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D-threo-isocitric acid (CHEBI:151)

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ChEBI Name D-threo-isocitric acid
ChEBI ID CHEBI:151
ChEBI ASCII Name D-threo-isocitric acid
Definition The D-threo-diastereomer of isocitric acid.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
See structure as:  Image  Applet
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Formula Source
C6H8O7 KEGG COMPOUND
Net Charge 0
Average Mass 192.12352
InChI
InChI=1S/C6H8O7/c7-3(8)1-2(5(10)11)4(9)6(12)13/h2,4,9H,1H2,(H,7,8)(H,10,11)(H,12,13)/t2-,4+/m0/s1
InChIKey
ODBLHEXUDAPZAU-ZAFYKAAXSA-N
SMILES
O[C@H]([C@H](CC(O)=O)C(O)=O)C(O)=O
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): fundamental metabolite
Any metabolite produced by all living cells.
(via isocitric acid )
View more on the ChEBI Ontology
ChEBI Ontology
Outgoing D-threo-isocitric acid (CHEBI:151) is a isocitric acid (CHEBI:30887)
D-threo-isocitric acid (CHEBI:151) is conjugate acid of D-threo-isocitrate(3−) (CHEBI:15562)
D-threo-isocitric acid (CHEBI:151) is enantiomer of L-threo-isocitric acid (CHEBI:30889)
Incoming D-threo-isocitrate(3−) (CHEBI:15562) is conjugate base of D-threo-isocitric acid (CHEBI:151)
L-threo-isocitric acid (CHEBI:30889) is enantiomer of D-threo-isocitric acid (CHEBI:151)
IUPAC Names
(1R,2S)-1-hydroxypropane-1,2,3-tricarboxylic acid
3-carboxy-2,3-dideoxy-L-threo-pentaric acid
Synonyms Sources
(+)-threo-isocitric acid HMDB
D-threo-Isocitric acid KEGG COMPOUND
ISOCITRIC ACID PDBeChem
Database Links Databases
C00001188 KNApSAcK
C00451 KEGG COMPOUND
HMDB01874 HMDB
ICT PDBeChem
THREO-DS-ISO-CITRATE MetaCyc
View more database links
Registry Numbers Types Sources
1220309 Gmelin Registry Number Gmelin
1727947 Reaxys Registry Number Reaxys
1727947 Beilstein Registry Number Beilstein
6061-97-8 CAS Registry Number KEGG COMPOUND
Citation Waiting for Citations Type Source
17439666 PubMed citation CiteXplore
Last Modified
17 July 2014

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