Drug General Information
Drug ID
D0D3ID
Former ID
DNC004037
Drug Name
GAMMA-AMINO-BUTANOIC ACID
Drug Type
Small molecular drug
Indication Discovery agent Investigative [528408]
Structure
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2D MOL

3D MOL

Formula
C4H9NO2
Canonical SMILES
C(CC(=O)O)CN
InChI
1S/C4H9NO2/c5-3-1-2-4(6)7/h1-3,5H2,(H,6,7)
InChIKey
BTCSSZJGUNDROE-UHFFFAOYSA-N
PubChem Compound ID
Target and Pathway
Target(s) Gamma-aminobutyric acid receptor subunit gamma-2 Target Info Inhibitor [528408]
Gamma-aminobutyric acid B receptor Target Info Inhibitor [528071]
GABA transporter-3 Target Info Inhibitor [533538]
Gamma-aminobutyric-acid receptor alpha-2 subunit Target Info Inhibitor [533580]
Gamma-aminobutyric-acid receptor alpha-3 subunit Target Info Inhibitor [533580]
Gamma-aminobutyric acid receptor Target Info Inhibitor [528408]
Gamma-aminobutyric acid receptor subunit beta-2 Target Info Inhibitor [528408]
Gamma-aminobutyric acid receptor subunit alpha-1 Target Info Inhibitor [528408]
Gamma-aminobutyric-acid receptor alpha-5 subunit Target Info Inhibitor [533580]
Sodium- and chloride-dependent GABA transporter 1 Target Info Inhibitor [527271]
KEGG Pathway Neuroactive ligand-receptor interaction
Retrograde endocannabinoid signaling
GABAergic synapse
Morphine addiction
Nicotine addictionhsa04024:cAMP signaling pathway
Estrogen signaling pathway
Morphine addictionhsa04080:Neuroactive ligand-receptor interaction
Nicotine addictionhsa04080:Neuroactive ligand-receptor interaction
Serotonergic synapse
Nicotine addictionhsa04727:GABAergic synapse
Reactome Ligand-gated ion channel transport
GABA A receptor activationR-HSA-1296041:Activation of G protein gated Potassium channels
G alpha (i) signalling events
Class C/3 (Metabotropic glutamate/pheromone receptors)
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunitsR-HSA-975298:Ligand-gated ion channel transport
GABA A receptor activationR-HSA-975298:Ligand-gated ion channel transport
GABA A receptor activationR-HSA-442660:Na+/Cl- dependent neurotransmitter transporters
WikiPathways Neurotransmitter Receptor Binding And Downstream Transmission In The Postsynaptic Cell
Iron uptake and transportWP501:GPCRs, Class C Metabotropic glutamate, pheromone
Potassium Channels
GPCR ligand binding
GPCR downstream signalingWP2754:Neurotransmitter Receptor Binding And Downstream Transmission In The Postsynaptic Cell
Iron uptake and transportWP2754:Neurotransmitter Receptor Binding And Downstream Transmission In The Postsynaptic Cell
Iron uptake and transportWP706:SIDS Susceptibility Pathways
Iron uptake and transportWP727:Monoamine Transport
NRF2 pathway
References
Ref 528408J Med Chem. 2006 Sep 7;49(18):5571-7.3-demethoxy-3-glycosylaminothiocolchicines: Synthesis of a new class of putative muscle relaxant compounds.
Ref 527271J Med Chem. 2004 Nov 4;47(23):5620-9.Novel secoergoline derivatives inhibit both GABA and glutamate uptake in rat brain homogenates: synthesis, in vitro pharmacology, and modeling.
Ref 528071J Med Chem. 1991 Aug;34(8):2557-60.3-Thienyl- and 3-furylaminobutyric acids. Synthesis and binding GABAB receptor studies.
Ref 528408J Med Chem. 2006 Sep 7;49(18):5571-7.3-demethoxy-3-glycosylaminothiocolchicines: Synthesis of a new class of putative muscle relaxant compounds.
Ref 533538J Med Chem. 1981 Jul;24(7):788-94.Epimeric cis-decahydroquinoline-5-carboxylic acids: effects on gamma-aminobutyric acid uptake and receptor binding in vitro.
Ref 533580J Med Chem. 1980 Jun;23(6):702-4.New anticonvulsants: Schiff bases of gamma-aminobutyric acid and gamma-aminobutyramide.

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