A new series of resveratrol analogues was designed, synthesized, and demonstrated to be
tubulin polymerization inhibitors. Most of these compounds exhibited antiproliferative activity …

Magnetically recoverable and reusable CuFe2O4 nanoparticles are shown to be highly
efficient catalysts for the one‐pot synthesis of biologically important 1, 4‐diaryl‐1, 2, 3 …

A novel series of nitrostyrene-based spirooxindoles were synthesized via the reaction of
substituted isatins 1a–b, a number of α-amino acids 2a–e and (E)-2-aryl-1-nitroethenes 3a …

In continuation of our investigation of pharmacologically-motivated natural products, we
have isolated bergenin (1) as a major compound from Mallotus philippensis, which is …

A new series of Schizandrin (1) derivatives were synthesized utilizing the C-9 position of the
Schizandrin core and evaluated for their cytotoxic activities against HeLa (cervical cancer) …

A series of phenstatin/isocombretastatin–chalcones were synthesized and screened for their
cytotoxic activity against various human cancer cell lines. Some representative compounds …

In an attempt to develop potent and selective anticancer agents, a series of twenty
arylpyrazole linked benzimidazole conjugates (10a–t) were designed and synthesized as …

We present a new class of derivatives of noscapine, 1, 3-diynyl-noscapinoids of an
antitussive plant alkaloid, noscapine based on our in silico efforts that binds tubulin and …

Bcl homologs prominently contribute to apoptotic resistance in cancer cells and serve as
molecular targets in treatment of various cancers. Herein, we report the synthesis of biphenyl …

The Suzuki cross‐coupling reaction of various aryl and heteroaryl halides with arylboronic
and heteroarylboronic acids was studied using a titania‐supported palladium (0) catalyst at …