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| 目录号 | 产品名称 | 产品描述 |
| R10005 | AT-406 (Synonyms: SM-406; Debio-1143) | 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， |
| R10039 | Venetoclax; ABT-199; GDC-0199 | Venetoclax (ABT-199, GDC-0199) is a Bcl-2-selective inhibitor with Ki of 4800-fo |
| R10094 | NSC 652287 | RITA (NSC 652287) induces both DNA-protein and DNA-DNA cross-links with no detec |
| R10095 | Tenovin1 | Tenovin-1 protects against MDM2-mediated p53 degradation, which involves ubiquit |
| R10119 | PAC-1 (Synonyms: Procaspase activating compound 1) | PAC-1 是一种 procaspase-3 激活剂，诱导癌细胞凋亡，EC50 为 2.08 μM。 |
| R10257 | VX765; Belnacasan | Belnacasan (VX-765) is a potent and selective inhibitor of caspase-1 with Ki of |
| R10333 | Navitoclax (Synonyms: ABT-263) | 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 |
| R10350 | UMI-77 | UMI-77 is a selective Mcl-1 inhibitor with Ki of 490 nM, showing selectivity ove |
| R10362 | GSK2606414 | GSK2606414 is an orally available, potent, and selective PERK inhibitor. |
| R10370 | GSK2656157 | GSK2656157 is an ATP-competitive inhibitor of PERK enzyme activity with an IC(50 |
| R10425 | Spautin1 | Spautin-1 is a novel autophagy inhibitor, IM inhibited the growth of K562 cells |
| R10511 | Lenalidomide; CC5013 | Lenalidomide (CC-5013) is a TNF-α secretion inhibitor with IC50 of 13 nM in PBMC |
| R10553 | Venetoclax; ABT199 | Venetoclax (ABT-199; GDC-0199) 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。 |
| R10603 | JNJ26854165 | JNJ-26854165 (Serdemetan) acts as a HDM2 ubiquitin ligase antagonist and also in |
| R10628 | Apoptosis Activator2 | Apoptosis Activator 2 strongly induces caspase-3 activation, PARP cleavage, and |
| R10655 | Necrostatin-1 | Necrostatin-1 is a specific RIP1 inhibitor and inhibits TNF-α-induced necroptosi |
| R10763 | Kevetrin hydrochloride; NSC525990 | Kevetrin hydrochloride is a small molecule and activator of the tumor suppressor |
| R10786 | FMK | FMK is a RSK2 kinase inhibitor. |
| R10798 | LCL161 | LCL161 is an orally bioavailable second mitochondrial-derived activator of caspa |
| R10799 | LCL161 Enantiomer | LCL161 is an orally bioavailable second mitochondrial-derived activator of caspa |
| R10802 | Nutlin-3 | MDM2 antagonist nutlin-3 is a potent inducer of apoptosis. |
| R10827 | RG7112 (Synonyms: RO5045337) | RG7112 是有效的、选择性的、第一个用于临床的、可口服的、可透过血脑屏障的、 MDM2-p53 抑制剂，IC50 值为 18 nM，结合到MDM2 的KD |
| R11535 | NSC59984 | NSC59984 is a p53 pathway activator via induction of mutant p53 protein degradat |
| R11566 | Tasisulam | Tasisulam is an antitumor agent and an apoptosis inducer via the intrinsic pathw |
| R11638 | Emricasan, (IDN-6556; PF-03491390) | Emricasan (PF 03491390)是不可逆的 pan-caspase 抑制剂。 |
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