Target
Zinc finger and BTB domain-containing protein 16
Ligand
BDBM50239362
Substrate
n/a
Meas. Tech.
ChEMBL_1665992 (CHEMBL4015788)
IC50
>30000±n/a nM
Citation
 McCoull, WAbrams, RDAnderson, EBlades, KBarton, PBox, MBurgess, JByth, KCao, QChuaqui, CCarbajo, RJCheung, TCode, EFerguson, ADFillery, SFuller, NOGangl, EGao, NGrist, MHargreaves, DHoward, MRHu, JKemmitt, PDNelson, JEO'Connell, NPrince, DBRaubo, PRawlins, PBRobb, GRShi, JWaring, MJWhittaker, DWylot, MZhu, X Discovery of Pyrazolo[1,5-a]pyrimidine B-Cell Lymphoma 6 (BCL6) Binders and Optimization to High Affinity Macrocyclic Inhibitors. J Med Chem 60:4386-4402 (2017) [PubMed]  Article 
Target
Name:
Zinc finger and BTB domain-containing protein 16
Synonyms:
PLZF | Promyelocytic leukemia zinc finger protein | ZBT16_HUMAN | ZBTB16 | ZNF145 | Zinc finger and BTB domain-containing protein 16 | Zinc finger protein 145 | Zinc finger protein PLZF
Type:
PROTEIN
Mol. Mass.:
74272.31
Organism:
Homo sapiens
Description:
ChEMBL_117331
Residue:
673
Sequence:
MDLTKMGMIQLQNPSHPTGLLCKANQMRLAGTLCDVVIMVDSQEFHAHRTVLACTSKMFEILFHRNSQHYTLDFLSPKTFQQILEYAYTATLQAKAEDLDDLLYAAEILEIEYLEEQCLKMLETIQASDDNDTEATMADGGAEEEEDRKARYLKNIFISKHSSEESGYASVAGQSLPGPMVDQSPSVSTSFGLSAMSPTKAAVDSLMTIGQSLLQGTLQPPAGPEEPTLAGGGRHPGVAEVKTEMMQVDEVPSQDSPGAAESSISGGMGDKVEERGKEGPGTPTRSSVITSARELHYGREESAEQVPPPAEAGQAPTGRPEHPAPPPEKHLGIYSVLPNHKADAVLSMPSSVTSGLHVQPALAVSMDFSTYGGLLPQGFIQRELFSKLGELAVGMKSESRTIGEQCSVCGVELPDNEAVEQHRKLHSGMKTYGCELCGKRFLDSLRLRMHLLAHSAGAKAFVCDQCGAQFSKEDALETHRQTHTGTDMAVFCLLCGKRFQAQSALQQHMEVHAGVRSYICSECNRTFPSHTALKRHLRSHTGDHPYECEFCGSCFRDESTLKSHKRIHTGEKPYECNGCGKKFSLKHQLETHYRVHTGEKPFECKLCHQRSRDYSAMIKHLRTHNGASPYQCTICTEYCPSLSSMQKHMKGHKPEEIPPDWRIEKTYLYLCYV
  
Inhibitor
Name:
BDBM50239362
Synonyms:
CHEMBL4064865
Type:
Small organic molecule
Emp. Form.:
C31H31ClN6O4
Mol. Mass.:
587.069
SMILES:
[H][C@]12C[C@@H](CO)N(C1)c1cc(Nc3cc4CCC(=O)N(Cc5ccccc5)c4c(OC\C=C\CO2)c3)n2ncc(Cl)c2n1 |r,t:34|
Structure:
Search PDB for entries with ligand similarity: