Drug Information

Drug General Information
Drug ID
D0A6AX
Former ID
DNC011402
Drug Name
(9H-beta-Carbolin-3-yl)-carbamic acid ethyl ester
Drug Type
Small molecular drug
Indication Discovery agent Investigative [533400]
Structure
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2D MOL

3D MOL
Formula
C14H13N3O2
Canonical SMILES
CCOC(=O)NC1=NC=C2C(=C1)C3=CC=CC=C3N2
InChI
1S/C14H13N3O2/c1-2-19-14(18)17-13-7-10-9-5-3-4-6-11(9)16-12(10)8-15-13/h3-8,16H,2H2,1H3,(H,15,17,18)
InChIKey
ABHBEIYQTPYXQQ-UHFFFAOYSA-N
PubChem Compound ID
355090
Target and Pathway
Target(s) Gamma-aminobutyric acid receptor Target Info Inhibitor [533400]
Gamma-aminobutyric acid receptor subunit alpha-1 Target Info Inhibitor [533400]
KEGG Pathway Neuroactive ligand-receptor interaction
Retrograde endocannabinoid signaling
GABAergic synapse
Morphine addiction
Nicotine addiction
Reactome Ligand-gated ion channel transport
GABA A receptor activation
WikiPathways SIDS Susceptibility Pathways
Neurotransmitter Receptor Binding And Downstream Transmission In The Postsynaptic Cell
Iron uptake and transport
References
Ref 533400J Med Chem. 1985 Jun;28(6):824-8.3-Amino-beta-carboline derivatives and the benzodiazepine receptor. Synthesis of a selective antagonist of the sedative action of diazepam.
Ref 533400J Med Chem. 1985 Jun;28(6):824-8.3-Amino-beta-carboline derivatives and the benzodiazepine receptor. Synthesis of a selective antagonist of the sedative action of diazepam.

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