Reaction Details Report a problem with these data
Target
Prostaglandin G/H synthase 2
Ligand
BDBM50182351
Substrate
n/a
Meas. Tech.
ChEMBL_344386 (CHEMBL865438)
IC50
<50±n/a nM
Citation
 Cheng, H; Lundy DeMello, KM; Li, J; Sakya, SM; Ando, K; Kawamura, K; Kato, T; Rafka, RJ; Jaynes, BH; Ziegler, CB; Stevens, R; Lund, LA; Mann, DW; Kilroy, C; Haven, ML; Nimz, EL; Dutra, JK; Li, C; Minich, ML; Kolosko, NL; Petras, C; Silvia, AM; Seibel, SB Synthesis and SAR of heteroaryl-phenyl-substituted pyrazole derivatives as highly selective and potent canine COX-2 inhibitors. Bioorg Med Chem Lett 16:2076-80 (2006) [PubMed]  Article 
Target
Name:
Prostaglandin G/H synthase 2
Synonyms:
Cyclooxygenase-2 | Prostaglandin G/H synthase-2
Type:
PROTEIN
Mol. Mass.:
68982.35
Organism:
Canis familiaris
Description:
ChEMBL_344386
Residue:
604
Sequence:
MLARALVLCAALAVVRAANPCCSHPCQNQGICMSTGFDQYKCDCTRTGFYGENCSTPEFLTRIKLYLKPTPNTVHYILTHFKGVWNIVNNIPFLRNTIMKYVLTSRSHLIESPPTYNVNYGYKSWEAFSNLSYYTRALPPVPDDCPTPMGVKGKKELPDSKEIVEKFLLRRKFIPDPQGTNMMFAFFAQHFTHQFFKTDHKRGPAFTKGLGHGVDLNHVYGETLDRQHKLRLFKDGKMKYQVIDGEVYPPTVKDTQVEMIYPPHVPEHLQFAVGQEVFGLVPGLMMYATIWLREHNRVCDVLKQEHPEWDDERLFQTSRLILIGETIKIVIEDYVQHLSGYHFKLKFDPELLFNQQFQYQNRIAAEFNTLYHWHPLLPDTLQIDDQEYNFQQFIYNNSILLEHGLTQFVESFSRQIAGRVAGGRNVPAAVQQVAKASIDQSRQMKYQSLNEYRKRFRLKPYTSFEELTGEKEMAAGLEALYGDIDAMELYPALLVEKPRPDAIFGETMVEMGAPFSLKGLMGNPICSPDYWKPSTFGGEVGFKIINTASIQSLICNNVKGCPFTAFSVQDGQLTKTVTINASSSHSGLDDINPTVLLKERSTEL
  
Inhibitor
Name:
BDBM50182351
Synonyms:
2-(5-(3-chloro-4-(thiazol-4-yl)phenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)-5-(methylsulfonyl)pyridine | CHEMBL377797
Type:
Small organic molecule
Emp. Form.:
C19H12ClF3N4O2S2
Mol. Mass.:
484.902
SMILES:
CS(=O)(=O)c1ccc(nc1)-n1nc(cc1-c1ccc(-c2cscn2)c(Cl)c1)C(F)(F)F
Structure:
Search PDB for entries with ligand similarity: