| | GABAergics
- 2-Hydroxysaclofen
Selective GABAB antagonist, more potent than saclofen| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202011 | 117354-64-0 | C9H12CINO4S | 10 mg/50 mg |
- 3-Methyl-GABA
Activator of GABA aminotransferase. Anticonvulsant.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203471 | 71424-95-8 | C5H11NO2 | 10 mg/50 mg |
- 3α,12α-Dihydroxy-5β-pregnan-20-one 3,12-diacetate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-226347 | 15991-93-2 | C25H38O5 | 50 mg |
- 5α-Pregnan-3β-ol-20-one 3β-acetate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-233497 | 906-83-2 | C23H36O3 | 5 g |
- 6,2'-Dihydroxyflavone
This is a partial inverse agonist at GABAA receptors with a-subunit selectivity.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300048 | n.n. | C15H10O4 | 5 mg |
- 16-Dehydropregnenolone acetate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-224976 | 979-02-2 | C23H32O3 | 10 g |
- 16,17-Epoxy-21-acetoxypregnenolone
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-224977 | 28444-97-5 | C23H32O5 | 1 g |
- 16α,17α-Epoxypregnenolone
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-223173 | 974-23-2 | C21H30O3 | 5 g/10 g |
- 16α,17α-Epoxypregnenolone acetate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-224978 | 34209-81-9 | C23H32O4 | 5 g |
- 17-PA
A steroid analog that selectively antagonizes potentiation of GABA responses by 5α-reduced potentiating neurosteroids.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361075 | 694438-95-4 | C25H34O | 10 mg/50 mg |
- 17α-Hydroxypregnenolone
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-223186 | 387-79-1 | C21H32O3 | 5 g |
- 17α-Hydroxypregnenolone 3-acetate
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-224980 | 41906-06-3 | C23H34O4 | 5 g |
- Alphaxalone
A neurosteroid anesthetic that directly activates and potentiates GABAA receptor-activated membrane current (IGABA). Efficacy but not potency is determined by the alpha subunit of the receptor (EC50 values are 1.4, 1.8, 2.1, 2.4 and 2.5 μM for α1β1γ3, α1β1γ1, β1γ1, α2β1γ2L and α1β1γ2L isoforms respectively).| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203814 | 23930-19-0 | C21H32O3 | 10 mg/50 mg |
- β-CCB
Benzodiazepine inverse agonist, putative endogenous ligand| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204429 | 84454-35-3 | C16H16N2O2 | 10 mg/50 mg |
- (±)-Baclofen
A selective agonist of the GABAB metabotropic receptor. Produces muscle relaxant and antispastic effects. Prototypic agonist at GABAB.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200464 | 1134-47-0 | C10H12ClNO2 | 1 g/5 g |
- (+)-Bicuculline
An antagonist of the GABAA receptor. Blocks the neurotransmission inhibition action of the GABA system, producing an artificial epileptic state in laboratory studies.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202498 | 485-49-4 | C20H17NO6 | 50 mg/250 mg |
- (-)-Bicuculline methiodide
An N-methylated water-soluble derivative of the GABAA antagonist bicuculline. Demonstrates blockade of Ca2+-activated K+ channel-mediated afterhyperpolarization, unobserved with the parent compound.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200485 | 40709-69-1 | C21H20INO6 | 50 mg |
- (-)-Bicuculline methobromide
An N-methylated water-soluble derivative of the GABAA antagonist bicuculline. Demonstrates blockade of Ca2+-activated K+ channel-mediated afterhyperpolarization, unobserved with the parent compound.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200436 | 73604-30-5 | C21H20BrNO6 | 50 mg |
- (-)-Bicuculline methochloride
Methochloride salt of (+)-bicuculline. Water-soluble GABAA antagonist. More stable than bicuculline. Non-GABA receptor-mediated actions reported.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203528 | 53552-05-9 | C21H20ClNO6 | 10 mg/50 mg |
