CHEBI:16255 - L-histidinol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name L-histidinol
ChEBI ASCII Name L-histidinol
Definition An amino alcohol that is propanol substituted by 1H-imidazol-4-yl group at position 3 and an amino group at position 2 (the 2S stereoisomer).
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:6241, CHEBI:13118, CHEBI:21326
Supplier Information
Download Molfile XML SDF
Formula C6H11N3O
Net Charge 0
Average Mass 141.17116
Monoisotopic Mass 141.09021
InChI InChI=1S/C6H11N3O/c7-5(3-10)1-6-2-8-4-9-6/h2,4-5,10H,1,3,7H2,(H,8,9)/t5-/m0/s1
SMILES N[C@H](CO)Cc1c[nH]cn1
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): EC (glycylpeptide N-tetradecanoyltransferase) inhibitor
An EC 2.3.1.* (acyltransferase transferring other than amino-acyl group) inhibitor that interferes with the action of glycylpeptide N-tetradecanoyltransferase (EC
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-histidinol (CHEBI:16255) has role Escherichia coli metabolite (CHEBI:76971)
L-histidinol (CHEBI:16255) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
L-histidinol (CHEBI:16255) has role EC (glycylpeptide N-tetradecanoyltransferase) inhibitor (CHEBI:78691)
L-histidinol (CHEBI:16255) has role human metabolite (CHEBI:77746)
L-histidinol (CHEBI:16255) is a amino alcohol (CHEBI:22478)
L-histidinol (CHEBI:16255) is a imidazoles (CHEBI:24780)
L-histidinol (CHEBI:16255) is conjugate base of L-histidinol(1+) (CHEBI:57699)
Incoming L-histidinol phosphate (CHEBI:16996) has functional parent L-histidinol (CHEBI:16255)
L-histidinol(1+) (CHEBI:57699) is conjugate acid of L-histidinol (CHEBI:16255)
Synonyms Sources
4-[(S)-2-amino-3-hydroxypropyl]imidazole ChEBI
Manual Xrefs Databases
C00007479 KNApSAcK
DB03811 DrugBank
HMDB0003431 HMDB
View more database links
Registry Numbers Types Sources
4836-52-6 CAS Registry Number KEGG COMPOUND
4836-52-6 CAS Registry Number ChemIDplus
81955 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1617631 PubMed citation Europe PMC
1768057 PubMed citation Europe PMC
21573440 PubMed citation Europe PMC
2292205 PubMed citation Europe PMC
2405251 PubMed citation Europe PMC
7042909 PubMed citation Europe PMC
8297120 PubMed citation Europe PMC
885850 PubMed citation Europe PMC
9042234 PubMed citation Europe PMC
9778369 PubMed citation Europe PMC
Last Modified
25 January 2016