Reaction Details |
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Target | P2X purinoceptor 1 |
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Ligand | BDBM50540456 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1981892 (CHEMBL4615154) |
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IC50 | 439±n/a nM |
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Citation | Tian, M; Abdelrahman, A; Baqi, Y; Fuentes, E; Azazna, D; Spanier, C; Densborn, S; Hinz, S; Schmid, R; Müller, CE Discovery and Structure Relationships of Salicylanilide Derivatives as Potent, Non-acidic P2X1 Receptor Antagonists. J Med Chem63:6164-6178 (2020) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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P2X purinoceptor 1 |
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Name: | P2X purinoceptor 1 |
Synonyms: | ATP receptor | P2RX1 | P2RX1_HUMAN | P2X1 | Purinergic receptor | Purinergic, P2X |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 44992.65 |
Organism: | Homo sapiens (Human) |
Description: | Purinergic, P2X 0 HUMAN::P51575 |
Residue: | 399 |
Sequence: | MARRFQEELAAFLFEYDTPRMVLVRNKKVGVIFRLIQLVVLVYVIGWVFLYEKGYQTSSG
LISSVSVKLKGLAVTQLPGLGPQVWDVADYVFPAQGDNSFVVMTNFIVTPKQTQGYCAEH
PEGGICKEDSGCTPGKAKRKAQGIRTGKCVAFNDTVKTCEIFGWCPVEVDDDIPRPALLR
EAENFTLFIKNSISFPRFKVNRRNLVEEVNAAHMKTCLFHKTLHPLCPVFQLGYVVQESG
QNFSTLAEKGGVVGITIDWHCDLDWHVRHCRPIYEFHGLYEEKNLSPGFNFRFARHFVEN
GTNYRHLFKVFGIRFDILVDGKAGKFDIIPTMTTIGSGIGIFGVATVLCDLLLLHILPKR
HYYKQKKFKYAEDMGPGAAERDLAATSSTLGLQENMRTS
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BDBM50540456 |
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n/a |
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Name | BDBM50540456 |
Synonyms: | CHEMBL2313133 |
Type | Small organic molecule |
Emp. Form. | C14H8ClF6NO3S |
Mol. Mass. | 419.727 |
SMILES | Oc1ccc(Cl)cc1S(=O)(=O)Nc1cc(cc(c1)C(F)(F)F)C(F)(F)F |
Structure |
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