CHEBI:32202 - tetracenomycin D3

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ChEBI Name tetracenomycin D3
ChEBI ID CHEBI:32202
Definition A tetracenomycin that is 1-methyl-6,11-dioxo-6,11-dihydrotetracene-2-carboxylic acid bearing four hydroxy substituents at positions 3, 8, 10 and 12.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C20H12O8
Net Charge 0
Average Mass 380.30448
Monoisotopic Mass 380.053
InChI InChI=1S/C20H12O8/c1-6-13-7(3-11(22)14(6)20(27)28)2-9-16(18(13)25)19(26)15-10(17(9)24)4-8(21)5-12(15)23/h2-5,21-23,25H,1H3,(H,27,28)
InChIKey OXCNORDLEQIUCT-UHFFFAOYSA-N
SMILES Cc1c(C(O)=O)c(O)cc2cc3C(=O)c4cc(O)cc(O)c4C(=O)c3c(O)c12
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): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via tetracenomycin )
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via tetracenomycin )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing tetracenomycin D3 (CHEBI:32202) is a hydroxy monocarboxylic acid (CHEBI:35868)
tetracenomycin D3 (CHEBI:32202) is a phenols (CHEBI:33853)
tetracenomycin D3 (CHEBI:32202) is a tetracenequinones (CHEBI:51286)
tetracenomycin D3 (CHEBI:32202) is a tetracenomycin (CHEBI:48132)
tetracenomycin D3 (CHEBI:32202) is conjugate acid of tetracenomycin D3(1−) (CHEBI:74934)
Incoming tetracenomycin D3 methyl ester (CHEBI:32203) has functional parent tetracenomycin D3 (CHEBI:32202)
tetracenomycin D3(1−) (CHEBI:74934) is conjugate base of tetracenomycin D3 (CHEBI:32202)
IUPAC Name
3,8,10,12-tetrahydroxy-1-methyl-6,11-dioxo-6,11-dihydrotetracene-2-carboxylic acid
Synonyms Sources
Tetracenomycin D(3) ChemIDplus
Tetracenomycin D3 KEGG COMPOUND
Database Links Databases
C00017937 KNApSAcK
C12368 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
117241-61-9 CAS Registry Number ChemIDplus
8807953 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
3170342 PubMed citation Europe PMC
Last Modified
28 July 2014