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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:73085 - colterol
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ChEBI Ontology
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ChEBI Name
colterol
ChEBI ID
CHEBI:73085
Definition
A member of the class of ethanolamines that is catechol in which the hydrogen at position 4 is replaced by a 2-(
tert
-butylamino)-1-hydroxyethyl group.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C12H19NO3
Net Charge
0
Average Mass
225.28420
Monoisotopic Mass
225.13649
InChI
InChI=1S/C12H19NO3/c1-12(2,3)13-7-11(16)8-4-5-9(14)10(15)6-8/h4-6,11,13-16H,7H2,1-3H3
InChIKey
PHSMOUBHYUFTDM-UHFFFAOYSA-N
SMILES
CC(C)(C)NCC(O)c1ccc(O)c(O)c1
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):
beta-adrenergic agonist
An agent that selectively binds to and activates
beta
-adrenergic receptors.
Application
(s):
beta-adrenergic agonist
An agent that selectively binds to and activates
beta
-adrenergic receptors.
anti-asthmatic drug
A drug used to treat asthma.
bronchodilator agent
An agent that causes an increase in the expansion of a bronchus or bronchial tubes.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
colterol (
CHEBI:73085
)
has role
β-adrenergic agonist (
CHEBI:35522
)
colterol (
CHEBI:73085
)
has role
anti-asthmatic drug (
CHEBI:49167
)
colterol (
CHEBI:73085
)
has role
bronchodilator agent (
CHEBI:35523
)
colterol (
CHEBI:73085
)
is a
catechols (
CHEBI:33566
)
colterol (
CHEBI:73085
)
is a
ethanolamines (
CHEBI:23981
)
colterol (
CHEBI:73085
)
is a
secondary alcohol (
CHEBI:35681
)
colterol (
CHEBI:73085
)
is a
secondary amino compound (
CHEBI:50995
)
colterol (
CHEBI:73085
)
is a
triol (
CHEBI:27136
)
IUPAC Name
4-[2-(
tert
-butylamino)-1-hydroxyethyl]benzene-1,2-diol
INNs
Sources
coltérol
WHO MedNet
colterol
WHO MedNet
colterol
ChemIDplus
colterolum
ChemIDplus
Synonyms
Sources
(±)-
N
-t-butylnoradrenaline
ChemIDplus
(±)-
N
-
tert
-butylarterenol
ChemIDplus
(+/-)-N-tert-butylarterenol
ChEBI
Registry Numbers
Types
Sources
18866-78-9
CAS Registry Number
ChemIDplus
2106130
Reaxys Registry Number
Reaxys
Citations
Types
Sources
473792
PubMed citation
Europe PMC
6345565
PubMed citation
Europe PMC
Last Modified
03 April 2013