santa cruz biotechnology, inc.
SCBT Logo

Willkommen!        Produkt(e) im Warenkorb.     Bestellen
 

GABAergics

  • 2-Hydroxysaclofen
    Selective GABAB antagonist, more potent than saclofen
    Katalog #CAS NummerSummenformelMenge
    sc-202011117354-64-0C9H12CINO4S10 mg/50 mg
  • 3-Methyl-GABA
    Activator of GABA aminotransferase. Anticonvulsant.
    Katalog #CAS NummerSummenformelMenge
    sc-20347171424-95-8C5H11NO210 mg/50 mg
  • 3α,12α-Dihydroxy-5β-pregnan-20-one 3,12-diacetate
    Katalog #CAS NummerSummenformelMenge
    sc-22634715991-93-2C25H38O550 mg
  • 5α-Pregnan-3β-ol-20-one 3β-acetate
    Katalog #CAS NummerSummenformelMenge
    sc-233497906-83-2C23H36O35 g
  • 6,2'-Dihydroxyflavone
    This is a partial inverse agonist at GABAA receptors with a-subunit selectivity.
    Katalog #CAS NummerSummenformelMenge
    sc-300048n.n.C15H10O45 mg
  • 16-Dehydropregnenolone acetate
    Katalog #CAS NummerSummenformelMenge
    sc-224976979-02-2C23H32O310 g
  • 16,17-Epoxy-21-acetoxypregnenolone
    Katalog #CAS NummerSummenformelMenge
    sc-22497728444-97-5C23H32O51 g
  • 16α,17α-Epoxypregnenolone
    Katalog #CAS NummerSummenformelMenge
    sc-223173974-23-2C21H30O35 g/10 g
  • 16α,17α-Epoxypregnenolone acetate
    Katalog #CAS NummerSummenformelMenge
    sc-22497834209-81-9C23H32O45 g
  • 17-PA
    A steroid analog that selectively antagonizes potentiation of GABA responses by 5α-reduced potentiating neurosteroids.
    Katalog #CAS NummerSummenformelMenge
    sc-361075694438-95-4C25H34O10 mg/50 mg
  • 17α-Hydroxypregnenolone
    Katalog #CAS NummerSummenformelMenge
    sc-223186387-79-1C21H32O35 g
  • 17α-Hydroxypregnenolone 3-acetate
    Katalog #CAS NummerSummenformelMenge
    sc-22498041906-06-3C23H34O45 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 NummerSummenformelMenge
    sc-20381423930-19-0C21H32O310 mg/50 mg
  • β-CCB
    Benzodiazepine inverse agonist, putative endogenous ligand
    Katalog #CAS NummerSummenformelMenge
    sc-20442984454-35-3C16H16N2O210 mg/50 mg
  • (±)-Baclofen
    A selective agonist of the GABAB metabotropic receptor. Produces muscle relaxant and antispastic effects. Prototypic agonist at GABAB.
    Katalog #CAS NummerSummenformelMenge
    sc-2004641134-47-0C10H12ClNO21 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 NummerSummenformelMenge
    sc-202498485-49-4C20H17NO650 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 NummerSummenformelMenge
    sc-20048540709-69-1C21H20INO650 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 NummerSummenformelMenge
    sc-20043673604-30-5C21H20BrNO650 mg
  • (-)-Bicuculline methochloride
    Methochloride salt of (+)-bicuculline. Water-soluble GABAA antagonist. More stable than bicuculline. Non-GABA receptor-mediated actions reported.
    Katalog #CAS NummerSummenformelMenge
    sc-20352853552-05-9C21H20ClNO610 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 NummerSummenformelMenge
    sc-20354357717-80-3C19H32O210 mg/50 mg
  • CGP 13501
    Positive allosteric modulator at GABAB receptors, potentiating the effects of GABA at this receptor type.
