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  • T64621(tBuBrettPhos Pd(allyl))TfOH salt；化合物 (tBuBrettPhos Pd(allyl))TfOH salt(tBuBrettPhos Pd(allyl))TfOH

    (tBuBrettPhos Pd(allyl))TfOH salt is a useful organic compound for research related to life sciences and the catalog number is T64621.

    价 格：￥电议型 号：T64621产 地：中国大陆

  • T6393ARQ 621；化合物ARQ 621ARQ 621

    ARQ 621 is an allosteric, and selective Eg5 mitotic motor protein inhibitor. Phase 1.

    价 格：￥电议型 号：T6393产 地：中国大陆

  • T63621LRRK2-IN-4；化合物 LRRK2-IN-4LRRK2-IN-4

    LRRK2-IN-4 is a potent, selective, orally active, leucine-rich repeat kinase 2 (LRRK2) inhibitor that crosses the blood-brain barrier with an IC50 value of 2.6 nM. LRRK2-IN-3 has shown investigational potential in Parkinson´s disease.

    价 格：￥电议型 号：T63621产 地：中国大陆

  • T62621pan-HER-IN-2；化合物 pan-HER-IN-2pan-HER-IN-2

    pan-HER-IN-2 (Compound C6) is an orally active, reversible, broad-spectrum HER inhibitor that acts on EGFR (IC50: 0.72 nM), HER4 (IC50: 2.0 nM), EGFRT790M (IC50: 8.2 nM), and L858R (IC50: 75.1 nM). pan-HER-IN-2 induces apoptosis and has anti-tumour effects.

    价 格：￥电议型 号：T62621产 地：中国大陆

  • T62199Talnetant hydrochloride；化合物 Talnetant hydrochlorideTalnetant hydrochloride

    Talnetant (SB 223412) hydrochloride is a selective NK3 receptor antagonist that acts in hNK-3-CHO cells (Ki: 1.4 nM). Talnetant hydrochloride is 100 times more selective for the hNK-3 receptor than the hNK-2 receptor and has no affinity for hNK-1 at a concentration of 100 μM.

    价 格：￥电议型 号：T62199产 地：中国大陆

  • T62198AR524；化合物 AR524AR524

    AR524 is a transgenic inhibitor with higher inhibitory activity than the known transgenic inhibitor kifunensine. AR524 inhibits the formation of human malignant cell spheroids at low concentrations (10 μM).

    价 格：￥电议型 号：T62198产 地：中国大陆

  • T62197Influenza virus-IN-4；化合物 Influenza virus-IN-4Influenza virus-IN-4

    Influenza virus-IN-4 (compound 11e) is a potent inhibitor of influenza virus neuraminidase, acting on H5N1 (IC50: 3.4 μM), H5N2 (IC50: 0.094 μM), H5N6 (IC50: 0.79 μM) and H5N8 (IC50: 0.077 μM). Influenza virus-IN-4 inhibits NA (neuraminidase) and has low cytotoxicity (CC50 > 200 μM). influenza virus-IN-4 is not significantly toxic to mice at 1500 mg/kg.

    价 格：￥电议型 号：T62197产 地：中国大陆

  • T62196CEP-9722；化合物 CEP-9722CEP-9722

    CEP-9722 is a prodrug of CEP-8983, a selective, orally active inhibitor of PARP-1 (IC50: 20 nM) and PARP-2 (IC50: 6 nM).CEP-9722 exhibits anticancer activity.

    价 格：￥电议型 号：T62196产 地：中国大陆

  • T62195Analgesic agent-1；化合物 Analgesic agent-1Analgesic agent-1

    Analgesic agent-1 is a potent analgesic that exhibits significant analgesic activity.

    价 格：￥电议型 号：T62195产 地：中国大陆

  • T62194MEIS-IN-3；化合物 MEIS-IN-3MEIS-IN-3

    MEIS-IN-3 is a potent inhibitor of MEIS.

