General Information of Drug (ID: DM03RIT)

Drug Name
Rp-5-OMe-UDPalphaB Drug Info
Synonyms 5-OMe-uridine-5'-O-(alpha-boranodiphosphate); compound 18a [PMID: 22901672]
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
91938091
TTD Drug ID
DM03RIT

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Discontinued Drug(s)
Investigative Drug(s)
Drug(s) Targeting P2Y purinoceptor 6 (P2RY6)
Drug Name Drug ID Indication ICD 11 Highest Status REF
GC021109 DMQBEYV Alzheimer disease 8A20 Phase 1 [3]
INS 316 DMTHMEI Lung cancer 2C25.0 Discontinued in Phase 3 [4]
adenosine diphosphate DMFUHKP N. A. N. A. Investigative [4]
2MeSATP DMUE0W6 Discovery agent N.A. Investigative [4]
RB 2 DMCEFUW Discovery agent N.A. Investigative [5]
PSB-0952 DMW19LB Discovery agent N.A. Investigative [5]
5BrUTP DMEVRH4 Discovery agent N.A. Investigative [4]
MRS2782 DMZSO4R Discovery agent N.A. Investigative [6]
MRS2578 DMKMPS6 Discovery agent N.A. Investigative [7]
UDP-beta-S DMMWHAV Discovery agent N.A. Investigative [8]
⏷ Show the Full List of 10 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
P2Y purinoceptor 6 (P2RY6) TTNVSKA P2RY6_HUMAN Agonist [2]

References

1 UDP made a highly promising stable, potent, and selective P2Y6-receptor agonist upon introduction of a boranophosphate moiety. Bioorg Med Chem. 2012 Sep 15;20(18):5483-95.
2 5-OMe-uridine-5'-O-(alpha-boranodiphosphate), a novel nucleotide derivative highly active at the human P2Y(6) receptor protects against death-receptor mediated glial apoptosis. Neurosci Lett. 2014 Aug 22;578:80-4.
3 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
4 Cloning, functional expression and tissue distribution of the human P2Y6 receptor. Biochem Biophys Res Commun. 1996 May 15;222(2):303-8.
5 Development of potent and selective inhibitors of ecto-5'-nucleotidase based on an anthraquinone scaffold. J Med Chem. 2010 Mar 11;53(5):2076-86.
6 Synthesis and potency of novel uracil nucleotides and derivatives as P2Y2 and P2Y6 receptor agonists. Bioorg Med Chem. 2008 Jun 15;16(12):6319-32.
7 Diisothiocyanate derivatives as potent, insurmountable antagonists of P2Y6 nucleotide receptors. Biochem Pharmacol. 2004 May 1;67(9):1763-70.
8 P2 receptors activated by uracil nucleotides--an update. Curr Med Chem. 2006;13(3):289-312.