    Katalog #CAS NummerSummenformelMenge
    sc-20354256189-68-5C19H30O210 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 NummerSummenformelMenge
    sc-203545111205-55-1C18H19N3O210 mg/50 mg
  • CGP 35348
    Katalog #CAS NummerSummenformelMenge
    sc-361138123690-79-9C8H20NO4P10 mg/50 mg
  • CGP 36216
    Katalog #CAS NummerSummenformelMenge
    sc-362724123691-29-2C5H14NO2P10 mg/50 mg
  • CGP 46381
    Katalog #CAS NummerSummenformelMenge
    sc-361140123691-14-5C10H22NO2P10 mg/50 mg
  • CGP 52432
    Katalog #CAS NummerSummenformelMenge
    sc-361141139667-74-6C15H24Cl2NO4P10 mg/50 mg
  • CGP 54626 Hydrochloride
    Katalog #CAS NummerSummenformelMenge
    sc-361142149184-21-4C18H28Cl2NO3P.HCl10 mg/50 mg
  • CGP 55845
    Katalog #CAS NummerSummenformelMenge
    sc-361143149184-22-5C18H22Cl2NO3P•HCl10 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 NummerSummenformelMenge
    sc-2035486001-74-7C6H8ClNS ·HCl10 mg/50 mg
  • Chlormezanone
    Skeletal muscle relaxant, acting at the benzodiazapine site of GABAA receptors
    Katalog #CAS NummerSummenformelMenge
    sc-20388780-77-3C11H12ClNO3S1 g
  • CI 966 hydrochloride
    Selective inhibitor of GAT-1 that is an anticonvulsive and neuroprotective.
    Katalog #CAS NummerSummenformelMenge
    sc-203891110283-66-4C23H22ClF6NO310 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 NummerSummenformelMenge
    sc-20355266548-69-4C13H9F3N410 mg/50 mg
  • Cloflubicyne
    Potent non-competitive GABA antagonist; convulsant; laboratory insecticide.
    Katalog #CAS NummerSummenformelMenge
    sc-300382224790-70-9C11H6Cl2F6N21 mg
  • D-Alanine
    Weak inhibitory glycine receptor agonist.
    Katalog #CAS NummerSummenformelMenge
    sc-203558338-69-2C3H7NO21 g
  • Dansyl-gamma-Amino-n-Butyric Acid Cyclohexylammonium Salt
    Katalog #CAS NummerSummenformelMenge
    sc-29426776563-43-4C16H20N2O4S ·C6H13N100 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 NummerSummenformelMenge
    sc-20257353-43-0C19H28O210 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 NummerSummenformelMenge
    sc-2039218067-24-1C33H45N5O5100 mg
  • DMCM hydrochloride
    Benzodiazepine inverse agonist. Exhibits strong convulsant and anxiogenic activity.
    Katalog #CAS NummerSummenformelMenge
    sc-20529582499-00-1C17H18N2O4 ·HCl10 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 NummerSummenformelMenge
    sc-2944791005-93-2C6H11O4P500 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 NummerSummenformelMenge
    sc-20357733125-97-2C14H16N2O210 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 NummerSummenformelMenge
    sc-20395278538-74-6C13H11N3O100 mg
  • FGIN-1-43
    Potent, specific ligand for mitochondrial diazepam binding inhibitor receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-203953145040-29-5C28H36Cl2N2O10 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 NummerSummenformelMenge
    sc-221630n.n.C6H15ClN4O25 mg
  • GABA
    The major inhibitory neurotransmitter in mammalian central nervous system.
    Katalog #CAS NummerSummenformelMenge
    sc-20305356-12-2C4H9NO210 g/25 g
  • gamma-Acetylenic GABA
    A GABA transaminase inhibitor
    Katalog #CAS NummerSummenformelMenge
    sc-29500257659-38-8C6H9NO21 mg/5 mg
  • Ganaxolone
    A synthetic neurosteroid which functions as a stereoselective positive allosteric modulator of GABAA receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-20358638398-32-2C22H36O210 mg/50 mg
  • GS 39783
    A compound that regulates GABAB receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-20358939069-52-8C15H23N5O2S10 mg/50 mg
  • GS 39783
    This product is a positive allosteric modulator of GABAB receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-30077339069-52-8C15H23N5O2S25 mg
  • Hispidulin
    Potent benzodiazepine (BZD) receptor ligand. Natural sage (Salvia officinalis) flavone. Also has antioxidant, antithrombotic, antifungal, and antiproliferative properties.
