Gomes Marcelo N, Muratov Eugene N, Pereira Maristela, Peixoto Josana C, Rosseto Lucimar P, Cravo Pedro V L, Andrade Carolina H, Neves Bruno J
Laboratory for Molecular Modeling and Drug Design, Faculty of Pharmacy, Universidade Federal de Goiás, Setor Leste Universitário, Goiânia 74605-510, Brazil.
Laboratory for Molecular Modeling, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC 27955-7568, USA.
Molecules. 2017 Jul 25;22(8):1210. doi: 10.3390/molecules22081210.
Medicinal chemists continue to be fascinated by chalcone derivatives because of their simple chemistry, ease of hydrogen atom manipulation, straightforward synthesis, and a variety of promising biological activities. However, chalcones have still not garnered deserved attention, especially considering their high potential as chemical sources for designing and developing new effective drugs. In this review, we summarize current methodological developments towards the design and synthesis of new chalcone derivatives and state-of-the-art medicinal chemistry strategies (bioisosterism, molecular hybridization, and pro-drug design). We also highlight the applicability of computer-assisted drug design approaches to chalcones and address how this may contribute to optimizing research outputs and lead to more successful and cost-effective drug discovery endeavors. Lastly, we present successful examples of the use of chalcones and suggest possible solutions to existing limitations.
由于查尔酮衍生物具有简单的化学结构、易于进行氢原子操作、合成方法直接以及多种有前景的生物活性,药物化学家们一直对其着迷。然而,查尔酮仍未得到应有的关注,尤其是考虑到它们作为设计和开发新型有效药物的化学来源具有很高的潜力。在这篇综述中,我们总结了目前用于设计和合成新型查尔酮衍生物的方法学进展以及最新的药物化学策略(生物电子等排体、分子杂交和前药设计)。我们还强调了计算机辅助药物设计方法在查尔酮上的适用性,并探讨了这如何有助于优化研究成果,从而带来更成功且成本效益更高的药物发现工作。最后,我们展示了使用查尔酮的成功案例,并针对现有局限性提出了可能的解决方案。