Details of the Drug-Related molecule(s) Interaction Atlas

General Information of Drug (ID: DM7KX2V)

Drug Name

N4-phenylethoxycytidine-5'-triphosphate Drug Info

Synonyms

N4-(phenylethoxy)-CTP; compound 15 [PMID:21528910]

Indication

Disease Entry	ICD 11	Status	REF
Discovery agent	N.A.	Investigative	[1]

Cross-matching ID

Molecule-Related Drug Atlas

Molecule Type:

DTT

Drug Status:

Discontinued Drug(s)

Investigative Drug(s)

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Drug(s) Targeting P2Y purinoceptor 4 (P2RY4)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
INS 316	DMTHMEI	Lung cancer	2C25.0	Discontinued in Phase 3	[2]
PPADS	DMWHN3T	Discovery agent	N.A.	Investigative	[3]
UTPgammaS	DMKLB4O	Discovery agent	N.A.	Investigative	[4]
CTP	DM4T62U	Discovery agent	N.A.	Investigative	[2]
ITP	DMVFITX	Discovery agent	N.A.	Investigative	[2]
2-amino-uridine-5'-monophosphate	DMO792L	Discovery agent	N.A.	Investigative	[5]
MRS2927	DMB2A7Q	Discovery agent	N.A.	Investigative	[1]
MRS4062	DMWKXGP	Discovery agent	N.A.	Investigative	[1]
(N)methanocarba-UTP	DM6SV7I	Discovery agent	N.A.	Investigative	[6]
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Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

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Drug Therapeutic Target (DTT)

References

1	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.
2	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.
3	Development of selective agonists and antagonists of P2Y receptors. Purinergic Signal. 2009 Mar;5(1):75-89.
4	Enzymatic synthesis of UTP gamma S, a potent hydrolysis resistant agonist of P2U-purinoceptors. Br J Pharmacol. 1996 Jan;117(1):203-9.
5	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.
6	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.