Amesilide, a New Bicyclic Polyketide from the Marine Fungus Amesia nigricolor MUT6601 Article Swipe
Giang Nam Pham
,
Matteo Florio Furno
,
Juan A. Garcia-Sanchez
,
Patrick Munro
,
Fatouma Mohamed Abdoul‐Latif
,
Laurent Boyer
,
Giovanna Cristina Varese
,
Mohamed Mehiri
·
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.3390/molecules30153169
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.3390/molecules30153169
A new bicyclic polyketide, amesilide (1), along with the previously reported metabolites, chamisides A (2), B (3), and E (4), chaetoconvosins B (5) and C (6), and chaetochromins A (7) and B (8), were isolated from the marine fungus Amesia nigricolor MUT6601. The structures of the compounds were determined by extensive spectrometric (HRMS) and spectroscopic (1D and 2D NMR) analyses, as well as specific rotation. Absolute configurations of the stereogenic centers of amesilide (1) were determined by a comparison of its experimental circular dichroism (CD) spectrum with its time-dependent density functional theory (TD-DFT) electronic circular dichroism (ECD) spectra. Among them, chaetochromins A (7) and B (8) showed strong antibacterial activity against Staphylococcus aureus S25 (MBC values of 12.50 µM and MIC values of 6.25 µM) and a moderate cytotoxicity against monocytes (THP-1) and peripheral blood cells (PBMC) (IC50 values of 33.65–40.01 µM).
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.3390/molecules30153169
- OA Status
- gold
- References
- 21
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4412867234
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4412867234Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.3390/molecules30153169Digital Object Identifier
- Title
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Amesilide, a New Bicyclic Polyketide from the Marine Fungus Amesia nigricolor MUT6601Work title
- Type
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articleOpenAlex work type
- Language
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enPrimary language
- Publication year
-
2025Year of publication
- Publication date
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2025-07-29Full publication date if available
- Authors
-
Giang Nam Pham, Matteo Florio Furno, Juan A. Garcia-Sanchez, Patrick Munro, Fatouma Mohamed Abdoul‐Latif, Laurent Boyer, Giovanna Cristina Varese, Mohamed MehiriList of authors in order
- Landing page
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https://doi.org/10.3390/molecules30153169Publisher landing page
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YesWhether a free full text is available
- OA status
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goldOpen access status per OpenAlex
- OA URL
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https://doi.org/10.3390/molecules30153169Direct OA link when available
- Concepts
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Stereocenter, Circular dichroism, Stereochemistry, Polyketide, Chemistry, Bicyclic molecule, Cytotoxicity, Antibacterial activity, Fungus, Absolute configuration, Biology, Bacteria, Enzyme, In vitro, Biochemistry, Biosynthesis, Enantioselective synthesis, Botany, Genetics, CatalysisTop concepts (fields/topics) attached by OpenAlex
- Cited by
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0Total citation count in OpenAlex
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21Number of works referenced by this work
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10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.and | 17, 23, 26, 30, 53, 56, 103, 119, 125, 132 |
| abstract_inverted_index.its | 80, 87 |
| abstract_inverted_index.new | 1 |
| abstract_inverted_index.the | 8, 36, 45, 68 |
| abstract_inverted_index.µM | 118 |
| abstract_inverted_index.(1), | 5 |
| abstract_inverted_index.(2), | 14 |
| abstract_inverted_index.(3), | 16 |
