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TargetUbiquitin carboxyl-terminal hydrolase isozyme L1
LigandBDBM53463
Substrate/Competitorn/a
Meas. Tech.Inhibition Activity Assay
pH7.6±0
Temperature298.15±0 K
IC50 5.2e+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 Biol10:837-46 (2003) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Ubiquitin carboxyl-terminal hydrolase isozyme L1
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:
MQLKPMEINPEMLNKVLAKLGVAGQWRFADVLGLEEETLGSVPSPACALLLLFPLTAQHE
NFRKKQIEELKGQEVSPKVYFMKQTIGNSCGTIGLIHAVANNQDKLEFEDGSVLKQFLSE
TEKLSPEDRAKCFEKNEAIQAAHDSVAQEGQCRVDDKVNFHFILFNNVDGHLYELDGRMP
FPVNHGASSEDSLLQDAAKVCREFTEREQGEVRFSAVALCKAA
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BDBM53463
n/a
NameBDBM53463
Synonyms:1-[[4-(1-adamantyl)phenyl]methylideneamino]thiourea | 4-(1-adamantyl)benzaldehyde thiosemicarbazone | MLS001000567 | O-acyl oxime isatin derivative, 45 | SMR000496110 | [[4-(1-adamantyl)benzylidene]amino]thiourea | [[4-(1-adamantyl)phenyl]methylideneamino]thiourea | cid_2839927
TypeSmall organic molecule
Emp. Form.C18H23N3S
Mol. Mass.313.46
SMILES[H]C12CC3([H])CC([H])(C1)CC(C2)(C3)c1ccc(C=NNC(N)=S)cc1 |w:18.21,TLB:8:1:12:6.9.5,8:6:12:1.11.2,THB:5:6:11:3.12.2|
Structure
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