Record Information
Version1.0
Creation date2015-10-09 22:29:10 UTC
Update date2017-01-19 02:36:16 UTC
FoodComEx IDPC000196
FoodDB RecordFDB022174
Chemical Information
NameIndolelactic acid
DescriptionIndolelactic acid is a tryptophan metabolite found in human plasma and serum and normal urine. Tryptophan is metabolized by two major pathways in humans, either through kynurenine or via a series of indoles, and some of its metabolites are known to be biologically active. Indolelactic acid is present in various amounts, significantly higher in umbilical foetal plasma than in maternal plasma in the protein-bound form. (PMID 2361979, 1400722, 3597614, 11060358, 1400722) [HMDB]
CAS Number1821-52-9
Structure
Thumb
Synonyms
SynonymSource
(+)-2-hydroxy-3-indol-3-yl-propionatehmdb
(+)-2-hydroxy-3-indol-3-yl-propionic acidhmdb
(+)-a-hydroxy-1H-indole-3-propanoatehmdb
(+)-a-hydroxy-1H-indole-3-propanoic acidhmdb
(+)-a-hydroxy-1H-indole-3-propionatehmdb
(+)-a-hydroxy-1H-indole-3-propionic acidhmdb
(+)-alpha-hydroxy-1H-indole-3-propanoatehmdb
(+)-alpha-hydroxy-1H-indole-3-propanoic acidhmdb
(+)-alpha-hydroxy-1H-indole-3-propionatehmdb
(+)-alpha-hydroxy-1H-indole-3-propionic acidhmdb
(S)-2-hydroxy-3-indol-3-yl-propionatehmdb
(S)-2-hydroxy-3-indol-3-yl-propionic acidhmdb
2-hydroxy-3-indol-3-yl-propionatehmdb
2-hydroxy-3-indol-3-yl-propionic acidhmdb
2-Hydroxy-3-indol-3-yl-propionsaeurehmdb
3-(indol-3-yl)LactateGenerator
3-(indol-3-yl)Lactic acidChEBI
a-Hydroxy-1H-indole-3-propanoateGenerator
a-Hydroxy-1H-indole-3-propanoic acidGenerator
alpha-Hydroxy-1H-indole-3-propanoateGenerator
alpha-Hydroxy-1H-indole-3-propanoic acidChEBI
DL-3-indolelactatehmdb
DL-3-indolelactic acidhmdb
Indole-3-lactateGenerator
Indole-3-lactic acidChEBI
Indolelactatehmdb
Indolelactic acidhmdb
α-hydroxy-1H-indole-3-propanoateGenerator
α-hydroxy-1H-indole-3-propanoic acidGenerator
Chemical FormulaNot Available
IUPAC nameNot Available
InChI IdentifierInChI=1S/C11H11NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,10,12-13H,5H2,(H,14,15)
InChI KeyXGILAAMKEQUXLS-UHFFFAOYSA-N
Isomeric SMILESOC(CC1=CNC2=C1C=CC=C2)C(O)=O
Average Molecular Weight205.2099
Monoisotopic Molecular Weight205.073893223
Chemical Taxonomy
Description Belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. Indolyl carboxylic acids and derivatives are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassIndoles and derivatives
Sub ClassIndolyl carboxylic acids and derivatives
Direct ParentIndolyl carboxylic acids and derivatives
Alternative Parents
Substituents
  • Indolyl carboxylic acid derivative
  • 3-alkylindole
  • Indole
  • Alpha-hydroxy acid
  • Hydroxy acid
  • Substituted pyrrole
  • Benzenoid
  • Pyrrole
  • Heteroaromatic compound
  • Secondary alcohol
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Azacycle
  • Hydrocarbon derivative
  • Alcohol
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Carbonyl group
  • Organic nitrogen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Physico-Chemical Properties - Experimental
PropertyValueReference
Experimental logPNot Available
Experimental Water SolubilityNot Available
Melting PointNot Available
Foods of Origin
FoodContent Range AverageReference
FoodReference
Production Data
Production Methodcommercial
Production Method ReferenceNot Available
Production Method Reference FileNot Available
Quantity AvailableProduction upon request, up to 100 mg
Delivery TimeNot Available
Storage Formsolid
Storage Conditions-80°C
StabilityNot Available
PurityNot Available
Spectra
Spectral Data Upon RequestNot Available
Provider Information
Contact NameContact InstitutionContact Email
Rosa Vazquez Fresnovazquezf@ualberta.ca
Commercial Vendors
AKSci 6637AH
Toronto Research Chemicals I627100