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  • T2039GSK923295GSK923295

    GSK923295 is a selective allosteric inhibitor of CENP-E kinesin motor ATPase(Ki=3.2 nM).

    价 格:¥电议型 号:T2039产 地:美洲

  • T2049GS967GS967,GS458967,

    GS967 is a potent, and selective inhibitor of cardiac late sodium current (late INa ).

    价 格:¥电议型 号:T2049产 地:美洲

  • T2073GSK-2636771GSK-2636771,GSK2636771,GSK 2636771

    GSK2636771, an effective, specific, orally bioavailable, PI3Kβ inhibitor, has been used in cancer, lymphoma, solid neoplasm, recurrent solid neoplasm, and advanced malignant neoplasm.

    价 格:¥电议型 号:T2073产 地:美洲

  • T2079GSK126GSK126,GSK2816126A,EZH2 inhibitor

    GSK126 is a excellently specific EZH2 methyltransferase inhibitor ( IC50=9.9 nM).

    价 格:¥电议型 号:T2079产 地:美洲

  • T2117PSI6206PSI6206,GS-331007,RO 2433

    PSI-6206 (RO2433) is a selective HCV RNA polymerase inhibitor.

    价 格:¥电议型 号:T2117产 地:美洲

  • T2120I-BET151I-BET151,GSK1210151A,

    I-BET151 (GSK1210151A) is a specific BET inhibitor for BRD2/3/4 (IC50: 0.5/0.25/0.79 μM, in cell-free assays).

    价 格:¥电议型 号:T2120产 地:美洲

  • T2125TrametinibTrametinib,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:美洲

  • T2240GSK2578215AGSK2578215A

    GSK2578215A is a potent and selective LRRK2 kinase inhibitor.

    价 格:¥电议型 号:T2240产 地:美洲

  • T2281GSK-2256098GSK-2256098,GSK2256098,GSK 2256098

    GSK-2256098 is a small molecule FAK kinase inhibitor.

    价 格:¥电议型 号:T2281产 地:美洲

  • T2315GSK-LSD1 dihydrochlorideGSK-LSD1 dihydrochloride,GSK-LSD1 2HCl,

    GSK-LSD1 2HCl is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).

    价 格:¥电议型 号:T2315产 地:美洲

  • T2329Dolutegravir sodiumDolutegravir sodium,GSK-1349572A,GSK1349572

    Dolutegravir sodium salt(DTG; GSK1349572) is an HIV integrase inhibitor(IC50: 2.7 nM), modest activity against raltegravir-resistant signature mutants Y143R, Q148K, N155H, and G140S/Q148H.

    价 格:¥电议型 号:T2329产 地:美洲

  • T2357GSK-1059615GSK-1059615,GSK1059615,GSK 1059615

    GSK1059615 has been used in trials studying the treatment of Lymphoma, Solid Tumours, Endometrial Cancer, Solid Tumor Cancer, and Metastatic Breast Cancer.

    价 格:¥电议型 号:T2357产 地:美洲

  • T2409Tenofovir alafenamideTenofovir alafenamide,GS-7340,

    Tenofovir Alafenamide (GS-7340) is a nucleotide reverse transcriptase inhibitor (NRTI) and a novel ester prodrug of the antiretroviral tenofovir.

    价 格:¥电议型 号:T2409产 地:美洲

  • T2436GSK2801GSK2801

    GSK2801 is an effective, specific and cell active acetyl-lysine competitive inhibitor of BAZ2A(Kd: 136 nM) and BAZ2B(Kd: 257 nM) bromodomains.

    价 格:¥电议型 号:T2436产 地:美洲

  • T2614GSK2606414GSK2606414

    GSK2606414 is an oral-available and specific PERK inhibitor (IC50=0.4 nM).

    价 格:¥电议型 号:T2614产 地:美洲

  • T2622GSK650394GSK650394

    GSK650394 is a serum- and glucocorticoid-regulated kinase-1 inhibitor.

    价 格:¥电议型 号:T2622产 地:美洲

  • T2633GSK429286AGSK429286A,RHO-15,

    GSK429286A is a specific inhibitor of ROCK1/2 (IC50: 14/63 nM).

    价 格:¥电议型 号:T2633产 地:美洲

  • T2654GSK2656157GSK2656157

    GSK2656157 is a highly specific and ATP-competitive PERK inhibitor (IC50: 0.9 nM) in a cell-free assay. The selectivty is 500-fold higher against a panel of 300 kinases.

    价 格:¥电议型 号:T2654产 地:美洲

  • T2674GSK0660GSK0660

    GSK0660 is an antagonist and inverse agonist of PPARβ/δ.

    价 格:¥电议型 号:T2674产 地:美洲

  • T2682AcalisibAcalisib,CAL-120,GS-9820

    Acalisib (GS-9820) is a potent and selective inhibitor of PI3Kδ.

    价 格:¥电议型 号:T2682产 地:美洲

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