Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Ranirestat effective and orally active aldose reductase inhibitor ( IC50s: 11 nM and 15 nM for rat lens AR and recombinant human AR, respectively and a Ki: 0.38 nM for recombinant human AR). Ranirestat has a neuroprotective effect on diabetic retinas.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
25 mg | 8-10 weeks | $ 691.00 | |
50 mg | 8-10 weeks | $ 898.00 | |
100 mg | 8-10 weeks | $ 1,440.00 |
Description | Ranirestat effective and orally active aldose reductase inhibitor ( IC50s: 11 nM and 15 nM for rat lens AR and recombinant human AR, respectively and a Ki: 0.38 nM for recombinant human AR). Ranirestat has a neuroprotective effect on diabetic retinas. |
Targets&IC50 | Aldose reductase (rat lens):11 nM, Aldose reductase (human recombinant):(ki)0.38 nM, Aldose reductase (human recombinant):15 nM |
In vitro | The potency of Ranirestat inhibition of sorbitol accumulation is similar between rat erythrocytes and sciatic nerves (IC50: 0.010 μM and 0.041 μM, respectively). Ranirestat concentration-dependently inhibits sorbitol accumulation in rat erythrocytes and sciatic nerves incubated in the high concentration (500 mg/dl) of glucose [1]. |
In vivo | Ranirestat also improves the STZ-induced decrease in motor nerve conduction velocity (MNCV) in a dose-dependent manner. Ranirestat (0.03-1.0 mg/kg;p.o.; once daily; for 3 weeks; male STD-Wistar rats) treatment dose-dependently reduces the elevated sorbitol and fructose levels in the rat sciatic nerves without affecting blood glucose level [1]. |
Synonyms | AS-3201 |
Molecular Weight | 420.19 |
Formula | C17H11BrFN3O4 |
CAS No. | 147254-64-6 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 50 mg/mL (118.99 mM)
You can also refer to dose conversion for different animals. More
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Ranirestat 147254-64-6 Others AS 3201 AS-3201 AS3201 inhibitor inhibit