Reaction Details |
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Target | Prostaglandin G/H synthase 1 |
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Ligand | BDBM50053410 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_158005 (CHEMBL768431) |
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IC50 | >100000±n/a nM |
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Citation | Boehm, JC; Smietana, JM; Sorenson, ME; Garigipati, RS; Gallagher, TF; Sheldrake, PL; Bradbeer, J; Badger, AM; Laydon, JT; Lee, JC; Hillegass, LM; Griswold, DE; Breton, JJ; Chabot-Fletcher, MC; Adams, JL 1-substituted 4-aryl-5-pyridinylimidazoles: a new class of cytokine suppressive drugs with low 5-lipoxygenase and cyclooxygenase inhibitory potency. J Med Chem39:3929-37 (1996) [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: | COX1 | Cyclooxygenase-1 | Cyclooxygenase-1 (COX-1) | PGH1_SHEEP | PTGS1 | Prostaglandin G/H synthase (cyclooxygenase) |
Type: | Protein |
Mol. Mass.: | 68868.60 |
Organism: | Ovis aries (Sheep) |
Description: | n/a |
Residue: | 600 |
Sequence: | MSRQSISLRFPLLLLLLSPSPVFSADPGAPAPVNPCCYYPCQHQGICVRFGLDRYQCDCT
RTGYSGPNCTIPEIWTWLRTTLRPSPSFIHFLLTHGRWLWDFVNATFIRDTLMRLVLTVR
SNLIPSPPTYNIAHDYISWESFSNVSYYTRILPSVPRDCPTPMDTKGKKQLPDAEFLSRR
FLLRRKFIPDPQSTNLMFAFFAQHFTHQFFKTSGKMGPGFTKALGHGVDLGHIYGDNLER
QYQLRLFKDGKLKYQMLNGEVYPPSVEEAPVLMHYPRGIPPQSQMAVGQEVFGLLPGLML
YATIWLREHNRVCDLLKAEHPTWGDEQLFQTARLILIGETIKIVIEEYVQQLSGYFLQLK
FDPELLFGAQFQYRNRIAMEFNQLYHWHPLMPDSFRVGPQDYSYEQFLFNTSMLVDYGVE
ALVDAFSRQPAGRIGGGRNIDHHILHVAVDVIKESRVLRLQPFNEYRKRFGMKPYTSFQE
LTGEKEMAAELEELYGDIDALEFYPGLLLEKCHPNSIFGESMIEMGAPFSLKGLLGNPIC
SPEYWKASTFGGEVGFNLVKTATLKKLVCLNTKTCPYVSFHVPDPRQEDRPGVERPPTEL
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BDBM50053410 |
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n/a |
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Name | BDBM50053410 |
Synonyms: | 4-(4-Fluorophenyl)-5-(pyridin-4-yl)-1H-imidazole | 4-[5-(4-Fluoro-phenyl)-3H-imidazol-4-yl]-pyridine | CHEMBL63135 |
Type | Small organic molecule |
Emp. Form. | C14H10FN3 |
Mol. Mass. | 239.2477 |
SMILES | Fc1ccc(cc1)-c1[nH]cnc1-c1ccncc1 |
Structure |
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