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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BA3252 PBENZ-DBRMDSummary: PBENZ-DBRMD is a potent inhibitor of iodothyronine deiodinase type 3. -
BA3253 VallesiachotamineSummary: Vallesiachotamine is a familiar monoterpene indole alkaloid with antitumor activity. -
BA3254 XylopineSummary: Xylopine is an aporphine alkaloid with cytotoxic activity against cancer cells. -
BA3255 CLEFMASummary: CLEFMA is a curcumin with anti-tumor activity. -
BA3256 TS-24Summary: TS-24 is a histone S inhibitor. -
BA3257 ChrysotoxineSummary: Chrysotoxine is a dual inhibitor. -
BA3258 ADPM06Summary: ADPM06, an azole pyrrolidomethyl, is a compound that can be used in photodynamic studies. -
BA3259 Thalidomide-O-PEG4-BocSummary: Thalidomide-O-PEG4-Boc is a synthetic E3 ligase ligand-linker coupler. -
BA3260 HBDDESummary: HBDDE, a derivative of Ellagicacid, is an isoform-selective and inhibitory agent. -
BA3261 NUN82647Summary: Inhibits the cell cycle and induces apoptosis in G2 phase.


