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CHEBI:16996 - L-histidinol phosphate

Default Structure
ChEBI IDCHEBI:16996
ChEBI NameL-histidinol phosphate
Stars
ASCII NameL-histidinol phosphate
DefinitionThe O-phospho derivative of L-histidinol.
Secondary ChEBI IDsCHEBI:6242, CHEBI:13119, CHEBI:21327, CHEBI:43319
Last Modified25 January 2016
DownloadsMolfile
FormulaC6H12N3O4P
Net Charge0
Average Mass221.153
Monoisotopic Mass221.05654
SMILESN[C@H](COP(=O)(O)O)Cc1cncn1
InChIInChI=1S/C6H12N3O4P/c7-5(3-13-14(10,11)12)1-6-2-8-4-9-6/h2,4-5H,1,3,7H2,(H,8,9)(H2,10,11,12)/t5-/m0/s1
InChIKeyCWNDERHTHMWBSI-YFKPBYRVSA-N
Species of MetaboliteComponentSourceComments
Escherichia coli (ncbitaxon:562) - PubMed (21988831)
Roles Classification
Biological Role:
Escherichia coli metabolite  Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
ChEBI Ontology
Outgoing Relation(s)
L-histidinol phosphate (CHEBI:16996) has functional parent L-histidinol (CHEBI:16255)
L-histidinol phosphate (CHEBI:16996) has role Escherichia coli metabolite (CHEBI:76971)
L-histidinol phosphate (CHEBI:16996) is a phosphoethanolamine (CHEBI:36711)
L-histidinol phosphate (CHEBI:16996) is conjugate acid of L-histidinol phosphate(1−) (CHEBI:57980)
Incoming Relation(s)
L-histidinol phosphate(1−) (CHEBI:57980) is conjugate base of L-histidinol phosphate (CHEBI:16996)
IUPAC Name 
(2S)-2-amino-3-(1H-imidazol-4-yl)propyl dihydrogen phosphate
Synonyms  Source
L-Histidinol phosphateKEGG COMPOUND
PHOSPHORIC ACID MONO-[2-AMINO-3-(3H-IMIDAZOL-4-YL)-PROPYL]ESTERPDBeChem
Manual XrefsDatabases
C00007480KNApSAcK
C01100KEGG COMPOUND
DB03997DrugBank
HSAPDBeChem
Registry NumbersSources
Beilstein:792319Beilstein
CAS:25679-93-0KEGG COMPOUND