Target
Ubiquitin carboxyl-terminal hydrolase isozyme L1
Ligand
BDBM53413
Substrate
n/a
Meas. Tech.
Inhibition Activity Assay
pH
7.6±0
Temperature
298.15±0 K
IC50
6e+3± 1e+3 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:
BDBM53413
Synonyms:
(2S)-2-[[[4-[(4-methylanilino)-oxomethyl]-1H-imidazol-5-yl]-oxomethyl]amino]-6-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]hexanoic acid tert-butyl ester | (2S)-6-(tert-butoxycarbonylamino)-2-[[4-(p-tolylcarbamoyl)-1H-imidazole-5-carbonyl]amino]hexanoic acid tert-butyl ester | ILP-IV-50 | Isatin, 1 | MLS000849601 | SMR000465892 | cid_16746604 | tert-butyl (2S)-2-[[4-[(4-methylphenyl)carbamoyl]-1H-imidazol-5-yl]carbonylamino]-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoate | tert-butyl (2S)-2-[[4-[(4-methylphenyl)carbamoyl]-1H-imidazole-5-carbonyl]amino]-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoate
Type:
Small organic molecule
Emp. Form.:
C27H39N5O6
Mol. Mass.:
529.6285
SMILES:
Cc1ccc(NC(=O)c2[nH]cnc2C(=O)N[C@@H](CCCCNC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)cc1
Structure:
Search PDB for entries with ligand similarity: