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TargetProstaglandin G/H synthase 2
LigandBDBM50097346
Substrate/Competitorn/a
Meas. Tech.ChEMBL_862249 (CHEMBL2172930)
IC50 3900±n/a nM
Citation Favia, ADHabrant, DScarpelli, RMigliore, MAlbani, CBertozzi, SMDionisi, MTarozzo, GPiomelli, DCavalli, ADe Vivo, M Identification and characterization of carprofen as a multitarget fatty acid amide hydrolase/cyclooxygenase inhibitor. J Med Chem55:8807-26 (2012) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Prostaglandin G/H synthase 2
Name:Prostaglandin G/H synthase 2
Synonyms:COX2 | Cyclooxygenase | Cyclooxygenase 2 (COX-2) | Cyclooxygenase-2 | Cyclooxygenase-2 (COX-2 AA) | Cyclooxygenase-2 (COX-2 AEA) | Cyclooxygenase-2 (COX-2) | PGH synthase 2 | PGH2_HUMAN | PGHS-2 | PHS II | PTGS2 | Prostaglandin E synthase/G/H synthase 2 | Prostaglandin H2 synthase 2 | Prostaglandin-endoperoxide synthase 2
Type:Enzyme
Mol. Mass.:69003.89
Organism:Homo sapiens (Human)
Description:Recombinant Cox-2 provided by Cayman (Cayman Chemical Co.,Ann Arbor, MI).
Residue:604
Sequence:
MLARALLLCAVLALSHTANPCCSHPCQNRGVCMSVGFDQYKCDCTRTGFYGENCSTPEFL
TRIKLFLKPTPNTVHYILTHFKGFWNVVNNIPFLRNAIMSYVLTSRSHLIDSPPTYNADY
GYKSWEAFSNLSYYTRALPPVPDDCPTPLGVKGKKQLPDSNEIVEKLLLRRKFIPDPQGS
NMMFAFFAQHFTHQFFKTDHKRGPAFTNGLGHGVDLNHIYGETLARQRKLRLFKDGKMKY
QIIDGEMYPPTVKDTQAEMIYPPQVPEHLRFAVGQEVFGLVPGLMMYATIWLREHNRVCD
VLKQEHPEWGDEQLFQTSRLILIGETIKIVIEDYVQHLSGYHFKLKFDPELLFNKQFQYQ
NRIAAEFNTLYHWHPLLPDTFQIHDQKYNYQQFIYNNSILLEHGITQFVESFTRQIAGRV
AGGRNVPPAVQKVSQASIDQSRQMKYQSFNEYRKRFMLKPYESFEELTGEKEMSAELEAL
YGDIDAVELYPALLVEKPRPDAIFGETMVEVGAPFSLKGLMGNVICSPAYWKPSTFGGEV
GFQIINTASIQSLICNNVKGCPFTSFSVPDPELIKTVTINASSSRSGLDDINPTVLLKER
STEL
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  Blast E-value cutoff:
BDBM50097346
n/a
NameBDBM50097346
Synonyms:(+/-)-2-(3-chloro-9H-carbazol-7-yl)propanoic acid | 2-(6-Chloro-9H-carbazol-2-yl)-propionic acid | 2-(6-Chloro-9H-carbazol-2-yl)-propionic acid(carprofen) | 2-(6-chloro-9H-carbazol-2-yl)propanoic acid | CARPROFEN | CHEMBL1316 | Rimadyl | Ro-20-5720/000
TypeSmall organic molecule
Emp. Form.C15H12ClNO2
Mol. Mass.273.714
SMILESCC(C(O)=O)c1ccc2c(c1)[nH]c1ccc(Cl)cc21
Structure
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