CHEBI:30347 - ethylenediamine

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ChEBI Name ethylenediamine
ChEBI ID CHEBI:30347
Definition An alkane-α,ω-diamine in which the alkane is ethane.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C2H8N2
Net Charge 0
Average Mass 60.09840
Monoisotopic Mass 60.06875
InChI InChI=1S/C2H8N2/c3-1-2-4/h1-4H2
InChIKey PIICEJLVQHRZGT-UHFFFAOYSA-N
SMILES NCCN
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): GABA agonist
A drug that binds to and activates gamma-aminobutyric acid receptors.
Application(s): GABA agonist
A drug that binds to and activates gamma-aminobutyric acid receptors.
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ChEBI Ontology
Outgoing ethylenediamine (CHEBI:30347) has parent hydride ethane (CHEBI:42266)
ethylenediamine (CHEBI:30347) has role GABA agonist (CHEBI:51373)
ethylenediamine (CHEBI:30347) is a alkane-α,ω-diamine (CHEBI:35411)
Incoming N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (CHEBI:88217) has functional parent ethylenediamine (CHEBI:30347)
ethylenebis(dithiocarbamic acid) (CHEBI:83986) has functional parent ethylenediamine (CHEBI:30347)
ethylenediamine derivative (CHEBI:31577) has functional parent ethylenediamine (CHEBI:30347)
ethylenediamine dihydrochloride (CHEBI:53626) has functional parent ethylenediamine (CHEBI:30347)
aminophylline (CHEBI:2659) has part ethylenediamine (CHEBI:30347)
IUPAC Name
ethane-1,2-diamine
Synonyms Sources
1,2-ethanediamine IUPAC
en IUPAC
ethylenediamine IUPAC
Manual Xrefs Databases
CPD-3682 MetaCyc
D01114 KEGG DRUG
EDN PDBeChem
Ethylenediamine Wikipedia
HMDB0031225 HMDB
View more database links
Registry Numbers Types Sources
107-15-3 CAS Registry Number ChemIDplus
107-15-3 CAS Registry Number NIST Chemistry WebBook
1098 Gmelin Registry Number Gmelin
605263 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
21616561 PubMed citation Europe PMC
3692019 PubMed citation Europe PMC
7070713 PubMed citation Europe PMC
Last Modified
16 February 2016