CHEBI:69475 - TAN-931

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ChEBI Name TAN-931
Definition A member of the class of benzoic acids that is benzoic acid substituted by a formyl group at position 3, a hydroxy group at position 5 and a 2,6-dihydroxybenzoyl group at position 4. Isolated from Penicillium purpurogenum, it exhibits antiviral activity.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C15H10O7
Net Charge 0
Average Mass 302.23570
Monoisotopic Mass 302.04265
InChI InChI=1S/C15H10O7/c16-6-8-4-7(15(21)22)5-11(19)12(8)14(20)13-9(17)2-1-3-10(13)18/h1-6,17-19H,(H,21,22)
SMILES OC(=O)c1cc(O)c(C(=O)c2c(O)cccc2O)c(C=O)c1
Metabolite of Species Details
Penicillium purpurogenum (NCBI:txid28575) Found in mycelium (BTO:0001436). Ethylacetate extract of fermentation broth and acetone extract of mycelia of strain JS03 21 See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): antiviral agent
A substance that destroys or inhibits replication of viruses.
EC (aromatase) inhibitor
An EC 1.14.14.* (oxidoreductase acting on paired donors, incorporating of 1 atom of oxygen, with reduced flavin or flavoprotein as one donor) inhibitor which interferes with the action of aromatase (EC and so reduces production of estrogenic steroid hormones.
Penicillium metabolite
Any fungal metabolite produced during a metabolic reaction in Penicillium.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing TAN-931 (CHEBI:69475) has role Penicillium metabolite (CHEBI:76964)
TAN-931 (CHEBI:69475) has role antiviral agent (CHEBI:22587)
TAN-931 (CHEBI:69475) has role EC (aromatase) inhibitor (CHEBI:50790)
TAN-931 (CHEBI:69475) is a benzaldehydes (CHEBI:22698)
TAN-931 (CHEBI:69475) is a benzoic acids (CHEBI:22723)
TAN-931 (CHEBI:69475) is a benzophenones (CHEBI:22726)
TAN-931 (CHEBI:69475) is a resorcinols (CHEBI:33572)
4-(2,6-dihydroxybenzoyl)-3-formyl-5-hydroxybenzoic acid
Synonym Source
Tan 931 ChemIDplus
Manual Xref Database
EP0342665 Patent
View more database links
Registry Numbers Types Sources
127448-92-4 CAS Registry Number ChemIDplus
21878450 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
2071487 PubMed citation Europe PMC
2071488 PubMed citation Europe PMC
21879714 PubMed citation Europe PMC
Last Modified
13 January 2014