Drug Information
Drug General Information | |||||
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Drug ID |
D0Z9CC
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Former ID |
DNC012865
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Drug Name |
ZONAMPANEL
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Drug Type |
Small molecular drug
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Indication | Discovery agent | Terminated | [1] | ||
Structure |
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Download2D MOL |
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Formula |
C13H9N5O6
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Canonical SMILES |
C1=CN(C=N1)C2=C(C=C3C(=C2)N(C(=O)C(=O)N3)CC(=O)O)[N+](=<br />O)[O-]
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InChI |
1S/C13H9N5O6/c19-11(20)5-17-8-4-9(16-2-1-14-6-16)10(18(23)24)3-7(8)15-12(21)13(17)22/h1-4,6H,5H2,(H,15,21)(H,19,20)
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InChIKey |
SPXYHZRWPRQLNS-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Glutamate receptor 1 | Target Info | Inhibitor | [2] | |
Glutamate receptor AMPA subtype | Target Info | Inhibitor | [2] | ||
KEGG Pathway | cAMP signaling pathway | ||||
Neuroactive ligand-receptor interaction | |||||
Circadian entrainment | |||||
Long-term potentiation | |||||
Retrograde endocannabinoid signaling | |||||
Glutamatergic synapse | |||||
Dopaminergic synapse | |||||
Long-term depression | |||||
Amyotrophic lateral sclerosis (ALS) | |||||
Amphetamine addiction | |||||
Nicotine addiction | |||||
PANTHER Pathway | Ionotropic glutamate receptor pathway | ||||
Metabotropic glutamate receptor group III pathway | |||||
Pathway Interaction Database | EPHB forward signaling | ||||
Reactome | COPII (Coat Protein 2) Mediated Vesicle Transport | ||||
Trafficking of AMPA receptors | |||||
Trafficking of GluR2-containing AMPA receptors | |||||
Unblocking of NMDA receptor, glutamate binding and activation | |||||
Cargo concentration in the ER | |||||
WikiPathways | Hypothetical Network for Drug Addiction | ||||
Neurotransmitter Receptor Binding And Downstream Transmission In The Postsynaptic Cell | |||||
Amyotrophic lateral sclerosis (ALS) | |||||
BDNF signaling pathway | |||||
References | |||||
REF 1 | Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800009224) | ||||
REF 2 | Bioorg Med Chem Lett. 2004 Oct 18;14(20):5107-11.Synthesis and AMPA receptor antagonistic activity of a novel 7-imidazolyl-6-trifluoromethyl quinoxalinecarboxylic acid with a substituted phenyl groupand improved its good physicochemical properties by introduced CF3 group. | ||||
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