Reaction Details |
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Target | Prostaglandin G/H synthase 2 [E165G] |
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Ligand | BDBM175281 |
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Substrate/Competitor | n/a |
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Meas. Tech. | In vitro Cyclooxygenase Inhibition Assay |
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IC50 | 6.1e+3±n/a nM |
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Citation | Abdellatif, KR; Abdelgawad, MA; Elshemy, HA; Alsayed, SS Design, synthesis and biological screening of new 4-thiazolidinone derivatives with promising COX-2 selectivity, anti-inflammatory activity and gastric safety profile. Bioorg Chem64:1-12 (2016) [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 [E165G] |
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Name: | Prostaglandin G/H synthase 2 [E165G] |
Synonyms: | COX2 | Cyclooxygenase-2 (COX-2) | PGH2_HUMAN | PTGS2 |
Type: | Protein |
Mol. Mass.: | 68932.84 |
Organism: | Homo sapiens (Human) |
Description: | P35354[E165G] |
Residue: | 604 |
Sequence: | MLARALLLCAVLALSHTANPCCSHPCQNRGVCMSVGFDQYKCDCTRTGFYGENCSTPEFL
TRIKLFLKPTPNTVHYILTHFKGFWNVVNNIPFLRNAIMSYVLTSRSHLIDSPPTYNADY
GYKSWEAFSNLSYYTRALPPVPDDCPTPLGVKGKKQLPDSNEIVGKLLLRRKFIPDPQGS
NMMFAFFAQHFTHQFFKTDHKRGPAFTNGLGHGVDLNHIYGETLARQRKLRLFKDGKMKY
QIIDGEMYPPTVKDTQAEMIYPPQVPEHLRFAVGQEVFGLVPGLMMYATIWLREHNRVCD
VLKQEHPEWGDEQLFQTSRLILIGETIKIVIEDYVQHLSGYHFKLKFDPELLFNKQFQYQ
NRIAAEFNTLYHWHPLLPDTFQIHDQKYNYQQFIYNNSILLEHGITQFVESFTRQIAGRV
AGGRNVPPAVQKVSQASIDQSRQMKYQSFNEYRKRFMLKPYESFEELTGEKEMSAELEAL
YGDIDAVELYPALLVEKPRPDAIFGETMVEVGAPFSLKGLMGNVICSPAYWKPSTFGGEV
GFQIINTASIQSLICNNVKGCPFTSFSVPDPELIKTVTINASSSRSGLDDINPTVLLKER
STEL
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BDBM175281 |
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n/a |
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Name | BDBM175281 |
Synonyms: | 2-(4-(4-Isobutylphenyl)thiazol-2-ylimino)thiazolidin-4-one (4b) |
Type | Small organic molecule |
Emp. Form. | C16H17N3OS2 |
Mol. Mass. | 331.456 |
SMILES | CC(C)Cc1ccc(cc1)-c1csc(N=C2NC(=O)CS2)n1 |w:14.14| |
Structure |
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