|T3714||SUN 11602||SUN11602 is a novel aniline compound, which mimics the neuroprotective mechanisms of ...||Nervous system|
|T3706||BDA-366||Small-molecule BDA-366 specifically targets the BH4 domain of Bcl2 BDA-366 suppresses...||Cancer|
|T3299||AT-406||AT-406, an orally active antagonist of multiple inhibitor of apoptosis proteins(IAP),...||Cancer|
|T3350||Selonsertib||Selonsertib, also known as GS-4997, is an orally bioavailable inhibitor of apoptosis ...||Metabolism|
ID5721353 is a B-Cell Lymphoma 6 Inhibitor (BCL6 inhibitor).
|T3668||Galangin||Galangin has anti-proliferation effect on HCC cells. Galangin elicits anti-inflammato...||Others|
|T3674||Hydroxysafflor yellow A||Hydroxysafflor yellow A inhibited adipogenesis by increasing HSL promoter activities....||Others|
|T3101||NQDI-1||Selective inhibitor of apoptosis signal-regulating kinase 1 (ASK1, MAP3K5) (IC50?= 3?...||Others|
|T3655||PD-1/PD-L1 inhibitor 1||PD1-PD-L1 inhibitor 1 (PD1-PD-L1-IN-1) is an inhibitor of the PD1-PD-L1 protein-prote...||Others|
|T1493||BH3I-1||BH3I-1 is a Bcl-2 family inhibitor. BH3I-1 appeared to induce a dose- and time-depend...||Others|
Inhibitor of p53; reversibly blocks p53-dependent transcriptional activation and a...
MX69 is the MDM2/XIAP inhibitor, used for cancer treatment. MX69 blocks the MDM2 p...
|T3053||CZC-25146?||CZC-25146 is a potent, selective and metabolically stable LRRK2 inhibitor with IC50 o...||Others|
|T7020||Z-VAD-FMK (Caspase Inhibitor VI)||
Z-VAD-FMK (Caspase Inhibitor VI) is an irreversible pan-caspase inhibitor.
|T7019||Z-IETD-FMK||Z-IETD-FMK is a specific Caspase-8 inhibitor.||Others|
|T7005||Ulixertinib (BVD-523, VRT752271)||Ulixertinib (BVD-523, VRT752271) is a potent and reversible ERK1/ERK2 inhibitor with ...||Others|
|T6965||RG-7112||RG7112 (RO5045337) is an orally bioavailable and selective p53-MDM2 inhibitor. Phase ...||Others|
|T6954||PRIMA-1||PRIMA-1 is a mutant p53 reactivator. It induces apoptosis and inhibits growth of huma...||Others|
|T6948||SC1||Pluripotin (SC1) is a dual inhibitor of extracellular signal-regulated kinase 1 (ERK1...||Others|
|T6910||NSC59984||NSC59984 is a p53 pathway activator via induction of mutant p53 protein degradation a...||Others|
|T6909||NSC348884||NSC348884, as a nucleophosmin inhibitor, inhibit cell proliferation and induce apopto...||Others|
|T6852||GSK481||GSK481 is a RIP1(Receptor Interacting Protein Kinase1) inhibitor. Inhibition of RIP1 ...||Others|
|T6826||Emricasan||Emricasan is a potent irreversible pan-caspase inhibitor.||Others|
|T6818||DEL-22379||DEL-22379 is a water-soluble ERK dimerization inhibitor with IC50 of ～0.5 μM.||Others|
|T6763||AT406 (SM-406, ARRY-334543)||AT406 (SM-406, ARRY-334543) is a potent Smac mimetic and an antagonist of IAP (inhibi...||Others|
|T6749||A-1331852||A-1331852 is a potent and selectiveBCL-XL inhibitor and may be useful in the treatmen...||Others|
|T6748||A-1155463||A-1155463, a highly potent and selective BCL-XL inhibitor, shows picomolar binding af...||Others|
|T3375||Verbascosidenew||Verbascoside has an antimicrobial activity, notably against Staphylococcus aureus. It...||Others|
|T3332||Isosteviol||Stevioside, a common natural sweetener, belongs to tetracyclic diterpene glycosides. ...||Metabolism|
|T3184||Kevetrin hydrochloride||Kevetrin hydrochloride is a small molecule and activator of the tumor suppressor prot...||Cancer|