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:73337 - (
R
)-α-methylhistamine
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
(
R
)-α-methylhistamine
ChEBI ID
CHEBI:73337
ChEBI ASCII Name
(R)-alpha-methylhistamine
Definition
An aralkylamino compound that is histamine bearing a methyl substituent at the α-position (the
R
-enantiomer).
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Margaret Duesbury
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
C6H11N3
Net Charge
0
Average Mass
125.17160
Monoisotopic Mass
125.09530
InChI
InChI=1S/C6H11N3/c1-5(7)2-6-3-8-4-9-6/h3-5H,2,7H2,1H3,(H,8,9)/t5-/m1/s1
InChIKey
XNQIOISZPFVUFG-RXMQYKEDSA-N
SMILES
C[C@@H](N)Cc1c[nH]cn1
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):
H3-receptor agonist
A histamine agonist that binds to and activates histamine H
3
-receptors.
Application
(s):
H3-receptor agonist
A histamine agonist that binds to and activates histamine H
3
-receptors.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(
R
)-α-methylhistamine (
CHEBI:73337
)
has role
H
3
-receptor agonist (
CHEBI:64154
)
(
R
)-α-methylhistamine (
CHEBI:73337
)
is a
aralkylamino compound (
CHEBI:64365
)
(
R
)-α-methylhistamine (
CHEBI:73337
)
is a
imidazoles (
CHEBI:24780
)
IUPAC Name
(2
R
)-1-(1
H
-imidazol-4-yl)propan-2-amine
Synonyms
Sources
(
R
)-(−)-4-(2-aminopropyl)imidazole
ChEBI
(
R
)-(−)-α-methylhistamine
ChEBI
(
R
)α-Me-histamine
ChEBI
Manual Xrefs
Databases
EP214058
Patent
US2002151576
Patent
US2003113309
Patent
US2005245587
Patent
US4767778
Patent
US5773457
Patent
View more database links
Registry Numbers
Types
Sources
6053636
Reaxys Registry Number
Reaxys
75614-87-8
CAS Registry Number
ChemIDplus
Citations
Types
Sources
23597562
PubMed citation
Europe PMC
7902173
PubMed citation
Europe PMC
Last Modified
01 May 2013