Record Information
Version1.0
StatusDetected and Quantified
Creation Date2021-11-17 23:52:45 UTC
Update Date2022-08-31 17:39:28 UTC
Metabolite IDMMDBc0030069
Metabolite Identification
Common NameIndoleglycerol phosphate
DescriptionIndoleglycerol phosphate is a member of the chemical class known as Indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. Indoleglycerol phosphate is involved in tryptophan biosynthesis. The latter is the competent substrate of indoleglycerol phosphate synthase, which catalyzes the subsequent step of tryptophan biosynthesis. (PMID 7727401 ) alphaTS by itself catalyzes the cleavage of indole-3-glycerol phosphate to glyceraldehyde-3-phosphate and indole, which is converted to tryptophan in tryptophan biosynthesis. (PMID 15879705 )
Structure
Synonyms
ValueSource
(3-Indolyl)-glycerol phosphateChEBI
1-C-(indol-3-yl)Glycerol 3-phosphateChEBI
C1-(3-Indolyl)-glycerol 3-phosphateChEBI
(1S,2R)-1-C-(indol-3-yl)Glycerol 3-phosphateKegg
(3-Indolyl)-glycerol phosphoric acidGenerator
1-C-(indol-3-yl)Glycerol 3-phosphoric acidGenerator
C1-(3-Indolyl)-glycerol 3-phosphoric acidGenerator
(1S,2R)-1-C-(indol-3-yl)Glycerol 3-phosphoric acidGenerator
Indole-3-glycerol phosphoric acidGenerator
Indole-3-glycerophosphateMeSH
Indoleglycerol phosphateMeSH
Indole-3-glycerol phosphateChEBI, KEGG
Indoleglycerol phosphoric acidGenerator
Molecular FormulaC11H14NO6P
Average Mass287.2057
Monoisotopic Mass287.055873697
IUPAC Name[(2R,3S)-2,3-dihydroxy-3-(1H-indol-3-yl)propoxy]phosphonic acid
Traditional Nameindole-3-glycerol phosphate
CAS Registry Number4220-97-7
SMILES
[H][C@@](O)(COP(O)(O)=O)[C@@]([H])(O)C1=CNC2=C1C=CC=C2
InChI Identifier
InChI=1S/C11H14NO6P/c13-10(6-18-19(15,16)17)11(14)8-5-12-9-4-2-1-3-7(8)9/h1-5,10-14H,6H2,(H2,15,16,17)/t10-,11+/m1/s1
InChI KeyNQEQTYPJSIEPHW-MNOVXSKESA-N