GABA Receptor
Gamma-aminobutyric acid Receptor; γ-Aminobutyric acid Receptor
GABA receptors are a class of receptors that respond to the neurotransmitter gamma-aminobutyric acid (GABA), the chief inhibitory neurotransmitter in the vertebrate central nervous system. There are two classes of GABA receptors: GABAA and GABAB. GABAA receptors are ligand-gated ion channels (also known as ionotropic receptors), whereas GABAB receptors are G protein-coupled receptors (also known asmetabotropic receptors). It has long been recognized that the fast response of neurons to GABA that is blocked by bicuculline and picrotoxin is due to direct activation of an anion channel. This channel was subsequently termed the GABAA receptor. Fast-responding GABA receptors are members of family of Cys-loop ligand-gated ion channels. A slow response to GABA is mediated by GABAB receptors, originally defined on the basis of pharmacological properties.
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GABA Receptor Inhibitors
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GABA Receptor Agonists
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GABA Receptor Antagonists
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GABA Receptor Activators
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GABA Receptor Modulators
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GABA Receptor Controls
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GABA Receptor Ligands
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GABA Receptor Verwandte Produkte (789)
Verwandte Produkte (789)
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Antibodies (14)
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Related Compound Screening Libraries (1)
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Org 21465
0 ImagesArt. -Nr.: HY-106965CAS. Nr.: 167946-96-5Org 21465 is an agent that can relieve pain. Org 21465 causes no cardiovascular or respiratory depression. Org 21465 can inhibit GABAA receptor in vivo.
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Broflanilide (Standard)
0 ImagesBroflanilide (Standard) is the analytical standard of Broflanilide. This product is intended for research and analytical applications. Broflanilide is a potential insecticide and metabolized to Desmethyl-Broflanilide, which is a potent antagonist at the insect resistant-to-dieldrin (RDL) GABA Receptor, and inhibits S. litura RDL GABAR, with an IC50 value of 1.3 nM.
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CGP44532
0 ImagesArt. -Nr.: HY-116197CAS. Nr.: 133345-68-3CGP44532 is a GABAB receptor agonist with a pEC50 (geometric mean of the half-maximal effective concentration) value of 5.63 μM.
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Propofol-d14
0 ImagesArt. -Nr.: HY-W707528CAS. Nr.: 2514564-65-7Synonyms: 2,6-Diisopropylphenol-d14
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GABA receptor Antagonist 1
0 ImagesArt. -Nr.: HY-156339GABA receptor Antagonist 1 (compound 7w) inhibits Px RDL1 GABAR with an IC50 value of 7.08 nmol/L. GABA receptor Antagonist 1 shows insecticide activity against P. xylostella, S. frugiperda, S. exigua, and S. litura, with LC50 of 0.09, 0.84, 0.87, and 0.68 mg/L respectively. GABA receptor Antagonist 1 shows a medium toxicity to honeybee (48 h, ID50 = 2.22 μg/adult), and low toxicity to zebrafish (LC50: 42.4 mg/L).
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NO-711ME
0 ImagesArt. -Nr.: HY-129464CAS. Nr.: 127586-66-7NO-711ME is a prodrug of NO-711. NO-711 is a potent and selective GABA uptake inhibitor.
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COR627
0 ImagesArt. -Nr.: HY-119256CAS. Nr.: 329221-34-3COR627 is a GABA receptor positive allosteric modulator with the ability to enhance GABA activity. COR627 exhibits effects on GABA and baclofen stimulation in rat cortical membranes and can increase its affinity for GABA(B) receptors. In vivo experiments have shown that COR627 can enhance the sedative/hypnotic effects of baclofen at pretreatment ineffective doses.
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Fengabine
0 ImagesArt. -Nr.: HY-123478CAS. Nr.: 80018-06-0Synonyms: SL 79229Fengabine is a GABAergic antidepressant agent. Fengabine can be used for the research of depression.
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SSR180575
0 ImagesArt. -Nr.: HY-W436366CAS. Nr.: 220448-02-2SSR180575 is a specific and potent peripheral benzodiazepine receptor ligand. SSR180575 irreversibly and specifically binds with high affinity on rat heart mitochondria (Kd = 1.95 nM). SSR180575 can be used in the research of cardiovascular diseases.
