Quinoline is an efficient scaffold for anticancer drug development as its derivatives have
shown potent results through several mechanisms like growth regulators through “apoptosis …

The quinoline scaffolds are privileged for their numerous biological activities in the
pharmaceutical field. This moiety constitutes a well‐known space in several marketed …

Heterocyclic compounds are a class of compounds of natural origin with favorable
properties and hence have major pharmaceutical significance. They have an exceptional …

Here in, we report the design, synthesis and in vitro anticancer activity of a novel series of 24
quinoline analogues of substituted amide and sulphonamide derivatives. The anticancer …

A novel series of pyrimido [5, 4-c] quinoline derivatives variously substituted at positions 2
and 5 have been synthesized, in good to excellent yields, via rapid base-catalyzed …

The third-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs)
have accomplished impressive clinical achievements in the treatment of non-small-cell lung …

A novel series of substituted thiazolo [5, 4-b] pyridine analogues were rationally designed
and synthesized via a multi-step synthetic pathway, including Suzuki cross-coupling …

In this study, different assortments of 2-arylquinolines and 2, 6-diarylquinolines have been
developed. Recently, we have developed a new series of 6, 7-dimethoxy-4-alkoxy-2 …

Two different schemes of novel substituted quinoline derivatives were designed and
synthesized via simple reaction steps and conditions. A comparative molecular docking …

The role of epidermal growth factor receptor (EGFR) in non-small cell lung cancer (NSCLC)
has been vastly studied over the last decade. This has led to the rapid development of many …