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ER-000444793

    
98.00%

ER-000444793

源叶(MedMol)
S86536 一键复制产品信息
792957-74-5
C23H18N2O2
354.40122
ER-000444793(792957-74-5)
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S86536-1mg
98.00%

¥150.00

9 - - - -
S86536-5mg
98.00%

¥270.00

7 - - - -
S86536-10mg
98.00%

¥500.00

6 - - - -
S86536-25mg
98.00%

¥790.00

5 - - - -
产品描述: ER-000444793 is a potent inhibitor of mitochondrial permeability transition pore (mPTP) opening. ER-000444793 inhibits mPTP with an IC50 of 2.8 μM.
靶点: IC50: 2.8 μM (mPTP);MitochondrialMetabolism
体外研究: ER-000444793 is a small molecule, non-toxic mPTP inhibitor with a mechanism of action independent of CypD inhibition. ER-000444793 potently and dose-dependently inhibits Ca2+-induced mPT. ER-000444793 binds CypD, a CsA/CypD homogenous time-resolved fluorescence (HTRF) assay is used to study compound binding. Both CsA and SfA dose-dependently decrease HTRF signal, suggesting displacement of labelled CsA from rhCypD protein (CsA IC50=23 nM and SfA IC50= 5 nM). In contrast, ER-000444793 has no effect up to a concentration of 50 μM, indicating lack of displacement of labelled-CsA from rhCypD protein. Together, these data suggest the mechanism of ER-000444793 in delaying mPT is independent of CypD functional inhibition
参考文献: 1. Briston T, et al. Identification of ER-000444793, a Cyclophilin D-independent inhibitor of mitochondrial permeability transition, using a high-throughput screen in cryopreserved mitochondria. Sci Rep. 2016 Nov 25;6:37798.
溶解性: soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.822 ml 14.108 ml 28.217 ml
5 mM 0.564 ml 2.822 ml 5.643 ml
10 mM 0.282 ml 1.411 ml 2.822 ml
50 mM 0.056 ml 0.282 ml 0.564 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

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