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Lirequinil
0 ImagesArt. -Nr.: HY-106917CAS. Nr.: 143943-73-1Synonyms: Ro 41-3696Lirequinil (Ro 41-3696) is an orally active partial agonist of the benzodiazepine (BDZ) receptor. Lirequinil has the effect of promoting sleep.
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GABAA receptor agent 6
0 ImagesArt. -Nr.: HY-145258CAS. Nr.: 1808463-81-1GABAA receptor agent 6 (compound 2027) is a potent γ-GABAAR antagonist with an Ki of 0.56 µM. GABAA receptor agent 6 shows γ-GABAAR antagonist activity with low cellular membrane permeability.
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γ-Aminobutyric acid-4,4-d2
0 ImagesArt. -Nr.: HY-N0067S2CAS. Nr.: 107022-06-0Synonyms: 4-Aminobutyric acid-4,4-d2γ-Aminobutyric acid-4,4-d2 is the deuterium labeled γ-Aminobutyric acid. γ-Aminobutyric acid (4-Aminobutyric acid) is a major inhibitory neurotransmitter in the adult mammalian brain[1][2], binding to the ionotropic GABA receptors (GABAA receptors) and metabotropic receptors (GABAB receptors)[2].
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Xilmenolone
0 ImagesArt. -Nr.: HY-147421CAS. Nr.: 2368807-26-3Xilmenolone is a GABAA receptor positive allosteric modulator.
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Sch 50910
0 ImagesArt. -Nr.: HY-115856CAS. Nr.: 790633-59-9Sch 50910 is a GABA(B) receptor antagonist with some activity in inhibiting GABA(B) autoreceptors. Sch 50910 had no effect on electrically stimulated release at a concentration of 100 μM. The activity of Sch 50910 suggests that it may not have a significant role in studies of GABA(B) receptor function.
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Jujuboside A (Standard)
0 ImagesArt. -Nr.: HY-N0659RCAS. Nr.: 55466-04-1Jujuboside A (Standard) is the analytical standard of Jujuboside A. This product is intended for research and analytical applications. Jujuboside A is a glycoside extracted from Semen Ziziphi Spinosae, a Chinese herbal medicine used to treat insomnia and anxiety.
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GABAA receptor agonist 1
0 ImagesArt. -Nr.: HY-147735GABAA receptor agonist 1 (compound 3e) is a potent GABAA receptor agonist. GABAA receptor agonist 1 shows anti-depression activities in classical mouse models of depression of FST and TST. GABAA receptor agonist 1 binds at the GABA binding site of GABAA receptor in order to produce GABAergic effects. GABAA receptor agonist 1 has the potential for the research of depression.
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U-90042
0 ImagesArt. -Nr.: HY-103496CAS. Nr.: 134516-99-7U-90042 is a gamma-aminobutyric acidA receptor agonist of α1, α3 and α6 subtypes with Ki values of 7.8 nM, 9.5 nM and 11.0 nM, respectively. U-90042 suppresses locomotor activity and impairs rotarod performance in mice. U-90042 produces sedation and ataxia and prolongs sleeping time in mice, rats and monkeys. U-90042 can be used as a sedative and hypnotic agent.
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Loreclezole hydrochloride
0 ImagesArt. -Nr.: HY-105272ACAS. Nr.: 2227372-56-5Synonyms: R 72063 hydrochlorideLoreclezole hydrochloride, an antiepileptic compound, is a selective GABAA receptor modulator and acts as a positive allosteric modulator of β2 or β3-subunit containing receptors.
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Nerisopam
0 ImagesArt. -Nr.: HY-113726CAS. Nr.: 102771-12-0Synonyms: GYKI52322; EGIS-6775Nerisopam is an orally active gamma-aminobutyric acid (GABA) receptor agonist. Nerisopam is an anxiolytic and antipsychotic homophthalazine. Nerisopam induces rapid, intense expression of Fos-like immunoreactivity in the rostral, dorsomedial and lateral parts of the striatum in the rat.
