CHEBI:32202 - tetracenomycin D3

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name tetracenomycin D3
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
Download Molfile XML SDF
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)
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)
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
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