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Bioactive Secondary Metabolites Isolated from the Antarctic Lichen Himantormia lugubris
Two new depsidones, himantormiones A and B (1 and 2) were isolated and identified from the Antarctic lichen, Himantormia lugubris (Parmeliaceae), with seven known compounds (3–9). The structures of two new compounds (1 and 2) were determined by means of spectroscopic analyses, including 1D and 2D NM...
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Published in: | Chemistry & biodiversity 2022-10, Vol.19 (10), p.e202200374-n/a |
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creator | Hyung Koo, Man Shin, Min‐Ji Ju Kim, Min Lee, Seulah Eun So, Jae Hee Kim, Ji Hyuck Lee, Jun Suh, Sung‐Suk Joung Youn, Ui |
description | Two new depsidones, himantormiones A and B (1 and 2) were isolated and identified from the Antarctic lichen, Himantormia lugubris (Parmeliaceae), with seven known compounds (3–9). The structures of two new compounds (1 and 2) were determined by means of spectroscopic analyses, including 1D and 2D NMR and HR‐MS. The isolated compounds were tested for antimicrobial and cytotoxic activities, where himantormione B (2) exhibited inhibitory effect against Staphylococcus aureus with the IC50 value of 7.01±0.85 mM. Compound 2 also exhibited strong cytotoxic activity against HCT116 cells (colon cancer) with the EC50 value of 1.11±0.85 μM, where that of the positive control, 5‐fluouracil, was 9.4±1.90 μM. |
doi_str_mv | 10.1002/cbdv.202200374 |
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Compound 2 also exhibited strong cytotoxic activity against HCT116 cells (colon cancer) with the EC50 value of 1.11±0.85 μM, where that of the positive control, 5‐fluouracil, was 9.4±1.90 μM.</description><identifier>ISSN: 1612-1872</identifier><identifier>EISSN: 1612-1880</identifier><identifier>DOI: 10.1002/cbdv.202200374</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Antiinfectives and antibacterials ; antimicrobial ; Antimicrobial agents ; Colon ; Colon cancer ; Cytotoxicity ; depsidone ; Himantormia ; Himantormia lugubris ; lichen ; Lichens ; Metabolites ; NMR ; Nuclear magnetic resonance ; Polar environments ; Secondary metabolites ; Two dimensional analysis</subject><ispartof>Chemistry & biodiversity, 2022-10, Vol.19 (10), p.e202200374-n/a</ispartof><rights>2022 Wiley‐VHCA AG, Zurich, Switzerland</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2804-dcb89109825d2ab2f2789c680fe38c40aa15ea732ac415a6cc25666f0c115d923</citedby><cites>FETCH-LOGICAL-c2804-dcb89109825d2ab2f2789c680fe38c40aa15ea732ac415a6cc25666f0c115d923</cites><orcidid>0000-0002-3217-1010</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Hyung Koo, Man</creatorcontrib><creatorcontrib>Shin, Min‐Ji</creatorcontrib><creatorcontrib>Ju Kim, Min</creatorcontrib><creatorcontrib>Lee, Seulah</creatorcontrib><creatorcontrib>Eun So, Jae</creatorcontrib><creatorcontrib>Hee Kim, Ji</creatorcontrib><creatorcontrib>Hyuck Lee, Jun</creatorcontrib><creatorcontrib>Suh, Sung‐Suk</creatorcontrib><creatorcontrib>Joung Youn, Ui</creatorcontrib><title>Bioactive Secondary Metabolites Isolated from the Antarctic Lichen Himantormia lugubris</title><title>Chemistry & biodiversity</title><description>Two new depsidones, himantormiones A and B (1 and 2) were isolated and identified from the Antarctic lichen, Himantormia lugubris (Parmeliaceae), with seven known compounds (3–9). The structures of two new compounds (1 and 2) were determined by means of spectroscopic analyses, including 1D and 2D NMR and HR‐MS. The isolated compounds were tested for antimicrobial and cytotoxic activities, where himantormione B (2) exhibited inhibitory effect against Staphylococcus aureus with the IC50 value of 7.01±0.85 mM. Compound 2 also exhibited strong cytotoxic activity against HCT116 cells (colon cancer) with the EC50 value of 1.11±0.85 μM, where that of the positive control, 5‐fluouracil, was 9.4±1.90 μM.</description><subject>Antiinfectives and antibacterials</subject><subject>antimicrobial</subject><subject>Antimicrobial agents</subject><subject>Colon</subject><subject>Colon cancer</subject><subject>Cytotoxicity</subject><subject>depsidone</subject><subject>Himantormia</subject><subject>Himantormia lugubris</subject><subject>lichen</subject><subject>Lichens</subject><subject>Metabolites</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Polar environments</subject><subject>Secondary metabolites</subject><subject>Two dimensional analysis</subject><issn>1612-1872</issn><issn>1612-1880</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAQhi0EEqWwMltiYUmxL4njjG35aKUiBr7GyHEc6iqJi-0U9d_jqqhILEx3Oj3P6e5F6JKSESUEbmRZbUZAAAiJs-QIDSijEFHOyfGhz-AUnTm3CnyY8wF6n2gjpNcbhZ-VNF0l7BY_Ki9K02ivHJ470wivKlxb02K_VHjceWGDIvFCy6Xq8Ey3ovPGtlrgpv_oS6vdOTqpRePUxU8dotf7u5fpLFo8Pcyn40UkgZMkqmTJc0pyDmkFooQaMp5LxkmtYi4TIgRNlchiEDKhqWBSQsoYq4mkNK1yiIfoer93bc1nr5wvWu2kahrRKdO7AjISBzOjPKBXf9CV6W0XrgsUMJqwPGeBGu0paY1zVtXF2ob_7LagpNjlXOxyLg45ByHfC1-6Udt_6GI6uX37db8BeR-BJg</recordid><startdate>202210</startdate><enddate>202210</enddate><creator>Hyung Koo, Man</creator><creator>Shin, Min‐Ji</creator><creator>Ju Kim, Min</creator><creator>Lee, Seulah</creator><creator>Eun So, Jae</creator><creator>Hee Kim, Ji</creator><creator>Hyuck Lee, Jun</creator><creator>Suh, Sung‐Suk</creator><creator>Joung Youn, Ui</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3217-1010</orcidid></search><sort><creationdate>202210</creationdate><title>Bioactive Secondary Metabolites Isolated from the Antarctic Lichen Himantormia lugubris</title><author>Hyung Koo, Man ; 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The structures of two new compounds (1 and 2) were determined by means of spectroscopic analyses, including 1D and 2D NMR and HR‐MS. The isolated compounds were tested for antimicrobial and cytotoxic activities, where himantormione B (2) exhibited inhibitory effect against Staphylococcus aureus with the IC50 value of 7.01±0.85 mM. Compound 2 also exhibited strong cytotoxic activity against HCT116 cells (colon cancer) with the EC50 value of 1.11±0.85 μM, where that of the positive control, 5‐fluouracil, was 9.4±1.90 μM.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/cbdv.202200374</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-3217-1010</orcidid></addata></record> |
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subjects | Antiinfectives and antibacterials antimicrobial Antimicrobial agents Colon Colon cancer Cytotoxicity depsidone Himantormia Himantormia lugubris lichen Lichens Metabolites NMR Nuclear magnetic resonance Polar environments Secondary metabolites Two dimensional analysis |
title | Bioactive Secondary Metabolites Isolated from the Antarctic Lichen Himantormia lugubris |
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