Reaction Details |
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Target | Prostaglandin G/H synthase 2 |
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Ligand | BDBM50331892 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_687200 (CHEMBL1291825) |
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IC50 | >50000±n/a nM |
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Citation | Lai, Y; Ma, L; Huang, W; Yu, X; Zhang, Y; Ji, H; Tian, 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 |
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More Info.: | Get all data from this article, Assay Method |
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Prostaglandin G/H synthase 2 |
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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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BDBM50331892 |
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n/a |
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Name | BDBM50331892 |
Synonyms: | CHEMBL1290779 | E-5-Methyl-3-[[4-(sulfamoyl)phenyl]methylene]-indolin-2-one |
Type | Small organic molecule |
Emp. Form. | C16H14N2O3S |
Mol. Mass. | 314.359 |
SMILES | Cc1ccc2NC(=O)\C(=C\c3ccc(cc3)S(N)(=O)=O)c2c1 |
Structure |
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