| abstract_inverted_index.(4), | 19 |
| abstract_inverted_index.(6), | 25 |
| abstract_inverted_index.(8), | 32 |
| abstract_inverted_index.(CD) | 84 |
| abstract_inverted_index.(MBC | 114 |
| abstract_inverted_index.6.25 | 123 |
| abstract_inverted_index.NMR) | 58 |
| abstract_inverted_index.from | 35 |
| abstract_inverted_index.well | 61 |
| abstract_inverted_index.were | 33, 47, 74 |
| abstract_inverted_index.with | 7, 86 |
| abstract_inverted_index.µM) | 124 |
| abstract_inverted_index.(ECD) | 96 |
| abstract_inverted_index.(IC50 | 137 |
| abstract_inverted_index.12.50 | 117 |
| abstract_inverted_index.Among | 98 |
| abstract_inverted_index.along | 6 |
| abstract_inverted_index.blood | 134 |
| abstract_inverted_index.cells | 135 |
| abstract_inverted_index.them, | 99 |
| abstract_inverted_index.µM). | 141 |
| abstract_inverted_index.(HRMS) | 52 |
| abstract_inverted_index.(PBMC) | 136 |
| abstract_inverted_index.Amesia | 39 |
| abstract_inverted_index.aureus | 112 |
| abstract_inverted_index.fungus | 38 |
| abstract_inverted_index.marine | 37 |
| abstract_inverted_index.showed | 106 |
| abstract_inverted_index.strong | 107 |
| abstract_inverted_index.theory | 91 |
| abstract_inverted_index.values | 115, 121, 138 |
| abstract_inverted_index.(THP-1) | 131 |
| abstract_inverted_index.against | 110, 129 |
| abstract_inverted_index.centers | 70 |
| abstract_inverted_index.density | 89 |
| abstract_inverted_index.(TD-DFT) | 92 |
| abstract_inverted_index.Absolute | 65 |
| abstract_inverted_index.MUT6601. | 41 |
| abstract_inverted_index.activity | 109 |
| abstract_inverted_index.bicyclic | 2 |
| abstract_inverted_index.circular | 82, 94 |
| abstract_inverted_index.isolated | 34 |
| abstract_inverted_index.moderate | 127 |
| abstract_inverted_index.reported | 10 |
| abstract_inverted_index.specific | 63 |
| abstract_inverted_index.spectra. | 97 |
| abstract_inverted_index.spectrum | 85 |
| abstract_inverted_index.amesilide | 4, 72 |
| abstract_inverted_index.analyses, | 59 |
| abstract_inverted_index.compounds | 46 |
| abstract_inverted_index.dichroism | 83, 95 |
| abstract_inverted_index.extensive | 50 |
| abstract_inverted_index.monocytes | 130 |
| abstract_inverted_index.rotation. | 64 |
| abstract_inverted_index.chamisides | 12 |
| abstract_inverted_index.comparison | 78 |
| abstract_inverted_index.determined | 48, 75 |
| abstract_inverted_index.electronic | 93 |
| abstract_inverted_index.functional | 90 |
| abstract_inverted_index.nigricolor | 40 |
| abstract_inverted_index.peripheral | 133 |
| abstract_inverted_index.previously | 9 |
| abstract_inverted_index.structures | 43 |
| abstract_inverted_index.polyketide, | 3 |
| abstract_inverted_index.stereogenic | 69 |
| abstract_inverted_index.cytotoxicity | 128 |
| abstract_inverted_index.experimental | 81 |
| abstract_inverted_index.metabolites, | 11 |
| abstract_inverted_index.33.65–40.01 | 140 |
| abstract_inverted_index.antibacterial | 108 |
| abstract_inverted_index.spectrometric | 51 |
| abstract_inverted_index.spectroscopic | 54 |
| abstract_inverted_index.Staphylococcus | 111 |
| abstract_inverted_index.chaetochromins | 27, 100 |
| abstract_inverted_index.configurations | 66 |
| abstract_inverted_index.time-dependent | 88 |
| abstract_inverted_index.chaetoconvosins | 20 |
| cited_by_percentile_year | |
| corresponding_author_ids | https://openalex.org/A5029466059 |
| countries_distinct_count | 3 |
| institutions_distinct_count | 8 |
| corresponding_institution_ids | https://openalex.org/I1294671590, https://openalex.org/I201841394, https://openalex.org/I4210086528 |
| sustainable_development_goals[0].id | https://metadata.un.org/sdg/14 |
| sustainable_development_goals[0].score | 0.8899999856948853 |
| sustainable_development_goals[0].display_name | Life below water |
| citation_normalized_percentile.value | 0.35408747 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |