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| Main Authors: | , , , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
Organic letters
2025
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| Subjects: | |
| Online Access: | https://pubmed.ncbi.nlm.nih.gov/40526409/ |
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| _version_ | 1868266191323136001 |
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| author | Hagihara, Masahiro Mehjabin, Jakia Jerin Vairappan, Charles S Okino, Tatsufumi Suenaga, Kiyotake Iwasaki, Arihiro |
| author_facet | Hagihara, Masahiro Mehjabin, Jakia Jerin Vairappan, Charles S Okino, Tatsufumi Suenaga, Kiyotake Iwasaki, Arihiro Hagihara, Masahiro Mehjabin, Jakia Jerin Vairappan, Charles S Okino, Tatsufumi Suenaga, Kiyotake Iwasaki, Arihiro |
| collection | PubMed - marine biology |
| contents | Isolation and Computer-Based Structural Determination of Madangolide B. Hagihara, Masahiro Mehjabin, Jakia Jerin Vairappan, Charles S Okino, Tatsufumi Suenaga, Kiyotake Iwasaki, Arihiro Cyanobacteria Molecular Structure Biological Products Magnetic Resonance Spectroscopy Molecular Conformation Madangolide () is a 17-membered cyclic enamide isolated from the marine cyanobacterium . Since its discovery in 1999, the relative and absolute configurations of have remained unknown. Here, we report the isolation, structural determination, and biological activity of a new analog of madangolide (), madangolide B (), from a marine sp. cyanobacterium. The planar structure of was established using conventional two-dimensional NMR spectroscopy. The absolute configuration was clarified by comparing the experimental and theoretical data, including the chemical shifts, homonuclear and heteronuclear coupling constants, and ECD spectra. Based on the similarity of the NMR data, we proposed an absolute configuration of madangolide () and verified it through degradation and derivatization reactions. This study demonstrates the effectiveness of modern computational chemistry in revealing the stereochemistry of complex natural products with conformational flexibility. |
| format | Artículo científico |
| id | pubmed_40526409 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | Organic letters |
| record_format | pubmed |
| spellingShingle | Isolation and Computer-Based Structural Determination of Madangolide B. Hagihara, Masahiro Mehjabin, Jakia Jerin Vairappan, Charles S Okino, Tatsufumi Suenaga, Kiyotake Iwasaki, Arihiro Cyanobacteria Molecular Structure Biological Products Magnetic Resonance Spectroscopy Molecular Conformation Isolation and Computer-Based Structural Determination of Madangolide B. Hagihara, Masahiro Mehjabin, Jakia Jerin Vairappan, Charles S Okino, Tatsufumi Suenaga, Kiyotake Iwasaki, Arihiro Cyanobacteria Molecular Structure Biological Products Magnetic Resonance Spectroscopy Molecular Conformation Madangolide () is a 17-membered cyclic enamide isolated from the marine cyanobacterium . Since its discovery in 1999, the relative and absolute configurations of have remained unknown. Here, we report the isolation, structural determination, and biological activity of a new analog of madangolide (), madangolide B (), from a marine sp. cyanobacterium. The planar structure of was established using conventional two-dimensional NMR spectroscopy. The absolute configuration was clarified by comparing the experimental and theoretical data, including the chemical shifts, homonuclear and heteronuclear coupling constants, and ECD spectra. Based on the similarity of the NMR data, we proposed an absolute configuration of madangolide () and verified it through degradation and derivatization reactions. This study demonstrates the effectiveness of modern computational chemistry in revealing the stereochemistry of complex natural products with conformational flexibility. |
| title | Isolation and Computer-Based Structural Determination of Madangolide B. |
| topic | Cyanobacteria Molecular Structure Biological Products Magnetic Resonance Spectroscopy Molecular Conformation |
| url | https://pubmed.ncbi.nlm.nih.gov/40526409/ |