Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:16255 -
L
-histidinol
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
L
-histidinol
ChEBI ID
CHEBI:16255
ChEBI ASCII Name
L-histidinol
Definition
An amino alcohol that is propanol substituted by 1
H
-imidazol-4-yl group at position 3 and an amino group at position 2 (the 2
S
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
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
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
InChIKey
ZQISRDCJNBUVMM-YFKPBYRVSA-N
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 (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
EC 2.3.1.97 (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 2.3.1.97).
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 2.3.1.97 (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
)
IUPAC Name
(2
S
)-2-amino-3-(1
H
-imidazol-4-yl)propan-1-ol
Synonyms
Sources
4-[(
S
)-2-amino-3-hydroxypropyl]imidazole
ChEBI
L-Histidinol
KEGG COMPOUND
Manual Xrefs
Databases
C00007479
KNApSAcK
C00860
KEGG COMPOUND
DB03811
DrugBank
HISTIDINOL
MetaCyc
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
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