Lee Sukhyun, Eubanks Lisa M, Janda Kim D
Department of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Re-search and Medicine (WIRM), The Scripps Research Institute, La Jolla, CA 92037, United States.
Department of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Re-search and Medicine (WIRM), The Scripps Research Institute, La Jolla, CA 92037, United States.
Bioorg Med Chem Lett. 2025 Dec 15;129:130387. doi: 10.1016/j.bmcl.2025.130387. Epub 2025 Aug 23.
Pyrrole derivatives represent a privileged scaffold in medicinal chemistry due to their frequent presence in biologically active compounds. Herein, we report the solid-phase synthesis of a combinatorial library consisting of 211 pyrrole derivatives using a split-and-pool strategy based on the Hantzsch pyrrole synthesis. The pooled compounds were evaluated in a cell proliferation assay using the human lymphoblastoid cell line P493-6, a model with Myc-regulated growth. Four pools exhibited notable inhibitory activity, and subsequent deconvolution and synthesis of 16 individual pyrrole derivatives led to the identification of several compounds with potent antiproliferative profiles.
由于吡咯衍生物频繁出现在生物活性化合物中,它们在药物化学领域是一种具有优势的骨架结构。在此,我们报道了基于汉茨希吡咯合成法,采用混合-均分策略固相合成一个由211种吡咯衍生物组成的组合库。使用人淋巴母细胞系P493-6(一种受Myc调控生长的模型)对混合化合物进行细胞增殖测定评估。四个混合物表现出显著的抑制活性,随后对16种单个吡咯衍生物进行反卷积和合成,从而鉴定出几种具有强效抗增殖特性的化合物。