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TargetProstaglandin G/H synthase 2
LigandBDBM50331892
Substrate/Competitorn/a
Meas. Tech.ChEMBL_687200 (CHEMBL1291825)
IC50>50000±n/a nM
Citation Lai, YMa, LHuang, WYu, XZhang, YJi, HTian, J Synthesis and biological evaluation of 3-[4-(amino/methylsulfonyl)phenyl]methylene-indolin-2-one derivatives as novel COX-1/2 and 5-LOX inhibitors. Bioorg Med Chem Lett20:7349-53 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Prostaglandin G/H synthase 2
Name:Prostaglandin G/H synthase 2
Synonyms:COX-2 | COX2 | PGH synthase 2 | PGH2_RABIT | PGHS-2 | PHS II | PTGS2 | Prostaglandin H2 synthase 2 | Prostaglandin-endoperoxide synthase 2
Type:PROTEIN
Mol. Mass.:69015.55
Organism:Oryctolagus cuniculus
Description:ChEMBL_687200
Residue:604
Sequence:
MLARALLLCAAVALSHAANPCCSNPCQNRGVCMTMGFDQYKCDCTRTGFYGENCSTPEFL
TRIKLLLKPTPDTVHYILTHFKGVWNIVNSIPFLRNSIMKYVLTSRSHMIDSPPTYNVHY
NYKSWEAFSNLSYYTRALPPVADDCPTPMGVKGKKELPDSKDVVEKLLLRRKFIPDPQGT
NMMFAFFAQHFTHQFFKTDLKRGPAFTKGLGHGVDLNHIYGETLDRQHKLRLFKDGKMKY
QVIDGEVYPPTVKDTQVEMIYPPHIPAHLQFAVGQEVFGLVPGLMMYATIWLREHNRVCD
VLKQEHPEWDDEQLFQTSRLILIGETIKIVIEDYVQHLSGYHFKLKFDPELLFNQQFQYQ
NRIAAEFNTLYHWHPLLPDTFQIDDQQYNYQQFLYNNSILLEHGLTQFVESFTRQIAGRV
AGGRNVPPAVQKVAKASIDQSRQMKYQSLNEYRKRFLLKPYESFEELTGEKEMAAELEAL
YGDIDAVELYPALLVERPRPDAIFGESMVEMGAPFSLKGLMGNPICSPNYWKPSTFGGEV
GFKIVNTASIQSLICNNVKGCPFTSFNVPDPQLTKTVTINASASHSRLEDINPTVLLKGR
STEL
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  Blast E-value cutoff:
BDBM50331892
n/a
NameBDBM50331892
Synonyms:CHEMBL1290779 | E-5-Methyl-3-[[4-(sulfamoyl)phenyl]methylene]-indolin-2-one
TypeSmall organic molecule
Emp. Form.C16H14N2O3S
Mol. Mass.314.359
SMILESCc1ccc2NC(=O)\C(=C\c3ccc(cc3)S(N)(=O)=O)c2c1
Structure
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