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Balicatib Sale

(Synonyms: 巴利卡替; AAE581) 目录号 : GC12751

A cathepsin K inhibitor

Balicatib Chemical Structure

Cas No.:354813-19-7

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥747.00
现货
5mg
¥738.00
现货
10mg
¥918.00
现货
50mg
¥2,763.00
现货

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Sample solution is provided at 25 µL, 10mM.

Description

Balicatib is an inhibitor of cathepsin K with IC50 value of 1.4nM [1].

Balicatib is highly selective against cathepsin K over cathepsin B, L and S in the in vitro enzyme assay. However, the selectivity is not so high in cell-based enzyme assay. The lysosomotropic character of balicatib results in its accumulation in lysosomes and the subsequent nonselective off-target effects. The off-target effects also cause the skin adverse events of balicatib [1, 2].

As a cathepsin K inhibitor, balicatib is developed for osteoporosis. It has been reported to reduce the biochemical markers of bone resorption and increase bone mineral density in ovariectomized monkeys. In addition, balicatib shows benefits in new bone formation of postmenopausal women [2].

References:
[1] Black WC. Peptidomimetic inhibitors of cathepsin K. 2010;10(7):745-51.
[2] Brömme D, Lecaille F. Cathepsin K inhibitors for osteoporosis and potential off-target effects. Expert Opin Investig Drugs. 2009 May;18(5):585-600.

化学性质

Cas No. 354813-19-7 SDF
别名 巴利卡替; AAE581
化学名 N-[1-(cyanomethylcarbamoyl)cyclohexyl]-4-(4-propylpiperazin-1-yl)benzamide
Canonical SMILES CCCN1CCN(CC1)C2=CC=C(C=C2)C(=O)NC3(CCCCC3)C(=O)NCC#N
分子式 C23H33N5O2 分子量 411.54
溶解度 ≥ 17mg/mL in DMSO 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.4299 mL 12.1495 mL 24.299 mL
5 mM 0.486 mL 2.4299 mL 4.8598 mL
10 mM 0.243 mL 1.2149 mL 2.4299 mL
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