LY 3000328

小分子

LY 3000328

L655759-1ml

1ml

10mM in DMSO

-80℃储存

超低温冰袋运输

LY 3000328 (Z-FL-COCHO) is a potent and selective Cathepsin S (Cat S) inhibitor with IC 50 s of 7.7 and 1.67 nM for hCat S and mCat S, respectively. In Vitro LY 3000328 maintains excellent in vitro potency and selectivity. LY 3000328 shows low in vitro CYP450 inhibition ( 4%). At a 100 μM concentration of LY 3000328 there is only 6% displacement of [ 3 H]-astemizole in an assay with HEK293 membrane preparation, indicating low potential of hERG blockade. LY 3000328 is a potent and specific inhibitor of cathepsin S (CatS). Inhibition of CatS activity in plasma would be 50% of maximal when LY 3000328 plasma concentration is approximately 60 ng/mL. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo The efficacies of LY 3000328 is studied in a mouse model of abdominal aortic aneurysm (AAA). In this model, inflammation is induced using CaCl 2 applied to the ablumenal surface. It is shown that features of the disease state in this model resemble those of human AAA. LY 3000328 exhibits a dose-responsive aortic diameter reduction at 1, 3, 10, and 30 mg/kg. At the lowest dose of 1 mg/kg of LY 3000328, the aortic diameter is reduced by 58%, then 83% at 3 mg/kg, and 87% at 10 mg/kg. The exposure (AUC) for both compounds increased in a dose-dependent manner, suggesting that the drug disposition properties of LY 3000328 are favorable . MCE has not independently confirmed the accuracy of these methods. They are for reference only. IC50& Target:cathepsin S

LY 3000328（Z-FL-COCHO）是一种强效的选择性胰蛋白酶 S（Cat S）抑制剂，对 hCat S 和 mCat S 的 IC 50 s 分别为 7.7 和 1.67 nM。

1373215-15-6(DMSO)

C25H29FN4O5

484.5 g/mol

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