配体生长实验表明4-氨基和4-脲基吡嗪-3(2H)- 1是抑制FABP4的新型支架。

Letizia Crocetti, Giuseppe Floresta, Chiara Zagni, Divya Merugu, Francesca Mazzacuva, Renan Rodrigues de Oliveira Silva, Claudia Vergelli, Maria Paola Giovannoni, Agostino Cilibrizzi
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引用次数: 3

摘要

脂肪酸结合蛋白(FABP4)抑制剂是合成和治疗的兴趣,正在进行的临床研究表明,它们可能是治疗癌症和其他疾病的希望。作为开发更有效的FABP4抑制剂的更广泛研究工作的一部分,我们试图通过基于共结晶配体支架的两步计算辅助分子设计来识别新的结构。利用这种方法开发出了新型有效的FABP4抑制剂,本文报道了基于4-氨基和4-脲基吡啶酮的系列抑制剂的合成、生物学评价和分子对接。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ligand Growing Experiments Suggested 4-amino and 4-ureido pyridazin-3(2<i>H</i>)-one as Novel Scaffold for FABP4 Inhibition.

Ligand Growing Experiments Suggested 4-amino and 4-ureido pyridazin-3(2<i>H</i>)-one as Novel Scaffold for FABP4 Inhibition.

Ligand Growing Experiments Suggested 4-amino and 4-ureido pyridazin-3(2<i>H</i>)-one as Novel Scaffold for FABP4 Inhibition.

Ligand Growing Experiments Suggested 4-amino and 4-ureido pyridazin-3(2H)-one as Novel Scaffold for FABP4 Inhibition.

Fatty acid binding protein (FABP4) inhibitors are of synthetic and therapeutic interest and ongoing clinical studies indicate that they may be a promise for the treatment of cancer, as well as other diseases. As part of a broader research effort to develop more effective FABP4 inhibitors, we sought to identify new structures through a two-step computing assisted molecular design based on the established scaffold of a co-crystallized ligand. Novel and potent FABP4 inhibitors have been developed using this approach and herein we report the synthesis, biological evaluation and molecular docking of the 4-amino and 4-ureido pyridazinone-based series.

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