Reaction Details |
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Target | Prostaglandin G/H synthase 1 |
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Ligand | BDBM50177395 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_334864 (CHEMBL871167) |
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IC50 | 221300±n/a nM |
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Citation | Crespo, A; Meyers, C; Coelho, A; Yáñez, M; Fraiz, N; Sotelo, E; Maes, BU; Laguna, R; Cano, E; Lemière, GL; Raviña, E Pyridazines part 41: synthesis, antiplatelet activity and SAR of 2,4,6-substituted 5-(3-oxo-3-phenylprop-1-en-1-yl)- or 5-(3-phenylprop-2-enoyl)pyridazin-3(2H)-ones. Bioorg Med Chem Lett16:1080-3 (2006) [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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BDBM50177395 |
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n/a |
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Name | BDBM50177395 |
Synonyms: | 4-(dimethylamino)-2-methyl-5-(3-oxo-3-phenylprop-1-enyl)pyridazin-3(2H)-one | CHEMBL202451 |
Type | Small organic molecule |
Emp. Form. | C16H17N3O2 |
Mol. Mass. | 283.3251 |
SMILES | CN(C)c1c(\C=C\C(=O)c2ccccc2)cnn(C)c1=O |
Structure |
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