Target
Ubiquitin carboxyl-terminal hydrolase 21
Ligand
BDBM50612973
Substrate
n/a
Meas. Tech.
ChEMBL_2290626
IC50
>25000±n/a nM
Citation
 Göricke, FVu, VSmith, LScheib, UBöhm, RAkkilic, NWohlfahrt, GWeiske, JBömer, UBrzezinka, KLindner, NLienau, PGradl, SBeck, HBrown, PJSanthakumar, VVedadi, MBarsyte-Lovejoy, DArrowsmith, CHSchmees, NPetersen, K Discovery and Characterization of BAY-805, a Potent and Selective Inhibitor of Ubiquitin-Specific Protease USP21. J Med Chem 66:3431-3447 (2023) [PubMed]
Target
Name:
Ubiquitin carboxyl-terminal hydrolase 21
Synonyms:
Deubiquitinating enzyme 21 | UBP21_HUMAN | USP21 | USP23 | Ubiquitin thioesterase 21 | Ubiquitin-specific-processing protease 21
Type:
PROTEIN
Mol. Mass.:
62692.84
Organism:
Homo sapiens (Human)
Description:
ChEMBL_105198
Residue:
565
Sequence:
MPQASEHRLGRTREPPVNIQPRVGSKLPFAPRARSKERRNPASGPNPMLRPLPPRPGLPDERLKKLELGRGRTSGPRPRGPLRADHGVPLPGSPPPTVALPLPSRTNLARSKSVSSGDLRPMGIALGGHRGTGELGAALSRLALRPEPPTLRRSTSLRRLGGFPGPPTLFSIRTEPPASHGSFHMISARSSEPFYSDDKMAHHTLLLGSGHVGLRNLGNTCFLNAVLQCLSSTRPLRDFCLRRDFRQEVPGGGRAQELTEAFADVIGALWHPDSCEAVNPTRFRAVFQKYVPSFSGYSQQDAQEFLKLLMERLHLEINRRGRRAPPILANGPVPSPPRRGGALLEEPELSDDDRANLMWKRYLEREDSKIVDLFVGQLKSCLKCQACGYRSTTFEVFCDLSLPIPKKGFAGGKVSLRDCFNLFTKEEELESENAPVCDRCRQKTRSTKKLTVQRFPRILVLHLNRFSASRGSIKKSSVGVDFPLQRLSLGDFASDKAGSPVYQLYALCNHSGSVHYGHYTALCRCQTGWHVYNDSRVSPVSENQVASSEGYVLFYQLMQEPPRCL
  
Inhibitor
Name:
BDBM50612973
Synonyms:
CHEMBL5266408
Type:
Small organic molecule
Emp. Form.:
C20H25N5O4S
Mol. Mass.:
431.509
SMILES:
CC(C)C(NC(=O)C1CCCC1)C(=O)Nc1nnc(Cc2ccc(cc2)[N+]([O-])=O)s1
Structure:
Search PDB for entries with ligand similarity: