Reaction Details |
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Target | Prostaglandin G/H synthase 1 |
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Ligand | BDBM50136106 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_158601 (CHEMBL766823) |
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IC50 | 25000±n/a nM |
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Citation | Khanapure, SP; Garvey, DS; Young, DV; Ezawa, M; Earl, RA; Gaston, RD; Fang, X; Murty, M; Martino, A; Shumway, M; Trocha, M; Marek, P; Tam, SW; Janero, DR; Letts, LG Synthesis and structure-activity relationship of novel, highly potent metharyl and methcycloalkyl cyclooxygenase-2 (COX-2) selective inhibitors. J Med Chem46:5484-504 (2003) [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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BDBM50136106 |
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n/a |
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Name | BDBM50136106 |
Synonyms: | 4-(6-Benzyl-benzo[1,3]dioxol-5-yl)-benzenesulfonamide | CHEMBL151042 |
Type | Small organic molecule |
Emp. Form. | C20H17NO4S |
Mol. Mass. | 367.418 |
SMILES | NS(=O)(=O)c1ccc(cc1)-c1cc2OCOc2cc1Cc1ccccc1 |
Structure |
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