Search results for '1.'

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  • SCH 39166 hydrobromide

    SCH 39166 hydrobromide is a high affinity dopamine D1/D5 receptor antagonist which displays Ki values of 1.2, 2, 980, 5520, 80 and 731 nM for binding to D1, D5, D2, D4, 5-HT and α2a receptors, respectively. Learn More

    Starting at: $149.00

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  • PF 04885614

    PF 04885614 is a potent NaV1.8 inhibitor (IC50 = 53 nM for human NaV1.8 channel), which exhibits selectivity for hNaV1.8 over hNaV1.6, hNaV1.7, hNaV1.1, hNaV1.2 and hNaV1.5 (IC50 values are 4.2, 7.0, 11, 16 and 27 μM respectively). Learn More

    Starting at: $125.00

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  • XAC

    XAC is an adenosine receptor antagonist (IC50 values are 1.8 and 114 nM at A1 and A2 receptors respectively). Learn More

    Starting at: $95.00

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  • NS 11021

    NS 11021 is an activator of large-conductance Ca2+-activated potassium channels (BKCa, KCa1.1). Learn More

    Starting at: $139.00

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  • PI 828

    PI 828 is a PI 3-Kinase inhibitor with IC50 values of 0.098, 0.183, 0.227 and 1.967 μM for p110β, p110α, p110δ and p110γ respectively. Learn More

    Starting at: $69.00

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  • G-1

    G-1 is a potent and selective GPR30 receptor agonist that increases cytosolic Ca2+ and inhibits migration of SKBr3 cells and MCF-7 cells in response to chemoattractants with IC50 values of 0.7 and 1.6 nM respectively in vitro. Learn More

    Starting at: $139.00

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  • ML 221

    ML 221 is an apelin receptor (APJ) antagonist with IC50 values of 0.70 and 1.75 μM in a cAMP assay and β-arrestin assay, respectively). Learn More

    Starting at: $139.00

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  • ZK 756326

    ZK 756326 is a selective, non-peptide CCR8 chemokine receptor agonist with IC50 values of 1.8 and 2.6 μM for human and mouse receptors respectively. Learn More

    Starting at: $105.00

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  • AC 261066

    AC 261066 is a potent RARβ2 agonist with a pEC50 value of 8.1. Learn More

    Starting at: $139.00

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  • A 844606

    A 844606 is a selective α7 nicotinic acetylcholine receptor (nAChR) agonist with EC50 values of 1.4 and 2.2 μM at human and rat receptors respectively. Learn More

    Starting at: $129.00

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  • ARP 101

    ARP 101 is a selective inhibitor of MMP-2 that displays ~ 600-fold selectivity over MMP-1. Learn More

    Starting at: $115.00

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  • CI 898 trihydrochloride

    CI 898 trihydrochloride is a potent lipophilic inhibitor of dihydrofolate reductase (DHFR) that inhibits protozoal, bacterial and human DHFR with IC50 values of 1.4, 6.1 and 3.2 nM respectively. Learn More

    Starting at: $139.00

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  • Iloprost

    Iloprost is a prostacyclin (PGI2) analog that inhibits platelet aggregation induced by collagen, thrombin and ADP with IC50 values of 0.24, 0.71 and 1.07 nM respectively. Learn More

    Starting at: $239.00

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  • K 858

    K 858 is a selective ATP-uncompetitive mitotic kinesin Eg5 inhibitor that induces mitotic arrest, caspase-3 activation and cell growth inhibition in HCT116 cells with a IC50 value of 1.3 μM. Learn More

    Starting at: $99.00

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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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  • Bucindolol

    Bucindolol is a non-selective β-adrenoceptor antagonist with additional α1-adrenoceptor blocking activity. Ki values are 1.61, 1.20 and 68.9 nM for β1-, β2- and α1-adrenoceptors respectively. Learn More

    Starting at: $139.00

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  • NS 3763

    NS 3763 is a selective non-competitive kainate receptor antagonist that displays selectivity for GLUK5 subunit-containing receptors with IC50 values of 1.6 and > 30 μM for homomeric GLUK5 and GLUK6 receptors respectively. Learn More

    Starting at: $99.00

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  • SCH 202676 hydrobromide

    SCH 202676 hydrobromide is a sulphydryl-reactive compound that inhibits agonist and antagonist binding to G-protein-coupled receptors that inhibits a variety of GPCRs including adenosine, opioid, muscarinic, adrenergic and dopaminergic receptors IC50 values of 0.1-1.8 μM. Learn More

    Starting at: $115.00

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  • Chlorisondamine diiodide

    Chlorisondamine diiodide is an exceptionally long lasting nicotinic antagonist with IC50 value of ~1.6 mM. Learn More

    Starting at: $99.00

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  • GBR 12783 dihydrochloride

    GBR 12783 dihydrochloride is a potent and selective inhibitor of dopamine uptake with IC50 value of 1.8 nM for inhibition of [3H]-dopamine uptake in rat striatal synaptosomes. Learn More

    Starting at: $99.00

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