Target
Ubiquitin carboxyl-terminal hydrolase isozyme L1
Ligand
BDBM53474
Substrate
n/a
Meas. Tech.
Inhibition Activity Assay
pH
7.6±0
Temperature
298.15±0 K
IC50
6.1e+3±n/a nM
Citation
 Liu, YLashuel, HAChoi, SXing, XCase, ANi, JYeh, LACuny, GDStein, RLLansbury, PT Discovery of inhibitors that elucidate the role of UCH-L1 activity in the H1299 lung cancer cell line. Chem Biol 10:837-46 (2003) [PubMed]  Article 
Target
Name:
Ubiquitin carboxyl-terminal hydrolase isozyme L1
Synonyms:
UCH-L1 | UCHL1_MOUSE | Ubiquitin carboxyl-terminal hydrolase isozyme L1 (UCH-L1) | Ubiquitin thioesterase L1 | Uchl1
Type:
Protein
Mol. Mass.:
24830.93
Organism:
Mus musculus (Mouse)
Description:
Q9R0P9
Residue:
223
Sequence:
MQLKPMEINPEMLNKVLAKLGVAGQWRFADVLGLEEETLGSVPSPACALLLLFPLTAQHENFRKKQIEELKGQEVSPKVYFMKQTIGNSCGTIGLIHAVANNQDKLEFEDGSVLKQFLSETEKLSPEDRAKCFEKNEAIQAAHDSVAQEGQCRVDDKVNFHFILFNNVDGHLYELDGRMPFPVNHGASSEDSLLQDAAKVCREFTEREQGEVRFSAVALCKAA
  
Inhibitor
Name:
BDBM53474
Synonyms:
1-butyl-2-hydroxy-4-oxo-N-(phenylmethyl)-3-quinolinecarboxamide | 1-butyl-2-oxidanyl-4-oxidanylidene-N-(phenylmethyl)quinoline-3-carboxamide | BRD-K11460778-001-04-0 | N-benzyl-1-butyl-2-hydroxy-4-keto-quinoline-3-carboxamide | N-benzyl-1-butyl-2-hydroxy-4-oxoquinoline-3-carboxamide | O-acyl oxime isatin derivative, 16 | cid_1897110
Type:
Small organic molecule
Emp. Form.:
C21H22N2O3
Mol. Mass.:
350.411
SMILES:
CCCCn1c2ccccc2c(O)c(C(=O)NCc2ccccc2)c1=O
Structure:
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