The book “Key Heterocyclic Cores for Smart Anticancer Drug–Design Part I” is an overview of various green methodologies for the synthesis of these heterocyclic cores. Furthermore, we also looked at ...

In this articale, we have described a new practical cyclocondensation synthesis for a series of [1,2,4]triazolo[4,3-c]pyrido[3,2-e] pyrimidine and pyrido[2',3':4,5] pyrimido[6,1-c][1,2,4] triazine ...

Recent investigations into heterocyclic compounds have yielded promising antimicrobial agents through innovative synthetic strategies and advanced computational methods. These compounds, distinguished ...

The book "Key Heterocyclic Cores for Smart Anticancer Drug–Design Part I" is an overview of various green methodologies for the synthesis of these heterocyclic cores. Furthermore, we also looked at ...

Researchers have pioneered a new catalytic transformation that converts epoxides into fluorinated oxetanes, a coveted but difficult-to-make class of drug molecules that escaped synthetic preparation ...

In a recent Food Science and Human Wellness study, researchers review the carcinogenic and mutagenic properties of heterocyclic aromatic amines (HAAs), which are common contaminants present in various ...

Pyrimidines are a class of heterocyclic aromatic organic compounds, characterized by a single six-membered ring structure composed of four carbon atoms and two nitrogen atoms. They are one of the two ...

1-Diazidocarbamoyl-5-azidotetrazole, informally called “azidoazide azide”, is a heterocyclic organic compound crammed with 14 nitrogen atoms. Because of the large number of high-energy nitrogen bonds, ...

Co. Ltd. has disclosed heterocyclic compounds acting as protein arginine N-methyltransferase 5 (PRMT5) inhibitors reported to be useful for the treatment of cancer.