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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BA3100 HS-1793Summary: HS-1793 is a Resveratrol analog with antitumor activity in a variety of cancer cells. -
BA3101 SKI-ISummary: SKI-I is a potent and selective inhibitor of human sphingosine kinase. -
BA3102 KumatakeninSummary: Kumatakenin, a flavonoid isolated from cloves, is known to induce apoptosis in ovarian cancer cells. -
BA3103 FuranodienoneSummary: Furanodienone is one of the main bioactive ingredients derived from turmeric rhizomes. -
BA3104 CDK8-IN-13Summary: CDK8-IN-13 is a potent, selective, orally active inhibitor. -
BA3106 PinobanksinSummary: Apoptosis-inducing effect on B-cell lymphoma cell lines. -
BA3107 Thalidomide-propargylSummary: Thalidomide-propargyl is a Thalidomide-based, ligand that recruits CRBN proteins. -
BA3108 MillepachineSummary: Millepachine is a bioactive natural chalcone from the herb Benth. -
BA3111 DCZ5418Summary: DCZ5418 is an inhibitor. -
BA3112 M47Summary: M47 is a small molecule that selectively destabilizes cryptorchidin 1 (CRY1) and increases the degradation of CRY1 in the nucleus.


