Recent advances in the environmentally benign synthesis of aromatic N-heterocycles are
reviewed, focusing primarily on the application of catalytic methods and non-traditional …

Thiazolines and their derivatives hold significant importance in the field of medicinal
chemistry due to their promising potential as pharmaceutical agents. These molecular …

c-Met tyrosine kinase plays a key role in the oncogenic process. Inhibition of the c-Met has
emerged as an attractive target for human cancer treatment. This work deals with the design …

Toxicity and resistance to newly synthesized anticancer drugs represent a challenging
phenomenon of intensified concern arising from variation in drug targets and consequently …

The observed toxicity of newly designed anticancer drugs is considered as an impediment
challenging phenomenon of intense concern arising from diversity in drug targets and the …

Three novel Cd (II) metal complexes 1–3 have been synthesized with different derivatives of
thiazoline, hydrazide and carbodithioate. These metal complexes are abbreviated as [Cd …

New sulfonamide-triazole-glycoside hybrids derivatives were designed, synthesised, and
investigated for anticancer efficacy. The target glycosides' cytotoxic activity was studied with …

The proviral integration for the Moloney murine leukemia virus (PIM) kinases, belonging to
serine/threonine kinase family, have been found to be overexpressed in various types of …

Over the past decades, cancer has been a challenging domain for medicinal chemists as it
is an international health concern. In association, small molecules such as 2 …

The current study focuses on developing a single molecule that acts as an antiproliferative
agent with dual or multi-targeted action, reducing drug resistance and adverse effects. A …