SML3973
Fidarestat
≥98% (HPLC)
Synonym(s):
(2S,4S)- 6-Fluoro-2,3-dihydro-2′,5′-dioxo-spiro[4H-1-benzopyran-4,4′-imidazolidine]-2-carboxamide, (2S,4S)-6-Fluoro-2′,5′-dioxospiro[chroman-4,4′-imidazolidine]-2-carboxamide, SNK-860
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About This Item
Empirical Formula (Hill Notation):
C12H10FN3O4
CAS Number:
Molecular Weight:
279.22
MDL number:
Quality Level
Assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
H2O: 2 mg/mL, clear
storage temp.
2-8°C
Biochem/physiol Actions
Active site-targeting, potent and selective aldose reductase (AR) inhibitor with >100-fold selectivity over aldehyde reductase (AHR).
Fidarestat inhibits Aldose Reductase (AR) involved in the rate limiting step in the conversion of glucose to sorbitol under hyperglycemic conditions. Aldose reductase has been the target of multiple clinical investigatons to treat diabetic neuropathy and retinopathy. Fidarestat has recently been shown to prevent inflammatory signals (TNF-α, LPS) that cause cancer (colon, breast, prostate and lung), metastasis, asthma, and other inflammatory diseases, as well as being useful for treatment of diabetic neuropathy.
Fidarestat inhibits Aldose Reductase (AR) involved in the rate limiting step in the conversion of glucose to sorbitol under hyperglycemic conditions. Aldose reductase has been the target of multiple clinical investigatons to treat diabetic neuropathy and retinopathy. Fidarestat has recently been shown to prevent inflammatory signals (TNF-α, LPS) that cause cancer (colon, breast, prostate and lung), metastasis, asthma, and other inflammatory diseases, as well as being useful for treatment of diabetic neuropathy.
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