Reaction Details |
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Target | Prostaglandin G/H synthase 1 |
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Ligand | BDBM50002861 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1912679 (CHEMBL4415262) |
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IC50 | 740±n/a nM |
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Citation | Kramer, JS; Woltersdorf, S; Duflot, T; Hiesinger, K; Lillich, FF; Knöll, F; Wittmann, SK; Klingler, FM; Brunst, S; Chaikuad, A; Morisseau, C; Hammock, BD; Buccellati, C; Sala, A; Rovati, GE; Leuillier, M; Fraineau, S; Rondeaux, J; Hernandez-Olmos, V; Heering, J; Merk, D; Pogoryelov, D; Steinhilber, D; Knapp, S; Bellien, J; Proschak, E Discovery of the First in Vivo Active Inhibitors of the Soluble Epoxide Hydrolase Phosphatase Domain. J Med Chem62:8443-8460 (2019) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Prostaglandin G/H synthase 1 |
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Name: | Prostaglandin G/H synthase 1 |
Synonyms: | COX-1 | COX1 | Cyclooxygenase | Cyclooxygenase-1 | Cyclooxygenase-1 (COX-1) | PGH1_HUMAN | PTGS1 | Prostaglandin G/H synthase (cyclooxygenase) |
Type: | Enzyme |
Mol. Mass.: | 68692.62 |
Organism: | Homo sapiens (Human) |
Description: | P23219 |
Residue: | 599 |
Sequence: | MSRSLLLWFLLFLLLLPPLPVLLADPGAPTPVNPCCYYPCQHQGICVRFGLDRYQCDCTR
TGYSGPNCTIPGLWTWLRNSLRPSPSFTHFLLTHGRWFWEFVNATFIREMLMRLVLTVRS
NLIPSPPTYNSAHDYISWESFSNVSYYTRILPSVPKDCPTPMGTKGKKQLPDAQLLARRF
LLRRKFIPDPQGTNLMFAFFAQHFTHQFFKTSGKMGPGFTKALGHGVDLGHIYGDNLERQ
YQLRLFKDGKLKYQVLDGEMYPPSVEEAPVLMHYPRGIPPQSQMAVGQEVFGLLPGLMLY
ATLWLREHNRVCDLLKAEHPTWGDEQLFQTTRLILIGETIKIVIEEYVQQLSGYFLQLKF
DPELLFGVQFQYRNRIAMEFNHLYHWHPLMPDSFKVGSQEYSYEQFLFNTSMLVDYGVEA
LVDAFSRQIAGRIGGGRNMDHHILHVAVDVIRESREMRLQPFNEYRKRFGMKPYTSFQEL
VGEKEMAAELEELYGDIDALEFYPGLLLEKCHPNSIFGESMIEIGAPFSLKGLLGNPICS
PEYWKPSTFGGEVGFNIVKTATLKKLVCLNTKTCPYVSFRVPDASQDDGPAVERPSTEL
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BDBM50002861 |
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n/a |
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Name | BDBM50002861 |
Synonyms: | 3-(4,5-Diphenyl-oxazol-2-yl)-propionic acid | CHEMBL1071 | Daypro | OXAPROZIN | WY-21743 | oxaprosin |
Type | Small organic molecule |
Emp. Form. | C18H15NO3 |
Mol. Mass. | 293.3166 |
SMILES | OC(=O)CCc1nc(c(o1)-c1ccccc1)-c1ccccc1 |
Structure |
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