Reaction Details |
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Target | Prostaglandin G/H synthase 1 |
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Ligand | BDBM50330852 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_685631 (CHEMBL1285409) |
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IC50 | 7200±n/a nM |
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Citation | Yamakawa, N; Suemasu, S; Matoyama, M; Kimoto, A; Takeda, M; Tanaka, K; Ishihara, T; Katsu, T; Okamoto, Y; Otsuka, M; Mizushima, T Properties and synthesis of 2-{2-fluoro (or bromo)-4-[(2-oxocyclopentyl)methyl]phenyl}propanoic acid: nonsteroidal anti-inflammatory drugs with low membrane permeabilizing and gastric lesion-producing activities. J Med Chem53:7879-82 (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 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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BDBM50330852 |
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n/a |
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Name | BDBM50330852 |
Synonyms: | 2-(2-bromo-4-(((1,2-cis)-2-hydroxycyclopentyl)methyl)phenyl)propanoic acid | CHEMBL1275971 |
Type | Small organic molecule |
Emp. Form. | C15H19BrO3 |
Mol. Mass. | 327.214 |
SMILES | CC(C(O)=O)c1ccc(C[C@@H]2CCC[C@@H]2O)cc1Br |r| |
Structure |
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