1. Signaling Pathways
  2. Apoptosis
    Immunology/Inflammation
  3. Pyroptosis

Pyroptosis (细胞焦亡)

Pyroptosis is a type of programmed cell death that features pore formation on the plasma membrane, cell swelling and plasma membrane disruption. Pyroptosis is a form of lytic programmed cell death initiated by inflammasomes, which detect cytosolic contamination or perturbation.

Gasdermin D (GSDMD), as the executive protein of pyroptosis, is activated and transferred to the membrane to induce glial rupture, resulting in the release of more inflammatory mediators.

Inflammasome is an intracellular signaling complex of the innate immune system. Activation of inflammasomes promotes the secretion of IL-1β/IL-18 and triggers pyroptosis. The proinflammatory effect of IL-1β/IL-18 and pyroptosis contributes to the development of autoimmune and inflammatory diseases.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-156154
    Caspase-3 activator 1 Inducer
    Caspase-3 activator 1 (compound 4b) 是 Ru(III) 金属复合物,抑制胃肿瘤生长和转移。Caspase-3 activator 1 介导 caspase-3 裂解,进而使 Caspase-3 剪切 gasdermin E (GSDME) 产生 GSDME-N 末端,造成胃肿瘤细胞膜穿孔。Caspase-3 activator 1 能够诱导焦亡 (pyroptosis) 和焦亡诱导的免疫反应,可以与地西他滨 DCT (HY-A0004) 组装为 4b-DCT-Lip 脂质递送系统。
    Caspase-3 activator 1
  • HY-150971
    ICy-Q Inducer
    ICy-Q 是一种醌氧化还原酶 1 (NQO-1) 激活的近红外 (NIR) 试剂,通过与 NQO-1 反应释放还原产物 ICy-OH。 ICy-OH 可通过诱导细胞焦亡 (pyroptosis) 途径选择性地诱导胰腺癌细胞死亡。ICy-Q 可以作为快速、准确地诊断术中病理切片的有效工具。
    ICy-Q
  • HY-150752
    BTK-IN-15 Inducer
    BTK-IN-15 (compound 42) 是一种新型的布鲁顿酪氨酸激酶 (BTK) 抑制剂,具有良好口服活性。BTK-IN-15 抑制 BTKIC50 为 0.7 nM,并具有良好的激酶选择性和抗肿瘤活性,能诱导癌细胞凋亡 (apoptosis)。
    BTK-IN-15
  • HY-161332
    Antitumor agent-143 Inducer
    Antitumor agent-143 (compound 2c) 是一种抗肿瘤剂,可阻断 A549 细胞 S 期的细胞增殖并诱导早期凋亡 (apoptosis)。Antitumor agent-143 通过铁死亡 (ferroptosis) 诱导细胞死亡,通过 ROS 介导的线粒体功能障碍途径诱导细胞凋亡,以及 GSDMD 介导的细胞焦亡 (pyroptosis)。
    Antitumor agent-143
  • HY-P3434
    Ac-FEID-CMK Inhibitor
    Ac-FEID-CMK 是一种有效的斑马鱼特异性 GSDMEb 衍生肽抑制剂。Ac-FEID-CMK 可减轻感染性休克的死亡率和肾损伤。Ac-FEID-CMK 在体内可抑制焦亡,减轻败血性 AKI (急性肾损伤)。Ac-FEID-CMK 可抑制 caspy2 介导的非典型炎症小体通路。
    Ac-FEID-CMK
  • HY-117532
    PenCB

    2,3',4,4',5-五氯联苯标准溶液

    Inducer
    PenCB (PCB 118) could induce pyroptosis by priming and activating NFκB-dependent NLRP3 inflammasome. PCB 118 induces oxidative stress and pyroptosis are dependent on Aryl hydrocarbon receptor (AhR) activation and subsequent cytochrome P450 1A1 upregulation.
    PenCB
  • HY-156374
    D359-0396 Inhibitor
    D359-0396 是一种具有口服活性的 NLRP3 炎性体抑制剂。D359-0396 抑制巨噬细胞焦亡 (pyroptosis) 和 IL-1β 释放。D359-0396 还抑制 NLRP3、ASC 的寡聚化和 GSDMD 的裂解。D359-0396 可缓解小鼠 EAE,也可提高小鼠感染性休克后的存活率。
    D359-0396
  • HY-138071
    8α-Tigloyloxyhirsutinolide 13-O-acetate Inducer
    8α-Tigloyloxyhirsutinolide 13-O-acetate (8αTGH) 是一种口服有效的 STAT3 抑制剂。8α-Tigloyloxyhirsutinolide 13-O-acetate 在 TNBC 细胞中诱导早期氧化应激和细胞焦亡 (pyroptosis),以及晚期 DNA 损伤、细胞周期停滞、细胞凋亡 (apoptosis)。 8α-Tigloyloxyhirsutinolide 13-O-acetate 在体外和体内可抑制肿瘤细胞生长。
    8α-Tigloyloxyhirsutinolide 13-O-acetate
  • HY-163179
    NLRP3-IN-28 Inhibitor
    NLRP3-IN-28 (compound N77) 是有效的 NLRP3 抑制剂。NLRP3-IN-28 抑制Nigericin (HY-127019) 诱导的焦亡,其 EC50 为0.07 μM。NLRP3-IN-28 在体内可减轻炎症反应。
    NLRP3-IN-28
  • HY-161043
    ECDD-S16 Inhibitor
    ECDD-S16 是有效的 pyroptosis 抑制剂。ECDD-S16 能抑制表面和内体 TLR 配体激活的 Raw264.7 细胞焦亡
    ECDD-S16
目录号 产品名 / 同用名 应用 反应物种