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TargetP2X purinoceptor 5
LigandBDBM50596625
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2221596 (CHEMBL5134930)
IC50 12339±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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BDBM50596625
n/a
NameBDBM50596625
Synonyms:CHEMBL5174645
TypeSmall organic molecule
Emp. Form.C18H20Cl2N2O2S
Mol. Mass.399.335
SMILESOc1c(Cl)cc(NC(=S)NC(=O)C23CC4CC(CC(C4)C2)C3)cc1Cl |TLB:19:18:21:15.14.13,19:14:21:18.20.17,THB:17:18:21.16.15:13,17:16:18.20.19:13|
Structure
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