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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BA3438 Suc-Ala-Leu-Pro-Phe-pNASummary: A substrate for FK-506 binding protein. -
BA3439 ElteN378Summary: ElteN378 is an inhibitor. -
BA3440 dTAGV-1-NEGSummary: dTAGV-1-NEG is a diastereoisomer and a heterobifunctional negative control for dTAGV-1. -
BA3453 CUDC-427Summary: CUDC-427 (GDC-0917) is a potent inhibitor. -
BA3454 MX69Summary: MX69 is an inhibitor. -
BA3455 SBP-0636457Summary: SBP-0636457 (SB1-0636457) is a SMAC analog that is antagonistic. -
BA3456 UC2288Summary: UC2288 is a novel, cell permeable and orally active attenuating reagent (with relatively selective activity against p21) based on the structural synthesis of sorafenib. -
BA3457 MD-224Summary: MD-224 is a highly efficient small molecule degrader based on protein hydrolysis-targeted chimeras (PROTAC). -
BA3458 SulanemadlinSummary: Sulanemadlin (ALRN-6924) is a cell membrane-penetrating, potent p53-based peptidomimetic macrocycle. -
BA3459 MB710Summary: MB710, an aminobenzothiazole derivative, is a stabilizer of the oncogenic p53 mutant Y220C.


