Reaction Details |
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Target | Prostaglandin G/H synthase 1 |
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Ligand | BDBM50330853 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_762068 (CHEMBL1816060) |
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IC50 | 24000±n/a nM |
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Citation | Yamakawa, N; Suemasu, S; Matoyama, M; Tanaka, K; Katsu, T; Miyata, K; Okamoto, Y; Otsuka, M; Mizushima, T Synthesis and biological evaluation of loxoprofen derivatives. Bioorg Med Chem19:3299-311 (2011) [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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BDBM50330853 |
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n/a |
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Name | BDBM50330853 |
Synonyms: | CHEMBL66552 | Sodium; 2-[4-(2-oxo-cyclopentylmethyl)-phenyl]-propionate; hydrate | loxoprofen sodium |
Type | Small organic molecule |
Emp. Form. | C15H17O3 |
Mol. Mass. | 245.2942 |
SMILES | CC(C([O-])=O)c1ccc(CC2CCCC2=O)cc1 |
Structure |
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