<noframes id="zd9f3">

    <address id="zd9f3"></address>

    <address id="zd9f3"></address>
    <address id="zd9f3"></address>

    <address id="zd9f3"><nobr id="zd9f3"><meter id="zd9f3"></meter></nobr></address>
    1. Apoptosis
    2. Apoptosis


    Apoptosis is a distinctive form of cell death exhibiting specific morphological and biochemical characteristics, including cell membrane blebbing, chromatin condensation, genomic DNA fragmentation, and exposure of specific phagocytosis signaling molecules on the cell surface. Cells undergoing apoptosis differ from those dying through necrosis. Necrotic cells are usually recognized by the immune system as a danger signal and, thus, resulting in inflammation; in contrast, apoptotic death is quiet and orderly.

    There are two major pathways of apoptotic cell death induction: The intrinsic pathway, also called the Bcl-2-regulated or mitochondrial pathway, is activated by various developmental cues or cytotoxic insults, such as viral infection, DNA damage and growth-factor deprivation, and is strictly controlled by the BCL-2 family of proteins. The extrinsic or death-receptor pathway is triggered by ligation of death receptors (members of the tumor necrosis factor (TNF) receptor family, such as Fas or TNF receptor-1 (TNFR1)) that contain an intracellular death domain, which can recruit and activate caspase-8 through the adaptor protein Fas-associated death domain (FADD; also known as MORT1) at the cell surface. This recruitment causes subsequent activation of downstream (effector) caspases, such as caspase-3, -6 or -7, without any involvement of the BCL-2 family.

    Studies suggest that alterations in cell survival contribute to the pathogenesis of a number of human diseases, including cancer, viral infections, autoimmune diseases, neurodegenerative disorders, and AIDS (acquired immunodeficiency syndrome). Treatments designed to specifically alter the apoptotic threshold may have the potential to change the natural progression of some of these diseases.

    Apoptosis 相关产品 (43):

    Cat. No. Product Name Effect Purity
    • HY-101103
    • HY-N0848
      Epibrassinolide Activator >98.00%
      Epibrassinolide 是一种天然油菜素类固醇(BR)衍生物,是一种植物调节剂,具有与哺乳动物类固醇相似的结构。Epibrassinolide在各种癌细胞中是一种潜在的凋亡诱导剂,而不影响非肿瘤细胞生长。
    • HY-12033
      2-Methoxyestradiol Activator 99.82%
      2-Methoxyestradiol是血管生成抑制剂和凋亡诱导剂,具有有效的抗肿瘤活性。 2-Methoxyestradiol也可破坏微管的稳定。
    • HY-12040
      Elesclomol Activator 99.80%
    • HY-N0052A
      Sanguinarine chloride Activator 99.80%
      Sanguinarine chloride 是一种来源于 Sanguinaria Canadensis 的生物碱,可通过激活活性氧 (ROS) 的产生来刺激细胞凋亡。Sanguinarine 诱导的细胞凋亡与 JNK 和 NF-κB 的活化有关。
    • HY-Y0892
      4-Hydroxybenzyl alcohol Inhibitor 99.60%
      4-Hydroxybenzyl alcohol是广泛分布于各种植物中的酚类化合物。 具有抗炎,抗氧化,抗伤害感受活性。 神经保护作用。 抑制肿瘤血管生成和生长。
    • HY-122910
      RIPGBM Activator
      RIPGBM 是一种选择性的细胞凋亡 (apoptosis) 诱导剂,诱导多形性成胶质细胞瘤 (GBM) 癌症干细胞 (CSCs) 凋亡,EC50≤500 nM。
    • HY-111617
      BTR-1 Activator 99.96%
      BTR-1 是一种活性抗癌剂,能够诱导细胞周期 S 期停滞,影响 DNA 复制。BTR-1 可激活凋亡 (apoptosis),导致细胞死亡。
    • HY-15097
      Myricetin Activator 99.41%
    • HY-50936
      Trabectedin Activator 99.83%
      Trabectedin (Ecteinascidin-743 or ET-743)是海洋来源的抗癌剂。
    • HY-10529
      Betulinic acid Activator 98.58%
      Betulinic acid 是一种天然的五环三萜类化合物,为真核细胞拓扑异构酶 I (topoisomerase I) 的抑制剂,IC50 值为 5 μM,具有抗炎,抗疟疾,抗艾滋病和抗肿瘤等活性。
    • HY-14808
      Adarotene Activator 99.15%
      Adarotene 是一种有效的 apoptosis 诱导剂,通过产生 DNA 损伤,来阻止人类肿瘤细胞的增殖。
    • HY-N0605
      Ginsenoside Rh2 Activator >98.0%
      Ginsenoside Rh2 是从 Ginseng 根中分离出来的。Ginsenoside Rh2 诱导 caspase-8caspase-9 活化。Ginsenoside Rh2 以多途径方式诱导癌细胞凋亡。
    • HY-N2027
      Taurochenodeoxycholic acid Activator 99.80%
      Taurochenodeoxycholic acid是动物胆汁酸的主要生物活性物质之一。
    • HY-N0011
      Baohuoside I Activator 98.96%
      Baohuoside I 是从朝鲜淫羊藿中得到的黄酮类化合物,作为 CXCR4 的抑制剂,能够抑制 CXCR4 的表达,诱导凋亡,具有抗肿瘤活性。
    • HY-N0036
      Costunolide Activator 99.84%
    • HY-N0083
      Betulin Activator >98.0%
      Betulin是一种SREBP抑制剂,在K562细胞中的IC50值是14.5 μM。
    • HY-N0120A
      Polydatin 98.42%
    • HY-100738
      Ubiquitin Isopeptidase Inhibitor I, G5 Activator >98.0%
      Ubiquitin Isopeptidase Inhibitor I, G5 (NSC 144303)是凋亡不依赖的半胱天冬酶和细胞凋亡的激活剂,对E1A和E1A/C9DN细胞的IC50值分别为1.76和1.6 μM。
    • HY-14615
      [6]-Gingerol Activator 98.01%
    Isoform Specific Products

    Your Search Returned No Results.

    Sorry. There is currently no product that acts on isoform together.

    Please try each isoform separately.