CHEBI:5296 - gemfibrozil

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name gemfibrozil
ChEBI ID CHEBI:5296
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C15H22O3
Net Charge 0
Average Mass 250.33338
Monoisotopic Mass 250.15689
InChI InChI=1S/C15H22O3/c1-11-6-7-12(2)13(10-11)18-9-5-8-15(3,4)14(16)17/h6-7,10H,5,8-9H2,1-4H3,(H,16,17)
InChIKey HEMJJKBWTPKOJG-UHFFFAOYSA-N
SMILES Cc1ccc(C)c(OCCCC(C)(C)C(O)=O)c1
Roles Classification
Application(s): antilipemic drug
A substance used to treat hyperlipidemia (an excess of lipids in the blood).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing gemfibrozil (CHEBI:5296) has functional parent valeric acid (CHEBI:17418)
gemfibrozil (CHEBI:5296) has role antilipemic drug (CHEBI:35679)
gemfibrozil (CHEBI:5296) is a aromatic ether (CHEBI:35618)
IUPAC Name
5-(2,5-dimethylphenoxy)-2,2-dimethylpentanoic acid
INNs Sources
gemfibrozil ChemIDplus
Gemfibrozilo ChemIDplus
gemfibrozilum ChemIDplus
Synonyms Sources
2,2-Dimethyl-5-(2,5-dimethylphenoxy)valeriansäure ChemIDplus
2,2-Dimethyl-5-(2,5-xylyloxy)valeriansäure ChemIDplus
2,2-Dimethyl-5-(2,5-xylyloxy)valeric acid ChemIDplus
Gemfibrozil KEGG DRUG
Brand Name Source
Lopid DrugBank
Manual Xrefs Databases
1285 DrugCentral
D00334 KEGG DRUG
DB01241 DrugBank
DE1925423 Patent
Gemfibrozil Wikipedia
LSM-2227 LINCS
US3674836 Patent
US4126637 Patent
View more database links
Registry Numbers Types Sources
1881200 Beilstein Registry Number Beilstein
25812-30-0 CAS Registry Number KEGG DRUG
25812-30-0 CAS Registry Number ChemIDplus
Last Modified
22 February 2017