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TargetUbiquitin carboxyl-terminal hydrolase isozyme L1
LigandBDBM445091
Substrate/Competitorn/a
Meas. Tech.USP30 Biochemical IC50 Assay
IC50 550±n/a nM
Citation Kemp, MStockley, MJones, A Cyanopyrrolidines as dub inhibitors for the treatment of cancer US Patent US11319287 Publication Date 5/3/2022
More Info.:Get all data from this article,  Assay Method
 
Ubiquitin carboxyl-terminal hydrolase isozyme L1
Name:Ubiquitin carboxyl-terminal hydrolase isozyme L1
Synonyms:Neuron cytoplasmic protein 9.5 | PGP 9.5 | PGP9.5 | UCH-L1 | UCHL1 | UCHL1_HUMAN | Ubiquitin thioesterase L1
Type:PROTEIN
Mol. Mass.:24819.03
Organism:Homo sapiens (Human)
Description:ChEMBL_974327
Residue:223
Sequence:
MQLKPMEINPEMLNKVLSRLGVAGQWRFVDVLGLEEESLGSVPAPACALLLLFPLTAQHE
NFRKKQIEELKGQEVSPKVYFMKQTIGNSCGTIGLIHAVANNQDKLGFEDGSVLKQFLSE
TEKMSPEDRAKCFEKNEAIQAAHDAVAQEGQCRVDDKVNFHFILFNNVDGHLYELDGRMP
FPVNHGASSEDTLLKDAAKVCREFTEREQGEVRFSAVALCKAA
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  Blast E-value cutoff:
BDBM445091
n/a
NameBDBM445091
Synonyms:(S)-4,4-difluoro-2-(4-(5-methyl-1H-pyrazol-4-yl)indoline-1-carbonyl)pyrrolidine-1-carbonitrile | US10669234, Example 30 | US11319287, Example 30
TypeSmall organic molecule
Emp. Form.C18H17F2N5O
Mol. Mass.357.3573
SMILESCc1[nH]ncc1-c1cccc2N(CCc12)C(=O)[C@@H]1CC(F)(F)CN1C#N
Structure
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