Search results for 'PR 171'

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  • 3-pyr-Cytisine

    3-pyr-Cytisine is a high affinity α4β2 partial agonist that exhibits antidepressant-like effects in mouse models of antidepressant efficacy. Learn More

    Starting at: $139.00

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  • Levcromakalim

    Levcromakalim is an active enantiomer of the prototypical Kir6 (KATP) channel opener cromakalim. Learn More

    Starting at: $169.00

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  • Cromakalim

    Cromakalim is a prototypical Kir6 (KATP) channel opener that relaxes rabbit isolated portal vein with an IC50 value of 21 nM . Learn More

    Starting at: $139.00

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  • Zatebradine hydrochloride

    Zatebradine hydrochloride is a bradycardic agent that produces use-dependent inhibition of hyperpolarization-activated current If (HCN channel) in sinoatrial node cells and Purkinje fibres. Learn More

    Starting at: $109.00

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  • UCL 2077

    UCL 2077 is a slow afterhyperpolarization (sAHP) channel blocker that reduces sAHP in hippocampal slice preparations. Learn More

    Starting at: $105.00

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  • Zacopride hydrochloride

    Zacopride hydrochloride is a highly potent 5-HT3 receptor antagonist and 5-HT4 receptor agonist with Ki values of 0.38nM and 373nM respectively. Learn More

    Starting at: $105.00

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  • 6-Iodonordihydrocapsaicin

    6-Iodonordihydrocapsaicin is a potent competitive vanilloid TRPV1 (VR1) receptor antagonist that inhibits capsaicin-induced [Ca2+]i increase in rat DRG neurons, and guinea pig bladder and trachea contractions in vitro. Learn More

    Starting at: $115.00

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  • Mirtazapine

    Mirtazapine is an antidepressant agent that enhances noradrenalin (NA) release in rat brain via inhibition of α2-adrenergic autoreceptors and displays only weak affinity for monoamine transporters. Learn More

    Starting at: $85.00

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  • Mecamylamine hydrochloride

    Mecamylamine hydrochloride is a non-competitive nicotinic acetylcholine receptor antagonist that displays antidepressant-like effects in mice. Learn More

    Starting at: $75.00

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  • N20C hydrochloride

    N20C hydrochloride is a selective, non-competitive NMDA receptor antagonist that binds to the receptor-associated ion channel and prevents glutamate-induced Ca2+ influx. Learn More

    Starting at: $99.00

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  • Cesium chloride

    Cesium chloride is a potassium channel blocker that prevents activation of caspase-3 and neuronal apoptosis in serum- and potassium-deprived cerebellar granule neurons by inactivating GSK-3β. Learn More

    Starting at: $39.00

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  • threo Ifenprodil hemitartrate

    threo Ifenprodil hemitartrate is a potent σ receptor agonist and NR2B subunit-selective NMDA receptor antagonist. Learn More

    Starting at: $109.00

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  • Piracetam

    Piracetam is a nootropic that displays cognitive enhancing properties.It facilitates efficiency of cholinergic neurotransmission at muscarinic receptors. Learn More

    Starting at: $55.00

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  • Bepridil hydrochloride

    Bepridil hydrochloride is a calcium channel blocker that inhibits Na+/Ca2+ exchange (NCX), sodium channels and cardiac sarcolemmal KATP channels. Learn More

    Starting at: $75.00

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  • (RS)-AMPA

    (RS)-AMPA is a prototypical and defining agonist for the AMPA subgroup of ionotropic glutamate receptors. Learn More

    Starting at: $139.00

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  • Psora 4

    Psora 4 is a potent KV1.3 channel blocker (EC50 = 3 nM) that preferentially binds the C-type inactivated state of the channel. Learn More

    Starting at: $145.00

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  • PPDA

    PPDA is a subtype-selective NMDA receptor antagonist that preferentially binds to NR2C/NR2D-containing receptors. Learn More

    Starting at: $119.00

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  • Nonactin

    Nonactin is a monovalent cation ionophore that displays selectivity for K+ and NH4+. It also inhibits P-glycoprotein-mediated efflux of chemotherapeutic agents in multiple-drug resistant cancer cells. Learn More

    Starting at: $99.00

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  • Dextromethorphan hydrobromide

    Dextromethorphan hydrobromide is a Non-competitive, low affinity NMDA receptor antagonist with the effect of antitussive, anticonvulsive and neuroprotective. Learn More

    Starting at: $42.00

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  • TNP-ATP triethylammonium salt

    TNP-ATP triethylammonium salt is a high affinity, selective P2X receptor antagonist that inhibits ATP-induced currents in cells expressing P2X1, P2X3 and heteromeric P2X2/3 receptors with IC50 values of 6, 0.9 and 7 nM respectively. Learn More

    Starting at: $189.00

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