(Q410677)

Alternariol (English)

7 October 2016

chemical formula

C₁₄H₁₀O₅

1 reference

Alternariol (English)

7 October 2016

canonical SMILES

CC1=CC(=CC2=C1C3=CC(=CC(=C3C(=O)O2)O)O)O

1 reference

Studies in the biochemistry of microorganisms. 90. Alternariol and alternariol monomethyl ether, metabolic products of Alternaria tenuis

Alternariol (English)

7 October 2016

9 references

Degradation of the Alternaria mycotoxins alternariol, alternariol monomethyl ether, and altenuene upon bread baking

The Alternaria mycotoxins alternariol and alternariol methyl ether induce cytochrome P450 1A1 and apoptosis in murine hepatoma cells dependent on the aryl hydrocarbon receptor

Cell death induced by the Alternaria mycotoxin Alternariol

Heptaketides with antiviral activity from three endolichenic fungal strains Nigrospora sp., Alternaria sp. and Phialophora sp.

Biosynthesis and preparation of fiveAlternaria metabolites

Alternariol is not biosynthesised via norlichexanthone

Metabolites produced by an endophyte Alternaria alternata isolated from Maytenus hookeri

Alternaria dauci

6 references

Studies in the biochemistry of microorganisms. 90. Alternariol and alternariol monomethyl ether, metabolic products of Alternaria tenuis

Degradation of the Alternaria mycotoxins alternariol, alternariol monomethyl ether, and altenuene upon bread baking

The Alternaria mycotoxins alternariol and alternariol methyl ether induce cytochrome P450 1A1 and apoptosis in murine hepatoma cells dependent on the aryl hydrocarbon receptor

Cell death induced by the Alternaria mycotoxin Alternariol

Heptaketides with antiviral activity from three endolichenic fungal strains Nigrospora sp., Alternaria sp. and Phialophora sp.

Alternaria cucumerina

7 references

Studies in the biochemistry of microorganisms. 90. Alternariol and alternariol monomethyl ether, metabolic products of Alternaria tenuis

Degradation of the Alternaria mycotoxins alternariol, alternariol monomethyl ether, and altenuene upon bread baking

The Alternaria mycotoxins alternariol and alternariol methyl ether induce cytochrome P450 1A1 and apoptosis in murine hepatoma cells dependent on the aryl hydrocarbon receptor

Cell death induced by the Alternaria mycotoxin Alternariol

Heptaketides with antiviral activity from three endolichenic fungal strains Nigrospora sp., Alternaria sp. and Phialophora sp.

Identification of some metabolites of Alternaria cucumerina (E. & E.) Ell.

Alternaria tenuis

7 references

Studies in the biochemistry of microorganisms. 90. Alternariol and alternariol monomethyl ether, metabolic products of Alternaria tenuis

Degradation of the Alternaria mycotoxins alternariol, alternariol monomethyl ether, and altenuene upon bread baking

The Alternaria mycotoxins alternariol and alternariol methyl ether induce cytochrome P450 1A1 and apoptosis in murine hepatoma cells dependent on the aryl hydrocarbon receptor

Cell death induced by the Alternaria mycotoxin Alternariol

Heptaketides with antiviral activity from three endolichenic fungal strains Nigrospora sp., Alternaria sp. and Phialophora sp.

Alternariol is not biosynthesised via norlichexanthone

Alternaria

4 references

Xanalteric Acids I and II and Related Phenolic Compounds from an EndophyticAlternariasp. Isolated from the Mangrove PlantSonneratia alba

Cytotoxic metabolites from the fungal endophyte Alternaria sp. and their subsequent detection in its host plant Polygonum senegalense

Protein Kinase Inhibitors from the Endophytic Fungus Alternaria sp. isolated from Polygonum senegalense Growing in Egypt

Metabolites of Alternaria in grain sorghum. Compounds which could be mistaken for zearalenone and aflatoxin

Allographa cognata

1 reference

6H-dibenzo[b,d]pyran-6-one derivatives from the cultured lichen mycobionts of Graphis spp. and their biosynthetic origin

Sorghum bicolor

1 reference

Metabolites of Alternaria in grain sorghum. Compounds which could be mistaken for zearalenone and aflatoxin

