NCBI Taxonomy: 498170
Xylaria obovata (ncbi_taxid: 498170)
found 79 associated metabolites at species taxonomy rank level.
Ancestor: Xylaria
Child Taxonomies: none taxonomy data.
Ergosterol
Ergosterol is a phytosterol consisting of ergostane having double bonds at the 5,6-, 7,8- and 22,23-positions as well as a 3beta-hydroxy group. It has a role as a fungal metabolite and a Saccharomyces cerevisiae metabolite. It is a 3beta-sterol, an ergostanoid, a 3beta-hydroxy-Delta(5)-steroid and a member of phytosterols. A steroid of interest both because its biosynthesis in FUNGI is a target of ANTIFUNGAL AGENTS, notably AZOLES, and because when it is present in SKIN of animals, ULTRAVIOLET RAYS break a bond to result in ERGOCALCIFEROL. Ergosterol is a natural product found in Gladiolus italicus, Ramaria formosa, and other organisms with data available. ergosterol is a metabolite found in or produced by Saccharomyces cerevisiae. A steroid occurring in FUNGI. Irradiation with ULTRAVIOLET RAYS results in formation of ERGOCALCIFEROL (vitamin D2). See also: Reishi (part of). Ergosterol, also known as provitamin D2, belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Thus, ergosterol is considered to be a sterol lipid molecule. Ergosterol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Ergosterol is the biological precursor to vitamin D2. It is turned into viosterol by ultraviolet light, and is then converted into ergocalciferol, which is a form of vitamin D. Ergosterol is a component of fungal cell membranes, serving the same function that cholesterol serves in animal cells. Ergosterol is not found in mammalian cell membranes. A phytosterol consisting of ergostane having double bonds at the 5,6-, 7,8- and 22,23-positions as well as a 3beta-hydroxy group. Ergosterol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=57-87-4 (retrieved 2024-07-12) (CAS RN: 57-87-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects.
Cerevisterol
An ergostanoid that is (22E)-ergosta-7,22-diene substituted by hydroxy groups at positions 3, 5 and 6 (the 3beta,5alpha,6beta stereoisomer). It has been isolated from the fungus, Xylaria species. Cerevisterol is a steroid isolated from the fruiting bodies of Agaricus blazei[1]. Cerevisterol is a steroid isolated from the fruiting bodies of Agaricus blazei[1].
Methyl indole-3-carboxylate
The methyl ester of indole-3-carboxylic acid. Methyl indole-3-carboxylate is a natural product isolated from Sorangium cellulosum strain Soce895. Methyl indole-3-carboxylate shows a weak activity against the Gram-positive Nocardia sp with a MIC value of 33.33 μg/mL[1]. Methyl indole-3-carboxylate is a natural product isolated from Sorangium cellulosum strain Soce895. Methyl indole-3-carboxylate shows a weak activity against the Gram-positive Nocardia sp with a MIC value of 33.33 μg/mL[1].
Ergosterol
Indicator of fungal contamination, especies in cereals. Occurs in yeast and fungi. The main fungal steroidand is also found in small amts. in higher plant prods., e.g. palm oil [DFC]. D018977 - Micronutrients > D014815 - Vitamins > D000072664 - Provitamins Disclaimer: While authors make an effort to ensure that the content of this record is accurate, the authors make no representations or warranties in relation to the accuracy or completeness of the record. This record do not reflect any viewpoints of the affiliation and organization to which the authors belong. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects.
