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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BA3132 CycloartenolSummary: Cycloartenol is a phytosterol compound, one of the key precursor substances for the biosynthesis of many sterols. -
BA3133 LevomenolSummary: Levomenol ((-)-α-Bisabolol) is a monocyclic sesquiterpene alcohol with antioxidant, anti-inflammatory and anti-apoptotic properties. -
BA3134 MC1742Summary: MC1742 is a potent inhibitor. -
BA3135 TrilexiumSummary: Trilexium (TRX-E-009-1) is a third-generation benzopyran with a structure related to TRX-E-002-1. -
BA3136 API-1Summary: API-1 is a potent inhibitor that binds to the PH structural domain and inhibits membrane translocation. -
BA3137 SchinifolineSummary: A derivative of quinolinone derived from Sieb -
BA3138 FalcarinolSummary: Falcarinol (Panaxynol) is a natural, orally active inhibitor that targets the N- and C-termini with limited toxicity. -
BA3139 RGB-286147Summary: RGB-286147 is a selective and ATP-competitive and related kinase inhibitor. -
BA3140 AmsilaroteneSummary: Amsilarotene (TAC-101; Am555S) is a synthetic retinoid with oral activity. -
BA3142 Mps-BAY2aSummary: Mps-BAY2a is an inhibitor.


