Lizzadro Luca, Spieß Oliver, Reinecke Silke, Stadler Marc, Schinzer Dieter
Medicinal Chemistry and Chemical Biology Laboratory, School of Pharmacy, University of California San Francisco, 600 16th St., San Francisco, CA 94158, USA.
Chemisches Institut, Otto-von-Guericke-Universität, Universitätsplatz 2, 39106 Magdeburg, Germany.
Molecules. 2024 Mar 1;29(5):1123. doi: 10.3390/molecules29051123.
The synthesis of a novel disorazole C analogue is described, and its biological activity as a cytotoxic compound is reported. Based on our convergent and flexible route to the disorazole core, we wish to report a robust strategy to synthesize a non-symmetrical disorazole in which we couple one half of the molecule containing the naturally occurring oxazole heterocycle and the second half of the disorazole macrocycle containing a thiazole heterocycle. This resulted in a very unusual non-symmetrical disorazole C analogue containing two different heterocycles, and its biological activity was studied. This provided exciting information about SAR (structure-activity-relationship) for this highly potent class of antitumor compounds.
本文描述了一种新型地索拉唑C类似物的合成,并报道了其作为细胞毒性化合物的生物活性。基于我们合成地索拉唑核心的汇聚且灵活的路线,我们希望报告一种合成非对称地索拉唑的稳健策略,其中我们将含有天然存在的恶唑杂环的分子的一半与含有噻唑杂环的地索拉唑大环的另一半偶联。这产生了一种非常不寻常的含有两种不同杂环的非对称地索拉唑C类似物,并对其生物活性进行了研究。这为这类高效抗肿瘤化合物的构效关系(SAR)提供了令人兴奋的信息。