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    1. Apoptosis
    2. Bcl-2 Family

    Bcl-2 Family

    Bcl-2 is a family of evolutionarily related proteins. These proteins govern mitochondrial outer membrane permeabilization (MOMP) and can be either pro-apoptotic (Bax, Bad, Bak and Bok among others) or anti-apoptotic (including Bcl-2 proper, Bcl-xL, and Bcl-w, among an assortment of others). There are a total of 25 genes in the Bcl-2 family known to date. Human genes encoding proteins that belong to this family include: Bak1, Bax, Bal-2, Bok, Mcl-1.

    View Bcl-2 Family Pathway Map

    Bcl-2 Family 相关产品 (53):

    Cat. No. Product Name Effect Purity
    • HY-15531
      Venetoclax Inhibitor 99.95%
      Venetoclax (GDC-0199; ABT-199) 是一种高效,有选择性和口服活性的 Bcl-2 抑制剂,Ki 小于0.01 nM。
    • HY-10087
      Navitoclax Inhibitor 99.97%
      Navitoclax (ABT-263) 是有效,可口服的 Bcl-2 抑制剂,可与Bcl-xL,Bcl-2, Bcl-w等多种Bcl-2家族蛋白结合,Ki 值小于 1 nM。
    • HY-100741
      S63845 Inhibitor 99.94%
      S63845是有效的选择性骨髓细胞白血病1 (MCL1) 抑制剂,结合人MCL1的Kd 值为0.19 nM。
    • HY-50907
      ABT-737 Inhibitor 99.59%
      ABT-737 是一种类似 BH3 的 Bcl-xLBcl-2Bcl-w 的抑制剂,EC50 值分别为 78.7 nM,30.3 nM 和 197.8 nM。
    • HY-10969
      Obatoclax Inhibitor 99.20%
      Obatoclax是 BCL-2 家族蛋白的抑制剂。它与 BCL-2 结合的Ki 为220 nM。
    • HY-101565
      AMG-176 Inhibitor 98.96%
      AMG-176 是一种有效的、有口服活性的、骨髓细胞因子 1 (MCL-1) 的选择性抑制剂,其 Ki 值为 0.13 nM。
    • HY-112859
      VU0661013 Inhibitor 98.42%
      VU661013 是一种有效的选择性 MCL-1 抑制剂。
    • HY-101533
      AZD-5991 Inhibitor
      AZD-5991 是一种有效的选择性 Mcl-1 抑制剂,FRET 实验检测的 IC50 为 0.7 nM, SPR 实验检测的 Kd 为 0.17 nM。
    • HY-12468
      A-1210477 Inhibitor 98.89%
      A-1210477 是一种有效,选择性的 MCL-1 抑制剂,Ki 值为 0.45 nM。
    • HY-19741
      A-1331852 Inhibitor 99.21%
      A-1331852是具有口服活性的BCL-XL选择性抑制剂,Ki值小于10 pM。
    • HY-19725
      A-1155463 Inhibitor 98.55%
      A-1155463是高效选择性的 BCL-XL 抑制剂,在Molt-4细胞中的EC50值为70 nM。
    • HY-15607A
      WEHI-539 hydrochloride Inhibitor
      WEHI-539 hydrochloride 是一种选择性的 Bcl-XL 抑制剂,IC50 为 1.1 nM。
    • HY-P0081
      Bax inhibitor peptide V5 Inhibitor 99.79%
      Bax inhibitor peptide V5 是一种 Bax 诱导凋亡的抑制剂,主要用于癌症研究。
    • HY-102027
      FX1 Inhibitor >98.0%
      FX1 是一种强效且特异性的 BCL6 抑制剂, IC50 大约为 35 μM。
    • HY-18628
      UMI-77 Inhibitor 98.04%
      UMI-77是一种选择性的 Mcl-1 抑制剂,对 Mcl-1 具有高亲和力 (IC50= 0.31 μM)。UMI-77 结到 Mcl-1 的 BH3 结合沟, Ki 值为 490 nM,比作用于 Bcl-2 家族其他成员的选择性高。
    • HY-17510
      Gossypol acetic acid Inhibitor 99.42%
      Gossypol acetic acid 是一种从棉籽和根中分离出来的天然产物,分别与 Bcl-xL 蛋白和 Bcl-2 蛋白结合,Ki 值分别为 0.5-0.6 μM 和 0.2-0.3 mM。
    • HY-12020
      TW-37 Inhibitor 98.50%
      TW-37 是一种有效的 Bcl-2 抑制剂,作用于 Mcl-1Bcl-2Bcl-xLKi 值分别为 260,290 和 1110 nM。
    • HY-N0087
      Gambogic Acid Inhibitor
      Gambogic acid 来自 Garcinia hanburyi 树的藤黄树脂。Gambogic acid 抑制 Bcl-XLBcl-2Bcl-WBcl-BBfl-1Mcl-1IC50 分别为 1.47 μM,1.21 μM,2.02 μM,0.66 μM,1.06 μM 和 0.79 μM。
    • HY-12011
      HA14-1 Inhibitor >98.0%
      HA14-1 是一种 Bcl-2/Bcl-xL 拮抗剂。HA14-1 与 Bcl-2 上的特定口袋结合, IC50 约为 9 μM,并抑制 Bcl-2 功能。
    • HY-15464A
      (R)-(-)-Gossypol acetic acid Inhibitor
      (R)-(-)-Gossypol acetic acid (AT-101 (acetic acid)) 是天然产物 Gossypol 的左旋异构体。AT-101 结合到 Bcl-2Mcl-1Bcl-xL 蛋白,Ki 值分别为 260±30 nM,170±10 nM 和 480±40 nM。