(1r,2s,3s,5r,6r,8s,10e,12r,13s,15r,16s,17r,18s)-18-benzyl-6,20-dihydroxy-6,8,15,16-tetramethyl-7-oxo-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-2-yl acetate
18-benzyl-20-hydroxy-6,8,15,16-tetramethyl-7-oxo-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-2-yl acetate
C30H37NO6 (507.26207420000003)
(1r,2s,3r,5s,6s,8s,10e,12r,13s,15r,16s,17s,18s)-18-benzyl-20-hydroxy-6,8,15,16-tetramethyl-7-oxo-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-2-yl acetate
C30H37NO6 (507.26207420000003)
17-benzyl-5,19-dihydroxy-5,7,14,15-tetramethyl-6-oxo-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-2-yl acetate
C30H37NO6 (507.26207420000003)
(1r,2s,3s,5r,6r,8s,10e,12r,13s,15r,16s,17s,18s)-18-benzyl-6,20-dihydroxy-6,8,15,16-tetramethyl-7-oxo-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-2-yl acetate
6-ethyl-3-methylidene-dihydro-3ah-furo[2,3-c]furan-2,4-dione
(1r,2r,3e,5r,7s,9e,11r,12s,14r,15s,16s,17s)-17-benzyl-5,19-dihydroxy-5,7,14,15-tetramethyl-6-oxo-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-2-yl acetate
C30H37NO6 (507.26207420000003)
18-benzyl-6,20-dihydroxy-6,8,15,16-tetramethyl-7-oxo-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-2-yl acetate
(1r,2s,3s,5r,6r,8s,10e,12r,13s,16s,17s)-17-benzyl-2,6,13,19-tetrahydroxy-6,8,14,15-tetramethyl-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,14,18-trien-7-one
C28H35NO6 (481.24642500000004)
1-(5,6-dimethylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
4-(3-acetyl-2,6-dihydroxy-5-methylphenyl)-4-hydroxy-2-methoxybutanoic acid
(1r,2s,3s,5r,6r,8s,10e,12r,13s,15r,16s,17s,18s)-18-benzyl-2,6,20-trihydroxy-6,8,15,16-tetramethyl-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-7-one
C28H35NO6 (481.24642500000004)
(1r,2s,3s,5r,6r,8s,10e,12r,13s,16s,17s)-17-benzyl-6,13,19-trihydroxy-6,8,14,15-tetramethyl-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,14,18-trien-2-yl acetate
17-benzyl-6,13,19-trihydroxy-6,8,14,15-tetramethyl-7-oxo-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,14,18-trien-2-yl acetate
(1as,6r,7r,7ar,7br)-6-hydroxy-1a-[(2s)-2-(hydroxymethyl)oxiran-2-yl]-7,7a-dimethyl-4h,5h,6h,7h,7bh-naphtho[1,2-b]oxiren-2-one
18-benzyl-2,6,20-trihydroxy-6,8,15,16-tetramethyl-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-7-one
C28H35NO6 (481.24642500000004)
(1r,2s,3r,6s,8s,10z,12r,13s,15r,17s,18s)-18-benzyl-20-hydroxy-6,8,15,16-tetramethyl-7-oxo-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-2-yl acetate
C30H37NO6 (507.26207420000003)
17-benzyl-2,6,13,19-tetrahydroxy-6,8,14,15-tetramethyl-4-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0³,⁵]nonadeca-10,14,18-trien-7-one
C28H35NO6 (481.24642500000004)
6-hydroxy-1a-[2-(hydroxymethyl)oxiran-2-yl]-7,7a-dimethyl-4h,5h,6h,7h,7bh-naphtho[1,2-b]oxiren-2-one
(2s,4e,6e,8r,10e)-trideca-4,6,10,12-tetraene-2,8-diol
(1r,2r,3e,5r,7s,9e,11r,12s,14r,15s,16r,17s)-17-benzyl-5,19-dihydroxy-5,7,14,15-tetramethyl-6-oxo-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-2-yl acetate
C30H37NO6 (507.26207420000003)
5-(3-acetyl-2,6-dihydroxy-5-methylphenyl)-3-methoxyoxolan-2-one
(1r,2s,3s,5r,6r,8s,10e,12r,13s,15r,16s,17r,18s)-18-benzyl-2,6,20-trihydroxy-6,8,15,16-tetramethyl-4,14-dioxa-19-azapentacyclo[10.8.0.0¹,¹⁷.0³,⁵.0¹³,¹⁵]icosa-10,19-dien-7-one
C28H35NO6 (481.24642500000004)