Target
P2Y purinoceptor 4
Ligand
BDBM50319140
Substrate
n/a
Meas. Tech.
ChEMBL_635652 (CHEMBL1119544)
EC50
300±n/a nM
Citation
 Maruoka, HBarrett, MOKo, HTosh, DKMelman, ABurianek, LEBalasubramanian, RBerk, BCostanzi, SHarden, TKJacobson, KA Pyrimidine ribonucleotides with enhanced selectivity as P2Y(6) receptor agonists: novel 4-alkyloxyimino, (S)-methanocarba, and 5'-triphosphate gamma-ester modifications. J Med Chem 53:4488-501 (2010) [PubMed]  Article 
Target
Name:
P2Y purinoceptor 4
Synonyms:
NRU | P2P | P2RY4 | P2RY4_HUMAN | P2Y purinoceptor 4 | P2Y4 | Pyrimidinergic receptor P2Y4 | UNR | Uridine nucleotide receptor
Type:
PROTEIN
Mol. Mass.:
40977.17
Organism:
Homo sapiens (Human)
Description:
ChEMBL_751027
Residue:
365
Sequence:
MASTESSLLRSLGLSPGPGSSEVELDCWFDEDFKFILLPVSYAVVFVLGLGLNAPTLWLFIFRLRPWDATATYMFHLALSDTLYVLSLPTLIYYYAAHNHWPFGTEICKFVRFLFYWNLYCSVLFLTCISVHRYLGICHPLRALRWGRPRLAGLLCLAVWLVVAGCLVPNLFFVTTSNKGTTVLCHDTTRPEEFDHYVHFSSAVMGLLFGVPCLVTLVCYGLMARRLYQPLPGSAQSSSRLRSLRTIAVVLTVFAVCFVPFHITRTIYYLARLLEADCRVLNIVNVVYKVTRPLASANSCLDPVLYLLTGDKYRRQLRQLCGGGKPQPRTAASSLALVSLPEDSSCRWAATPQDSSCSTPRADRL
  
Inhibitor
Name:
BDBM50319140
Synonyms:
(S)-Methanocarbauridine5'-Triphosphate TriethylammoniumSalt | CHEMBL1083148
Type:
Small organic molecule
Emp. Form.:
C11H17N2O14P3
Mol. Mass.:
494.179
SMILES:
O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H]2C[C@]2([C@@H]1O)n1ccc(=O)[nH]c1=O |r|
Structure:
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