“AZ 960”的搜索结果

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  1. Pifithrin-alpha

    Catalog No. A12451
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    p53 抑制剂
    Pifithrin-alpha是p53介导的细胞凋亡和p53依赖性基因转录(如细胞周期蛋白G,p21/waf1和mdm2表达)的可逆抑制剂。 了解更多
  2. Nec-4

    Catalog No. A21033
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    RIP1 inhibitor
    Nec-4, a tricyclic derivative, is a potent receptor interacting protein 1 (RIP1) inhibitor, with an IC50 of 2.6 μM, Ki of 0.46 μM. 了解更多
  3. Pifithrin-β

    Catalog No. A22006
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    p53 inhibitor
    Pifithrin-β (PFT β) is a potent p53 inhibitor with an IC50 of 23 μM. 了解更多
  4. cis-Pralsetinib

    Catalog No. A21586
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    RET inhibitor
    cis-Pralsetinib (cis-BLU-667) is a highly potent and selective inhibitor of rearranged during transfection (RET), with IC50s ranging from 0.3 to 0.4 nM for WT RET and four enzyme variants (V804L, V804M, M918T, CCDC6-RET), and with broad, robust and anti-tumor activity against multiple RET-driven solid tumor types. 了解更多
  5. APG-115

    Catalog No. A12575
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    MDM2 inhibitor
    APG-115 (AA-115) is an orally active MDM2 protein inhibitor binding to MDM2 protein with IC50 and Ki values of 3.8 nM and 1 nM, respectively. 了解更多
  6. MA242

    Catalog No. A13480
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    dual MDM2/NFAT1 inhibitor
    MA242 is a dual inhibitor of murine double minute 2 (MDM2) and nuclear factor of activated T cells 1 (NFAT1) for Pancreatic Cancer Therapy. 了解更多
  7. Bax-activator-106

    Catalog No. A18406
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    Bax agonist
    Bax-activator-106 is a specific Bax agonist. It acts by promoting Bax-dependent but not Bak-dependent apoptosis. 了解更多
  8. PROTAC MDM2 Degrader-4

    Catalog No. A18877
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    MDM2 inhibitor
    PROTAC MDM2 Degrader-4 is a MDM2 degrader based on PROTAC technology. PROTAC MDM2 Degrader-4 composes of a potent MDM2 inhibitor, linker, and the MDM2 ligand for E3 ubiquitin ligase. 了解更多
  9. PROTAC MDM2 Degrader-3

    Catalog No. A18883
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    MDM2 degrader
    PROTAC MDM2 Degrader-3 is a MDM2 degrader based on PROTAC technology. PROTAC MDM2 Degrader-3 composes of a potent MDM2 inhibitor, linker, and the MDM2 ligand for E3 ubiquitin ligase. 了解更多
  10. PROTAC MDM2 Degrader-2

    Catalog No. A18890
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    MDM2 inhibitor
    PROTAC MDM2 Degrader-2 is a MDM2 degrader based on PROTAC technology. PROTAC MDM2 Degrader-2 composes of a potent MDM2 inhibitor, linker, and the MDM2 ligand for E3 ubiquitin ligase. 了解更多
  11. PROTAC MDM2 Degrader-1

    Catalog No. A18897
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    MDM2 degrader
    PROTAC MDM2 Degrader-1 is a MDM2 degrader based on PROTAC technology. PROTAC MDM2 Degrader-1 composes of a potent MDM2 inhibitor, linker, and the MDM2 ligand for E3 ubiquitin ligase. 了解更多
  12. Nutlin carboxylic acid

    Catalog No. A18917
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    Nutlin 3-based MDM2 ligand
    Nutlin carboxylic acid (MDM2 ligand 1) is the Nutlin 3-based MDM2 ligand. Nutlin carboxylic acid (MDM2 ligand 1) can be connected to the ligand for protein by a linker to form PROTACs. 了解更多
  13. (4R,5S)-nutlin carboxylic acid

    Catalog No. A18924
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    Nutlin 3-based MDM2 ligand
    (4R,5S)-nutlin carboxylic acid (MDM2 ligand 2) is the Nutlin 3-based MDM2 ligand. (4R,5S)-nutlin carboxylic acid can be connected to the ligand for protein by a linker to form PROTACs. 了解更多
  14. RET-IN-1

    Catalog No. A19015
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    RET inhibitor
    RET-IN-1 is a RET kinase inhibitor extracted from patent WO2018071447A1, Compound Example 552, has IC50s of 1 nM, 7 nM, and 101 nM for RET (WT), RET (V804M) , and RET (G810R), respectively . 了解更多
  15. RIPK1-IN-3

    Catalog No. A19023
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    RIPK1 inhibitor
    RIPK1-IN-3 (Example 38), a RIPK1 inhibitor, extracted from patent WO2018148626A1, possesses anti-inflammatory proprieties. 了解更多
  16. AZD-4320

    Catalog No. A17171
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    Bcl-2/Bcl-XL 抑制剂
    AZD-4320是BH3模拟物和双重Bcl-2/Bcl-XL抑制剂。AZD4320 对于 KPUM-MS3,KPUM-UH1,和 STR-428 细胞系的 IC50 分别为 26 nM,17 nM,和 170 nM。 了解更多
  17. AZD5991

    Catalog No. A16880
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    Mcl-1 抑制剂
    AZD-5991是一种有效的选择性Mcl-1抑制剂,在FRET分析中的IC50为0.7 nM,在表面等离子体共振(SPR)分析中的Kd为0.17 nM。 了解更多
  18. WEHI-539 hydrochloride

    Catalog No. A13327
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    Bcl-xL 抑制剂
    WEHI-539 hydrochloride是BCL-xL的小分子抑制剂,IC50值为1.1 nM。 了解更多
  19. Azoramide

    Catalog No. A16075
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    UPR modulator
    Azoramide是具有抗糖尿病活性的未折叠蛋白应答的小分子调节剂。 了解更多
  20. GSK481

    Catalog No. A12615
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    RIP1 抑制剂
    GSK481是新型的RIP1抑制剂苯并a庚酮(BOAz)系列。受体相互作用蛋白激酶1(RIP1)已被认为是通过调节程序性坏死调节炎症的关键因素。已显示对该激酶的抑制作用可阻止细胞坏死,从而将RIP1确定为潜在治疗多种炎性疾病的可行靶标。 了解更多
  21. AZ 10417808

    Catalog No. A15294
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    Caspase-3 抑制剂
    AZ 10417808,caspase-3的选择性非肽抑制剂(Ki = 247 nM);相对于半胱氨酸蛋白酶1、2、6、7和8(Ki> 10 uM)显示的选择性> 40倍。 了解更多

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