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Sparsentan (RE-021)

Cat. No. M20689
Sparsentan (RE-021) Structure
Synonym:

PS-433540; RE-021; DARA-a; BMS-346567

Size Price Availability Quantity
5mg USD 105  USD105 In stock
10mg USD 170  USD170 In stock
25mg USD 340  USD340 In stock
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Quality Control & Documentation
Biological Activity

Sparsentan (PS-433540, RE-021, DARA) is a first-in-class, orally active, high-affinity dual antagonist of the endothelin type A receptor (ETA) and Angiotensin II type 1 (AT1) receptor, with Ki values of 9.3 and 0.8 nM, respectively. Sparsentan dose dependently antagonizes the angiotensin II-induced pressor response with an ED50 value of 0.8 µmol/kg iv and 3.6 µmol/kg po. Sparsentan also shows efficacious and long acting in the big ET-1-induced pressor model.

Sparsentan causes a significant lowering of blood pressure at the lowest dose tested (10 µmol/kg/day) in spontaneously hypertensive rats. Sparsentan shows good oral bioavailability in rats, dogs, and monkeys, averaging 40%, 86%, and 21% F, respectively. At 100 µmol/kg/day, Sparsentan reduces the blood pressure from 170 to less than 100 mmHg during the course of the compound’s pharmacokinetic duration. Sparsentan at 100 µmol/kg/day essentially converts the spontaneously hypertensive rats into normotensive rats during the course of its pharmacokinetic duration.

Chemical Information
Molecular Weight 592.75
Formula C32H40N4O5S
CAS Number 254740-64-2
Solubility (25°C) DMSO 90 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Efren Chavez, et al. Front Med (Lausanne). Novel Therapies for Alport Syndrome

[2] Howard Trachtman, et al. J Am Soc Nephrol. DUET: A Phase 2 Study Evaluating the Efficacy and Safety of Sparsentan in Patients with FSGS

[3] Isaac D Liu, et al. Cochrane Database Syst Rev. Interventions for idiopathic steroid-resistant nephrotic syndrome in children

[4] Elisabeth M Hodson, et al. Cochrane Database Syst Rev. Interventions for focal segmental glomerulosclerosis in adults

[5] Liang Li, et al. Mol Ther. Targeting tissue-resident memory CD8+ T cells in the kidney is a potential therapeutic strategy to ameliorate podocyte injury and glomerulosclerosis

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Keywords: Sparsentan (RE-021), PS-433540; RE-021; DARA-a; BMS-346567 supplier, Endothelin Receptor, inhibitors, activators


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