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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BA2733 WM-3835Summary: WM-3835 is a potent, highly specific(or) inhibitor. -
BA2734 RaptinalSummary: Direct activation of Raptinal initiates apoptosis-dependent endogenous pathways. -
BA2735 HA15Summary: HA15 is a potent and specific inhibitor of endoplasmic reticulum chaperonin. -
BA2736 TakinibSummary: Takinib (EDHS-206) is a potent and selective inhibitor (=9.5nM) -
BA2738 DB2313Summary: DB2313 is a potent inhibitor of transcription factors. -
BA2739 ACBI1Summary: ACBI1 is a potent, technology-based BAFATPase subunit and degrader. -
BA2740 3BDOSummary: 3BDO is a new type of activator. -
BA2741 APTO-253Summary: APTO-253 (LOR-253) is a small molecule that inhibits expression, stabilizes G-quadruplex DNA and induces cell cycle arrest and apoptosis in AML cells. -
BA2742 AZD5582Summary: AZD5582 is an antagonist. -
BA2743 BarbadinSummary: Barbadin is a selective interaction inhibitor with values of 19.1 μM and 15.6 μM for β-arrestin1 and β-arrestin2, respectively.


