1,8-Naphthalimide derivatives: new leads against dynamin I GTPase activity?
Organic & Biomolecular Chemistry Pub Date: 2015-06-16 DOI: 10.1039/C5OB00751H
Abstract
Fragment-based in silico screening against dynamin I (dynI) GTPase activity identified the 1,8-naphthalimide framework as a potential scaffold for the design of new inhibitors targeting the GTP binding pocket of dynI. Structure-based design, synthesis and subsequent optimization resulted in the development of a library of 1,8-naphthalimide derivatives, called the Naphthaladyn? series, with compounds 23 and 29 being the most active (IC50 of 19.1 ± 0.3 and 18.5 ± 1.7 μM respectively). Compound 29 showed effective inhibition of clathrin-mediated endocytosis (IC50(CME) 66 μM). The results introduce 29 as an optimised GTP-competitive lead Naphthaladyn? compound for the further development of naphthalimide-based dynI GTPase inhibitors.
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Journal Name：Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4
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