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Home»Science»Unlocking the Secrets of ‘Mirror Molecules’ for Innovative Medicines
Science

Unlocking the Secrets of ‘Mirror Molecules’ for Innovative Medicines

October 11, 2024No Comments4 Mins Read
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Researchers have developed a groundbreaking new chemical reaction that enables the synthesis of specific versions of “mirror molecules” found in nature. This discovery has the potential to revolutionize the development of novel treatments for a wide range of conditions, including cancer, infections, depression, and inflammation. By selectively producing the desired enantiomers, scientists can now explore the therapeutic potential of these natural compounds more efficiently. Enantiomers are “mirror image” molecules that have the same chemical properties but can react differently in the human body.

A look into 'mirror molecules' may lead to new medicines
University of Texas at Dallas chemist Dr. Filippo Romiti, assistant professor of chemistry and biochemistry, and his colleagues have developed a new chemical reaction that will allow researchers to synthesize selectively the left-handed or right-handed versions of “mirror molecules” found in nature and assess them for potential use against cancer, infection, depression, inflammation and a host of other conditions. The research was published in the Oct. 11, 2024, issue of the journal Science. Credit: The University of Texas at Dallas

Revolutionizing Medicinal Chemistry with ‘Mirror Molecules’

A team of researchers, led by Dr. Filippo Romiti from the University of Texas at Dallas, has made a significant breakthrough in the field of medicinal chemistry. They have developed a new chemical reaction that allows for the selective synthesis of left-handed or right-handed versions of “mirror molecules” found in nature.

These mirror molecules, or enantiomers, are critically important in the development of new medicines. While they have identical chemical properties, their interactions within the human body can differ. Identifying the specific enantiomer with the desired biological effect is essential for creating effective and safe drugs. The researchers’ new method enables the efficient and scalable production of a pure sample of the desired enantiomer, as opposed to a mixture of both versions.

Harnessing Nature’s Synthetic Prowess for Drug Discovery

Naturally occurring compounds are a rich source of potential new medicines, but accessing them in sufficient quantities has been a longstanding challenge. The researchers’ discovery addresses this issue by providing a cost-effective and energy-efficient way to synthesize large amounts of these biologically active molecules.

The new chemical reaction involves adding prenyl groups – molecules composed of five carbon atoms – to enones, a process that mimics the way nature assembles these mirror molecules. “Nature is the best synthetic chemist of all; she’s way ahead of us,” said Dr. Romiti, a corresponding author of the study published in the journal Science. “This research represents a paradigm shift in the way we can now synthesize large quantities of biologically active molecules and test them for therapeutic activity.”

Unlocking the Therapeutic Potential of Mirror Molecules

The researchers demonstrated the versatility of their new method by synthesizing enantiomers of eight polycyclic polyprenylated acylphloroglucinols (PPAPs), a class of natural products with a wide range of bioactivities. One of the compounds they produced, nemorosonol, has previously been shown to have antibiotic properties, but it was unclear which enantiomer was responsible for this activity.

By testing their pure enantiomer of nemorosonol, the researchers found that it had promising effects against lung and breast cancer cell lines. This discovery highlights the importance of studying the individual enantiomers, as the therapeutic potential of these mirror molecules may vary significantly.

The researchers believe that their new synthesis method will enable more efficient drug discovery and development, allowing for the exploration of a vast array of natural product analogs – optimized versions of the natural compounds that may be more potent or selective in their biological effects. “We now have access to potent natural products that we previously could not synthesize in the lab,” said Dr. Romiti, emphasizing the transformative potential of this breakthrough.

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Tech enthusiast by profession, passionate blogger by choice. When I'm not immersed in the world of technology, you'll find me crafting and sharing content on this blog. Here, I explore my diverse interests and insights, turning my free time into an opportunity to connect with like-minded readers.

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