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CHEBI:41582 - D-pipecolic acid

ChEBI IDCHEBI:41582
ChEBI NameD-pipecolic acid
Stars
ASCII NameD-pipecolic acid
DefinitionThe D-enantiomer of pipecolic acid.
Secondary ChEBI IDsCHEBI:18704, CHEBI:41574
Last Modified22 August 2024
DownloadsMolfile
FormulaC6H11NO2
Net Charge0
Average Mass129.159
Monoisotopic Mass129.07898
SMILESO=C(O)[C@H]1CCCCN1
InChIInChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m1/s1
InChIKeyHXEACLLIILLPRG-RXMQYKEDSA-N
Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606) - PubMed (2871866)
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
ChEBI Ontology
Outgoing Relation(s)
D-pipecolic acid (CHEBI:41582) has role human metabolite (CHEBI:77746)
D-pipecolic acid (CHEBI:41582) is a pipecolic acid (CHEBI:17964)
D-pipecolic acid (CHEBI:41582) is conjugate acid of D-pipecolate (CHEBI:18703)
D-pipecolic acid (CHEBI:41582) is enantiomer of L-pipecolic acid (CHEBI:30913)
Incoming Relation(s)
D-pipecolate (CHEBI:18703) is conjugate base of D-pipecolic acid (CHEBI:41582)
L-pipecolic acid (CHEBI:30913) is enantiomer of D-pipecolic acid (CHEBI:41582)
IUPAC Name 
(2R)-piperidine-2-carboxylic acid
Synonyms  Source
(R)-piperidine-2-carboxylic acidChemIDplus
6-CARBOXYPIPERIDINEPDBeChem
(R)-pipecolic acidChEBI
Manual XrefsDatabases
CPIPDBeChem
HMDB0005960HMDB
Registry NumbersSources
Beilstein:81094Beilstein
Beilstein:4291592Beilstein
Reaxys:81094Reaxys
CAS:1723-00-8ChemIDplus
Citations