Reaction Details |
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Target | Prostaglandin G/H synthase 2 |
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Ligand | BDBM113767 |
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Substrate/Competitor | n/a |
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Meas. Tech. | COX-2 Activity Assay |
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pH | 8±n/a |
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Temperature | 298.15±n/a K |
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IC50 | 2.2e+3± 1.2e+3 nM |
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Comments | extracted |
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Citation | Chicca, A; Caprioglio, D; Minassi, A; Petrucci, V; Appendino, G; Taglialatela-Scafati, O; Gertsch, J Functionalization of ß-Caryophyllene Generates Novel Polypharmacology in the Endocannabinoid System. ACS Chem Biol9:1499-507 (2014) [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: | 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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BDBM113767 |
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n/a |
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Name | BDBM113767 |
Synonyms: | (E)-6-((1R,2R)-3,3-Dimethyl-2-(3-methylbut-3-enyl)cyclobutyl)-N-(4-hydroxy-3-methoxybenzyl)hepta-2,6-dienamide (11e) |
Type | Small organic molecule |
Emp. Form. | C26H37NO3 |
Mol. Mass. | 411.5769 |
SMILES | COc1cc(CNC(=O)\C=C\CCC(=C)[C@@H]2CC(C)(C)[C@@H]2CCC(C)=C)ccc1O |
Structure |
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