51猎奇入口

As the world faces new and often untreatable viral threats, 51猎奇入口 researchers have found a way to cut years off the time it takes to discover antiviral drugs.

The research enables scientists to quickly create large libraries of nucleoside analogs (NAs), compounds that mimic the building blocks of DNA and RNA and are widely used to treat cancer and viral infections such as HIV and hepatitis.

The new method could significantly reduce the time and resources needed for early-stage drug discovery.

鈥淭his is a game changer for making and modifying nucleosides,鈥� explains Robert Britton, chemistry professor and lead author of the study. 鈥淚n an emerging outbreak, the more compounds you can screen, the better your chances of finding something effective. With this method, we can produce libraries 10 to 100 times larger in just weeks, rather than months or years.鈥�

鈥淲e have lots of pain killers and a wide collection of antibiotics, but we don鈥檛 have a good of a panel of antivirals, which is why viral outbreaks like COVID-19, or Ebola, or hantavirus scare people so much,鈥� says Britton. 鈥淔inding viable drug candidates is extremely challenging.鈥�

To identify new treatments, scientists typically screen libraries of molecules to find promising 鈥渉its鈥� for further development. This approach helped companies like Merck & Co. and Gilead Sciences develop early COVID-19 treatments.

But in antiviral discovery, scale matters. Generating large libraries of molecules to screen has been limited by complex chemistry.

In published in Science, Britton and his research team which included scientists at the drug company Merck, began with a single, scalable building block 鈥� one versatile molecular starting point that can be produced in large quantities.

Using a light-driven reaction, the team attached different nucleobases to this core structure, quickly generating a library of more than 70 NAs.

To test whether the approach could find useful drug candidates, the researchers screened the library against HIV. Three compounds showed activity comparable to approved HIV therapies.

鈥淢ost of the compounds in our library were entirely new,鈥� Britton says. 鈥淎 few had been made before, but it took other groups longer to synthesize those molecules, and they were not able to modify and improve them as readily.鈥