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Target
Ubiquitin carboxyl-terminal hydrolase isozyme L3
Ligand
BDBM53449
Substrate
n/a
Meas. Tech.
Inhibition Activity Assay
pH
7.6±0
Temperature
298.15±0 K
IC50
3.2e+4±n/a nM
Citation
 Liu, Y; Lashuel, HA; Choi, S; Xing, X; Case, A; Ni, J; Yeh, LA; Cuny, GD; Stein, RL; Lansbury, 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 L3
Synonyms:
UCH-L3 | UCHL3_MOUSE | Ubiquitin carboxyl-terminal hydrolase isozyme L3 (UCH-L3) | Ubiquitin thioesterase L3 | Uchl3
Type:
Protein
Mol. Mass.:
26139.77
Organism:
Mus musculus (Mouse)
Description:
Q9JKB1
Residue:
230
Sequence:
MEGQRWLPLEANPEVTNQFLKQLGLHPNWQFVDVYGMEPELLSMVPRPVCAVLLLFPITEKYEVFRTEEEEKIKSQGQDVTSSVYFMKQTISNACGTIGLIHAIANNKDKMHFESGSTLKKFLEESVSMSPEERAKFLENYDAIRVTHETSAHEGQTEAPSIDEKVDLHFIALVHVDGHLYELDGRKPFPINHGKTSDETLLEDAIEVCKKFMERDPDELRFNAIALSAA
  
Inhibitor
Name:
BDBM53449
Synonyms:
4-(4-bromophenyl)-2-(o-toluoylamino)-3-thenoic acid | 4-(4-bromophenyl)-2-[(2-methylbenzoyl)amino]-3-thiophenecarboxylic acid | 4-(4-bromophenyl)-2-[(2-methylbenzoyl)amino]thiophene-3-carboxylic acid | 4-(4-bromophenyl)-2-[(2-methylphenyl)carbonylamino]thiophene-3-carboxylic acid | 4-(4-bromophenyl)-2-[[(2-methylphenyl)-oxomethyl]amino]-3-thiophenecarboxylic acid | MLS001179267 | O-acyl oxime isatin derivative, 1 | SMR000475976 | cid_1724426
Type:
Small organic molecule
Emp. Form.:
C19H14BrNO3S
Mol. Mass.:
416.288
SMILES:
Cc1ccccc1C(=O)Nc1scc(c1C(O)=O)-c1ccc(Br)cc1
Structure:
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