Apoptosis
Apoptosis, also known as programmed cell death, is rigorously controlled process of cell death that leads to phagocytosis of unwanted cell. It is triggered after sufficient cellular damage and activated through extrinsic or intrinsic pathways. The intrinsic pathway is mainly occurs via release of cytochrome c from the mitochondria and regulates mitochondrial outer membrane permeabilization by Bcl-2 family proteins. The extrinsic pathway is induced by ligand binding to death receptor, such as Fas, TNFαR, DR3, DR4, and DR5. Caspases then cleave target proteins and nuclear lamins to promote DNA degradation, resulting apoptotic cells undergo phagocytosis. In addition, p53 has the ability to activate intrinsic and extrinsic pathways of apoptosis by inducing transcription of several proteins like Puma, Bid, Bax, TRAIL-R2, and CD95.
Some Inhibitors of apoptosis proteins (IAPs), such as XIAP/BIRC4 and Bruce/BIRC6, can block casapse activity through direct binding, while other IAPs, such as cIAP1/BIRC2, cIAP2/BIRC3, act as ubiquitin ligases that target caspases for ubiquitin-mediated degradation. Apoptosis is essential for growth, development and aging in multicellular organisms. Any alterations or abnormalities occurring in apoptotic processes contribute to development of human diseases, including cancer.
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BA3111 DCZ5418Summary: DCZ5418 is an inhibitor. -
BA3112 M47Summary: M47 is a small molecule that selectively destabilizes cryptorchidin 1 (CRY1) and increases the degradation of CRY1 in the nucleus. -
BA3113 DesacetylcinobufotalinSummary: Desacetylcinobufotalin is an apoptosis inducer. -
BA3114 GM-90257Summary: GM-90257 is a microtubule acetylation inhibitor that binds directly to alpha-microtubule proteins. -
BA3115 AZD4877Summary: AZD4877 is another conformation and is a spindle kinesin inhibitor. -
BA3116 Nampt-IN-3Summary: Nampt-IN-3 simultaneously inhibits nicotinamide phosphoribosyltransferase. -
BA3117 XMU-MP-3Summary: XMU-MP-3 is a potent non-covalent inhibitor. -
BA3118 EL-102Summary: EL-102 is an inhibitor of hypoxia-induced factor1. -
BA3119 Thalidomide-O-C8-BocSummary: Thalidomide-O-C8-Boc is a Thalidomide-based, ligand that recruits CRBN proteins. -
BA3120 AlteminostatSummary: Alteminostat (CKD-581) is a potent inhibitor.


