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TargetP2X purinoceptor 5
LigandBDBM50596630
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2221596 (CHEMBL5134930)
IC50 9037±n/a nM
Citation Mahmood, AAli Shah, SJIqbal, 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
More Info.:Get all data from this article,  Assay Method
 
P2X purinoceptor 5
Name:P2X purinoceptor 5
Synonyms:ATP receptor | P2RX5 | P2RX5_HUMAN | P2X5 | Purinergic receptor
Type:PROTEIN
Mol. Mass.:47208.74
Organism:Homo sapiens (Human)
Description:ChEMBL_612725
Residue:422
Sequence:
MGQAGCKGLCLSLFDYKTEKYVIAKNKKVGLLYRLLQASILAYLVVWVFLIKKGYQDVDT
SLQSAVITKVKGVAFTNTSDLGQRIWDVADYVIPAQGENVFFVVTNLIVTPNQRQNVCAE
NEGIPDGACSKDSDCHAGEAVTAGNGVKTGRCLRRENLARGTCEIFAWCPLETSSRPEEP
FLKEAEDFTIFIKNHIRFPKFNFSKSNVMDVKDRSFLKSCHFGPKNHYCPIFRLGSVIRW
AGSDFQDIALEGGVIGINIEWNCDLDKAASECHPHYSFSRLDNKLSKSVSSGYNFRFARY
YRDAAGVEFRTLMKAYGIRFDVMVNGKGAFFCDLVLIYLIKKREFYRDKKYEEVRGLEDS
SQEAEDEASGLGLSEQLTSGPGLLGMPEQQELQEPPEAKRGSSSQKGNGSVCPQLLEPHR
ST
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BDBM50596630
n/a
NameBDBM50596630
Synonyms:CHEMBL5172961
TypeSmall organic molecule
Emp. Form.C19H23BrN2OS
Mol. Mass.407.368
SMILESCc1ccc(NC(=S)NC(=O)C23CC4CC(CC(C4)C2)C3)c(Br)c1 |TLB:18:17:20:14.13.12,18:13:20:17.19.16,THB:16:17:20.15.14:12,16:15:17.19.18:12|
Structure
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