General Information of DTT (ID: TT24DGP)

DTT Name P2Y purinoceptor 4 (P2RY4) DTT Info
Gene Name P2RY4

Molecule-Related Drug & Molecule List

Molecule-Related Drug List
Molecule Type:
DTT
DTP
DME
Drug Status:
Discontinued Drug(s)
Investigative Drug(s)
1 Discontinued Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
INS 316 DMTHMEI Lung cancer 2C25.0 Discontinued in Phase 3 [1]
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9 Investigative Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
(N)methanocarba-UTP DM6SV7I Discovery agent N.A. Investigative [2]
2-amino-uridine-5'-monophosphate DMO792L Discovery agent N.A. Investigative [3]
CTP DM4T62U Discovery agent N.A. Investigative [1]
ITP DMVFITX Discovery agent N.A. Investigative [1]
MRS2927 DMB2A7Q Discovery agent N.A. Investigative [4]
MRS4062 DMWKXGP Discovery agent N.A. Investigative [4]
N4-phenylethoxycytidine-5'-triphosphate DM7KX2V Discovery agent N.A. Investigative [4]
PPADS DMWHN3T Discovery agent N.A. Investigative [5]
UTPgammaS DMKLB4O Discovery agent N.A. Investigative [6]
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⏷ Show the Full List of 9 Investigative Drug(s)
Molecule Interaction Atlas

References

1 ATP, an agonist at the rat P2Y(4) receptor, is an antagonist at the human P2Y(4) receptor. Mol Pharmacol. 2000 May;57(5):926-31.
2 Methanocarba modification of uracil and adenine nucleotides: high potency of Northern ring conformation at P2Y1, P2Y2, P2Y4, and P2Y11 but not P2Y6 receptors. J Med Chem. 2002 Jan 3;45(1):208-18.
3 Structural modifications of UMP, UDP, and UTP leading to subtype-selective agonists for P2Y2, P2Y4, and P2Y6 receptors. J Med Chem. 2011 Apr 28;54(8):2878-90.
4 Pyrimidine nucleotides with 4-alkyloxyimino and terminal tetraphosphate delta-ester modifications as selective agonists of the P2Y(4) receptor. J Med Chem. 2011 Jun 23;54(12):4018-33.
5 Development of selective agonists and antagonists of P2Y receptors. Purinergic Signal. 2009 Mar;5(1):75-89.
6 Enzymatic synthesis of UTP gamma S, a potent hydrolysis resistant agonist of P2U-purinoceptors. Br J Pharmacol. 1996 Jan;117(1):203-9.