxy-5-(3-hydroxy-2-methylprop-1-en-1-yl)-16'-(2-hydroxyethyl)-3,4',7'-trimethyl-2'-oxa-16'-azaspiro[oxolane-2,10'-tetracyclo[12.3.0.0¹,⁵.0⁷,¹¹]heptadecane]-15',17'-dione

(1'r,2s,3s,4's,5r,5'r,7'r,11'r,14'r)-4'-hydroxy-5-(3-hydroxy-2-methylprop-1-en-1-yl)-16'-(2-hydroxyethyl)-3,4',7'-trimethyl-2'-oxa-16'-azaspiro[oxolane-2,10'-tetracyclo[12.3.0.0¹,⁵.0⁷,¹¹]heptadecane]-15',17'-dione

C27H41NO7 (491.2883)

6,8-dimethyldeca-2,4,6-trienamide

C12H19NO (193.1467)

methyl 1-(3,4-dihydroxy-2-methylbutan-2-yl)indole-3-carboxylate

C15H19NO4 (277.1314)

4-[(2r)-oxiran-2-yl]-2-[(2e)-5-oxofuran-2-ylidene]but-3-yn-1-yl acetate

C12H10O5 (234.0528)

(2r,4ar,4bs,5s,10ar,12ar)-5-hydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-4a,10a-dimethyl-8-[(2s,4e)-4-methyl-3-oxohex-4-en-2-yl]-2,3,4,4b,5,11,12,12a-octahydro-1,10-dioxatetraphene-6,9-dione

C29H40O8 (516.2723)

5-(3-hydroxy-2-methylprop-1-en-1-yl)-3,3',14'-trimethyl-12'-oxospiro[oxolane-2,6'-tricyclo[9.3.0.0³,⁷]tetradecane]-9',13'-diene-10'-carbaldehyde

C25H34O4 (398.2457)

(1's,2s,3s,3'r,5r,7'r,13's,15'r)-15'-hydroxy-12'-(2-hydroxyethyl)-3,3',15'-trimethyl-5-(2-methylprop-1-en-1-yl)-12'-azaspiro[oxolane-2,6'-tetracyclo[8.5.1.0³,⁷.0¹³,¹⁶]hexadecan]-10'(16')-en-11'-one

(1's,2s,3s,3'r,5r,7'r,13's,15'r)-15'-hydroxy-12'-(2-hydroxyethyl)-3,3',15'-trimethyl-5-(2-methylprop-1-en-1-yl)-12'-azaspiro[oxolane-2,6'-tetracyclo[8.5.1.0³,⁷.0¹³,¹⁶]hexadecan]-10'(16')-en-11'-one

C27H41NO4 (443.3035)