Search results for 'inhibit'

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  • ML 298 hydrochloride

    ML 298 hydrochloride is a selective inhibitor of phospholipase D2 (PLD2) (IC50 values are 355 and >20,000 nM for PLD2 and PLD1, respectively), which decreases invasive migration in U87-MG glioblastoma cells, without affecting cell viability. Learn More

    Starting at: $125.00

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  • L-651,582

    L-651,582 is an orally active Ca2+ channel blocker which inhibits K+- and carbachol-stimulated Ca2+ influx (IC50 values are 500 and 935 nM respectively). Learn More

    Starting at: $149.00

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  • AMTB hydrochloride

    AMTB hydrochloride is a TRPM8 channel blocker that inhibits icilin- induced TRPM8 channel activation in a rat model. 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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  • Benidipine hydrochloride

    Benidipine hydrochloride is an orally active antihypertensive agent that inhibits L-, N- and T-type Ca2+ channels and also inhibits aldosterone-induced mineralocorticoid receptor activation. Learn More

    Starting at: $109.00

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  • HC 067047

    HC 067047 is a potent and selective TRPV4 antagonist that reversibly inhibits currents through mouse, human and rat TRPV4 orthologs. Learn More

    Starting at: $139.00

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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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  • DCPIB

    DCPIB is a potent, selective blocker of the volume-sensitive anion channel (VSAC) that reverses cell swelling-induced action potential duration shortening in atrial myocytes and inhibits astroglial swelling in vitro. Learn More

    Starting at: $109.00

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  • A 784168

    A 784168 is a potent TRPV1 antagonist with an IC50 value of 25 nM for inhibition of TRPV1 activation by 50 nM capsaicin. Learn More

    Starting at: $139.00

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  • JNJ 17203212

    JNJ 17203212 is a reversible, competitive and potent TRPV1 antagonist that inhibits capsaicin- and H+-induced channel activation and exhibits antitussive and analgesic activity in vivo. Learn More

    Starting at: $119.00

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  • MG 624

    MG 624 inhibits α-Bgtx binding to chick α7 and α4β2 subtypes with Ki values of 106 nM and 84 μM respectively. Learn More

    Starting at: $99.00

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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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  • 9-AC

    9-AC is a Cl- transport inhibitor with a moderate to strong inhibitory action on PKA activated cardiac IcI. Learn More

    Starting at: $65.00

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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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  • 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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  • PNU 37883 hydrochloride

    PNU 37883 hydrochloride acts as a novel antagonist selective for the vascular form of Kir6 (KATP) channel. It inhibits Kir6 currents in isolated mesenteric artery smooth muscle cells (Kd = 65 nM) but not in cardiac or skeletal myocytes. Learn More

    Starting at: $125.00

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  • L-Serine

    L-Serine is an endogenous agonist at the inhibitory glycine receptor. Learn More

    Starting at: $33.00

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  • L-Alanine

    L-Alanine is an Agonist at the inhibitory glycine receptor. Learn More

    Starting at: $33.00

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  • T16Ainh-A01

    T16Ainh-A01 is an inhibitor of Ca2+-dependent Cl- channel (CaCC) transmembrane protein 16A (TMEM16A) (IC50 = 1.8 μM in A253 salivary gland epithelial cells). Learn More

    Starting at: $119.00

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