| Reaction Details |
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 | Report a problem with these data |
| Target | P2X purinoceptor 5 |
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| Ligand | BDBM50179360 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_2221596 (CHEMBL5134930) |
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| IC50 | 16070±n/a nM |
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| Citation |  Mahmood, A; Ali Shah, SJ; Iqbal, J Design and synthesis of adamantane-1-carbonyl thiourea derivatives as potent and selective inhibitors of h-P2X4 and h-P2X7 receptors: An Emerging therapeutic tool for treatment of inflammation and neurological disorders. Eur J Med Chem231:0 (2022) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| P2X purinoceptor 5 |
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| Name: | P2X purinoceptor 5 |
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| Synonyms: | ATP receptor | P2RX5 | P2RX5_HUMAN | P2X5 | Purinergic receptor |
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| Type: | PROTEIN |
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| Mol. Mass.: | 47208.74 |
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| Organism: | Homo sapiens (Human) |
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| Description: | ChEMBL_612725 |
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| Residue: | 422 |
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| Sequence: | MGQAGCKGLCLSLFDYKTEKYVIAKNKKVGLLYRLLQASILAYLVVWVFLIKKGYQDVDT
SLQSAVITKVKGVAFTNTSDLGQRIWDVADYVIPAQGENVFFVVTNLIVTPNQRQNVCAE
NEGIPDGACSKDSDCHAGEAVTAGNGVKTGRCLRRENLARGTCEIFAWCPLETSSRPEEP
FLKEAEDFTIFIKNHIRFPKFNFSKSNVMDVKDRSFLKSCHFGPKNHYCPIFRLGSVIRW
AGSDFQDIALEGGVIGINIEWNCDLDKAASECHPHYSFSRLDNKLSKSVSSGYNFRFARY
YRDAAGVEFRTLMKAYGIRFDVMVNGKGAFFCDLVLIYLIKKREFYRDKKYEEVRGLEDS
SQEAEDEASGLGLSEQLTSGPGLLGMPEQQELQEPPEAKRGSSSQKGNGSVCPQLLEPHR
ST
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| BDBM50179360 |
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| n/a |
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| Name | BDBM50179360 |
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| Synonyms: | CHEMBL3040216 |
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| Type | Small organic molecule |
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| Emp. Form. | C51H40N6O23S6 |
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| Mol. Mass. | 1297.28 |
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| SMILES | CC1=CCC(=C\C1=N\C(=O)C1=CC=C\C(C1)=N/C(=O)/N=C1/CC(=CC=C1)C(=O)\N=C1\CC(=CC=C1C)C(=O)\N=C1/CC=C(c2cc(cc(c12)S(O)(=O)=O)S(O)(=O)=O)S(O)(=O)=O)C(=O)\N=C1/CC=C(c2cc(cc(c12)S(O)(=O)=O)S(O)(=O)=O)S(O)(=O)=O |c:4,13,24,26,34,36,45,72,t:1,11| |
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| Structure | 
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