- CGP 7930
Positive allosteric modulator of GABAB receptors. Increases the potency and efficacy of GABA at both native and recombinant GABAB receptors (EC50 values are 5.37 and 4.60μM respectively) and enhances the inhibitory effect of the agonist L-baclofen in cultured cortical neurons. Reduces operant self-administration of ethanol in alcohol-preferring rats following i.p. administration.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203543 | 57717-80-3 | C19H32O2 | 10 mg/50 mg |
- CGP 13501
Positive allosteric modulator at GABAB receptors, potentiating the effects of GABA at this receptor type.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203542 | 56189-68-5 | C19H30O2 | 10 mg/50 mg |
- CGS 20625
Anti-anxiety drug used in research, acts as a central benzodiazepine receptor partial agonist, but is classified as a nonbenzodiazepine drug. Does not have sedative effect.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203545 | 111205-55-1 | C18H19N3O2 | 10 mg/50 mg |
- CGP 35348
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361138 | 123690-79-9 | C8H20NO4P | 10 mg/50 mg |
- CGP 36216
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-362724 | 123691-29-2 | C5H14NO2P | 10 mg/50 mg |
- CGP 46381
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361140 | 123691-14-5 | C10H22NO2P | 10 mg/50 mg |
- CGP 52432
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361141 | 139667-74-6 | C15H24Cl2NO4P | 10 mg/50 mg |
- CGP 54626 Hydrochloride
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361142 | 149184-21-4 | C18H28Cl2NO3P.HCl | 10 mg/50 mg |
- CGP 55845
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361143 | 149184-22-5 | C18H22Cl2NO3P•HCl | 10 mg/50 mg |
- Chlormethiazole hydrochloride
Potentiates GABAA receptor function. Sedative and anticonvulsant which is neuroprotective in a number of animal models. Prevents degeneration of serotonergic nerve terminals induced by MDMA ('Ecstasy').| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203548 | 6001-74-7 | C6H8ClNS ·HCl | 10 mg/50 mg |
- Chlormezanone
Skeletal muscle relaxant, acting at the benzodiazapine site of GABAA receptors| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203887 | 80-77-3 | C11H12ClNO3S | 1 g |
- CI 966 hydrochloride
Selective inhibitor of GAT-1 that is an anticonvulsive and neuroprotective.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203891 | 110283-66-4 | C23H22ClF6NO3 | 10 mg/50 mg |
- CL 218872
Benzodiazepine agonist displaying selectivity for α1 subunit-containing GABAA receptors (Ki values are 130, 1820, 1530, > 10000, 490 and > 10000 nM for α1, α2, α3, α4, α5 and α6-subunit containing receptors respectively). Orally active anxiolytic and anticonvulsant in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203552 | 66548-69-4 | C13H9F3N4 | 10 mg/50 mg |
- Cloflubicyne
Potent non-competitive GABA antagonist; convulsant; laboratory insecticide.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300382 | 224790-70-9 | C11H6Cl2F6N2 | 1 mg |
- D-Alanine
Weak inhibitory glycine receptor agonist.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203558 | 338-69-2 | C3H7NO2 | 1 g |
- Dansyl-gamma-Amino-n-Butyric Acid Cyclohexylammonium Salt
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-294267 | 76563-43-4 | C16H20N2O4S ·C6H13N | 100 mg/250 mg |
- DHEA
Major secretory steroidal product of the adrenal gland. DHEA and its sulfated metabolite, DHEA-S, are negative modulators of GABAA receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202573 | 53-43-0 | C19H28O2 | 10 g |
- Dihydroergotoxine mesylate
