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Quinolone antibiotic derivatives as new selective Axl kinase inhibitors.

Abstract：

:Axl is a new promising molecular target for antineoplastic therapies. A series of quinolone antibiotic derivatives were designed and synthesized as new selective Axl inhibitors. One of the most promising compound 8i bound tightly to Axl with a Kd value of 1.1 nM, and inhibited its kinase activity with an IC50 value of 26 nM. The compound also significantly inhibited the phosphorylation of Axl and dose dependently inhibited cell invasion and migration in TGF-β1 induced MDA-MD-231 breast cancer cells. In addition, 8i demonstrated reasonable pharmacokinetic properties and exhibited extraordinary target selectivity over 468 kinases except for Flt3 (IC50 = 50 nM)), with a S(10) and S(35) value of 0.022 and 0.42 at 1.0 μM, respectively. Compound 8i may serve as a new valuable lead compound for future anticancer drug discovery.

journal_name

Eur J Med Chem

journal_title

European journal of medicinal chemistry

authors

Tan L,Zhang Z,Gao D,Chan S,Luo J,Tu ZC,Zhang ZM,Ding K,Ren X,Lu X

doi

10.1016/j.ejmech.2019.01.065

subject

Has Abstract

pub_date

2019-03-15 00:00:00

pages

318-327

eissn

0223-5234

issn

1768-3254

pii

S0223-5234(19)30085-6

journal_volume

166

pub_type

杂志文章

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