Drug Synthesis

As biocompatible linkers, triazoles are stable to metabolic degradation and capable of readily combining with biological targets, through hydrogen bonding and dipole-dipole interactions^[1]. In addition, they possess high tolerance to a wide range of acidic and alkaline conditions, as well as oxidation and reduction conditions. Therefore, triazoles have received extensive attention in pharmaceutical science. Click chemistry is a promising approach to the rapid synthesis of triazoles due to its high efficiency, reliability and stereoselectivity. These triazoles are powerful and versatile tools and can be used in the synthesis of antiviral agents, anticancer agents, and antibacterial agents. Alfa Chemistry is an expert in click chemistry. We provide you with technical support and services so that you explore the application of click chemistry in drug synthesis. To learn more about the role of click chemistry in drug synthesis, please click on the links below.

Antiviral Agent Synthesis

Click chemistry has become the preferred choice for the synthesis of antiviral agents because of its convenience and effectiveness.

Anticancer Agent Synthesis

Click chemistry is widely used in the synthesis of anticancer agents because it can attach small units to produce more complicated molecules.

Antibacterial Agent Synthesis

Click chemistry provides a new approach to the efficient and clean creation of antibacterial agents under extremely mild conditions.

Reference

1. Kaur, J.; et al. An overview of recent advances in biomedical applications of click chemistry. Bioconjugate Chemistry. 2021, 8(32): 1455-1471.