Binds with high affinity to GABAA receptor Cl- channel. Interacts with central dopaminergic, serotonergic and adrenergic (a1) receptors. Exhibits antirproliferative activity in vitro. Displays cognition-enhancing, anticonvulsant and sedative activity in vivo. Active orally.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203921 | 8067-24-1 | C33H45N5O5 | 100 mg |
- DMCM hydrochloride
Benzodiazepine inverse agonist. Exhibits strong convulsant and anxiogenic activity.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-205295 | 82499-00-1 | C17H18N2O4 ·HCl | 10 mg/50 mg |
- Etbicyphat
A synthetic, non-competitive GABA antagonist suggested to operate by blocking GABA-gated Cl- channels. Also shown to inhibit dihydropicrotoxin and t-butylbicyclo-phosphorothionate binding.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-294479 | 1005-93-2 | C6H11O4P | 500 mg |
- Etomidate
General anesthetic with GABA modulatory and GABA-mimetic actions. Interacts selectively with β2- and β3-subunit containing GABAA receptors. Short acting and potent hypnotic; low toxicity.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203577 | 33125-97-2 | C14H16N2O2 | 10 mg |
- FG 7142
Anxiogenic agent and Benzodiazepine inverse agonist. Shows increase in Tyr hydroxylation and exhibits upregulation of b-adrenoceptors in the cerebral cortex in mice.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203952 | 78538-74-6 | C13H11N3O | 100 mg |
- FGIN-1-43
Potent, specific ligand for mitochondrial diazepam binding inhibitor receptor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203953 | 145040-29-5 | C28H36Cl2N2O | 10 mg/50 mg |
- FrPbAII
A component of the Parawixia bistriata spider venom which has been shown to selectively inhibitf GABA and glycine uptake (IC50=65 µM and 62 µM respectively) with little or no effect on monoamine or glutamate transporters. It produces neuroprotective effects in a rat retinal ischemia/reperfusion model displaying remarkable reduction in cell death1. It also abolishes convulsive tonic-clonic seizures induced by bicuculline (SCBT Catalog # sc-200485) in rats.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-221630 | n.n. | C6H15ClN4O2 | 5 mg |
- GABA
The major inhibitory neurotransmitter in mammalian central nervous system.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203053 | 56-12-2 | C4H9NO2 | 10 g/25 g |
- gamma-Acetylenic GABA
A GABA transaminase inhibitor| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-295002 | 57659-38-8 | C6H9NO2 | 1 mg/5 mg |
- Ganaxolone
A synthetic neurosteroid which functions as a stereoselective positive allosteric modulator of GABAA receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203586 | 38398-32-2 | C22H36O2 | 10 mg/50 mg |
- GS 39783
A compound that regulates GABAB receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203589 | 39069-52-8 | C15H23N5O2S | 10 mg/50 mg |
- GS 39783
This product is a positive allosteric modulator of GABAB receptors.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-300773 | 39069-52-8 | C15H23N5O2S | 25 mg |
- Hispidulin
Potent benzodiazepine (BZD) receptor ligand. Natural sage (Salvia officinalis) flavone. Also has antioxidant, antithrombotic, antifungal, and antiproliferative properties. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203999 | 1447-88-7 | C16H12O6 | 10 mg |
- Hypotaurine
Endogenous inhibitory amino acid.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204005 | 300-84-5 | C2H7NO2S | 100 mg |
- Indiplon
Potent GABAAreceptor positive allosteric modulator. Exhibits sedative, hypnotic, anxiolytic and anticonvulsant activity in vivo and is orally active.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204011 | 325715-02-4 | C20H16N4O2S | 10 mg/50 mg |
- Isoguvacine·HCl
