(Q104909073)

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Aspergillus Toxins

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Aspergillus Toxins (English)

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http://api.crossref.org/works/10.1016%2Fb978-0-12-179760-7.50023-1

Aspergillus melleus

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Aspergillus versicolor

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Aspergillus nidulans

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Aspergillus striatus

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Aspergillus stellatus

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Aspergillus parasiticus

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Aspergillus clavatus

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Aspergillus ostianus

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Aspergillus chevalieri

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Aspergillus unguis

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Aspergillus flavus

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Aspergillus nomiae

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Aspergillus amstelodami

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Aspergillus caespitosus

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Aspergillus ustus

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Aspergillus desertorum

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Aspergillus alliaceus

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Aspergillus giganteus

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Aspergillus quadrilineatus

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Aspergillus fumigatus

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Aspergillus foveolatus

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Aspergillus terreus

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Aspergillus ochraceus

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Aspergillus nomius

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Aspergillus ruber

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Aspergillus echinulatus

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Aspergillus sclerotiorum

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Aspergillus multicolor

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(2S,3'S,3aR,4S)-2-methyl-3'-(4-oxoquinazolin-3-yl)spiro[3,3a-dihydro-2H-imidazo[1,2-a]indole-4,5'-oxolane]-1,2'-dione

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nortryptoquivalone

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tryptoquivaline f

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(8beta,9beta)-6,8-Dimethylergolin-9-ol

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(+/-)-nidurufin

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5b-Hydroxy-2,2,13b,13c-tetramethyl-2,3,5b,6,7,7a,8,13,13b,13c,14,15-dodecahydro-4h-3,15a-epoxy[1]benzoxepino[6',7':6,7]indeno[1,2-b]indol-4-one

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[(1R)-1-[3-[(3'R,3aS,4S)-2,2-dimethyl-1,2'-dioxospiro[3,3a-dihydroimidazo[1,2-a]indole-4,5'-oxolane]-3'-yl]-4-oxoquinazolin-2-yl]-2-methylpropyl] acetate

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(3R,7R)-3-hydroxy-11,15-dimethoxy-6,8,20-trioxapentacyclo[10.8.0.02,9.03,7.014,19]icosa-1,4,9,11,14(19),15,17-heptaen-13-one

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(±)-aflatoxin G1

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[(1R)-1-[3-[(2S,3'R,3aR,4R)-2-methyl-1,2'-dioxospiro[3,3a-dihydro-2H-imidazo[1,2-a]indole-4,5'-oxolane]-3'-yl]-4-oxoquinazolin-2-yl]-2-methylpropyl] acetate

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(3S,7R)-15-hydroxy-11,18-dimethoxy-6,8,20-trioxapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,4,9,11,14,16,18-heptaen-13-one

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8-O-methylsterigmatocystin

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(3'R,3aS,4S)-3-hydroxy-2,2-dimethyl-3'-[2-(2-methylpropanoyl)-4-oxoquinazolin-3-yl]spiro[3aH-imidazo[1,2-a]indole-4,5'-oxolane]-1,2'-dione

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sterigmatocystin

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4b-Hydroxy-2-(1-hydroxy-1-methylethyl)-12b,12c-dimethyl-5,6,6a,7,12,12b,12c,13,14,14a-decahydro-2H-chromeno[5',6':6,7]indeno[1,2-b]indol-3(4bH)-one

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8-O-methyldihydrosterigmatocystin

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dihydrosterigmatocystin

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ent-Neoechinulin A

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(3S)-3alpha-Methyl-6beta-[[2-(1,1-dimethyl-2-propenyl)-1H-indole-3-yl]methyl]hexahydropyrazine-2,5-dione

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4,6,8-Trihydroxy-3a,12a-dihydroanthra[2,3-b]furo[3,2-d]furan-5,10-dione

