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  • T12853SBI-477

    SBI-477 is a chemical probe stimulated insulin signaling by deactivating the transcription factor MondoA. SBI-477 coordinately inhibits triacylglyceride (TAG) synthesis and enhances basal glucose uptake in human skeletal myocytes.

    价 格：￥电议型 号：T12853产 地：中国大陆

  • T1258NabumetoneBRL14777；萘丁美酮

    Nabumetone(BRL14777) is a non-steroidal anti-inflammatory drug and its active metabolite 6MNA inhibits the enzymes cyclo-oxygenase I and II.

    价 格：￥电议型 号：T1258产 地：中国大陆

  • T12477Uzansertib phosphateINCB053914 phosphate

    INCB053914 phosphate is an orally active, ATP-competitive inhibitor of pan-PIM kinase(PIM1, PIM2, PIM3 with IC50s of 0.24 nM, 30 nM, 0.12 nM , respectively).

    价 格：￥电议型 号：T12477产 地：中国大陆

  • T10590ZatolmilastBPN14770

    BPN14770 is an allosteric inhibitor of selective phosphodiesterase 4D (PDE4D; IC50s: 7.8 nM and 7.4 nM for PDE4D7 and PDE4D3).

    价 格：￥电议型 号：T10590产 地：中国大陆

  • T10477BAY-985

    BAY-985 is a potent, selective, and orally active ATP-competitive dual inhibitor of TBK1 and IKKε (IC50s: 2/30 and 2 nM for TBK1 (low/high ATP) and IKKε) with antitumor efficacy.

    价 格：￥电议型 号：T10477产 地：中国大陆

  • T0477Zileuton齐留通；A 64077；Abbott 64077

    Zileuton is a synthetic derivative of hydroxyurea with antiasthmatic properties. The leukotriene inhibitor zileuton blocks 5-lipoxygenase, which catalyzes the formation of leukotrienes from arachidonic acid; causes bronchodilation; decreases bronchial muc

    价 格：￥电议型 号：T0477产 地：中国大陆

  • T0178Saxagliptin hydrate沙格列汀单水化合物；BMS-477118 hydrate；Onglyza hydrate

    Saxagliptin is a selective and reversible DPP4 inhibitor (IC50: 26 nM; Ki: 1.3 nM).

    价 格：￥电议型 号：T0178产 地：中国大陆

  • T0178Saxagliptin hydrateSaxagliptin hydrate,BMS-477118 hydrate,Onglyza hydrate

    Saxagliptin is a selective and reversible DPP4 inhibitor (IC50: 26 nM; Ki: 1.3 nM).

    价 格：￥电议型 号：T0178产 地：美洲

  • T0477ZileutonZileuton,Abbott 64077,A 64077

    Zileuton is a synthetic derivative of hydroxyurea with antiasthmatic properties. The leukotriene inhibitor zileuton blocks 5-lipoxygenase, which catalyzes the formation of leukotrienes from arachidonic acid; causes bronchodilation; decreases bronchial muc

    价 格：￥电议型 号：T0477产 地：美洲

  • T10477BAY-985BAY-985

    BAY-985 is a potent, selective, and orally active ATP-competitive dual inhibitor of TBK1 and IKKε (IC50s: 2/30 and 2 nM for TBK1 (low/high ATP) and IKKε) with antitumor efficacy.

    价 格：￥电议型 号：T10477产 地：美洲

  • T11477GSK1059865GSK1059865

    GSK1059865 is a potent orexin 1 receptor antagonist.

    价 格：￥电议型 号：T11477产 地：美洲

  • T12193NCGC00247743NCGC00247743

    NCGC00247743 is an inhibitor of histone lysine demethylase KDM4.

    价 格：￥电议型 号：T12193产 地：美洲

  • T12477INCB053914 phosphateINCB053914 phosphate

    INCB053914 phosphate is an orally active, ATP-competitive inhibitor of pan-PIM kinase(PIM1, PIM2, PIM3 with IC50s of 0.24 nM, 30 nM, 0.12 nM , respectively).

    价 格：￥电议型 号：T12477产 地：美洲

  • T1258NabumetoneNabumetone,BRL14777,

    Nabumetone(BRL14777) is a non-steroidal anti-inflammatory drug and its active metabolite 6MNA inhibits the enzymes cyclo-oxygenase I and II.

    价 格：￥电议型 号：T1258产 地：美洲

  • T12853SBI-477SBI-477

    SBI-477 is a chemical probe stimulated insulin signaling by deactivating the transcription factor MondoA. SBI-477 coordinately inhibits triacylglyceride (TAG) synthesis and enhances basal glucose uptake in human skeletal myocytes.

    价 格：￥电议型 号：T12853产 地：美洲

  • T14774Bragsin1Bragsin1

    Bragsin1 is a potent, selective and noncompetitive inhibitor of the ArfGEF BRAG2. Which inhibits Arf GTPase activation, with an IC50 of 3 μM. Bragsin1 has no effect on the Sec7 domain of human ArfGEFs. Anti-cancer activity[1]. Bragsin1 binds to PH domain

    价 格：￥电议型 号：T14774产 地：美洲

  • T14779BRD7389BRD7389

    BRD7389 is a small-molecule inducer of insulin expression in pancreatic α-cells and it is a specific RSK family kinase inhibitor with IC50s of 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3, respectively.

    价 格：￥电议型 号：T14779产 地：美洲

  • T15477Hexaminolevulite hydrochlorideHexaminolevulite hydrochloride,Hexaminolevulinate hydrochloride,Hexyl

    Hexaminolevulinate hydrochloride has approved for cystoscopic detection of papillary bladder cancer and it also is a fluorescent agent.

    价 格：￥电议型 号：T15477产 地：美洲

  • T16145MS-444MS-444,BE-34776,

    MS-444 suppresses the activity of purified smooth muscle myosin light chain kinase (MLCK) (IC50: 10 μM).

    价 格：￥电议型 号：T16145产 地：美洲

  • T16332NKH477NKH477,Colforsin dapropate hydrochloride,

    NKH477 is a novel water-soluble forskolin derivative that improves cardiac failure mainly through its beneficial effects on diastolic cardiac function. NKH477 shows an antiproliferative effect in vivo with an altered cytokine profile to inhibit the acute

    价 格：￥电议型 号：T16332产 地：美洲

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