    Katalog #CAS NummerSummenformelMenge
    sc-2039991447-88-7C16H12O610 mg
  • Hypotaurine
    Endogenous inhibitory amino acid.
    Katalog #CAS NummerSummenformelMenge
    sc-204005300-84-5C2H7NO2S100 mg
  • Indiplon
    Potent GABAAreceptor positive allosteric modulator. Exhibits sedative, hypnotic, anxiolytic and anticonvulsant activity in vivo and is orally active.
    Katalog #CAS NummerSummenformelMenge
    sc-204011325715-02-4C20H16N4O2S10 mg/50 mg
  • Isoguvacine·HCl
    Isoguvacine is an agonist of Gamma-amino butyric acid (GABA) with similar biochemical features.
    Katalog #CAS NummerSummenformelMenge
    sc-20045164603-90-3C5H10NO2 ·HCl10 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 NummerSummenformelMenge
    sc-204040130477-52-0C18H19N3O410 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 NummerSummenformelMenge
    sc-204061117857-45-1C10H7Cl4N310 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 NummerSummenformelMenge
    sc-2953761449-89-4C5H9O4P500 mg
  • Muscimol
    A structural analog of GABA and a potent, selective agonist of the GABAA receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-2004602763-96-4C4H6N2O25 mg/25 mg
  • NCS-382 Sodium Salt
    γ-Hydroxybutyric acid antagonist, anticonvulsant.
    Katalog #CAS NummerSummenformelMenge
    sc-203444131733-92-1C13H13NaO310 mg/50 mg
  • NCS-382 hydrate
    This product is a γ-Hydroxybutyrate (GHB) receptor antagonist. It displays anti-convulsant activity.
    Katalog #CAS NummerSummenformelMenge
    sc-301458131733-92-1C13H15NaO410 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 NummerSummenformelMenge
    sc-20364560252-41-7C6H11NO2100 mg
  • NNC 05-2090 hydrochloride
    GABA uptake inhibitor; displays moderate selectivity for BGT-1 (mGAT-2) transporters.
    Katalog #CAS NummerSummenformelMenge
    sc-204131184845-43-0C27H30N2O2 ·HCl10 mg/50 mg
  • NNC 711
    Potent and selective inhibitor of GABA uptake by GAT-1. Anticonvulsant following systemic administration in vivo.
    Katalog #CAS NummerSummenformelMenge
    sc-204132145645-62-1C21H22N2O3•HCl10 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 NummerSummenformelMenge
    sc-204150187652-71-7C25H40ClNO310 mg/50 mg
  • Phaclofen
    A selective GABAB receptor antagonist. The phosphonic acid derivative of Baclofen.
    Katalog #CAS NummerSummenformelMenge
    sc-200462114012-12-3C9H13ClNO3P5 mg/25 mg
  • Pregnenolone sulfate sodium salt
    Neurosteroid that has been demonstrated to antagonize the GABAA receptor chloride channel.
    Katalog #CAS NummerSummenformelMenge
    sc-3016091852-38-6C21H31NaO5S25 mg
  • Primidone
    Anticonvulsant. Potentiates GABAA receptor function.
    Katalog #CAS NummerSummenformelMenge
    sc-204861125-33-7C12H14N2O2100 mg
  • Propybicyphat
    Demonstrated GABA-gated chloride channel blocker, non-competitive GABA antagonist in mammals.
