CHEBI:2663 - amiodarone

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ChEBI Name amiodarone
ChEBI ID CHEBI:2663
Definition A member of the class of 1-benzofurans that is 1-benzofuran substituted by a butyl group at position 2 and a 4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl group at position 3. It is a cardiovascular drug used for the treatment of cardiac dysrhythmias.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C25H29I2NO3
Net Charge 0
Average Mass 645.31160
InChI InChI=1S/C25H29I2NO3/c1-4-7-11-22-23(18-10-8-9-12-21(18)31-22)24(29)17-15-19(26)25(20(27)16-17)30-14-13-28(5-2)6-3/h8-10,12,15-16H,4-7,11,13-14H2,1-3H3
InChIKey IYIKLHRQXLHMJQ-UHFFFAOYSA-N
SMILES CCCCc1oc2ccccc2c1C(=O)c1cc(I)c(OCCN(CC)CC)c(I)c1
Roles Classification
Application(s): cardiovascular drug
A drug that affects the rate or intensity of cardiac contraction, blood vessel diameter or blood volume.
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ChEBI Ontology
Outgoing amiodarone (CHEBI:2663) has role cardiovascular drug (CHEBI:35554)
amiodarone (CHEBI:2663) is a 1-benzofurans (CHEBI:38830)
amiodarone (CHEBI:2663) is a aromatic ketone (CHEBI:76224)
amiodarone (CHEBI:2663) is a organoiodine compound (CHEBI:37142)
amiodarone (CHEBI:2663) is a tertiary amino compound (CHEBI:50996)
IUPAC Name
(2-butyl-1-benzofuran-3-yl){4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl}methanone
INNs Sources
amiodarona ChemIDplus
amiodaronum ChemIDplus
Synonyms Sources
2-Butyl-3-(3,5-diiodo-4-(2-diethylaminoethoxy)benzoyl)benzofuran ChemIDplus
2-Butyl-3-benzofuranyl 4-(2-(diethylamino)ethoxy)-3,5-diiodophenyl ketone ChemIDplus
2-n-Butyl-3',5'-diiodo-4'-N-diethylaminoethoxy-3-benzoylbenzofuran ChemIDplus
Amiodarone KEGG COMPOUND
Database Links Databases
Amiodarone Wikipedia
C06823 KEGG COMPOUND
CA2826272 Patent
D02910 KEGG DRUG
DB01118 DrugBank
HMDB15250 HMDB
TW201400111 Patent
View more database links
Registry Numbers Types Sources
1271711 Beilstein Registry Number Beilstein
1951-25-3 CAS Registry Number KEGG COMPOUND
1951-25-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10188629 PubMed citation CiteXplore
16479044 PubMed citation CiteXplore
18368867 PubMed citation CiteXplore
Last Modified
09 février 2015