Reaction Details |
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Target | Prostaglandin G/H synthase 1 |
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Ligand | BDBM50387595 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_830632 (CHEMBL2061525) |
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IC50 | 3600±n/a nM |
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Citation | Hansen, FK; Khankischpur, M; Tolaymat, I; Mesaros, R; Dannhardt, G; Geffken, D Efficient synthesis and 5-LOX/COX-inhibitory activity of some 3-hydroxybenzo[b]thiophene-2-carboxylic acid derivatives. Bioorg Med Chem Lett22:5031-4 (2012) [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 | PGH1_BOVIN | PTGS1 |
Type: | PROTEIN |
Mol. Mass.: | 68814.10 |
Organism: | Bos taurus |
Description: | ChEMBL_547440 |
Residue: | 600 |
Sequence: | MSRQGISLRFPLLLLLLSPSPVLPADPGAPAPVNPCCYYPCQHQGICVRFGLDRYQCDCT
RTGYYGPNCTIPEIWTWLRTTLRPSPSFVHFLLTHGRWLWDFVNATFIRDKLMRLVLTVR
SNLIPSPPTYNVAHDYISWESFSNVSYYTRILPSVPRDCPTPMGTKGKKQLPDAEFLSRR
FLLRRKFIPDPQGTNLMFAFFAQHFTHQFFKTSGKMGPGFTKALGHGVDLGHIYGDNLER
QYQLRLFKDGKLKYQMLNGEVYPPSVEEAPVLMHYPRGIPPQSQMAVGQEVFGLLPGLMV
YATIWLREHNRVCDLLKAEHPTWGDEQLFQTARLILIGETIKIVIEEYVQQLSGYFLQLK
FDPELLFGAQFQYRNRIAMEFNQLYHWHPLMPDSFRVGPQDYSYEQFLFNTSMLVDYGVE
ALVDAFSRQPAGRIGGGRNIDHHILHVAVDVIKESRELRLQPFNEYRKRFGMKPYTSFQE
LTGEKEMAAELEELYGDIDALEFYPGLLLEKCHPNSIFGESMIEMGAPFSLKGLLGNPIC
SPEYWKASTFGGDVGFNLVKTATLKKLVCLNTKTCPYVSFHVPDPHREDRPGVERPPTEL
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BDBM50387595 |
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n/a |
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Name | BDBM50387595 |
Synonyms: | CHEMBL2057739 |
Type | Small organic molecule |
Emp. Form. | C10H8O4S |
Mol. Mass. | 224.233 |
SMILES | COc1cccc2c(O)c(sc12)C(O)=O |
Structure |
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