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Scalable synthesis of withanolides: A significant development in cancer research<\/h1>E-News<\/a>, Molecular Diagnostics<\/a> <\/span><\/span><\/header>\n<\/div><\/section>
\nResearchers at Moffitt Cancer Center have developed a novel method for the scalable synthesis of withanolides, a class of naturally occurring compounds with significant potential in cancer treatment. This groundbreaking approach, published in Science Advances [1], could revolutionise cancer research by providing a reliable and efficient means of producing these vital compounds in large quantities.<\/strong><\/p>\n
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Withanolides have long been a focus of cancer research due to their ability to inhibit cancer cell growth, induce cell death, and prevent metastasis. However, the difficulty of obtaining enough of these compounds from plants has hindered research and therapeutic development. The new synthesis route developed by the Moffitt team addresses this challenge, enabling the production of withanolides on a gram scale.<\/p>\n
A bioinspired approach<\/h4>\nThe key to this innovative synthesis is a bioinspired photooxygenation-allylic hydroperoxide rearrangement sequence. This approach facilitates the introduction of functional groups at the late stages of the synthesis, ensuring scalability and allowing for the concise preparation of numerous different withanolides from the same synthesis. Dr Justin M. Lopchuk, lead author and associate member of the Drug Discovery Department at Moffitt, said: “Our new synthesis route represents a major step forward in the field of withanolide chemistry. By enabling the diversifiable production of these compounds on a gram scale, we can now support more extensive biological research and medicinal chemistry efforts.”<\/p>\n<\/div><\/section>
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Researchers at Moffitt Cancer Center have developed a novel method for the scalable synthesis of withanolides, a class of naturally occurring compounds with significant potential in cancer treatment. This groundbreaking approach, published in Science Advances [1], could revolutionise cancer research by providing a reliable and efficient means of producing these vital compounds in large quantities.<\/strong><\/p>\n
<\/p>\n
Withanolides have long been a focus of cancer research due to their ability to inhibit cancer cell growth, induce cell death, and prevent metastasis. However, the difficulty of obtaining enough of these compounds from plants has hindered research and therapeutic development. The new synthesis route developed by the Moffitt team addresses this challenge, enabling the production of withanolides on a gram scale.<\/p>\n
A bioinspired approach<\/h4>\nThe key to this innovative synthesis is a bioinspired photooxygenation-allylic hydroperoxide rearrangement sequence. This approach facilitates the introduction of functional groups at the late stages of the synthesis, ensuring scalability and allowing for the concise preparation of numerous different withanolides from the same synthesis. Dr Justin M. Lopchuk, lead author and associate member of the Drug Discovery Department at Moffitt, said: “Our new synthesis route represents a major step forward in the field of withanolide chemistry. By enabling the diversifiable production of these compounds on a gram scale, we can now support more extensive biological research and medicinal chemistry efforts.”<\/p>\n<\/div><\/section>
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