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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N2901 Ginsenoside Rk3Summary: A saponin NF-κB transcriptional activity inhibitor derived from ginseng root. -
B8757 AmcinonideSummary: An effective corticosteroid hormone receptor agonist. -
BA7642 GuaiazuleneSummary: A bicyclic sesquiterpene with anti-inflammatory, antioxidant, hepatoprotective, antibacterial, and antitumor activities, also used as a cosmetic colorant -
BA8500 IproniazidSummary: An orally active, nonselective irreversible monoamine oxidase (MAO) inhibitor. -
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C9051 IACS-010759Summary: A selective Complex I inhibitor for research on the mechanisms of mitochondrial oxidative phosphorylation, for research use only. -
C9054 Ammonium tetrathiomolybdateSummary: A research-grade copper chelator and conditional sulfide donor for in vitro studies of copper-dependent enzymes and mitochondria. -
C9057 PHA-767491 HClSummary: An ATP-competitive dual-target DDK/CDK9 inhibitor for cell cycle and transcription research.


