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  • T5193Danirixin；化合物DanirixinGSK1325756；GSK1325756

    Danirixin (GSK1325756) is a potent antagonist of CXCR2 that inhibits IL-8 binding to CXCR2 (IC50: 12.5 nM).

    价 格：￥电议型 号：T5193产 地：中国大陆

  • T5097Ezatiostat；化合物EzatiostatTER199(free base)|||TLK199；TER199(free base)|||TLK199

    Ezatiostat (TER199(free base)) is a tripeptide analog of glutathione that can selectively inhibit GSTP1-1 catalytic activity.

    价 格：￥电议型 号：T5097产 地：中国大陆

  • T5093Pim1/AKK1-IN-1；化合物Pim1/AKK1-IN-1LKB1/AAK1 dual inhibitor|||MDK-2275；LKB1/AAK1 dual inhibitor|||MDK-2

    Pim1/AKK1-IN-1 (LKB1/AAK1 dual inhibitor) 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；化合物PK11000PK11000

    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

  • T4198T.cruzi-IN-1；T.cruzi InhibitorMDK1088|||T.cruzi Inhibitor；MDK1088|||T.cruzi Inhibitor

    T.cruzi-IN-1 (MDK1088) is a Trypanosoma cruzi inhibitor.

    价 格：￥电议型 号：T4198产 地：中国大陆

  • T41166NVS PAK1 C；NVS PAK1 CNVS PAK1 C

    NVS PAK1 C is a negative control of NVS PAK1 1, a potent and selective PAK1 inhibitor.

    价 格：￥电议型 号：T41166产 地：中国大陆

  • T41124Kizuta saponin K11；Kizuta saponin K11Kizuta saponin K11

    Kizuta saponin K11 is a saponin derived from Kalopanax pictum var. maximowiczii leaves, which is a widely used Korean medicinal plant.

    价 格：￥电议型 号：T41124产 地：中国大陆

  • T41085UK122UK122UK122

    UK122 is a highly effective and specific inhibitor of urokinase-type plasminogen activator (uPA) with an IC50 value of 0.2 μM. It displays negligible to minimal inhibition towards tissue-type plasminogen activator (tPA), plasmin, thrombin, and trypsin (all IC50 >100 μM). Functioning as a 4-oxazolidinone analogue, UK122 is an anticancer agent that effectively inhibits cancer cell migration and invasion.

    价 格：￥电议型 号：T41085产 地：中国大陆

  • T40577TAK1-IN-3；TAK1 抑制剂3TAK1-IN-3；TAK1-IN-3

    TAK1-IN-3 is a novel ATP-competitive TAK1 inhibitor for the study of cancer.

    价 格：￥电议型 号：T40577产 地：中国大陆

  • T4046BX517；化合物BX517PDK1 inhibitor 2|||BX 517|||BX-517；PDK1 inhibitor 2|||BX 517|||BX-517

    BX517 (PDK1 inhibitor 2) is a potent and selective inhibitor of PDK1.

    价 格：￥电议型 号：T4046产 地：中国大陆

  • T40396FgGpmk1-IN-1FgGpmk1-IN-1FgGpmk1-IN-1

    FgGpmk1-IN-1 is a new inhibitor of the fusarium graminearum mitogen-activated protein kinase (FgGpmk1), displaying a potency with an EC50 value of 3.46 μg/mL.

    价 格：￥电议型 号：T40396产 地：中国大陆

  • T40350HPK1-IN-4；化合物HPK1-IN-4HPK1-IN-4；HPK1-IN-4

    HPK1-IN-4 is an HPK1 (MAPK41) inhibitor with an IC 50 of 0.061 nM. HPK1-IN-4 is often used as a preclinical immunotherapy tool compound.

    价 格：￥电议型 号：T40350产 地：中国大陆

  • T40348TTBK1-IN-1；TTBK1-IN-1TTBK1-IN-1；TTBK1-IN-1

    TTBK1-IN-1 is a highly potent and selective inhibitor of tau tubulin kinase 1 (TTBK1), capable of penetrating the blood-brain barrier with ease. With an IC 50 value of 2.7 nM, TTBK1-IN-1 exhibits strong inhibitory activity against TTBK1. This compound holds great promise for advancing research in Alzheimer´s disease and other tauopathies.

    价 格：￥电议型 号：T40348产 地：中国大陆

  • T40290CDK12-IN-5；CDK12-IN-5CDK12-IN-5；CDK12-IN-5

    CDK12-IN-5 is a pyrazolotriazine compound that effectively inhibits CDK12, with an IC50 value of 23.9 nM at a high ATP concentration of 2 mM. However, CDK12-IN-5 does not exhibit inhibitory effects on CDK2/Cyclin E (IC50 = 173 μM) and CDK9/Cyclin T1 (IC50 = 127 μM) at the same high ATP concentration of 2 mM, as stated in WO2021116178A1.

    价 格：￥电议型 号：T40290产 地：中国大陆

  • T40289CDK12-IN-6CDK12-IN-6CDK12-IN-6

    CDK12-IN-6, a pyrazolotriazine compound, is a powerful inhibitor of CDK12. Its inhibitory activity is significant with an IC50 value of 1.19 μM when tested at high ATP concentration (2 mM). Notably, CDK12-IN-6 does not exhibit any inhibitory effect on CDK2/Cyclin E (IC50 >20 μM) and CDK9/Cyclin T1 (IC50 >20 μM) when tested under the same high ATP conditions (2 mM) (WO2021116178A1).

    价 格：￥电议型 号：T40289产 地：中国大陆

  • T40288CDK12-IN-4CDK12-IN-4CDK12-IN-4

    CDK12-IN-4, a pyrazolotriazine compound, exhibits potent inhibition of CDK12 by achieving an IC50 value of 0.641 μM, utilizing high ATP levels (2 mM). Notably, CDK12-IN-4 does not impact CDK2/Cyclin E (IC50 > 20 μM) or CDK9/Cyclin T1 (IC50 > 20 μM) under the influence of high ATP (2 mM) levels (WO2021116178A1).

    价 格：￥电议型 号：T40288产 地：中国大陆

  • T40265PLK1-IN-2PLK1-IN-2PLK1-IN-2

    PLK1-IN-2 is a PLK1 kinase inhibitor with an IC 50 value of 0.384 μM.

    价 格：￥电议型 号：T40265产 地：中国大陆

  • T40188HPK1-IN-20HPK1-IN-20HPK1-IN-20

    HPK1-IN-19 is a potent inhibitor of hematopoietic progenitor kinase 1 (HPK1).

    价 格：￥电议型 号：T40188产 地：中国大陆

  • T40091Chk1-IN-6Chk1-IN-6Chk1-IN-6

    Chk1-IN-6 is a potent, selective, and orally bioavailable CHK1 inhibitor candidate.

    价 格：￥电议型 号：T40091产 地：中国大陆

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