Isoguvacine is an agonist of Gamma-amino butyric acid (GABA) with similar biochemical features.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200451 | 64603-90-3 | C5H10NO2 ·HCl | 10 mg/50 mg |
- L-655,708
Potent and selective inverse agonist for the benzodiazepine site of α5-containing GABAA receptors. Displays high selectivity over GABAA receptors containing α1, α2, α3 or α6 subunits in combination with β3 and γ2.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204040 | 130477-52-0 | C18H19N3O4 | 10 mg/50 mg |
- Loreclezole hydrochloride
Subtype-selective GABAA receptor agonist. Positive allosteric modulator of β2 or β3-subunit containing receptors. Also acts as a negative modulator at a novel regulatory site, enhancing GABAA receptor sensitization. Inhibits homomeric ρ1 GABAC receptors. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204061 | 117857-45-1 | C10H7Cl4N3 | 10 mg/50 mg |
- Mebicyphat
Shown to be a non-competitive GABA antagonist. Blocks GABA gated Cl- channels, and is shown to inhibit dihydropicrotoxin binding and t-butylbicyclophosphorothionate binding.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-295376 | 1449-89-4 | C5H9O4P | 500 mg |
- Muscimol
A structural analog of GABA and a potent, selective agonist of the GABAA receptor. | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200460 | 2763-96-4 | C4H6N2O2 | 5 mg/25 mg |
- NCS-382 Sodium Salt
γ-Hydroxybutyric acid antagonist, anticonvulsant.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203444 | 131733-92-1 | C13H13NaO3 | 10 mg/50 mg |
- NCS-382 hydrate
This product is a γ-Hydroxybutyrate (GHB) receptor antagonist. It displays anti-convulsant activity.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-301458 | 131733-92-1 | C13H15NaO4 | 10 mg |
- (±)-Nipecotic acid
GABA uptake inhibitor. IC50 values are 8, 38, 106 and 2370 mM for hGAT-1, rGAT-2, hGAT-3 and hBGT-1 respectively.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203645 | 60252-41-7 | C6H11NO2 | 100 mg |
- NNC 05-2090 hydrochloride
GABA uptake inhibitor; displays moderate selectivity for BGT-1 (mGAT-2) transporters.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204131 | 184845-43-0 | C27H30N2O2 ·HCl | 10 mg/50 mg |
- NNC 711
Potent and selective inhibitor of GABA uptake by GAT-1. Anticonvulsant following systemic administration in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204132 | 145645-62-1 | C21H22N2O3•HCl | 10 mg/50 mg |
- Org 20599
Positive allosteric modulator. Direct agonist of GABAAreceptors at higher concentrations. Anesthetic steroid. Shown to induce hypnosis and lost of righting reflexes in mice.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204150 | 187652-71-7 | C25H40ClNO3 | 10 mg/50 mg |
- Phaclofen
A selective GABAB receptor antagonist. The phosphonic acid derivative of Baclofen.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200462 | 114012-12-3 | C9H13ClNO3P | 5 mg/25 mg |
- Pregnenolone sulfate sodium salt
Neurosteroid that has been demonstrated to antagonize the GABAA receptor chloride channel.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-301609 | 1852-38-6 | C21H31NaO5S | 25 mg |
- Primidone
Anticonvulsant. Potentiates GABAA receptor function.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204861 | 125-33-7 | C12H14N2O2 | 100 mg |
- Propybicyphat
Demonstrated GABA-gated chloride channel blocker, non-competitive GABA antagonist in mammals.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-301615 | 51486-74-9 | C7H13O4P | 1 mg |
- R-(+)-Baclofen (free base)
Selective GABAB receptor agonist. Skeletal muscle relaxant. The more active enantiomer of (±)-Baclofen (sc-200464)| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203228 | 69308-37-8 | C10H12ClNO2 | 10 mg/50 mg |
