Reaction Details |
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Target | Platelet-activating factor receptor |
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Ligand | BDBM50286012 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_155162 |
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Ki | 2.3±n/a nM |
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Citation | Davidsen, SK; Summers, JB; Sweeny, DJ; Holms, JH; Albert, DH; Carrera, GM; Tapang, P; Magoc, TJ; Conway, RG; Rhein, DA Synthesis of active metabolites of indole pyrrolothiazole paf antagonists Bioorg Med Chem Lett5:2909-2912 (1995) Article |
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More Info.: | Get all data from this article, Assay Method |
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Platelet-activating factor receptor |
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Name: | Platelet-activating factor receptor |
Synonyms: | PAF Platelet activating factor | PAF-R | PTAFR_RAT | Platelet activating factor receptor | Platelet-activating factor receptor | Ptafr |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 39221.53 |
Organism: | RAT |
Description: | PAF Platelet activating factor PTAFR RAT::P46002 |
Residue: | 341 |
Sequence: | MEQNGSFRVDSEFRYTLFPIVYSVIFVLGVVANGYVLWVFATLYPSKKLNEIKIFMVNLT
VADLLFLMTLPLWIVYYSNEGDWIVHKFLCNLAGCLFFINTYCSVAFLGVITYNRYQAVA
YPIKTAQATTRKRGITLSLVIWISIAATASYFLATDSTNVVPKKDGSGNITRCFEHYEPY
SVPILVVHIFITSCFFLVFFLIFYCNMVIIHTLLTRPVRQQRKPEVKRRALWMVCTVLAV
FVICFVPHHVVQLPWTLAELGYQTNFHQAINDAHQITLCLLSTNCVLDPVIYCFLTKKFR
KHLSEKFYSMRSSRKCSRATSDTCTEVMMPANQTPVLPLKN
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BDBM50286012 |
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n/a |
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Name | BDBM50286012 |
Synonyms: | 3-{(R)-7-[1-Dimethylcarbamoyl-6-(4-fluoro-phenyl)-1H-indole-3-carbonyl]-1H-pyrrolo[1,2-c]thiazol-3-yl}-1-hydroxy-pyridinium | 6-(4-Fluoro-phenyl)-3-[(R)-3-(1-oxy-pyridin-3-yl)-1H-pyrrolo[1,2-c]thiazole-7-carbonyl]-indole-1-carboxylic acid dimethylamide | CHEMBL317745 |
Type | Small organic molecule |
Emp. Form. | C29H23FN4O3S |
Mol. Mass. | 526.581 |
SMILES | CN(C)C(=O)n1cc(C(=O)c2ccn3[C@H](SCc23)c2ccc[n+]([O-])c2)c2ccc(cc12)-c1ccc(F)cc1 |
Structure |
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