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Bpsbioscience/LDN-57444/27706-1/10 mg

  
  2024-05-03
  
MW: 397.6 Da CAS Registry #: 668467-91-2 Formula: C17H11Cl3N2O3 Description:LDN-57444 is a cell permeable ubiquitin C-terminal hydrolase (UCH-L1) inhibitor (Ki=0.4 μM). Decreases proteasome activity and increases levels of ubiquitinated proteins. Induces apoptosis and causes dramatic alterations in synaptic protein distribution and spine morphology in vivo. LDN-57444 is a useful tool to study UCH-L1 in different pathological conditions such as cancer and neurodegeneration. Synonym(s): 1H–Indole–2,3–dione, 5–chloro–1–[(2,5–dichlorophenyl)methyl]–, 3–(O–acetyloxime) Purity: ≥98% by TLC. Solubility: Soluble in DMSO (20 mg/ml) Format: Yellow powder Storage / Stability:

Store at +4°C. Stable as supplied for up to 2 years when stored dessicated at +4°C. Store solutions at -20°C for up to 1 week.

Application(s): Useful for the inhibition of Ubiquitin C-terminal Hydrolase (UCH-L1) in drug discovery studies. Reference(s): 1. Tan, et al Endoplasmic reticulum stress contributes to the cell death induced by UCH-L1 inhibitor. Mol.Cell.Biochem. 318:109 (2008).2. Susor, A., et al., Proteomic analysis of porcine oocytes during in vitro maturation reveals essential role for the ubiquitin C-terminal hydrolase-L1. Reprod. 134:559 - 568, (2007) . Warning(s): Protect from moisture. Avoid freeze/thaw cycles. Scientific Category: Ubiquitin Enzymes Product Type: Inhibitors/Activators Data shown is lot-specific. Contact us for specific information on other lots.

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