1. Apoptosis
  2. IAP

IAP

IAP (Inhibitors of Apoptosis) is a family of functionally and structurally related proteins, which serve as endogenous inhibitors of programmed cell death (apoptosis). A common feature of all IAPs is the presence of a BIR in one to three copies. The human IAP family consists of 8 members, and IAP homologs have been identified in numerous organisms. The members of the IAPs included IAPs, Cp-IAP, Op-IAP, XIAP, c-IAPl, C-IAP2, NAIP, Livin and Survivin. The best characterized IAP is XIAP, which binds caspase-9, caspase-3 and caspase 7, thereby inhibiting their activation and preventing apoptosis. Also cIAP1 and cIAP2 have been shown to bind caspases, although how the IAPs inhibit apoptosis mechanistically at the molecular level is not completely understood.

IAP 相关产品 (13):

Cat. No. Product Name Effect Purity
  • HY-15518
    LCL161 Inhibitor 99.17%
    LCL161是 IAP 的抑制剂,抑制 HEK293 细胞中 XIAP 和 MDA-MB-231细胞中 cIAP1IC50 分别为 35 和 0.4 nM。
  • HY-16591
    Birinapant Antagonist 99.84%
    Birinapant是一种二价Smac模拟物, 是 XIAPcIAP1 的强效拮抗剂,Kd 值分别为45 nM和小于1 nM。
  • HY-16701
    BV6 Antagonist 99.25%
    BV6 是cIAP1XIAP拮抗剂。
  • HY-12600
    AZD5582 Antagonist 98.13%
    AZD5582是二聚化Smac mimetics,IAPs抑制剂,对cIAP1,cIAP2和XIAP的IC50值分别为15,21和15nM。
  • HY-15989
    SM-164 Antagonist >98.0%
    SM-164 是一种可渗透细胞的 Smac 类似物。SM-164 与含有 BIR2 和 BIR3 结构域的 XIAP 蛋白结合,IC50 值为 1.39 nM,SM-164 用作 XIAP 的强效拮抗剂。
  • HY-13638
    GDC-0152 Inhibitor 98.73%
    GDC-0152 是一种有效的 IAPs 抑制剂,能够分别与 XIAP BIR3 结合域,ML-IAP 的 BIR 结合域,cIAP1cIAP2 的 BIR3 结合域结合,Ki 值分别为 28,14,17 和 43 nM。
  • HY-17473
    Embelin Antagonist 98.02%
    Embelin是可渗透入细胞的,有抗癌特性的苯醌化合物。
  • HY-15835
    CUDC-427 Inhibitor 99.60%
    CUDC-427 是一种高效的 IAP 抑制剂,常用于各种癌症的治疗。
  • HY-15454
    AT-406 Antagonist 98.80%
    AT-406 是一种有效的,可口服的 Smac 模拟物,为 IAPs 的拮抗剂,能够抑制 XIAP,cIAP1 和 cIAP2 蛋白,Ki 值分别为 66.4,1.9 和 5.1 nM。
  • HY-109565
    ASTX660 Antagonist 98.79%
    ASTX660 是细胞凋亡蛋白抑制剂 (cIAP) 和 X 连锁凋亡抑制蛋白 (XIAP) 的口服生物可用的双重拮抗剂。
  • HY-100892
    MX69 Inhibitor 98.59%
    MX69 是一种 MDM2/XIAP 抑制剂,常用于抗癌研究。
  • HY-15989A
    SM-164 Hydrochloride Antagonist 98.84%
    SM-164 Hydrochloride 是一种可渗透细胞的 Smac 类似物。SM-164 与含有 BIR2 和 BIR3 结构域的 XIAP 蛋白结合,IC50 值为 1.39 nM,SM-164 用作 XIAP 的强效拮抗剂。
  • HY-12842
    UC-112 Inhibitor
    UC-112是凋亡抑制蛋白IAP新型高效抑制剂,癌细胞IC50值0.7-3.4uM。
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