Abstract
Abstract Narciclasine is a promising anti-cancer agent produced by plants of the family Amaryllidaceae. Narciclasine has been shown to be a potent anti-cancer agent against a variety of cancers carrying dismal outcomes, including glioblastoma, non-small cell lung cancer, and non-Hodgkin’s lymphoma. It is particularly effective in animal studies of brain cancer both primary, such as glioblastoma, metastatic tumors to the brain, such as melanoma and non-small cell lung cancer. Its isolation from plants has generally been accompanied with variable success as it depends on the plant species, their location and the time of plant collection. In this study, an optimized procedure for the extraction of narciclasine yielding 300 mg/kg of dried plant material. This represents a crucial step towards the development of optimized narciclasine derivatives, as the price of narciclasine from commercial sources ranges from $100-$500 per milligram. Additionally, clinical advancement of narciclasine and its derivatives has been severely thwarted, potentially owing to its sparing water-solubility. Insolubility in water makes administration at therapeutic dosages difficult and can lead to unfavorable pharmacokinetic and pharmacodynamic characteristics. To this effort, the synthesis of five prodrug esters of narciclasine is presented, with the target of a water-soluble narciclasine prodrug. Citation Format: Alexander Kornienko, Ryan Rutledge. Novel efficient isolation and water-soluble prodrug preparation of anti-cancer natural product narciclasine [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 1818.
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