FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Chemical: epalrestat
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General Information
Name
epalrestat
FlyBase ID
FBch0002143
ChEBI Name
epalrestat
ChEBI ID
PubChem Name
Epalrestat
PubChem ID
Chemical Structure
Chemical structure of epalrestat
epalrestat
InChIKey

CHNUOJQWGUIOLD-NFZZJPOKSA-N

Definition (ChEBI)

A monocarboxylic acid that is 1,3-thiazolidine which is substituted on the nitrogen by a carboxymethyl group, at positions 2 and 4 by thioxo and oxo groups, respectively, and at position 5 by a 2-methyl-3-phenylprop-2-en-1-ylidene group. It is an inhibitor of aldose reductase (which catalyses the conversion of glucose to sorbitol) and is used for the treatment of some diabetic complications, including neuropathy. ChEBI: Epalrestat is a monocarboxylic acid that is 1,3-thiazolidine which is substituted on the nitrogen by a carboxymethyl group, at positions 2 and 4 by thioxo and oxo groups, respectively, and at position 5 by a 2-methyl-3-phenylprop-2-en-1-ylidene group. It is an inhibitor of aldose reductase (which catalyses the conversion of glucose to sorbitol) and is used for the treatment of some diabetic complications, including neuropathy. It has a role as an EC 1.1.1.21 (aldehyde reductase) inhibitor. It is a member of thiazolidines and a monocarboxylic acid.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (17)
Synonyms
2-((z)-5-((e)-2-methyl-3-phenylallylidene)-4-oxo-2-thioxothiazolidin-3-yl)acetic acid
5-((1Z,2E)-2-methyl-3-phenylpropenylidene)-4-oxo-2-thioxo-3-thiazolidineacetic acid
5-((Z,E)-beta-methylcinnamylidene)-4-oxo-2-thioxo-3-thiazolidineacetic acid
82159-09-9
Epalrestat [INN]
Epalrestatum
Epalrestatum [Latin]
ONO-2235
Ono-2235
PubChem:1549120
epalrestatum
{(5Z)-5-[(2E)-2-methyl-3-phenylprop-2-en-1-ylidene]-4-oxo-2-thioxo-1,3-thiazolidin-3-yl}acetic acid
Secondary FlyBase IDs
    References (3)