| Drug General Information |
| Drug ID |
D01VEU
|
| Former ID |
DNC003566
|
| Drug Name |
9-Ethyl-8-phenylethynyl-9H-purin-6-ylamine
|
| Drug Type |
Small molecular drug
|
| Indication |
Discovery agent
|
Investigative |
[1]
|
|---|
| Structure |
|
Download
2D MOL
3D MOL
|
| Formula |
C15H13N5
|
| Canonical SMILES |
CCN1C(=NC2=C1N=CN=C2N)C#CC3=CC=CC=C3
|
| InChI |
1S/C15H13N5/c1-2-20-12(9-8-11-6-4-3-5-7-11)19-13-14(16)17-10-18-15(13)20/h3-7,10H,2H2,1H3,(H2,16,17,18)
|
| InChIKey |
AXENMZHFYBPHQF-UHFFFAOYSA-N
|
| PubChem Compound ID |
|
| Target and Pathway |
| Target(s) |
Adenosine A2a receptor |
Target Info |
Inhibitor |
[1]
|
|---|
| Adenosine A1 receptor |
Target Info |
Inhibitor |
[1]
|
| Adenosine A3 receptor |
Target Info |
Inhibitor |
[1]
|
|
KEGG Pathway
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Rap1 signaling pathway
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Calcium signaling pathway
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cAMP signaling pathway
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Neuroactive ligand-receptor interaction
|
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Vascular smooth muscle contraction
|
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Parkinson's disease
|
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Alcoholismhsa04022:cGMP-PKG signaling pathway
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Sphingolipid signaling pathway
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Morphine addiction
|
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NetPath Pathway
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TCR Signaling Pathway
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RANKL Signaling Pathway
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PANTHER Pathway
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Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway
|
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Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway
|
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Pathway Interaction Database
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HIF-2-alpha transcription factor network
|
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PathWhiz Pathway
|
Intracellular Signalling Through Adenosine Receptor A2a and Adenosine
|
|
Reactome
|
NGF-independant TRKA activation
|
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Adenosine P1 receptors
|
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G alpha (s) signalling events
|
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Surfactant metabolismR-HSA-417973:Adenosine P1 receptors
|
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G alpha (i) signalling eventsR-HSA-417973:Adenosine P1 receptors
|
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G alpha (i) signalling events
|
|
WikiPathways
|
Nucleotide GPCRs
|
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Monoamine Transport
|
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GPCRs, Class A Rhodopsin-like
|
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NGF signalling via TRKA from the plasma membrane
|
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GPCR ligand binding
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GPCR downstream signaling
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GPCRs, OtherWP80:Nucleotide GPCRs
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GPCR downstream signalingWP80:Nucleotide GPCRs
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|
GPCRs, Other
|
| References |
| REF 1 | Bioorg Med Chem Lett. 2001 Jul 23;11(14):1931-4.Introduction of alkynyl chains on C-8 of adenosine led to very selective antagonists of the A(3) adenosine receptor. |
|---|
