Bacterial infections have attracted the attention of researchers in recent decades, especially
due to the special problems they have faced, such as their increasing diversity and …

Herein, a one-pot synthesis of tetra-substituted imidazole, 4-chloro-2-(1-(4-methoxyphenyl)-
4, 5-diphenyl-1H-imidazol-2-yl) phenol (HL), is reported by the reaction of benzil, 5 …

Benzimidazole scaffolds have potent anticancer activity due to their structure similarity to
nucleoside. In addition, benzimidazoles could function as hydrogen donors or acceptors and …

Abstract Citral (1a), a bioactive component of Cymbopogon citratus (lemongrass) could be
isolated and semi‐synthetic analogs synthesized with improved therapeutic properties …

The worldwide impact of cancer is further compounded by the constraints of current
anticancer medications, which frequently exhibit a lack of selectivity, raise safety …

O-phenylenediamine and formic acid are condensed to create the commercially accessible
benzimidazole. The most common benzimidazole substance found in nature is N …

Diarylether (DE) is a privileged structure found in both natural products and synthetic
compounds including small molecule drugs. We present the synthesis of a series of 13 new …

Wild bitter gourd (Momordica charantia var. abbreviata Ser.) shows diverse pharmacological
effects, especially containing many phytocompounds with potential antidiabetic activity. Forty …

The main components of black ginger (Kaempferia parviflora Wall ex Baker.) show diverse
biological effects, especially potential anticancer activity. Thirty-five bioactive compounds …

Tóm tắt A novel series of s-triazine derivatives was designed and screened for in silico
anticancer activity in histone deacetylase 6 (HDAC6) target by molecular docking method …