General Information of Drug Therapeutic Target (DTT) (ID: TTYXPCO)

DTT Name P2Y purinoceptor 11 (P2RY11)
Synonyms P2Y11
Gene Name P2RY11
DTT Type
Discontinued target
[1]
UniProt ID
P2Y11_HUMAN
TTD ID
T92689
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Sequence
MAANVSGAKSCPANFLAAADDKLSGFQGDFLWPILVVEFLVAVASNGLALYRFSIRKQRP
WHPAVVFSVQLAVSDLLCALTLPPLAAYLYPPKHWRYGEAACRLERFLFTCNLLGSVIFI
TCISLNRYLGIVHPFFARSHLRPKHAWAVSAAGWVLAALLAMPTLSFSHLKRPQQGAGNC
SVARPEACIKCLGTADHGLAAYRAYSLVLAGLGCGLPLLLTLAAYGALGRAVLRSPGMTV
AEKLRVAALVASGVALYASSYVPYHIMRVLNVDARRRWSTRCPSFADIAQATAALELGPY
VGYQVMRGLMPLAFCVHPLLYMAAVPSLGCCCRHCPGYRDSWNPEDAKSTGQALPLNATA
APKPSEPQSRELSQ
Function Receptor for ATP and ADP coupled to G-proteins that activate both phosphatidylinositol-calcium and adenylyl cyclase second messenger systems. Not activated by UTP or UDP.
KEGG Pathway
Neuroactive ligand-receptor interaction (hsa04080 )
Reactome Pathway
P2Y receptors (R-HSA-417957 )
G alpha (s) signalling events (R-HSA-418555 )
ADORA2B mediated anti-inflammatory cytokines production (R-HSA-9660821 )
G alpha (q) signalling events (R-HSA-416476 )

Molecular Interaction Atlas (MIA) of This DTT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DTT
1 Discontinued Drug(s) Targeting This DTT
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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8 Investigative Drug(s) Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
2MeSATP DMUE0W6 Discovery agent N.A. Investigative [2]
ATPgammaS DMXHQIN Discovery agent N.A. Investigative [2]
BzATP DM37GYA Discovery agent N.A. Investigative [2]
dATP DMMXFBJ Discovery agent N.A. Investigative [2]
NAADP DM51DW6 Discovery agent N.A. Investigative [3]
NF157 DMGMH8T Discovery agent N.A. Investigative [4]
NF340 DMPSXR8 Discovery agent N.A. Investigative [5]
NF546 DMPZB31 Discovery agent N.A. Investigative [6]
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⏷ Show the Full List of 8 Investigative Drug(s)

References

1 Characterization of a Ca2+ response to both UTP and ATP at human P2Y11 receptors: evidence for agonist-specific signaling. Mol Pharmacol. 2003 Jun;63(6):1356-63.
2 Pharmacological characterization of the human P2Y11 receptor. Br J Pharmacol. 1999 Nov;128(6):1199-206.
3 NAADP+ is an agonist of the human P2Y11 purinergic receptor. Cell Calcium. 2008 Apr;43(4):344-55.
4 Synthesis and structure-activity relationships of suramin-derived P2Y11 receptor antagonists with nanomolar potency. J Med Chem. 2005 Nov 3;48(22):7040-8.
5 Invited Lectures : Overviews Purinergic signalling: past, present and future. Purinergic Signal. 2006 May;2(1):1-324.
6 NF546 [4,4'-(carbonylbis(imino-3,1-phenylene-carbonylimino-3,1-(4-methyl-phenylene)-carbonylimino))-bis(1,3-xylene-alpha,alpha'-diphosphonic acid) tetrasodium salt] is a non-nucleotide P2Y11 agonist and stimulates release of interleukin-8 from human monocyte-derived dendritic cells. J Pharmacol Exp Ther. 2010 Jan;332(1):238-47.