CHEBI:166870 - aminoethyl nitrate

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ChEBI Name aminoethyl nitrate
ChEBI ID CHEBI:166870
Definition A nitrate ester resulting from the formal condensation of the hydroxy group of ethanolamine with the hydroxy group of nitric acid. It causes vasodilation by generating nitric oxide and is used for the treatment of angina pectoris and ischemic heart disease.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C2H6N2O3
Net Charge 0
Average Mass 106.081
Monoisotopic Mass 106.03784
InChI InChI=1S/C2H6N2O3/c3-1-2-7-4(5)6/h1-3H2
InChIKey KZTZJUQNSSLNAG-UHFFFAOYSA-N
SMILES NCCO[N+]([O-])=O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Application(s): vasodilator agent
A drug used to cause dilation of the blood vessels.
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ChEBI Ontology
Outgoing aminoethyl nitrate (CHEBI:166870) has functional parent ethanolamine (CHEBI:16000)
aminoethyl nitrate (CHEBI:166870) has role vasodilator agent (CHEBI:35620)
aminoethyl nitrate (CHEBI:166870) is a nitrate ester (CHEBI:51080)
aminoethyl nitrate (CHEBI:166870) is a primary amino compound (CHEBI:50994)
Incoming itramin tosilate (CHEBI:136001) has part aminoethyl nitrate (CHEBI:166870)
IUPAC Name
2-aminoethyl nitrate
INNs Sources
aminoethyl nitrate WHO MedNet
aminoethylis nitras WHO MedNet
nitrate d'aminoéthyle WHO MedNet
nitrato de aminoetilo WHO MedNet
Synonyms Sources
2-aminoethanol nitrate ester ChEBI
2-nitratoethylamine ChEBI
CLC 1011 ChEBI
CLC-1011 ChEBI
itramin DrugBank
monoethanolamine nitrate ester ChEBI
nitrolamine ChemIDplus
Brand Name Source
Aramin ChemIDplus
Manual Xrefs Databases
24220 ChemSpider
DB13585 DrugBank
View more database links
Registry Number Type Source
646-02-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
19732062 PubMed citation Europe PMC
23711023 PubMed citation Europe PMC
23711024 PubMed citation Europe PMC
28988245 PubMed citation Europe PMC
2913756 PubMed citation Europe PMC
Last Modified
26 November 2020