LDN-57444

CAS No. 668467-91-2

LDN-57444 ( Ubiquitin C-terminal Hydrolase L1 Inhibitor; UCH-L1 Inhibitor )

Catalog No. M15554 CAS No. 668467-91-2

A reversible, competitive, active site-directed Uch-L1 inhibitor with IC50 of 0.88 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 31 In Stock
5MG 46 In Stock
10MG 83 In Stock
25MG 158 In Stock
50MG 282 In Stock
100MG 437 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    LDN-57444
  • Note
    Research use only, not for human use.
  • Brief Description
    A reversible, competitive, active site-directed Uch-L1 inhibitor with IC50 of 0.88 uM.
  • Description
    A reversible, competitive, active site-directed Uch-L1 inhibitor with IC50 of 0.88 uM; shows weak inhibition on Uch-L3 (IC50> 20 uM); causes cell death through the apoptosis pathway by decreasing the activity of ubiquitin proteasome system and increasing the levels of highly ubiquitinated proteins, both of which can activate UPR.
  • Synonyms
    Ubiquitin C-terminal Hydrolase L1 Inhibitor; UCH-L1 Inhibitor
  • Pathway
    Proteasome/Ubiquitin
  • Target
    DUB
  • Recptor
    UCH-L1;UCH-L3
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    668467-91-2
  • Formula Weight
    397.64
  • Molecular Formula
    C17H11Cl3N2O3
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O=C1N(CC2=CC(Cl)=CC=C2Cl)C3=C(C=C(Cl)C=C3)/C1=N/OC(C)=O
  • Chemical Name
    1H-Indole-2,3-dione, 5-chloro-1-[(2,5-dichlorophenyl)methyl]-, 3-(O-acetyloxime)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Gong B, et al. Cell. 2006 Aug 25;126(4):775-88.
2. Xie M, et al. J Alzheimers Dis. 2016;49(2):353-63.
3. Tan YY, et al. Mol Cell Biochem. 2008 Nov;318(1-2):109-15.
molnova catalog
related products
  • IU-1

    IU-1 (USP14 inhibitor IU1) is a specific, small molecule inhibitor of deubiquitinating enzyme USP14 with IC50 of 4-5 uM.

  • PR-619

    PR-619 is a non-selective, reversible inhibitor of the deubiquitinylating enzymes (DUBs) with EC50 of 1-20 μM in a cell-free assay.

  • GNE-6776

    GNE-6776 is a novel potent, specific, non-covalent, orally bioavailable USP7 inhibitor with IC50 of 1.34 uM.