KR-33494

Modify Date: 2024-01-06 11:09:14

KR-33494 Structure
KR-33494 structure
Common Name KR-33494
CAS Number 1021497-97-1 Molecular Weight 460.351
Density N/A Boiling Point N/A
Molecular Formula C20H18BrN3O3S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of KR-33494


KR-33493 is a potent inhibitor of Fas-mediated cell death (FAF1).

 Names

Name KR-33494
Synonym More Synonyms

 KR-33494 Biological Activity

Description KR-33493 is a potent inhibitor of Fas-mediated cell death (FAF1).
Related Catalog
Target

FAF1[1]

In Vivo Body weight changes of both sexes are not related to KR-33493 in all doses. In rats administrated KR-33493 for 4 weeks, no test article-related changes in any treated groups of either sex are found in hematology, serum biochemistry, and urinalysis. In dogs administrated KR-33493 for 2 weeks, red blood cell count (RBC) value in males is significantly higher at the 1000 mg/kg/day dose than that of the control group (i.e., 6.96±0.323 vs. 6.12±0.418). However, the change of RBC is recovered after the end of the administration period. The dose-normalized AUClast is not significantly different between the groups, suggesting that KR-33493 is governed by linear kinetics[1].
Animal Admin A total of 93 male and 93 female specific pathogen-free rats (6 weeks of age), and 16 male and 16 female beagle dogs (8 months of age) are used in this study. In a toxicokinetic study, rat blood samples (approximately 0.6 mL) are collected into tubes containing heparin from the lateral tail vein at 0, 0.5, 1, 2, 4, 8, 12, and 24 h after dosing with KR-33493 at doses of 50, 150, and 500 mg/kg/day on Day 1 and Week 4. Dog blood samples (approximately 0.6 mL) are collected into tubes containing EDTA-2K from the cephalic vein at 0, 0.5, 1, 2, 4, 6, 8, and 24 h after dosing at KR-33493 doses of 50, 250, and 1000 mg/kg/day on Day 1 and Week 2. The plasma is separated by centrifugation (approximately 132,000 g, 3 min, 4°C) and stored at approximately -80°C until analysis. The KR-33493 concentration in plasma is quantified[1].
References

[1]. Jeong JW, et al. Subacute toxicity evaluation of KR-33493, FAF1 inhibitor for a new anti-parkinson's disease agent, after oral administration in rats and dogs. Regul Toxicol Pharmacol. 2016 Nov;81:387-396.

 Chemical & Physical Properties

Molecular Formula C20H18BrN3O3S
Molecular Weight 460.351

 Synonyms

4-[2-(4-bromo-phenylsulfanyl)-acetylamino]-1-phenethyl-1H-pyrazole-3-carboxylic acid
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