About 31 results found for searched term "GABA Receptor" (0.046 seconds)
Cat.No. | Name | Target |
---|---|---|
M28615 | GABAA receptor agent 1 | GABA Receptor |
GABAA receptor agent 1 is a high affinity ligand for GABAA receptor, with potent anticonvulsant activity. | ||
M2005 | (R)-Baclofen | GABA Receptor |
STX 209; Arbaclofen | ||
(R)-baclofen, a gamma-aminobutyric acid derivative and agonist at GABA-B receptors, inhibits nerve conduction in the central nervous system and can be used in studies related to spasticity. | ||
M2347 | (+)-Bicuculline | GABA Receptor |
d-Bicuculline | ||
(+)-Bicuculline is a competitive antagonist of GABAA receptors with IC50 of 2 μM, also blocks Ca(2+)-activated potassium channels. | ||
M4013 | Glabridin | GABA Receptor |
Glabridin, one of the active phytochemicals in licorice extract, binds to and activates the ligand binding domain of PPARγ, as well as the full length receptor. It is also a GABAA receptor positive modulator promoting fatty acid oxidation and improving learning and memory. | ||
M4019 | Songorine | GABA Receptor |
Songorine is a diterpenoid alkaloid isolated from the genus Aconite. Songorine is a GABAA receptor antagonist in rat brain and has anticancer, anti-arrhythmia and anti-inflammatory activities. Songorine has potential to be used in epithelial ovarian cancer (EOC) studies. | ||
M4073 | Ginsenoside-Rc | GABA Receptor |
Panaxoside Rc | ||
Ginsenoside Rc is one of the major ginsenosides. Ginsenoside Rc enhances GABA receptor A (GABAA) -mediated ion channel (IGABA) currents. Ginsenoside Rc also inhibited TNF-α and IL-1β expression. | ||
M4950 | Topiramate | GluR |
McN 4853; RWJ 17021 | ||
Topiramate is an anticonvulsant that antagonizes GluR5 receptors and acts as a positive allosteric modulator of GABA receptor-mediated currents. | ||
M5378 | Acamprosate calcium | GABA Receptor |
Calcium N-acetylhomotaurinate | ||
Acamprosate calcium (Campral EC) is a GABA receptor agonist and glutamate system modulator. | ||
M5390 | Afloqualone | GABA Receptor |
Afloqualone is a agonist of GABA receptor . | ||
M5575 | Dihydroergotoxine mesylate | GABA Receptor |
Ergoloid mesylates | ||
Dihydroergotoxine mesylate is a complex of closely related alkaloid salts; Binds with high affinity to the GABAA receptor Cl- channel, producing an allosteric interaction with the benzodiazepine site. | ||
M5653 | Flumazenil | GABA Receptor |
Ro 15-1788 | ||
Flumazenil is a competitive GABAA receptor antagonist, used in the treatment of benzodiazepine overdoses. | ||
M5870 | Pentylenetetrazol | GABA Receptor |
Pentylenetetrazole, Metrazole, pentetrazol | ||
Pentylenetetrazol displays activity as a central nervous system and respiratory stimulant. It is considered a non-competitive GABA(A) receptor antagonist. | ||
M6385 | AA 29504 | Others |
AA 29504 is a positive allosteric modulator of GABA A receptors. | ||
M6583 | CGP 36216 hydrochloride | Others |
CGP 36216 hydrochloride is a gABA B antagonist; displays activity at presynaptic receptors. | ||
M6720 | Etifoxine hydrochloride | GABA Receptor |
HOE 36-801 | ||
Etifoxine hydrochloride is a ligand of the translocator protein (TSPO); also GABA A receptor potentiator. | ||
M6735 | Flupirtine maleate | Potassium Channel |
Flupirtine maleate is a selective potassium channel opener, NMDA receptor antagonist and GABAA receptor modulator. | ||
M6744 | Ganaxolone | GABA Receptor |
CCD 1042 | ||
Ganaxolone (CCD 1042) is A neuroactive steroid allopregnenolone analogue synthesized orally and is A selective, high-affinity positive sex modulator of γ -aminobutyrate-A (GABAA) receptor with anticonvulsant properties. Gannadone works through different binding sites with benzodiazepine binding sites and can be used in epilepsy studies related to cyclin-dependent kinase-like 5 (CDKL5) deficiency (CDD). | ||
M6828 | Indiplon | Others |
Indiplon is a subtype-selective GABA A receptor positive allosteric modulator. | ||
M6915 | Loreclezole hydrochloride | Others |
Loreclezole hydrochloride is a subtype-selective GABA A receptor modulator. | ||
M6961 | MK 0343 | Others |
MK 0343 is a subtype-selective GABA A receptor partial agonist. | ||
M7087 | Org 20599 | Others |
Org 20599 is a positive allosteric modulator and direct agonist of GABA A receptors. | ||
M7158 | Pregnanolone | Others |
Pregnanolone is a gABA A receptor positive allosteric modulator. | ||
M7252 | SB 205384 | GABA Receptor |
SB 205384 is a gABA A receptor modulator; slows current decay. | ||
M7381 | TCS 1105 | Others |
TCS 1105 is a gABA A α2 benzodiazepine receptor agonist. | ||
M7382 | TCS 1205 | Others |
TCS 1205 is a subtype-selective GABA A receptor agonist. | ||
M7420 | TP 003 | Others |
TP 003 is a functionally selective GABA A receptor (α3 subtype) partial agonist. | ||
M7441 | U 90042 | Others |
U 90042 is a gABA A receptor ligand. | ||
M7442 | U 93631 | GABA Receptor |
U 93631 is a gABA A receptor antagonist. | ||
M7691 | Chlormethiazole hydrochloride | GABA Receptor |
Chlormethiazole hydrochloride is a GABAA agonist; glycine receptor modulator. Clomethiazole hydrochloride is neuroprotective and prevents the degeneration of serotonergic nerve terminals induced by 3,4-methylenedioxymethamphetamine (MDMA). | ||
M7697 | Chlorprothixene hydrochloride | Others |
D2 dopamine receptor antagonist; blocks a subset of GABAA receptors in rat cortex that is also blocked by clozapine; thioxanthine antipsychotic. | ||
M7740 | DS1 | Others |
δ-GABAA receptors are emerging as an important pharmacological target. |
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