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ONO-5334
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
ONO-5334图片
CAS NO:868273-90-9

ONO-5334 是一种强效、选择性和口服活性的组织蛋白酶 K (cathepsin K) 抑制剂,对人、兔和大鼠组织蛋白酶 K 的作用值分别为 0.10 nM、0.049 nM 和 0.85 nM。ONO-5334 是一种有效的抗SAR-COV-2病毒活性的抗病毒化合物,其EC50值为 500 nM。ONO-5334 有潜力用于骨质疏松症以及 COVID-19 的相关研究。
生物活性

ONO-5334 is a potent, selective and orally activecathepsin Kinhibitor withKivalues of 0.10 nM, 0.049 nM and 0.85 nM for human, rabbit and ratcathepsin K, respectively. ONO 5334 is an effective antiviral compound againstSAR-COV-2virus activity with anEC50value of 500 nM. ONO-5334 has the potential for the study of osteoporosis and COVID-19 disease[1].

IC50& Target

cathepsin K

 

体外研究
(In Vitro)

ONO-5334 has inhibitory effects on human cathepsin S, human cathepsin L, human cathepsin B, porcine calpain Ι and porcine calpain II withKivalues of 0.83 nM, 1.7 nM, 32 nM, 82 nM and 69 nM, respectively[1].
ONO-5334 (0.1-1 μM; 24 hours) suppresses human osteoclast-mediated bone resorption. It potently reduces osteoclast-mediated release of CTX from bone slices as a dose dependent manner[1].
ONO-5334 (0-10 μM; pre-treated for 16 h) inhibits antiviral activities in a discernable dose-dependent manner in Vero E6 cells by designed to capture multicycle replication, exhibiting an EC50value of 0.5 μM[2]/

Cell Viability Assay[2]

Cell Line:Vero E6 cells
Concentration:0.001 μM, 0.003 μM, 0.1 μM, 0.3 μM, 1 μM, 2.5 μM
Incubation Time:Pre-treated for 16 h and then cultured for 24 hours
Result:Inhibited SARS-COV-2 virus replication in a dose-dependent manner.
体内研究
(In Vivo)

ONO-5334 (oral administration; 0.12-15 mg/kg; single dose) can dose-dependently reduce PTHrP-induced increase in plasma calcium with significant effect (86% reduction) at 15 mg/kg. It also reduces PTHrP-induced increase in plasma CTX level in TPTX rats by 90% at 15 mg/kg[1].
ONO-5334 (oral administration; 0.3-30 mg/kg; 7 consecutive days) at 3 mg/kg or 30 mg/kg significantly decreases CTX (a bone resorption marker) concentration. On day 7, the reduction in serum CTX concentration by ONO-5334 at 3 mg/kg and 30 mg/kg was 62% and 79%, respectively[1].

Animal Model:Monkey[1]
Dosage:0.3 mg/kg; 3 mg/kg
Administration:Oral administration; 7 consecutive days
Result:Reduced bone resorption markers but not bone formation markers in normal monkeys.
Clinical Trial
分子量

438.58

性状

Solid

Formula

C21H34N4O4S

CAS 号

868273-90-9

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
 
 
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