    Katalog #CAS NummerSummenformelMenge
    sc-30161551486-74-9C7H13O4P1 mg
  • R-(+)-Baclofen (free base)
    Selective GABAB receptor agonist. Skeletal muscle relaxant. The more active enantiomer of (±)-Baclofen (sc-200464)
    Katalog #CAS NummerSummenformelMenge
    sc-20322869308-37-8C10H12ClNO210 mg/50 mg
  • R-(+)-Baclofen hydrochloride
    Selective GABAB receptor agonist. Skeletal muscle relaxant. The more active enantiomer of (±)-Baclofen (sc-200464)
    Katalog #CAS NummerSummenformelMenge
    sc-20322963701-55-3C10H12ClNO2•HCl10 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 NummerSummenformelMenge
    sc-204228123557-91-5C17H21F3O310 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 NummerSummenformelMenge
    sc-20368391917-65-6C15H14N6O310 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 NummerSummenformelMenge
    sc-20368499632-94-7C15H17N3O3S10 mg/50 mg
  • S(+)-gamma-Vinyl-GABA
    Selective GABA transaminase inhibitor. Active enantiomer. Potential usefulness in treating cocaine addiction.
    Katalog #CAS NummerSummenformelMenge
    sc-22227974046-07-4C6H11NO25 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 NummerSummenformelMenge
    sc-204257157604-55-2C30H35NO610 mg/50 mg
  • Saclofen
    A selective antagonist of the GABAB receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-203252125464-42-8C9H12CINO3S10 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 NummerSummenformelMenge
    sc-204263160296-13-9C17H18N2O3S10 mg/50 mg
  • SCH 50911
    Katalog #CAS NummerSummenformelMenge
    sc-361352160415-07-6C8H15NO310 mg/50 mg
  • SCS
    Partial inhibitor of β1-containing GABAA receptors. May bind allosterically to a novel site on GABAA receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-2033753232-36-8C14H12N2O350 mg
  • SK&F 97541
    SK&F 97541 is a very potent GABAB agonist, at least ten times more active than baclofen.
    Katalog #CAS NummerSummenformelMenge
    sc-200469127729-35-5C4H12NO2P5 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 NummerSummenformelMenge
    sc-203701104104-50-9C15H17N3O3 ·HBr10 mg/50 mg
  • TACA
    GABAA and GABAC agonist. Also GABA-T substrate and GABA uptake inhibitor. Trans-isomer of CACA.
    Katalog #CAS NummerSummenformelMenge
    sc-20370538090-53-8C4H7NO210 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 NummerSummenformelMenge
    sc-204322207306-50-1C15H17NO2S310 mg/50 mg
  • Thiocolchicoside
    A potent, competitive antagonist of GABAA receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-202839602-41-5C27H33NO10S1 mg/5 mg
  • Thiomuscimol
    A structural analog of GABAA.
    Katalog #CAS NummerSummenformelMenge
    sc-21303562020-54-6C4H6N2OS10 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 NummerSummenformelMenge
    sc-20434264603-91-4C6H8N2O2 ·HCl50 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 NummerSummenformelMenge
    sc-204352182485-36-5C6H12NO2P10 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 NummerSummenformelMenge
    sc-20370941094-88-6C16H24N4O2•HCl•xH2O10 mg/50 mg
  • trans-4-Hydroxycrotonic acid
    Katalog #CAS NummerSummenformelMenge
    sc-20371024587-49-3C4H6O310 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 NummerSummenformelMenge
    sc-204361157013-32-6C16H23N5 ·HCl10 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 NummerSummenformelMenge
    sc-204362134516-99-7C17H13ClN6O10 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 NummerSummenformelMenge
    sc-204364152273-12-6C17H21N3O210 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 NummerSummenformelMenge
    sc-2043773569-10-6C15H22O21 mg
  • Vigabatrin
    Selective GABA-T inhibitor. Anticonvulsant.
    Katalog #CAS NummerSummenformelMenge
    sc-20438260643-86-9C6H11NO210 mg/50 mg
  • ZAPA sulfate
    A potent, selective GABAA receptor agonist. Demonstrates higher GABAA affinity than muscimol and GABA.
    Katalog #CAS NummerSummenformelMenge
    sc-20047192138-10-8C4H6N2O2S ·H2SO45 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 NummerSummenformelMenge
    sc-20442283910-44-5C23H22N2O4 ·HCl10 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 NummerSummenformelMenge
    sc-20372789592-45-0C18H20N2O3 ·HCl10 mg/50 mg