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  • T15664KIRA-7；化合物 T15664KIRA-7

    KIRA-7 is an imidazopyrazine compound. KIRA-7 has an anti-fibrotic effect. KIRA-7 binds the IRE1α kinase (IC50: 110 nM) to allosterically inhibit its RNase activity.

    价 格：￥电议型 号：T15664产 地：中国大陆

  • T15663Kinesore化合物 T15663Kinesore

    Kinesore is a KLC2-SKIP Interaction inhibitor.

    价 格：￥电议型 号：T15663产 地：中国大陆

  • T15662KIN1408；化合物 T15662KIN1408

    KIN1408 is an antiviral small molecule compound. KIN1408 also is an agonist of the RLR pathway.

    价 格：￥电议型 号：T15662产 地：中国大陆

  • T15661Kif15-IN-1；化合物 T15661Kif15-IN-1

    Kif15-IN-1, a mitotic Kinesin family member 15 (Kif15) inhibitor, is utilized in the study of cellular proliferative diseases.

    价 格：￥电议型 号：T15661产 地：中国大陆

  • T15660KHK-IN-1；化合物KHK-IN-1KHK-IN-8|||Ketohexokinase inhibitor 8；KHK-IN-8|||Ketohexokinase inhibitor 8

    KHK-IN-1 (KHK-IN-8) is a selective and cell membrane permeable inhibitor of ketohexokinase (KHK, IC50=12 nM; F=34%). KHK-IN-1 inhibits F1P production in HepG2 cell lysates with IC50 of 400 nM. KHK-IN-1 has potential for the study of obesity and diabetes.

    价 格：￥电议型 号：T15660产 地：中国大陆

  • T1566Aripiprazole；阿立哌唑OPC-14597；阿立哌唑|||OPC-14597

    Aripiprazole (OPC-14597) is an antipsychotic agent that is structurally related to piperazines and quinolones. It is a partial agonist of SEROTONIN RECEPTOR, 5-HT1A and DOPAMINE D2 RECEPTORS, where it also functions as a post-synaptic antagonist, and an antagonist of SEROTONIN RECEPTOR, 5-HT2A.

    价 格：￥电议型 号：T1566产 地：中国大陆

  • T15659KHK-IN-1 hydrochloride；化合物 T15659KHK-IN-1 hydrochloride

    KHK-IN-1 hydrochloride is a potent inhibitor of ketohexokinase (KHK) (IC50: 12 nM). In the ATP-binding region of KHK, KHK-IN-1 hydrochloride interacts with Asp-27B.

    价 格：￥电议型 号：T15659产 地：中国大陆

  • T15657KH-CB19；化合物 T15657KH-CB19

    KH-CB19 is an effective and highly specific inhibitor of the CDC2-like kinase isoforms 1 and 4 (CLK1/CLK4).

    价 格：￥电议型 号：T15657产 地：中国大陆

  • T15656KGA-2727；化合物KGA-2727KGA-2727

    KGA-2727 is a potent and selective SGLT1 inhibitor, with Kis of 97.4 nM and 43.5 nM for human and rat SGLT1, respectively. The selectivity ratios (Ki for SGLT2/Ki for SGLT1) of KGA-2727 are 140 (human) and 390 (rat). KGA-2727 for the treatment of diabete.

    价 格：￥电议型 号：T15656产 地：中国大陆

  • T15655KFM19；化合物KFM19KFM19

    KFM19 is a potent and selective adenosine receptor (A1-receptor) antagonist (IC50 : 50 nM) for the study of neurological disorders.

    价 格：￥电议型 号：T15655产 地：中国大陆

  • T15654Ketohexokinase inhibitor 1；化合物Ketohexokinase inhibitor 1PF-06835919；PF-06835919

    Ketohexokinase inhibitor 1 is a ketohexokinase inhibitor (IC50s: 8.4 nM and 66 nM for KHK-C and KHK-A, respectively).

    价 格：￥电议型 号：T15654产 地：中国大陆

  • T15653Ketocaine；凯托卡因Rec 7-0518；Rec 7-0518

    Ketocaine（Rec 7-0518） is a local anesthetic commonly used in animal experiments with potential antitumor activity for pain relief.

    价 格：￥电议型 号：T15653产 地：中国大陆

  • T15652Kelatorphan；化合物 T15652Kelatorphan

    Kelatorphan is an enkephalin degrading enzyme full inhibitor.

    价 格：￥电议型 号：T15652产 地：中国大陆

  • T15651KDU731；化合物 T15651KDU731

    KDU731 is a promising drug candidate for the treatment of diarrhea caused by Cryptosporidium and meets a broad range of safety. KDU731is an orally active C. parvum inhibitor of PI4K (IC50: 25 nM). KDU731 blocks Cryptosporidium infection in vitro and in vivo.

    价 格：￥电议型 号：T15651产 地：中国大陆

  • T15650KDM5A-IN-1；KDM5A抑制剂1KDM5A-IN-1

    KDM5A-IN-1 is an orally available, potent and selective inhibitor of the pan-histidine lysine demethylase 5 KDM5, inhibiting KDM5A, KDM5B, and KDM5C with IC50 values of 45 nM, 56 nM, and 55 nM, respectively.KDM5A-IN-1 inhibits PC9 H3K4Me3, and may be useful in cancer research.

    价 格：￥电议型 号：T15650产 地：中国大陆

  • T1565Deferiprone；去铁酮Deferidone|||CP20；去铁酮|||Deferidone|||CP20

    Deferiprone (Deferidone) is an Iron Chelator. The mechanism of action of deferiprone is as an Iron Chelating Activity.

    价 格：￥电议型 号：T1565产 地：中国大陆

  • T15649KDM5-IN-1；化合物KDM5-IN-1KDM5-IN-1

    KDM5-IN-1 is an effective and selective inhibitor of KDM5 with an IC50 of 15.1 nM.

    价 格：￥电议型 号：T15649产 地：中国大陆

  • T15648KDM5-C70；化合物KDM5-C70KDM5-C70

    KDM5-C70 is an ethyl ester derivative of KDM5-C49. KDM5-C70 is an effective, cell-permeable, and pan-KDM5 histone demethylase inhibitor. KDM5-C70 has an antiproliferative effect in myeloma cells, inducing a genome-wide elevation of H3K4me3 levels.

    价 格：￥电议型 号：T15648产 地：中国大陆

  • T15647Tipelukast；泰鲁司特MN 001|||KCA 757；MN 001|||KCA 757

    Tipelukast (KCA 757) is a novel orally available leukotriene receptor antagonist with anti-inflammatory activity that reduces fibrosis and down-regulates TIMP-1, type 1 collagen.Tipelukast is used in the study of asthma.

    价 格：￥电议型 号：T15647产 地：中国大陆

  • T15646KBU2046；化合物KBU2046KBU2046

    KBU2046 is an orally administered compound that inhibits cell motility and invasion, effectively suppressing cancer metastasis and extending lifespan. This compound uniquely targets and binds to chaperone heterocomplexes, selectively modifying the interaction of client proteins involved in motility regulation, while avoiding the characteristics typical of classical HSP90 inhibitors.

    价 格：￥电议型 号：T15646产 地：中国大陆

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