Target Validation Information | |||||
---|---|---|---|---|---|
Target ID | T62184 | ||||
Target Name | Sodium- and chloride-dependent GABA transporter 1 | ||||
Target Type | Successful |
||||
Drug Potency against Target | 4-Hydroxy-piperidine-3-carboxylic acid | Drug Info | IC50 = 11000 nM | [533544] | |
(S)-Piperidine-3-carboxylic acid | Drug Info | IC50 = 2660 nM | [527271] | ||
2,4-Diamino-butyric acid(GABA) | Drug Info | IC50 = 2000 nM | [533404] | ||
(R)-Piperidine-3-carboxylic acid | Drug Info | IC50 = 2600 nM | [527271] | ||
GAMMA-AMINO-BUTANOIC ACID | Drug Info | IC50 = 2640 nM | [527271] | ||
References | |||||
Ref 533544 | J Med Chem. 1982 Oct;25(10):1157-62.Hydroxy- and amino-substituted piperidinecarboxylic acids as gamma-aminobutyric acid agonists and uptake inhibitors. | ||||
Ref 527271 | J 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 533404 | J Med Chem. 1986 Feb;29(2):224-9.Glycine antagonists. Synthesis, structure, and biological effects of some bicyclic 5-isoxazolol zwitterions. | ||||
Ref 527271 | J 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 527271 | J 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. |
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