- R-(+)-Baclofen hydrochloride
Selective GABAB receptor agonist. Skeletal muscle relaxant. The more active enantiomer of (±)-Baclofen (sc-200464)| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203229 | 63701-55-3 | C10H12ClNO2•HCl | 10 mg/50 mg |
- rac BHFF
Potent and selective GABAB receptor positive allosteric modulator that increases the efficacy and potency of GABA ( > 149% and > 15-fold respectively). Orally active and exhibits anxiolytic activity in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204228 | 123557-91-5 | C17H21F3O3 | 10 mg/50 mg |
- RO 15-4513
A high affinity benzodiazepine ligand which acts as a partial inverse agonist at recombinant diazepam-sensitive (DS) benzodiazepine α1-, α2-, α3- and α5-GABAA receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203683 | 91917-65-6 | C15H14N6O3 | 10 mg |
- RO 19-4603
Benzodiazepine inverse agonist. Antagonizes effects of ethanol on locomotor behavior and suppresses ethanol intake in alcohol-preferring rats. Binds with high affinity to both diazepam-sensitive (DS) and diazepam-insensitive (DI) GABAA receptors (Ki values are ~ 0.2 and ~ 2.6 nM for DS and DI receptors respectively). | Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203684 | 99632-94-7 | C15H17N3O3S | 10 mg/50 mg |
- S(+)-gamma-Vinyl-GABA
Selective GABA transaminase inhibitor. Active enantiomer. Potential usefulness in treating cocaine addiction.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-222279 | 74046-07-4 | C6H11NO2 | 5 mg |
- (S)-SNAP 5114
GABA uptake inhibitor, showing selectivity for GAT-3 and GAT-2 (IC50 values are 5, 21 and 388 μM for hGAT-3, rGAT-2 and hGAT-1 respectively). Increases thalamic GABA levels and is an anticonvulsant following systemic administration in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204257 | 157604-55-2 | C30H35NO6 | 10 mg/50 mg |
- Saclofen
A selective antagonist of the GABAB receptor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203252 | 125464-42-8 | C9H12CINO3S | 10 mg |
- SB 205384
GABAA receptor modulator; slows current decay. Displays some specificity for α3-subunit-containing receptors (in particular α3β2γ2). Has little effect on receptors containing α1 or α2 subunits.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204263 | 160296-13-9 | C17H18N2O3S | 10 mg/50 mg |
- SCH 50911
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-361352 | 160415-07-6 | C8H15NO3 | 10 mg/50 mg |
- SCS
Partial inhibitor of β1-containing GABAA receptors. May bind allosterically to a novel site on GABAA receptor.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203375 | 3232-36-8 | C14H12N2O3 | 50 mg |
- SK&F 97541
SK&F 97541 is a very potent GABAB agonist, at least ten times more active than baclofen.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-200469 | 127729-35-5 | C4H12NO2P | 5 mg/25 mg |
- SR 95531 Hydrobromide
Selective GABAA receptor antagonist. Displaces [3H]-GABA from rat brain membranes with a Ki of 150 nM. Selectively antagonizes GABA-induced Cl- currents with little action on pentobarbitone-induced currents. Acts as a low affinity glycine receptor antagonist.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203701 | 104104-50-9 | C15H17N3O3 ·HBr | 10 mg/50 mg |
- TACA
GABAA and GABAC agonist. Also GABA-T substrate and GABA uptake inhibitor. Trans-isomer of CACA.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203705 | 38090-53-8 | C4H7NO2 | 10 mg/50 mg |
- TB 21007
GABAA receptor inverse agonist selective for the α5-subtype (Ki values are 1.6, 16, 20 and 20 nM for α5, α2, α1 and α3 subtypes respectively). Brain penetrant; enhances cognitive performance in rats in the delayed matching-to-place morris water maze test following i.p. administration.
