Target
Ubiquitin carboxyl-terminal hydrolase isozyme L1
Ligand
BDBM53041
Substrate
n/a
Meas. Tech.
Inhibition Activity Assay
pH
7.6±0
Temperature
298.15±0 K
IC50
1.6e+4±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:
BDBM53041
Synonyms:
MLS001181166 | N''''-[(E)-(3-chloranyl-5-nitro-6-oxidanylidene-cyclohexa-2,4-dien-1-ylidene)methyl]-2-oxidanyl-2,2-diphenyl-ethanehydrazide | N''''-[(E)-(3-chloro-5-nitro-6-oxo-1-cyclohexa-2,4-dienylidene)methyl]-2-hydroxy-2,2-diphenylacetohydrazide | N''''-[(E)-(3-chloro-5-nitro-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]-2-hydroxy-2,2-diphenylacetohydrazide | N''''-[(E)-(3-chloro-6-keto-5-nitro-cyclohexa-2,4-dien-1-ylidene)methyl]-2-hydroxy-2,2-diphenyl-acetohydrazide | N'-[(E)-(3-chloro-6-keto-5-nitro-cyclohexa-2,4-dien-1-ylidene)methyl]-2-hydroxy-2,2-diphenyl-acetohydrazide | O-acyl oxime isatin derivative, 41 | SMR000502198 | cid_5498930
Type:
Small organic molecule
Emp. Form.:
C21H16ClN3O5
Mol. Mass.:
425.822
SMILES:
OC(C(=O)N\[NH+]=C\[c-]1cc(Cl)cc([N+]([O-])=O)c1=O)(c1ccccc1)c1ccccc1
Structure:
Search PDB for entries with ligand similarity: