Furan and benzofuran scaffolds are privileged and well-studied heterocyclic rings for
designing and develo** new potential anticancer compounds. Previous literature showed …

One‐pot multi‐component reactions especially under transition‐metal‐free catalysis served
as an efficient, and environmentally friendly method for the construction of value‐added …

To overcome the shortcomings of traditional extraction methods, such as long extraction time
and low efficiency, and considering the low content and high complexity of total flavonoids in …

Of ChtI and Of Chi-h are considered potential targets for the control of Asian corn borer
(Ostrinia furnacalis). In this work, the previously reported Of ChtI inhibitor 5f was found to …

Peptide-based drugs are gaining significant momentum in the modern drug discovery, which
is witnessed by the approval of new drugs by the FDA in recent years. On the other hand …

An important group of heterocyclic compounds with significant biological characteristics are
furan derivatives. The creation of furan derivatives and their testing for various …

Antimicrobial peptides (AMPs) are a promising class of therapeutic alternatives with broad-
spectrum activity against resistant pathogens. Small AMPs like temporin-SHa (1) and its first …

A chiral Lewis acid-catalyzed enantioselective Friedel–Crafts furan alkylation with in situ-
generated o-quinone methides has been developed. In the presence of a chiral …

Background Therapeutic approaches based on glycolysis and energy metabolism of tumor
cells are new promising strategies for the treatment of cancer. Currently, researches on the …

A series of mixed-ligand Cu (II) complexes of the type [Cu (L 1-5)(diimine)(H 2 O)](ClO 4)(1–
5) and [Cu (L 6)(diimine)](ClO 4)(6), where HL 1-HL 4 are aminophenolate Schiff base …