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.
-
A4623 Glyphosate -
A4625 Flavokawain A -
A4627 2-Methoxycinnamaldehyde -
A4640 3-O-Methylgallic acid -
A4643 Importazole -
A4644 DIM-C-pPhOH -
C5297 Morin1 Citation -
BA2627 McMMAFSummary: McMMAF is composed of the highly efficient microtubule inhibitor MonomethylF (MMAF) coupled with the protecting group maleimidocaproyl, which can be used as the active molecular linker. -
BA2719 DT2216Summary: DT2216 is an effective, selective (family member) degrader of a class. -
BA2722 TAK-243Summary: TAK-243 (MLN7243) is a first-of-its-kind, selective ubiquitin-activating enzyme, inhibitor.


