Reaction Details |
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Target | Prostaglandin G/H synthase 1 |
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Ligand | BDBM50392664 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_854157 (CHEMBL2154078) |
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IC50 | >10000±n/a nM |
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Citation | Biava, M; Battilocchio, C; Poce, G; Alfonso, S; Consalvi, S; Porretta, GC; Schenone, S; Calderone, V; Martelli, A; Testai, L; Ghelardini, C; Di Cesare Mannelli, L; Sautebin, L; Rossi, A; Giordani, A; Patrignani, P; Anzini, M Improving the solubility of a new class of antiinflammatory pharmacodynamic hybrids, that release nitric oxide and inhibit cycloxygenase-2 isoenzyme. Eur J Med Chem58:287-98 (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-1 | PGH synthase 1 | PGH1_MOUSE | PGHS-1 | PHS 1 | Prostaglandin G/H synthase (cyclooxygenase) | Prostaglandin H2 synthase 1 | Prostaglandin-endoperoxide synthase 1 | Ptgs1 |
Type: | PROTEIN |
Mol. Mass.: | 69044.61 |
Organism: | Mus musculus |
Description: | ChEMBL_10575 |
Residue: | 602 |
Sequence: | MSRRSLSLWFPLLLLLLLPPTPSVLLADPGVPSPVNPCCYYPCQNQGVCVRFGLDNYQCD
CTRTGYSGPNCTIPEIWTWLRNSLRPSPSFTHFLLTHGYWLWEFVNATFIREVLMRLVLT
VRSNLIPSPPTYNSAHDYISWESFSNVSYYTRILPSVPKDCPTPMGTKGKKQLPDVQLLA
QQLLLRREFIPAPQGTNILFAFFAQHFTHQFFKTSGKMGPGFTKALGHGVDLGHIYGDNL
ERQYHLRLFKDGKLKYQVLDGEVYPPSVEQASVLMRYPPGVPPERQMAVGQEVFGLLPGL
MLFSTIWLREHNRVCDLLKEEHPTWDDEQLFQTTRLILIGETIKIVIEEYVQHLSGYFLQ
LKFDPELLFRAQFQYRNRIAMEFNHLYHWHPLMPNSFQVGSQEYSYEQFLFNTSMLVDYG
VEALVDAFSRQRAGRIGGGRNFDYHVLHVAVDVIKESREMRLQPFNEYRKRFGLKPYTSF
QELTGEKEMAAELEELYGDIDALEFYPGLLLEKCQPNSIFGESMIEMGAPFSLKGLLGNP
ICSPEYWKPSTFGGDVGFNLVNTASLKKLVCLNTKTCPYVSFRVPDYPGDDGSVLVRRST
EL
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BDBM50392664 |
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n/a |
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Name | BDBM50392664 |
Synonyms: | CHEMBL2153826 |
Type | Small organic molecule |
Emp. Form. | C23H24FN3O7S |
Mol. Mass. | 505.516 |
SMILES | Cc1c(cc(-c2ccc(cc2)S(C)(=O)=O)n1-c1cccc(F)c1)C(N)C(=O)OCCCO[N+]([O-])=O |
Structure |
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