Search results for 'inhibit'

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  • Decynium 22

    Decynium 22 is an inhibitor of the plasma membrane monoamine transporter (PMAT) (Ki = 0.10 μM). Learn More

    Starting at: $49.00

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  • (-)-5'-DMH-CBD

    (-)-5'-DMH-CBD is an anandamide membrane transport inhibitor (IC50 = 14 μM) that is relatively metabolically stable, which displays some affinity for CB2 receptors but has only weak affinity for CB1 receptors and has no activity at VR1 receptors or FAAH. Learn More

    Starting at: $149.00

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  • (±)-McN 5652

    (±)-McN 5652 is a potent, high affinity serotonin re-uptake inhibitor; selective in viv, and displays moderate selectivity over noradrenalin and dopamine re-uptake in vitro (Ki values are 0.68, 2.9 and 36.8 nM for inhibition of serotonin, noradrenalin and dopamine uptake respectively in rat brain synaptosomes). Learn More

    Starting at: $139.00

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  • (±)-MDMA hydrochloride

    (±)-MDMA hydrochloride is a hallucinogenic compound that inhibits 5-HT and dopamine uptake. Learn More

    Starting at: $105.00

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  • VU 0240551

    VU 0240551 is an inhibitor of the neuronal K-Cl cotransporter, KCC2 that also inhibits hERG and L-type Ca2+ channels. Learn More

    Starting at: $115.00

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  • Indatraline hydrochloride

    Indatraline hydrochloride is a potent monoamine uptake inhibitor that inhibits transporters for 5-HT (SERT), dopamine (DAT) and noradrenalin (NET). Learn More

    Starting at: $95.00

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  • WAY 213613

    WAY 213613 is a potent, non-substrate inhibitor of EAAT2 (GLT-1) that displays > 44-fold selectivity over EAAT1 and EAAT3. Learn More

    Starting at: $139.00

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  • LY 2365109 hydrochloride

    LY 2365109 hydrochloride is a potent and selective glycine transporter 1 (GlyT1) inhibitor that induces a dose-dependent elevation in CSF levels of glycine, and enhances acetylcholine and dopamine release in the striatum and prefrontal cortex respectively. Learn More

    Starting at: $149.00

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  • YM 244769

    YM 244769 is an inhibitor of the reverse mode of Na+/Ca2+ exchange (NCX) that inhibits Na+-dependent 45Ca2+ uptake with IC50 values of 18, 68 and 96 nM for CCL39 cells transfected with NCX3, NCX1 and NCX2 respectively. Learn More

    Starting at: $125.00

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  • Concanamycin A

    Concanamycin A is a specific inhibitor of V-type (vacuolar) H+-ATPase that blocks cell surface expression of virus envelope glycoproteins without affecting synthesis and exhibits cytotoxicity in several cell lines. Learn More

    Starting at: $99.00

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  • Sertraline hydrochloride

    Sertraline hydrochloride is a potent, orally active selective serotonin re-uptake inhibitor (SSRI). Learn More

    Starting at: $109.00

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  • GBR 13069 dihydrochloride

    GBR 13069 dihydrochloride is a potent inhibitor of dopamine uptake with an IC50 value of 40 nM. Learn More

    Starting at: $89.00

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  • SCH 28080

    SCH 28080 is a potent inhibitor of H+,K+-ATPase that binds to the K+ recognition site and is competitive with respect to K+. Learn More

    Starting at: $139.00

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  • cis-ACBD

    cis-ACBD is a potent, competitive and selective inhibitor of glutamate uptake. Learn More

    Starting at: $99.00

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  • L-(-)-threo-3-Hydroxyaspartic acid

    L-(-)-threo-3-Hydroxyaspartic acid is a potent, competitive, transportable EAAT1-4 inhibitor/non-transportable EAAT5 inhibitor. Learn More

    Starting at: $149.00

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  • STF 31

    STF 31 is an inhibitor of GLUT1 that inhibits glucose uptake in renal cell carcinoma (RCC) 4 cells. Learn More

    Starting at: $155.00

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  • Org 24598 lithium salt

    Org 24598 lithium salt is a selective inhibitor of the glial glycine transporter (GlyT1). pIC50 values are 6.9, <4 and <3 for GlyT1, GABA transporter and Glyt2 respectively. Learn More

    Starting at: $139.00

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  • Talopram hydrochloride

    Talopram hydrochloride is a potent, selective inhibitor of the noradrenalin transporter (NET) with selectivity for NET against SERT (5-HT transporters) and DAT (dopamine transporters). Learn More

    Starting at: $139.00

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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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  • L-trans-2,4-PDC

    L-trans-2,4-PDC is a potent, competitive, transportable EAAT1-4 inhibitor/non-transportable EAAT5 inhibitor. Learn More

    Starting at: $115.00

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