Virtual Screening of Bio-active Compounds as an Inhibitor of c-FLIP Protein for Cancer Treatment
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Published:19 Nov 2019
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Special Collection: 2019 ebook collection
P. Nagaraja, A. Guhathakurta, S. S. Baidya, and P. Krishnasamudram, in Conference on Drug Design and Discovery Technologies, ed. M. Murahari, L. Sundar, S. Chaki, V. Poongavanam, P. Bhat, and U. Y. Nayak, The Royal Society of Chemistry, 2019, pp. 21-24.
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Cellular FLICE (FADD-like IL-1β-converting enzyme)-inhibitory protein (c-FLIP) is an anti-apoptotic regulatory protein play an important role in cell maintenance and survival to regulate the activation of caspases-8 and -10 proteins in apoptotic signaling pathways. cFLIP mediates death receptors to apoptosis via FAS, TNFR, DR4/DR5, and TNF-related apoptosis-inducing ligand (TRAIL) with the process and activation of procaspase-8 and -10 are over expressed in down process and is the major potential drug targets for cancer therapy. Moreover, abnormal c-FLIP expression has been found in various diseases such as cancer, multiple sclerosis, Alzheimer’s disease, diabetes mellitus, and rheumatoid arthritis. Therefore, c-FLIP-has been identified as potential target for major cancer signaling pathways to inhibit the functions of c-FLIP by targeted therapy. Using computational methods, identified active lead molecules from chemical library databases for the design of potential c-FLIP inhibitors.