NCBI Taxonomy: 1934354
Arcopilus (ncbi_taxid: 1934354)
found 80 associated metabolites at genus taxonomy rank level.
Ancestor: Chaetomiaceae
Child Taxonomies: Arcopilus aureus, Arcopilus cupreus, Arcopilus globulus, Arcopilus amazonicus, Arcopilus flavigenus, Arcopilus fusiformis, Arcopilus megasporus, Arcopilus navicularis, environmental samples, Arcopilus eremanthusum, unclassified Arcopilus, Arcopilus purpurascens, Arcopilus turgidopilosus, Arcopilus macrostiolatus, Arcopilus tangerinicapillus
Sclerotiorin
C21H23ClO5 (390.12339380000003)
Rotiorinol A
An azaphilone that is 9,9a-dihydro-2H-furo[3,2-g]isochromen-2-one substituted by an acetyl group at position 3, a hydroxy group at position 9, a 3,5-dimethylhepta-1,3-dien-1-yl group at position 6 and a methyl group at position 9a. It has been isolated from Chaetomium cupreum and exhibits antifungal activity.
Rotiorinol C
An azaphilone that is 9,9a-dihydro-2H-furo[3,2-g]isochromen-2-one substituted by an acetyl group at position 3, a hydroxy group at position 9, a 7-hydroxy-3,5-dimethylhepta-1,3-dien-1-yl group at position 6 and a methyl group at position 9a. It has been isolated from Chaetomium cupreum and exhibits antifungal activity.
(-)-Rotiorin
An azaphilone that is 9,9a-dihydro-2H-furo[3,2-g]isochromen-2-one substituted by an acetyl group at position 3, an oxo group at position 9, a 3,5-dimethylhepta-1,3-dien-1-yl group at position 6 and a methyl group at position 9a. It has been isolated from Chaetomium cupreum and exhibits antifungal activity.
epi-isochromophilone II
C22H27ClO4 (390.15977720000006)
An azaphilone that is 7,8-dihydro-6H-isochromen-6-one substituted by a chloro group at position 5, a 3,5-dimethylhepta-1,3-dien-1-yl group at position 3, a hydroxy group at position 7, a methyl group at position 7 and a 2-oxopropyl group at position 8. Isolated from Chaetomium cupreum, it exhibits antifungal activity.
Rubrorotiorin
C23H23ClO5 (414.12339380000003)
An azaphilone that is 6,6a-dihydro-8H-furo[2,3-h]isochromen-6,8(6aH)-dione substituted by an acetyl group at position 9, a chloro group a position 5, a 3,5-dimethylhepta-1,3-dien-1-yl group at position 3 and a methyl group at position 6a. Isolated from Chaetomium cupreum, it exhibits antifungal activity.
5-hydroxy-6-(5-hydroxy-2-methyl-3-oxohexyl)-7-methoxy-2-methylchromen-4-one
(z)-3',5,5',6'-tetrahydroxy-4,4'-dimethyl-[1,1'-bi(cyclohexylidene)]-3',4,5'-triene-2,2',3,6-tetrone
3-acetyl-9-hydroxy-6-(7-hydroxy-3,5-dimethylhepta-1,3-dien-1-yl)-9a-methyl-9h-furo[3,2-g]isochromen-2-one
(2z,12z,14e)-16-(3,5-dihydroxyphenyl)-2-ethylidenehexadeca-12,14-dienoic acid
(1s,3s)-7,8-dihydroxy-1-methoxy-3-methyl-10-oxo-1h,3h,4h-pyrano[4,3-b]chromene-9-carboxylic acid
(7r)-5-chloro-3-[(1e,3e,5s)-3,5-dimethylhepta-1,3-dien-1-yl]-7-hydroxy-7-methylisochromene-6,8-dione
C19H21ClO4 (348.11282960000005)
(7r)-5-chloro-3-[(1e,3e,5s)-3,5-dimethylhepta-1,3-dien-1-yl]-2-(2-hydroxyethyl)-7-methyl-6,8-dioxoisoquinolin-7-yl acetate
C23H28ClNO5 (433.1655908000001)
3-acetyl-9-hydroxy-6-(5-hydroxy-3,5-dimethylhepta-1,3-dien-1-yl)-9a-methyl-9h-furo[3,2-g]isochromen-2-one
(9r,9ar)-3-acetyl-9-hydroxy-6-[(1e,3e,5s)-5-hydroxy-3,5-dimethylhepta-1,3-dien-1-yl]-9a-methyl-9h-furo[3,2-g]isochromen-2-one
3-acetyl-6-(3,5-dimethylhepta-1,3-dien-1-yl)-9a-methylfuro[3,2-g]isochromene-2,9-dione
(9r,9ar)-3-acetyl-9-hydroxy-6-[(1e,3e)-5-hydroxy-3,5-dimethylhepta-1,3-dien-1-yl]-9a-methyl-9h-furo[3,2-g]isochromen-2-one
9-acetyl-5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-6a-methylfuro[2,3-h]isochromene-6,8-dione
C23H23ClO5 (414.12339380000003)
(7r)-5-chloro-3-[(1e,3e,5s)-3,5-dimethylhepta-1,3-dien-1-yl]-7-methyl-6,8-dioxo-2h-isoquinolin-7-yl acetate
C21H24ClNO4 (389.13937740000006)
5-chloro-3-[(1e,3e)-3,5-dimethylhepta-1,3-dien-1-yl]-8a-hydroxy-7-methyl-6,8-dioxo-1h-isochromen-7-yl acetate
(12e)-13-({5,6'-dioxo-3',8'-dioxaspiro[oxolane-2,5'-tricyclo[5.1.0.0²,⁴]octan]-4-yl}-c-hydroxycarbonimidoyl)-13-methyltridec-12-enoic acid
C24H33NO8 (463.22060580000004)
16-(3,5-dihydroxyphenyl)-2-ethylidenehexadeca-12,14-dienoic acid
5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-hydroxy-7-methyl-8-(2-oxopropyl)-8h-isochromen-6-one
C22H27ClO4 (390.15977720000006)