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deoxynortryptoquivaline

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fumitremorgin a

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fumitremorgin b

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[(6Ar,9R,10S,10aR)-7,9-dimethyl-5-(2-methylbut-3-en-2-yl)-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinolin-10-yl] acetate

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(6Z)-5-hydroxy-6-{[6-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene}-1H-pyrazine-2,3-dione

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1-[3-(2,2-Dimethyl-3,5'-dioxo-1,2,3,9a-tetrahydrospiro[imidazo[1,2-a]indole-9,2'-oxolan]-4'-yl)-4-oxo-3,4-dihydroquinazolin-2-yl]-2-methylpropyl acetate

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fumitremorgin C

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

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(1R,17S)-3,7,9-trihydroxy-17-methyl-16,21-dioxapentacyclo[15.3.1.02,15.04,13.06,11]henicosa-2(15),3,6(11),7,9,13-hexaene-5,12-dione

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(12R,16S)-6-(2-hydroxyethyl)-8-methoxy-3,11,13-trioxatetracyclo[8.6.0.02,7.012,16]hexadeca-1,5,7,9,14-pentaen-4-one

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(Z)-penicillic acid

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(3R,7S)-15-hydroxy-11,18-dimethoxy-6,8,20-trioxapentacyclo[10.8.0.02,9.03,7.014,19]icosa-1,4,9,11,14,16,18-heptaen-13-one

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nortryptoquivaline A

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(3Z)-3-[[5-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene]-6-methylidenepiperazine-2,5-dione

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tryptoquivaline

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Tryptoquivaline L

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3-[[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene]-6-methylidenepiperazine-2,5-dione

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(-)-Neoechinulin A; Neoechinuline A

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3-[[2-(2-methylbut-3-en-2-yl)-5-(3-methylbut-2-enyl)-1H-indol-3-yl]methylidene]-6-methylidenepiperazine-2,5-dione

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(-)-Fumigaclavine B

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6-{[6-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene}piperazine-2,3,5-trione

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12alpha-Fumitremorgin C

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Alanyl-dimethylallyl-L-tryptophan anhydride

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2,5-Piperazinedione, 3-[[2-(1,1-dimethyl-2-propenyl)-5,7-bis(3-methyl-2-butenyl)-1H-indol-3-yl]methyl]-6-methyl-, (3S,6S)-

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3-methyl-6-[[2-(2-methylbut-3-en-2-yl)-5-(3-methylbut-2-enyl)-1H-indol-3-yl]methylidene]piperazine-2,5-dione

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Emericella desertorum

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Aspergillus sydowii

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Aspergillus tamarii

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author name string

RICHARD J. COLE

1

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http://api.crossref.org/works/10.1016%2Fb978-0-12-179760-7.50023-1

RICHARD H. COX

2

1 reference

http://api.crossref.org/works/10.1016%2Fb978-0-12-179760-7.50023-1

publication date

15 August 2014

1 reference

http://api.crossref.org/works/10.1016%2Fb978-0-12-179760-7.50023-1

753-822

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http://api.crossref.org/works/10.1016%2Fb978-0-12-179760-7.50023-1

Toluquinones from Aspergillus fumigatus.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.3891/ACTA.CHEM.SCAND.17-1771

Studies on the metabolic products of a strain of Aspergillus fumigatus DH 413. VI. Metabolic position of 3,4-dihydroxytoluquinone and fumigatin chlorohydrin in fumigatin biosynthesis.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.22.83

Studies on the Metabolic Products of a Strain of Aspergillus fumigatus DH 413. V. A New Metabolite produced by Ethionine Inhibition

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.20.931

METABOLITES OF PATHOGENIC FUNGI: V. ISOLATION AND TENTATIVE STRUCTURES OF VIOXANTHIN AND VIOPURPURIN, TWO COLORED METABOLITES OF TRICHOPHYTON VIOLACEUM

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1139/V66-427

Identifiers

10.1016/B978-0-12-179760-7.50023-1

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