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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BA8984 SoquelitinibSummary: An orally active and highly selective covalent interleukin-2-inducible kinase (ITK) inhibitor for T cell-mediated inflammatory disease -
BA8989 ZeteletinibSummary: Zeteletinib (BOS-172738; DS-5010) is an orally effective, selective kinase inhibitor with nanomolar potency against and >300-fold selectivity for VEGFR2. -
BA8996 BT-13Summary: BT-13 is a potent, selective agonist (acting independently of GDNF ligands). -
BA4734 XX-650-23Summary: XX-650-23 is a potent inhibitor. -
BA4772 NiCurSummary: NiCur is a potent and selective inhibitor. -
BA4887 CMLD-2Summary: CMLD-2 is an inhibitor. -
BA4971 SpisulosineSummary: Spisulosine (ES-285) is a marine-derived antiproliferative (antitumor) compound. -
BA5008 OxatomideSummary: Oxatomide is a potent orally active dual H1 histamine receptor and receptor antagonist with antihistamine and antiallergic activity. -
BA5103 ParoxetineSummary: Paroxetine, a phenylpiperidine derivative, is a potent selective serotonin reuptake inhibitor (SSRI). -
BA5212 VoacamineSummary: Voacamine is an indole alkaloid.


