CHEBI:90194 - laccaic acid D

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ChEBI Name laccaic acid D
Definition A trihydroxyanthraquinone that is that is 3,6,8-trihydroxy-9,10-anthraquinone substituted by methyl and carboxy groups at positions 1 and 2 respectively. A minor component of LAC dye together with laccaic acids A, B and C.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C16H10O7
Net Charge 0
Average Mass 314.247
Monoisotopic Mass 314.04265
InChI InChI=1S/C16H10O7/c1-5-11-8(4-10(19)12(5)16(22)23)14(20)7-2-6(17)3-9(18)13(7)15(11)21/h2-4,17-19H,1H3,(H,22,23)
SMILES C=1C(=C2C(C3=C(C=C(O)C(C(O)=O)=C3C)C(C2=CC1O)=O)=O)O
Metabolite of Species Details
Dactylopius coccus (NCBI:txid765876) 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): animal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
Application(s): dye

View more via ChEBI Ontology
ChEBI Ontology
Outgoing laccaic acid D (CHEBI:90194) has role animal metabolite (CHEBI:75767)
laccaic acid D (CHEBI:90194) has role dye (CHEBI:37958)
laccaic acid D (CHEBI:90194) is a monocarboxylic acid (CHEBI:25384)
laccaic acid D (CHEBI:90194) is a polyphenol (CHEBI:26195)
laccaic acid D (CHEBI:90194) is a trihydroxyanthraquinone (CHEBI:37488)
laccaic acid D (CHEBI:90194) is conjugate acid of laccaic acid D(1−) (CHEBI:149532)
Incoming LAC dye (CHEBI:90184) has part laccaic acid D (CHEBI:90194)
laccaic acid D(1−) (CHEBI:149532) is conjugate base of laccaic acid D (CHEBI:90194)
3,6,8-trihydroxy-1-methyl-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid
Synonyms Sources
9,10-Dihydro-3,6,8-trihydroxy-1-methyl-9,10-dioxo-2-anthracenecarboxylic acid HMDB
Flavokermesic acid HMDB
Xanthokermesic acid HMDB
Manual Xrefs Databases
C00051186 KNApSAcK
HMDB0029508 HMDB
View more database links
Registry Numbers Types Sources
18499-84-8 CAS Registry Number KNApSAcK
3122381 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
21271239 PubMed citation Europe PMC
24267092 PubMed citation Europe PMC
29215010 PubMed citation Europe PMC
30150747 PubMed citation Europe PMC
Last Modified
19 May 2020