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  • T5093Pim1/AKK1-IN-1LKB1/AAK1 dual inhibitor;MDK-2275

    Pim1/AKK1-IN-1 is a potent multi-kinase inhibitor with Kd values of 35 nM/53 nM/75 nM/380 nM for Pim1/AKK1/MST2/LKB1 respectively, and also inhibits MPSK1 and TNIK.

    价 格:¥电议型 号:T5093产 地:中国大陆

  • T4S1499Ginsenoside Rk1人参皂苷RK1;人参皂苷

    Ginsenoside Rk1 is a component created by processing the ginseng plant at high temperatures. Ginsenoside Rk1 has an anti-inflammatory effect, suppresses the activation of Jak2/Stat3 signaling pathway and NF-κB. It also has an anti-tumor effect.

    价 格:¥电议型 号:T4S1499产 地:中国大陆

  • T4459PK11000

    PK11000 is a p53 targeting compound, has anti-tumor activities through activation of unstable p53.

    价 格:¥电议型 号:T4459产 地:中国大陆

  • T4046BX517BX 517;BX-517;PDK1 inhibitor 2

    BX-517 is a potent and selective inhibitor of PDK1.

    价 格:¥电议型 号:T4046产 地:中国大陆

  • T3722MK-1064MK 1064;MK1064;Urokinase inhibitor 1

    MK-1064 is a selective orexin 2 receptor antagonist (2-SORA).

    价 格:¥电议型 号:T3722产 地:中国大陆

  • T3709XMD8-87ACK1-B19

    XMD8-87 is a TNK2 inhibitor with activity in the inhibition of TNK2 phosphorylation. XMD8-87 and XMD16-5 potently inhibit phosphorylation of TNK2 truncation mutations found in solid tumor types.

    价 格:¥电议型 号:T3709产 地:中国大陆

  • T3588JK184

    JK184 is a potent Hedgehog (Hh) pathway inhibitor.

    价 格:¥电议型 号:T3588产 地:中国大陆

  • T3513GSK180736AGSK180736

    GSK180736A is an effective and selective GRK2 inhibitor (IC50: 0.77 μM) and >100-fold selectivity over other GRKs. It is a weak inhibitor of PKA (IC50: 30 μM), but highly effective against ROCK1 (IC50: 100 nM).

    价 格:¥电议型 号:T3513产 地:中国大陆

  • T3171GSK137647AGSK 137647

    GSK137647A is a selective FFA4 agonist.

    价 格:¥电议型 号:T3171产 地:中国大陆

  • T3153SerabelisibINK1117;MLN1117;TAK-117

    MLN1117 (INK1117) is a p110α/β/γ/δ inhibitor (IC50: 15/4.5/1.9/13.39 μM).

    价 格:¥电议型 号:T3153产 地:中国大陆

  • T3113ForetinibGSK089;EXEL-2880;GSK1363089;XL880

    Foretinib is a broad-spectrum tyrosine kinase inhibitor with IC50s of 0.4 nM and 0.9 nM for Met and KDR.

    价 格:¥电议型 号:T3113产 地:中国大陆

  • T3105PFK-158PFK 158;PFK158

    PFK-158 is an effective and specific inhibitor PFKFB3.

    价 格:¥电议型 号:T3105产 地:中国大陆

  • T28972Tiaramide hydrochlorideFK 1160;FK-1160;FK1160;NTA-194;tiaramide

    Tiaramide hydrochloride is an anti-inflammatory drug that inhibits the action of mediators released from mast cells and has direct smooth muscle relaxant properties.

    价 格:¥电议型 号:T28972产 地:中国大陆

  • T28416PIK-108PIK108;PIK 108

    PIK-108 is an allosteric inhibitor of phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunits β and δ (PI3Kβ/δ).

    价 格:¥电议型 号:T28416产 地:中国大陆

  • T2704MLN0905PLK1 Inhibitor

    MLN0905 is an effective PLK1 inhibitor(IC50=2 nM).

    价 格:¥电议型 号:T2704产 地:中国大陆

  • T2701GSK1292263

    GSK1292263 is a GPR119 agonist and has been investigated for the treatment of DIABETES MELLITUS, TYPE 2.

    价 格:¥电议型 号:T2701产 地:中国大陆

  • T2508BinimetinibMEK162;ARRY-162;ARRY-438162

    Binimetinib (MEK162, ARRY-162, ARRY-438162) is an orally available inhibitor of MEK1/2 (IC50: 12 nM) in a cell-free assay.

    价 格:¥电议型 号:T2508产 地:中国大陆

  • T2455PFK-015PFK15;PFK 015;PFK015

    PFK-015 is an effective inhibitor of PFKFB3 (IC50: 110 nM) and inhibits PFKFB3 activity in Y cells (IC50: 20 nM).

    价 格:¥电议型 号:T2455产 地:中国大陆

  • T22254AlflutinibAST2818;ASK120067

    Alflutinib is an inhibitor of EGFR, and its targets including EGFR activating mutations and T790M, thus leading to tumor growth inhibition.

    价 格:¥电议型 号:T22254产 地:中国大陆

  • T2125Trametinib曲美替尼;JTP-74057;GSK1120212

    Trametinib is an ATP-noncompetitive inhibitor of MEK 1/2 (IC50s: 0.7/0.9 nM). It shows low inhibition for more than 180 kinases, including B-Raf, c-Raf, and MEK5.

    价 格:¥电议型 号:T2125产 地:中国大陆

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