| Literature DB >> 34917255 |
Emanuele M Gargano1, Abdelrahman Mohamed1,2, Ahmed S Abdelsamie3,4, Giuseppe F Mangiatordi5, Hanna Drzewiecka6, Paweł P Jagodziński6, Arcangela Mazzini1, Chris J van Koppen7, Matthias W Laschke8, Orazio Nicolotti5, Angelo Carotti5, Sandrine Marchais-Oberwinkler1, Rolf W Hartmann1,3, Martin Frotscher1.
Abstract
In the face of the clinical challenge posed by non-small cell lung cancer (NSCLC), the present need for new therapeutic approaches is genuine. Up to now, no proof existed that 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) is a viable target for treating this disease. Synthesis of a rationally designed library of 2,5-disubstituted furan derivatives followed by biological screening led to the discovery of 17β-HSD1 inhibitor 1, capable of fully inhibiting human NSCLC Calu-1 cell proliferation. Its pharmacological profile renders it eligible for further in vivo studies. The very high selectivity of 1 over 17β-HSD2 was investigated, revealing a rational approach for the design of selective inhibitors. 17β-HSD1 and 1 hold promise in fighting NSCLC.Entities:
Year: 2021 PMID: 34917255 PMCID: PMC8667298 DOI: 10.1021/acsmedchemlett.1c00462
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345