    价 格：￥电议型 号：T62194产 地：中国大陆

  • T62193PD-1/PD-L1-IN 5；化合物 PD-1/PD-L1-IN 5PD-1/PD-L1-IN 5

    PD-1/PD-L1-IN 5 is a potent PD-1/PD-L1 protein/protein interaction inhibitor (IC50 ≤ 100 nM).

    价 格：￥电议型 号：T62193产 地：中国大陆

  • T62192CDK4/6-IN-9；化合物 CDK4/6-IN-9CDK4/6-IN-9

    CDK4/6-IN-9 (compound 10) is a selective inhibitor of CDK4/6, capable of acting on CDK6/cyclin D1 (IC50: 905 nM). CDK4/6-IN-9 has potential research value in multiple myeloma (MM).

    价 格：￥电议型 号：T62192产 地：中国大陆

  • T62191DNA-PK-IN-5；化合物 DNA-PK-IN-5DNA-PK-IN-5

    DNA-PK-IN-5 is a potent inhibitor of DNA-PK. DNA-PK-IN-5 inhibits the activity of DNA-PKcs, significantly reduces tumour DNA repair and induces apoptosis. DNA-PK-IN-5 improves the sensitivity of tumour tissue to radiotherapy, overcomes drug resistance problems and improves the inhibition of many solid and haematological tumours.

    价 格：￥电议型 号：T62191产 地：中国大陆

  • T62190CSF1R-IN-7；化合物 CSF1R-IN-7CSF1R-IN-7

    CSF1R-IN-7 (Formula I) is a CSF-1R inhibitor that can be used to study Alzheimer´s disease.

    价 格：￥电议型 号：T62190产 地：中国大陆

  • T6219Azilsartan Medoxomil；阿齐沙坦酯TAK-491；TAK-491|||阿齐沙坦酯

    Azilsartan Medoxomil (TAK-491) is an orally administered angiotensin II receptor type 1 antagonist with IC50 of 0.62 nM, which used in the treatment of adults with essential hypertension.

    价 格：￥电议型 号：T6219产 地：中国大陆

  • T62188PIM1-IN-6；化合物 PIM1-IN-6PIM1-IN-6

    PIM1-IN-6 (compound 5h) is a potent inhibitor of PIM-1 (IC50: 0.60 μM).PIM1-IN-6 has a high cytotoxic effect on HCT-116 and MCF-7 cells with IC50 values of 1.51 and 15.2 μM, respectively.

    价 格：￥电议型 号：T62188产 地：中国大陆

  • T62187CSF1R-IN-6；化合物 CSF1R-IN-6CSF1R-IN-6

    CSF1R-IN-6 is a potent inhibitor of CSF1R. CSF1R-IN-6 is a potent inhibitor of CSF1R, which is expressed in macrophages and is dependent on the CSF-1/CSF-1R signalling pathway for survival and differentiation of macrophages. Compound 5).

    价 格：￥电议型 号：T62187产 地：中国大陆

  • T62186ART615；化合物 ART615ART615

    ART615 is a related isomer of ART558. ART615 inhibits Polθ by <10% at 12 μM and is able to act as a control for ART558 (IC50:7.9 nM).

    价 格：￥电议型 号：T62186产 地：中国大陆

  • T62185GABA-AT-IN-1；化合物 GABA-AT-IN-1GABA-AT-IN-1

    GABA-AT-IN-1 (Compound 6) is an inhibitor of γ-aminobutyric acid transaminase (GABA-AT) that crosses the blood-brain barrier.

    价 格：￥电议型 号：T62185产 地：中国大陆

  • T62184NRX-2663；化合物 NRX-2663NRX-2663

    NRX-2663 is an enhancer of the interaction of β-catenin with the homologous E3 ligaseSCFβ-TrCP and has an enhanced effect on the binding of β-catenin to β-TrCP (Kd: 54.8 nM, EC50: 22.9 nM).

    价 格：￥电议型 号：T62184产 地：中国大陆

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