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  • T4280Gcase activator 1LTI-291;LTI 291;LTI291

    LTI-291 is a glucocerebrosidase (Gcase) activator.

    价 格:¥电议型 号:T4280产 地:中国大陆

  • T2649Menin-MLL inhibitor MI-2MI-2;Menin-MLL inhibitor 2;Menin-MLL Inhibitor;MI 2;MI2

    MI-2 (Menin-MLL Inhibitor) is a potent menin-MLL interaction inhibitor with IC50 of 446 nM.

    价 格:¥电议型 号:T2649产 地:中国大陆

  • T2628RI-2RI 2;RI2

    RI-2 is an optimized RAD51 inhibitor with an IC50 of 44.17 μM in the standard DNA binding assay; specifically inhibits HR(Homologous recombination) repair in human cells.

    价 格:¥电议型 号:T2628产 地:中国大陆

  • T2505NSC 74859S3I201;S3I-201;S3I 201

    S3I-201 is a selective Stat3 inhibitor (IC50: 86±33 μM) and low effect towards STAT1/5.

    价 格:¥电议型 号:T2505产 地:中国大陆

  • T2442CPI203CPI 203;CPI-203

    CPI-203 is an effective BET bromodomain inhibitor (IC50: 37 nM for BRD4).

    价 格:¥电议型 号:T2442产 地:中国大陆

  • T2437O4I2

    O4I2 is an effective Oct3/4 inducer in various human cell lines including human fibroblasts.

    价 格:¥电议型 号:T2437产 地:中国大陆

  • T11689ITI-214ITI214

    ITI214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).

    价 格:¥电议型 号:T11689产 地:中国大陆

  • T0431Abexinostat阿贝司他;PCI-24781;CRA 24781;CRA 024781;PCI 24781;PCI24781

    PCI-24781 (Abexinostat) is a new pan-HDAC inhibitor mainly targeting HDAC1 (Ki: 7 nM), also have moderate inhibitory for HDACs 2, 3, 6, and 10 and greater than 40-fold selectivity against HDAC8. Phase 1/2.

    价 格:¥电议型 号:T0431产 地:中国大陆

  • T0162QuetiapineICI204636;Quetiapin;喹硫平

    Quetiapine is used for the therapy of schizophrenia, and for the treatment of acute manic episodes associated with bipolar I disorder. The mechanism of quetiapine´ action is thought by mediated through antagonist activity at serotonin and dopamine recepto

    价 格:¥电议型 号:T0162产 地:中国大陆

  • T0431PCI-24781PCI-24781,PCI24781,PCI 24781

    PCI-24781 (Abexinostat) is a new pan-HDAC inhibitor mainly targeting HDAC1 (Ki: 7 nM), also have moderate inhibitory for HDACs 2, 3, 6, and 10 and greater than 40-fold selectivity against HDAC8. Phase 1/2.

    价 格:¥电议型 号:T0431产 地:美洲

  • T11397GGTI298GGTI298

    GGTI298 is a CAAZ peptidomimetic geranylgeranyltransferase I (GGTase I) inhibitor, strongly inhibiting the processing of geranylgeranylated Rap1A with little effect on processing of farnesylated Ha-Ras, with IC50 values of 3 and >?20 μM in vivo, respectiv

    价 格:¥电议型 号:T11397产 地:美洲

  • T11594I2906I2906

    I2906 showed antimycobacterial and cytotoxic activity against mycobacterium tuberculosis.?IC50 Value: Target: Antibacterial Under in vitro conditions, I2906 showed excellent antimycobacterial activities and low cytotoxicity.?In a murine model infected wit

    价 格:¥电议型 号:T11594产 地:美洲

  • T11688ITI214 free baseITI214 free base

    ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).

    价 格:¥电议型 号:T11688产 地:美洲

  • T11689ITI214ITI214

    ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM).

    价 格:¥电议型 号:T11689产 地:美洲

  • T15238Epoprostenol sodiumEpoprostenol sodium,Prostaglandin I2 sodium salt,Prostacyclin sodium salt

    Epoprostenol sodium as a potent inhibitor of platelet aggregation is used in pulmonary hypertension and transplantation. Epoprostenol sodium, the synthetic form of the natural prostaglandin derivative prostacyclin, is registered worldwide for the treatmen

    价 格:¥电议型 号:T15238产 地:美洲

  • T2437O4I2O4I2

    O4I2 is an effective Oct3/4 inducer in various human cell lines including human fibroblasts.

    价 格:¥电议型 号:T2437产 地:美洲

  • T2505S3I-201S3I-201,S3I201,S3I 201

    S3I-201 is a selective Stat3 inhibitor (IC50: 86±33 μM) and low effect towards STAT1/5.

    价 格:¥电议型 号:T2505产 地:美洲

  • T2628RI-2RI-2,RI2,RI 2

    RI-2 is an optimized RAD51 inhibitor with an IC50 of 44.17 μM in the standard DNA binding assay; specifically inhibits HR(Homologous recombination) repair in human cells.

    价 格:¥电议型 号:T2628产 地:美洲

  • T2649MI-2MI-2,MI2,MI 2

    MI-2 (Menin-MLL Inhibitor) is a potent menin-MLL interaction inhibitor with IC50 of 446 nM.

    价 格:¥电议型 号:T2649产 地:美洲

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