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204322 | 207306-50-1 | C15H17NO2S3 | 10 mg/50 mg |
- Thiocolchicoside
A potent, competitive antagonist of GABAA receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-202839 | 602-41-5 | C27H33NO10S | 1 mg/5 mg |
- Thiomuscimol
A structural analog of GABAA.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-213035 | 62020-54-6 | C4H6N2OS | 10 mg |
- THIP hydrochloride
Systemically active GABAA receptor agonist and GABAC receptor antagonist. Displays anticonvulsant, antinociceptive and sedative effects. Hypnotic agent that enhances delta activity within non-REM sleep in rats.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204342 | 64603-91-4 | C6H8N2O2 ·HCl | 50 mg |
- TPMPA
Competitive, selective GABAC antagonist with minimal effects on GABAA and GABAB receptors (Kb values are 2.1 μM (antagonist), 320 μM (antagonist) and EC550 ~ 500 μM (weak agonist) respectively). Shows 8-fold selectivity for human recombinant ρ 1 receptors over ρ2 receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204352 | 182485-36-5 | C6H12NO2P | 10 mg/50 mg |
- Tracazolate hydrochloride
Subtype selective GABAA allosteric receptor modulator. Can potentiate or inhibit recombinant GABAA function depending on subunit combination. Enhances native GABAA receptor function and is anxiolytic following systemic administration in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203709 | 41094-88-6 | C16H24N4O2•HCl•xH2O | 10 mg/50 mg |
- trans-4-Hydroxycrotonic acid
| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-203710 | 24587-49-3 | C4H6O3 | 10 mg/50 mg |
- U 89843A
Positive allosteric modulator of GABAA receptors. Enhances GABA-induced Cl- currents in the α1β2γ2, α3β2γ2 and α6β2γ2 subtypes. Causes sedation in vivo following i.v. administration without losing "righting reflex". Also displays antioxidant activity.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204361 | 157013-32-6 | C16H23N5 ·HCl | 10 mg/50 mg |
- U 90042
GABAA receptor ligand that binds with comparable affinities to three receptor subtypes: α1β2γ2, α3β2γ2 and α6β2γ2 (Ki values are 7.8, 9.5 and 11.0 nM respectively). Potentiates GABA-induced chloride currents in α6β2γ2 receptors. Sedative/hypnotic compound.| Katalog # | CAS Nummer | Summenformel | Menge |
|---|
| sc-204362 | 134516-99-7 | C17H13ClN6O | 10 mg/50 mg |
- U 93631
GABAA receptor antagonist that binds picrotoxin site and stabilizes the inactive form of the channel via allosteric interaction. Accelerates decay of GABA-induced Cl- currents with little effect on peak amplitude. Also inhibits 5-HT3A receptors via similar mechanism.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204364 | 152273-12-6 | C17H21N3O2 | 10 mg/50 mg |
- Valerenic acid
Positive allosteric modulator of GABAA receptors that displays preference for β2 or β3 subunit receptors. Directly activates the receptor and also blocks the channel at high concentrations. Displays a anxiolytic and sedative activity in vivo. Also acts as a partial agonist of 5-HT5A receptors.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204377 | 3569-10-6 | C15H22O2 | 1 mg |
- Vigabatrin
Selective GABA-T inhibitor. Anticonvulsant.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204382 | 60643-86-9 | C6H11NO2 | 10 mg/50 mg |
- ZAPA sulfate
A potent, selective GABAA receptor agonist. Demonstrates higher GABAA affinity than muscimol and GABA. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-200471 | 92138-10-8 | C4H6N2O2S ·H2SO4 | 5 mg/25 mg |
- ZK 93423 hydrochloride
Potent benzodiazepine agonist. Non-selective with GABAAreceptors containing α1-, α2-, α3- and α5-subunits. Anxiolytic post systemic administration in vivo. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204422 | 83910-44-5 | C23H22N2O4 ·HCl | 10 mg/50 mg |
- ZK 93426 hydrochloride
Potent, selective and competitive benzodiazepine receptor antagonist (IC50 values are 0.4 and 0.7 nM for inhibition of [3H]-flunitrazepam binding to rat cerebellum and hippocampus respectively). Similar in vivo profile to flumazenil (Ro 15-1788); produces anxiogenic effects in some behavioral tests and anxiolytic effects in others. Orally active.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203727 | 89592-45-0 | C18H20N2O3 ·HCl | 10 mg/50 mg |
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