Aspergillus nidulans

1 reference

Illuminating the diversity of aromatic polyketide synthases in Aspergillus nidulans

Adenocarpus foliolosus

1 reference

Novel Highly Substituted Biraryl Ethers, Phomosines D-G, Isolated from the Endophytic FungusPhomopsis sp. fromAdenocarpus foliolosus

Alternaria porri

1 reference

New antitumour fungal metabolites from Alternaria porri

Gymnosporia oxyphylla

1 reference

Metabolites produced by an endophyte Alternaria alternata isolated from Maytenus hookeri

Sonneratia alba

1 reference

Xanalteric Acids I and II and Related Phenolic Compounds from an EndophyticAlternariasp. Isolated from the Mangrove PlantSonneratia alba

Gymnosporia acuminata

1 reference

Metabolites produced by an endophyte Alternaria alternata isolated from Maytenus hookeri

Rhizopycnis vagum

1 reference

Bioactive Dibenzo-α-pyrone Derivatives from the Endophytic Fungus Rhizopycnis vagum Nitaf22.

Penicillium concentricum

1 reference

Halogenated Compounds from Directed Fermentation of Penicillium concentricum, an Endophytic Fungus of the Liverwort Trichocolea tomentella

Streptomyces fradiae

1 reference

Phenolic polyketides from the co-cultivation of marine-derived Penicillium sp. WC-29-5 and Streptomyces fradiae 007.

Acrocalymma vagum

1 reference

Bioactive Dibenzo-α-pyrone Derivatives from the Endophytic Fungus Rhizopycnis vagum Nitaf22.

subject has role

acetylcholinesterase inhibitor

1 reference

InChI=1S/C14H10O5/c1-6-2-7(15)5-11-12(6)9-3-8(16)4-10(17)13(9)14(18)19-11/h2-5,15-17H,1H3

Medical Subject Headings

15 March 2018

0 references

0 references

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Alternariol

0 references

Identifiers

InChI

1 reference

Alternariol (English)

7 October 2016

2 references

Alternariol (English)

7 October 2016

ChEBI release 2020-09-01

2 references

alternariol (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=641-38-3

10 April 2021

1 reference

3,7,9-Trihydroxy-1-methyl-6H-benzo[c]chromen-6-one (English)

7 October 2016

1 reference

Alternariol (English)

7 October 2016

Reaxys registry number

244839

1 reference

alternariol (English)

7 October 2016

ChEBI ID

64983

mapping relation type

2 references

alternariol (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C14H10O5/c1-6-2-7(15)5-11-12(6)9-3-8(16)4-10(17)13(9)14(18)19-11/h2-5,15-17H,1H3

1 reference

splash10-0a4i-0290000000-913a843eb1fbe0ab9082

ALTERNARIOL (English)

7 October 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

splash10-0a4i-0490000000-4c5e72338325be202711

0 references

DSSTox substance ID

DTXSID80214305

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

DTXCID40136796

0 references

EC number

636-339-1

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.164.145

27 December 2018

ECHA Substance Infocard ID

3,7,9-trihydroxy-1-methyl-6H-benzo[c]chromen-6-one (English)

quotation

CAS no.: 641-38-3 (English)

100.164.145

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.164.145

27 December 2018

3,7,9-trihydroxy-1-methyl-6H-benzo[c]chromen-6-one (English)

quotation

CAS no.: 641-38-3 (English)

MeSH descriptor ID

C005197

1 reference

Medical Subject Headings

MeSH descriptor ID

C005197

Human Metabolome Database ID

14 March 2018

HMDB0030831

2 references

inferred from InChIKey

3 references

alternariol (English)

7 October 2016

inferred from InChIKey

1 reference

Global Substance Registration System

alternariol (English)

7 October 2016

2 references

UNII

KN9L4260JW

ALTERNARIOL (English)

7 October 2016

Natural Product Atlas ID

NPA020438

2 references

inferred from InChIKey

0 references

1 reference

Immune Epitope Database and Analysis Resource

alternariol (English)

7 October 2016

1 reference

1 March 2022

1 reference

6 April 2020

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

UMLS CUI

C0051493

1 reference

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023