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产品数:86101

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  • T10717CBP-IN-1CBP-IN-1

    CBP-IN-1 is a potent inhibitor of p300/CBP bromodomain.

    价 格:¥电议型 号:T10717产 地:美洲

  • T10721CD73-IN-1CD73-IN-1

    CD73-IN-1 is an inhibitor of CD73 with anticancer activity extracted from patent WO 2017153952 A1 (example 80).

    价 格:¥电议型 号:T10721产 地:美洲

  • T10723CDC25B-IN-1CDC25B-IN-1

    CDC25B-IN-1 is a potent inhibitor of cell division cycle 25B (CDC25B) phosphatase (Ki: 8.5 μM). It potently inhibits cell proliferation and colony formation.

    价 格:¥电议型 号:T10723产 地:美洲

  • T10724Cdc7-IN-1Cdc7-IN-1

    Cdc7-IN-1 is a highly selective and ATP competitive inhibitor of Cdc7 kinase (IC50: 0.6 nM at 1 mM ATP). It potently inhibits Cdc7 activity in cancer cells and effectively induces cell death.

    价 格:¥电议型 号:T10724产 地:美洲

  • T10740CDK8-IN-1CDK8-IN-1

    CDK8-IN-1 is a selective CDK8 inhibitor (IC50: 3 nM).

    价 格:¥电议型 号:T10740产 地:美洲

  • T10741CDK9-IN-1CDK9-IN-1

    CDK9-IN-1 is a novel, selective CDK9 inhibitor for the treatment of HIV infection (IC50: 39 nM for CDK9/CycT1).

    价 格:¥电议型 号:T10741产 地:美洲

  • T10765Cereblon modulator 1Cereblon modulator 1

    Cereblon modulator 1 is a cereblon (CRBN) E3 ligase modulator. It specifically binds to CRBN, thereby affecting the activity of the ubiquitin E3 ligase complex.

    价 格:¥电议型 号:T10765产 地:美洲

  • T10782CGP52411CGP52411,DAPH,

    CGP52411 (DAPH) is a highly selective, orally active, and ATP-competitive EGFR inhibitor (IC50: 0.3 μM). It blocks the toxic influx of Ca2+ ions into neuronal cells and dramatically inhibits and reverses the formation of β-amyloid (Aβ42) fibril aggregates

    价 格:¥电议型 号:T10782产 地:美洲

  • T10787Chitise-IN-1Chitise-IN-1,Chitinase-IN-1,

    Chitinase-IN-1 is an insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide.

    价 格:¥电议型 号:T10787产 地:美洲

  • T10836CLK1-IN-1CLK1-IN-1

    CLK1-IN-1 is a potent and selective inhibitor of the Cdc2-like kinase 1 (CLK1; IC50: 2 nM).

    价 格:¥电议型 号:T10836产 地:美洲

  • T10853CNT2 inhibitor-1CNT2 inhibitor-1

    CNT2 inhibitor-1 is a potent inhibitor of concentrative nucleoside transporter 2 (CNT2; IC50: 640 nM for hCNT2).

    价 格:¥电议型 号:T10853产 地:美洲

  • T10863Complement C5-IN-1Complement C5-IN-1

    Complement C5-IN-1 is a small-molecule inhibitor of complement component 5 protein (C5).

    价 格:¥电议型 号:T10863产 地:美洲

  • T10865Cot inhibitor-1Cot inhibitor-1

    Cot inhibitor-1 is an inhibitor of COT/Tpl2.

    价 格:¥电议型 号:T10865产 地:美洲

  • T10884CRAC intermediate 1CRAC intermediate 1

    CRAC intermediate 1 is a key intermediate in the chemical synthesis of a series of CRAC channel inhibitors.

    价 格:¥电议型 号:T10884产 地:美洲

  • T1092ZolmitriptanZolmitriptan,BW-311C90,311C90

    Zolmitriptan selectively binds to and activates serotonin (5-HT) 1B receptors expressed in intracranial arteries and 5-HT 1D receptors located on peripheral trigeminal sensory nerve terminals in the meninges and central terminals in brainstem sensory nucl

    价 格:¥电议型 号:T1092产 地:美洲

  • T13251UKI-1UKI-1,UKI-1C,

    UKI-1 is a urokinase-type plasminogen activator system synthetic inhibitor.

    价 格:¥电议型 号:T13251产 地:美洲

  • T13261CCK-B Receptor Antagonist 1CCK-B Receptor Antagonist 1

    CCK-B Receptor Antagonist 1 is an cholecystokinin B (CCK-B) receptorant agonist, and has the potential of reducing the secretion of gastric acid.

    价 格:¥电议型 号:T13261产 地:美洲

  • T13572Cancer-Targeting Compound 1Cancer-Targeting Compound 1

    Cancer-Targeting Compound 1, extracted from patent WO 2008021331 A2, is used in the research of hormone-related cancer.

    价 格:¥电议型 号:T13572产 地:美洲

  • T14860CaMKII-IN-1CaMKII-IN-1

    CaMKII-IN-1 is a potent and highly selective CaMKII inhibitor (IC50: 63 nM). It has significantly high selectivity against CaMKIV, MLCK, p38a, Akt1, and PKC.

    价 格:¥电议型 号:T14860产 地:美洲

  • T14960Chroman 1Chroman 1

    Chroman 1 is an inhibitor of ROCK2 (IC50: 1 nM).

    价 格:¥电议型 号:T14960产 地:美洲

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