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S80376

CA-074 ME

源叶(MedMol) 98%
  • 英文名:
  • CA-074 ME
  • 别名:
  • L-TRANS-环氧琥珀酸- ILE-PRO-OME丙醛;(L-3-反式-(丙基氨基甲酰)环氧乙烷-2-甲酰基)-L-异亮氨酰-L-脯氨酸甲酯;CA-074 甲酯;L-TRANS-EPOXYSUCCINYL-ILE-PRO-OME PROPYLAMIDE;L-TRANS-EPOXYSUCCINYL (PROPYLAMIDE)-ILE-PRO-OME;CA-074 ME;CATHEPSIN B IN
  • CAS号:
  • 147859-80-1
  • 分子式:
  • C19H31N3O6
  • 分子量:
  • 397.466
  • 核磁/质谱:
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源叶(MedMol) S80376-1mg 98% ¥400.00元 1 - - - EA 加入购物车
源叶(MedMol) S80376-5mg 98% ¥748.00元 4 - - - EA 加入购物车
源叶(MedMol) S80376-25mg 98% ¥2461.60元 5 - - - EA 加入购物车
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参考文献

质检证书(COA)

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  • 提示:详情请下载说明书。
  • 产品描述: CA-074 methyl ester is a specific inhibitor of Cathepsin B, which has potent bioactivities such as neuroprotective, anti-cancer, and anti-inflamatory effects.
  • 靶点: Cathepsin;CysteineProtease
  • 体内研究:
    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
  • 参考文献:
    1. Xu Y, et al. Protective mechanisms of CA074-me (other than cathepsin-B inhibition) against programmed necrosis induced by global cerebral ischemia/reperfusion injury in rats. Brain Res Bull. 2016 Jan;120:97-105 2. Patel N, et al. CA-074Me compound inhibits osteoclastogenesis via suppression of the NFATc1 and c-FOS signaling pathways. J Orthop Res. 2015 Oct;33(10):1474-86 3. Zhang L, et al. Treatment with CA-074Me, a Cathepsin B inhibitor, reduces lung interstitial inflammation and fibrosis in a rat model of polymyositis. Lab Invest. 2015 Jan;95(1):65-77
  • 溶解性: DMSO  :  100  mg/mL  (251.59  mM;  Need  ultrasonic)    H2O  :  <  0.1  mg/mL  (ultrasonic;warming;heat  to  60°C)  (insoluble)
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.516 ml 12.58 ml 25.159 ml
    5 mM 0.503 ml 2.516 ml 5.032 ml
    10 mM 0.252 ml 1.258 ml 2.516 ml
    50 mM 0.05 ml 0.252 ml 0.503 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)


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