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Mar. Drugs 2019, 17(1), 53; https://doi.org/10.3390/md17010053

Fragment-Based Structural Optimization of a Natural Product Itampolin A as a p38α Inhibitor for Lung Cancer

School of Pharmacy, China Medical University, Liaoning 110122, China
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Received: 1 December 2018 / Revised: 1 January 2019 / Accepted: 7 January 2019 / Published: 12 January 2019
(This article belongs to the Collection Marine Compounds and Cancer)
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Abstract

Marine animals and plants provide abundant secondary metabolites with antitumor activity. Itampolin A is a brominated natural tyrosine secondary metabolite that is isolated from the sponge Iotrochota purpurea. Recently, we have achieved the first total synthesis of this brominated tyrosine secondary metabolite, which was found to be a potent p38α inhibitor exhibiting anticancer effects. A fragment-based drug design (FBDD) was carried out to optimize itampolin A. Forty-five brominated tyrosine derivatives were synthesized with interesting biological activities. Then, a QSAR study was carried out to explore the structural determinants responsible for the activity of brominated tyrosine skeleton p38α inhibitors. The lead compound was optimized by a FBDD method, then three series of brominated tyrosine derivatives were synthesized and evaluated for their inhibitory activities against p38α and tumor cells. Compound 6o (IC50 = 0.66 μM) exhibited significant antitumor activity against non-small cell lung A549 cells (A549). This also demonstrated the feasibility of the FBDD method of structural optimization. View Full-Text
Keywords: itampolin A; FBDD; antitumor; p38α; novel inhibitor itampolin A; FBDD; antitumor; p38α; novel inhibitor
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Liang, J.-W.; Wang, M.-Y.; Wang, S.; Li, X.-Y.; Meng, F.-H. Fragment-Based Structural Optimization of a Natural Product Itampolin A as a p38α Inhibitor for Lung Cancer. Mar. Drugs 2019, 17, 53.

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