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将异己二醇单元引入内脂醇样喹诺酮骨架中。

Incorporation of an Isohexide Subunit into the Endochin-like Quinolone Scaffold.

机构信息

Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, 123 Bevier Road, Piscataway, NJ 08854, USA.

出版信息

Molecules. 2024 Jul 31;29(15):3615. doi: 10.3390/molecules29153615.

Abstract

In order to improve the drug-likeness qualities, the antimalarial endochin-like quinolone (ELQ) scaffold has been modified by replacing the 4-(trifluoromethoxy)phenyl portion with an isoidide unit that is further adjustable by varying the distal O-substituents. As expected, the water solubilities of the new analogs are greatly improved, and the melting points are lower. However, the antimalarial potency of the new analogs is reduced to EC > 1 millimolar, a result ascribable to the hydrophilic nature of the new substitution.

摘要

为了提高药物相似性质量,抗疟内源性啉类喹诺酮(ELQ)支架已通过用异亚单位取代 4-(三氟甲氧基)苯基部分进行修饰,通过改变远端 O-取代基进一步调节。正如预期的那样,新类似物的水溶性大大提高,熔点降低。然而,新类似物的抗疟效力降低到 EC>1 毫摩尔,这归因于新取代基的亲水性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc03/11314205/7f7850e4960d/molecules-29-03615-g001.jpg

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