    Bcl-2 family members have been grouped into three classes. The anti-apoptotic subfamily contains the Bcl-2, Bcl-XL, Bcl-w, Mcl-1, Bfl1/A-1, and Bcl-B proteins, which suppress apoptosis and contain all four Bcl-2 homology domains, designated BH1-4. The pro-apoptotic subfamily contain BH1-3 domains, such as Bax, Bak, and Bok. A third class of BH3 only proteins Bad, Bid, Bim, Noxa and Puma have a conserved BH3 domain that can bind and regulate the anti-apoptotic BCL-2 proteins to promote apoptosis [1].

    The intrinsic pathway is initiated by various signals, principally extracellular stimuli. BH3-only proteins (Bim, Bid, Bad, Noxa, Puma) engage with anti-apoptotic Bcl-2 family proteins to relieve their inhibition of Bax and Bak to activate them. Next, Bax and Bak are oligomerized and activated, leading to mitochondrial outer membrane permeabilization. Once mitochondrial membranes are permeabilized, cytochrome c and/or Smac/DIABLO is released into the cytoplasm, wherein they combine with an adaptor molecule, Apaf-1, and an inactive initiator Caspase, Pro-caspase 9, within a multiprotein complex called the apoptosome. Smac/DIABLO inhibits IAPs to activate Caspase 9. Caspase 9 activates Caspase 3, which is the initiation step for the cascade of Caspase activation. The extrinsic pathway can be activated by cell surface receptors, such as Fas and TNF Receptor, subsequently activating Caspase 8, and leads to Caspase 3 activation and cell demolition. Caspases in turn cleave a series of substrates, activate DNases and orchestrate the demolition of the cell. Bcl-2 family proteins are also found on the endoplasmic reticulum and the perinuclear membrane in hematopoietic cells, but they are predominantly localized to mitochondria [2]


    [1]. Cotter TG, et al. Apoptosis and cancer: the genesis of a research field. Nat Rev Cancer. 2009 Jul;9(7):501-7.

    [2]. Kang MH, et al. Bcl-2 inhibitors: targeting mitochondrial apoptotic pathways in cancer therapy. Clin Cancer Res. 2009 Feb 15;15(4):1126-32.

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