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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名：
CA-074Me
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- 规格：
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥1049.0 |
|---|---|---|---|
| 规格： | 1 mg | 产品价格： | ￥700.0 |
| 规格： | 5 mg | 产品价格： | ￥1200.0 |
| 规格： | 10 mg | 产品价格： | ￥2100.0 |
| 规格： | 25 mg | 产品价格： | ￥3900.0 |
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CA-074 methyl ester
CAS No. : 147859-80-1
MCE 国际站：CA-074 methyl ester
产品活性：CA-074 methyl ester 是一种特异性的 Cathepsin B 抑制剂，具有保护神经，抗癌、抗炎等多种生物活性。
研究领域：Metabolic Enzyme/Protease
作用靶点：Cathepsin
In Vitro: CA-074Me (5 μM and 50 μM) inhibits RANKL-induced osteoclastogenesis in BMM cells derived from C57BL/6J and NOD/ShiLtJ mice. CA-074Me exerts its anti-osteoclastogenic effect within 24 hours post-RANKL stimulation in vitro. CA-074Me does not exert its anti-osteoclastogenic effect via the MAPK-ERK signaling cascade. CA-074Me inhibits c-FOS upregulation and subsequent NFATc1 autoamplification following RANKL stimulation..
CA-074Me reduces apoptosis induced by CVB1.
In Vivo: Hippocampal CA1 neuronal programmed necrosis induced by global cerebral I/R injury is prevented by CA074-me (1 μg, 10 μg) both pre-treatment and post-treatment. The rupture of lysosomal membrane and the leakage of cathepsin-B, and this is strongly inhibited by CA074-me pre-treatment. The overexpression and nuclear translocation of RIP3 and the reduction of NAD+ level after I/R injury are also inhibited, while the upregulation of Hsp70 is strengthened by CA074-me pre-treatment.
CA-074Me (30 mg/kg) is capable of inhibiting osteoclastogenesis and bone degradation in vivo.
In the CVB+CA-074Me (4 mg/kg/day i.m.) guinea pigs group, the scores of inflammation significantly decrease in comparison with the CVB+None group. In CVB+CA-074Me group, the number of CD8+T cells decrease in comparison with the sham group.
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