Signal Transduction

Items 61 to 80 of 85 total

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  • CCG 50014

    CCG 50014 is a potent and selective inhibitor of regulator of G-protein signaling 4 (RGS4) protein that exhibits >20-fold selectivity for RGS4 over other RGS proteins. Learn More

    Starting at: $125.00

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  • SecinH3

    SecinH3 is a sec7-specific GEF inhibitor that inhibits insulin signaling via inhibition of insulin receptor substrate protein (IRS) phosphorylation. Learn More

    Starting at: $169.00

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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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  • 8-Bromo-cGMP, sodium salt

    Membrane permeable cGMP analog that activates protein kinase G (PKG). 4.3-fold more potent than cGMP in activating PKG1α and promotes relaxation of tracheal and vascular smooth muscle tissue in vitro. Learn More

    Starting at: $55.00

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  • Gue 1654

    Gue 1654 is an oxoeicosanoid receptor 1 (OXE-R) modulator, which selectively inhibits Gβγ but not Gαi signaling upon activation of the Gαi-βγ heterotrimer by OXE-R. Learn More

    Starting at: $90.00

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  • Gallein

    Gallein is an inhibitor of G protein βγ subunit-dependent signaling, which blocks PI 3-kinase and Rac1 activation in HL60 cells and chemotaxis in HL60 differentiated cells. Learn More

    Starting at: $55.00

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  • CCG 2046

    CCG 2046 is an inhibitor of regulator of G-protein signaling 4 (RGS4), which reduces the RGS4-Gαo protein-protein interaction signal. Learn More

    Starting at: $90.00

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  • SD 1008

    SD 1008 is a JAK2/STAT3 signaling pathway inhibitor, which inhibits activation of STAT3, JAK2 and Src. Learn More

    Starting at: $109.00

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  • MDL 28170

    MDL 28170 is a potent, selective inhibitor of calpain and cathepsin B that rapidly penetrates the blood-brain barrier following systemic administration and displays neuroprotective effects in vivo. Learn More

    Starting at: $65.00

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  • Calpeptin

    Calpeptin is a potent, cell-permeable inhibitor of the Ca2+-dependent protease, calpain. Prevents collagen- and thrombin-induced platelet aggregation, probably by blocking calpain induced phospholipase C and thromboxane synthase activation. Learn More

    Starting at: $90.00

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  • Carbenoxolone disodium

    Carbenoxolone disodium is a glucocorticoid that inhibits 11β-hydroxysteroid dehydrogenase (11-HSD) and blocks gap junction communication. Learn More

    Starting at: $65.00

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  • SR 11302

    SB 205384 is a GABAA receptor modulator; slows current decay. Learn More

    Starting at: $110.00

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  • HPI 1

    HPI 1, a Hedgehog (Hh) signaling inhibitor, inhibits Sonic hedgehog (Shh)-, SAG- and Gli-induced Hh pathway activation in Shh-LIGHT2 cells with IC50 values of 1.5, 1.5, 4 and 6 μM for Shh-, SAG-, Gli2- and Gli1-induced activation. Learn More

    Starting at: $129.00

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  • 20(S)-Hydroxycholesterol

    20(S)-Hydroxycholesterol is a allosteric activator of the Hedgehog signaling pathway Smoothened (Smo) oncoprotein that activates Hedgehog (Hh) signaling (EC50 ~ 3μM for induction of Hh reporter gene transcription in in NIH 3T3 cells). Learn More
  • Jervine

    Jervine is an inhibitor of Hedgehog signaling (IC50 = 500 - 700 nM), which binds directly to Smoothened (Smo), and inhibits the response of target tissues to Sonic hedgehog signaling, possibly via the sterol sensing domain of Patched. Learn More

    Starting at: $159.00

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  • AY 9944 dihydrochloride

    AY 9944 dihydrochloride is an inhibitor of hedgehog (Hh) signaling, possibly via several mechanisms, which inhibits Δ7-dehydrocholesterol reductase (IC50 = 13 nM), thus reduces cholesterol biosynthesis, and also inhibits cholesterol esterification. Learn More

    Starting at: $119.00

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  • SANT-2

    SANT-2 is an inhibitor of Sonic hedgehog (Shh) signaling; antagonizes smoothened receptor activity (KD = 12 nM), which displays allosteric binding characteristics similar to SANT-1. Displaces smo-[3H]SAG-1.3 and -[3H]Cyclopamine binding (Ki values are 7.8 nM and 8.4 nM respectively). Learn More

    Starting at: $139.00

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  • U 18666A

    U 18666A is an inhibitor of cholesterol synthesis and cellular transport, and weak inhibitor of hedgehog (Hh) signaling. Learn More

    Starting at: $139.00

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  • Ciliobrevin A

    Ciliobrevin A is a hedgehog (Hh) pathway antagonist which blocks Sonic hedgehog (Shh)-induced Hh pathway activation (IC50 = 7 μM) downstream of Smo. Learn More

    Starting at: $119.00

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  • MG 132

    MG 132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 μM) which inhibits TNF-α-induced NF-κB activation and IκBα degradation. Learn More

    Starting at: $75.00

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