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Isolation structural chracteristic and biological activity ( )-mikanokryptin. 


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The compound (-)-mikanokryptin, a cytotoxic guaianolide, has been extensively studied for its isolation, structural characteristics, and biological activity. The stereochemistry of mikanokryptin has been defined using X-ray diffraction analysis, revealing specific torsion angles and crystal structure details . Additionally, the compound has been synthesized through a total synthesis approach, showcasing its trans-fused 8,12-guaianolide structure derived from (+)-carvone . Studies on the isolation of biologically active compounds have highlighted the use of affinity chromatography for isolating such compounds from natural sources, emphasizing the importance of solid carriers in this process . Overall, the research on mikanokryptin underscores its structural complexity, synthesis pathways, and potential biological activities, contributing to the broader understanding of guaianolides as medicinal agents.

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(+)-Mikanokryptin, a trans-fused 8,12-guaianolide, was isolated in 1975. Its total synthesis from (+)-carvone was achieved in 10 steps, marking the first gram-scale synthesis of a guaianolide natural product.
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The X-ray crystallographic analysis of mikanokryptin revealed its structure, confirming its constitution and stereochemistry. The compound is a cytotoxic guaianolide with a defined molecular structure.
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