Reaction Details Report a problem with these data
Target
4-hydroxyphenylpyruvate dioxygenase
Ligand
BDBM50024731
Substrate
n/a
Meas. Tech.
ChEMBL_1438115 (CHEMBL3388490)
Ki
87±n/a nM
Citation
 Xu, YL; Lin, HY; Cao, RJ; Ming, ZZ; Yang, WC; Yang, GF Pyrazolone-quinazolone hybrids: a novel class of human 4-hydroxyphenylpyruvate dioxygenase inhibitors. Bioorg Med Chem 22:5194-211 (2014) [PubMed]  Article 
Target
Name:
4-hydroxyphenylpyruvate dioxygenase
Synonyms:
4-hydroxyphenylpyruvate dioxygenase | 4-hydroxyphenylpyruvic acid oxidase | 4HPPD | HPD | HPPD_HUMAN | PPD
Type:
PROTEIN
Mol. Mass.:
44937.33
Organism:
Homo sapiens (Human)
Description:
ChEMBL_123
Residue:
393
Sequence:
MTTYSDKGAKPERGRFLHFHSVTFWVGNAKQAASFYCSKMGFEPLAYRGLETGSREVVSHVIKQGKIVFVLSSALNPWNKEMGDHLVKHGDGVKDIAFEVEDCDYIVQKARERGAKIMREPWVEQDKFGKVKFAVLQTYGDTTHTLVEKMNYIGQFLPGYEAPAFMDPLLPKLPKCSLEMIDHIVGNQPDQEMVSASEWYLKNLQFHRFWSVDDTQVHTEYSSLRSIVVANYEESIKMPINEPAPGKKKSQIQEYVDYNGGAGVQHIALKTEDIITAIRHLRERGLEFLSVPSTYYKQLREKLKTAKIKVKENIDALEELKILVDYDEKGYLLQIFTKPVQDRPTLFLEVIQRHNHQGFGAGNFNSLFKAFEEEQNLRGNLTNMETNGVVPGM
  
Inhibitor
Name:
BDBM50024731
Synonyms:
CHEMBL3342428
Type:
Small organic molecule
Emp. Form.:
C22H19BrN4O3
Mol. Mass.:
467.315
SMILES:
Cc1nn(C)c(O)c1C(=O)c1ccc2nc(C)n(-c3ccc(C)cc3Br)c(=O)c2c1 |(19.9,-51.81,;18.73,-50.81,;17.23,-51.16,;16.44,-49.84,;14.91,-49.72,;17.44,-48.67,;17.09,-47.18,;18.86,-49.27,;20.18,-48.48,;20.15,-46.94,;21.53,-49.22,;21.56,-50.76,;22.91,-51.51,;24.22,-50.71,;25.58,-51.46,;26.91,-50.65,;28.26,-51.39,;26.87,-49.1,;28.19,-48.3,;29.53,-49.04,;30.85,-48.25,;30.81,-46.71,;32.13,-45.91,;29.45,-45.97,;28.14,-46.77,;26.79,-46.03,;25.51,-48.35,;25.47,-46.81,;24.19,-49.16,;22.84,-48.43,)|
Structure:
Search PDB for entries with ligand similarity: