Reaction Details Report a problem with these data
Target
4-hydroxyphenylpyruvate dioxygenase
Ligand
BDBM50024723
Substrate
n/a
Meas. Tech.
ChEMBL_1438115 (CHEMBL3388490)
Ki
38±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:
BDBM50024723
Synonyms:
CHEMBL3342601
Type:
Small organic molecule
Emp. Form.:
C21H18N4O4
Mol. Mass.:
390.392
SMILES:
COc1ccccc1-n1c(C)nc2ccc(cc2c1=O)C(=O)c1cnn(C)c1O |(24.63,-14.14,;23.28,-13.4,;23.25,-11.86,;24.57,-11.06,;24.54,-9.52,;23.18,-8.78,;21.87,-9.58,;21.91,-11.12,;20.59,-11.92,;20.63,-13.47,;21.98,-14.21,;19.3,-14.27,;17.95,-13.53,;16.63,-14.32,;15.28,-13.58,;15.25,-12.03,;16.56,-11.24,;17.91,-11.98,;19.23,-11.17,;19.19,-9.63,;13.91,-11.29,;13.87,-9.75,;12.59,-12.09,;12.46,-13.62,;10.96,-13.97,;10.16,-12.66,;8.63,-12.53,;11.16,-11.49,;10.81,-9.99,)|
Structure:
Search PDB for entries with ligand similarity: