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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BA3325 K-8012Summary: K-8012 is a sulindac analog and is a potent antagonist. -
BA3326 DMH2Summary: DMH2 is a potent receptor antagonist. -
BA3327 BTR-1Summary: BTR-1 is an active anticancer agent that induces cell cycle S-phase arrest and affects DNA replication. -
BA3328 OsajinSummary: Osajin is the main bioactive isoflavone present in the fruit. -
BA3329 BT2Summary: BT2 is a BCKDC kinase inhibitor. -
BA3330 AZD-5991Summary: AZD-5991 is a potent and selective inhibitor. -
BA3331 MIK665Summary: MIK665 (S-64315), a myeloid leukemia sequence 1 inhibitor. -
BA3332 BI-3802Summary: BI-3802 is a highly efficient degradation agent capable of inhibiting the Bric-à-brac (BTB) structural domain with values ≤3nM. -
BA3333 AZD4320Summary: AZD4320 is a novel analog of BH-3, a potent dual inhibitor. -
BA3334 BI-3812Summary: BI-3812 is a potent inhibitor.


