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Antimicrobial Dihydroflavonols and Isoflavans Isolated from the Root Bark of Dalbergia gloveri
Three new dihydroflavonols, gloverinols A–C (1–3), a new flavon-3-ol, gloverinol D (4), two new isoflavans, gloveriflavan A (5) and B (6), and seven known compounds were isolated from the root bark of Dalbergia gloveri. The structures of the isolates were elucidated by using NMR, ECD, and HRESIMS da...
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Published in: | Journal of natural products (Washington, D.C.) D.C.), 2024-09, Vol.87 (9), p.2263-2271 |
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creator | Kiganda, Ivan Wieske, Lianne H. E. Nchiozem-Ngnitedem, Vaderament-Alexe Chalo, Duncan Umereweneza, Daniel Ndakala, Albert Herrebout, Wouter Xiong, Ruisheng Karpiński, Tomasz M. Yenesew, Abiy Erdelyi, Mate |
description | Three new dihydroflavonols, gloverinols A–C (1–3), a new flavon-3-ol, gloverinol D (4), two new isoflavans, gloveriflavan A (5) and B (6), and seven known compounds were isolated from the root bark of Dalbergia gloveri. The structures of the isolates were elucidated by using NMR, ECD, and HRESIMS data analyses. Among the isolated compounds, gloverinol B (2), gloveriflavan B (6), and 1-(2,4-dihydroxyphenyl)-3-hydroxy-3-(4-hydroxyphenyl)-1-propanone (10) were the most active against Staphylococcus aureus, with MIC values of 9.2, 18.4, and 14.2 μM, respectively. |
doi_str_mv | 10.1021/acs.jnatprod.4c00690 |
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E. ; Nchiozem-Ngnitedem, Vaderament-Alexe ; Chalo, Duncan ; Umereweneza, Daniel ; Ndakala, Albert ; Herrebout, Wouter ; Xiong, Ruisheng ; Karpiński, Tomasz M. ; Yenesew, Abiy ; Erdelyi, Mate</creator><creatorcontrib>Kiganda, Ivan ; Wieske, Lianne H. E. ; Nchiozem-Ngnitedem, Vaderament-Alexe ; Chalo, Duncan ; Umereweneza, Daniel ; Ndakala, Albert ; Herrebout, Wouter ; Xiong, Ruisheng ; Karpiński, Tomasz M. ; Yenesew, Abiy ; Erdelyi, Mate</creatorcontrib><description>Three new dihydroflavonols, gloverinols A–C (1–3), a new flavon-3-ol, gloverinol D (4), two new isoflavans, gloveriflavan A (5) and B (6), and seven known compounds were isolated from the root bark of Dalbergia gloveri. The structures of the isolates were elucidated by using NMR, ECD, and HRESIMS data analyses. Among the isolated compounds, gloverinol B (2), gloveriflavan B (6), and 1-(2,4-dihydroxyphenyl)-3-hydroxy-3-(4-hydroxyphenyl)-1-propanone (10) were the most active against Staphylococcus aureus, with MIC values of 9.2, 18.4, and 14.2 μM, respectively.</description><identifier>ISSN: 0163-3864</identifier><identifier>ISSN: 1520-6025</identifier><identifier>EISSN: 1520-6025</identifier><identifier>DOI: 10.1021/acs.jnatprod.4c00690</identifier><identifier>PMID: 39255387</identifier><language>eng</language><publisher>United States: American Chemical Society and American Society of Pharmacognosy</publisher><subject>Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - isolation & purification ; Anti-Bacterial Agents - pharmacology ; bark ; Dalbergia ; Dalbergia - chemistry ; Flavonoids - chemistry ; Flavonoids - isolation & purification ; Flavonoids - pharmacology ; isoflavans ; Isoflavones - chemistry ; Isoflavones - isolation & purification ; Isoflavones - pharmacology ; Microbial Sensitivity Tests ; Molecular Structure ; Plant Bark - chemistry ; Plant Roots - chemistry ; Staphylococcus aureus ; Staphylococcus aureus - drug effects</subject><ispartof>Journal of natural products (Washington, D.C.), 2024-09, Vol.87 (9), p.2263-2271</ispartof><rights>2024 The Authors. 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The structures of the isolates were elucidated by using NMR, ECD, and HRESIMS data analyses. Among the isolated compounds, gloverinol B (2), gloveriflavan B (6), and 1-(2,4-dihydroxyphenyl)-3-hydroxy-3-(4-hydroxyphenyl)-1-propanone (10) were the most active against Staphylococcus aureus, with MIC values of 9.2, 18.4, and 14.2 μM, respectively.</abstract><cop>United States</cop><pub>American Chemical Society and American Society of Pharmacognosy</pub><pmid>39255387</pmid><doi>10.1021/acs.jnatprod.4c00690</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-0359-5970</orcidid><orcidid>https://orcid.org/0000-0002-3167-8944</orcidid><orcidid>https://orcid.org/0000-0003-4617-7605</orcidid><orcidid>https://orcid.org/0000-0002-1123-3200</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - isolation & purification Anti-Bacterial Agents - pharmacology bark Dalbergia Dalbergia - chemistry Flavonoids - chemistry Flavonoids - isolation & purification Flavonoids - pharmacology isoflavans Isoflavones - chemistry Isoflavones - isolation & purification Isoflavones - pharmacology Microbial Sensitivity Tests Molecular Structure Plant Bark - chemistry Plant Roots - chemistry Staphylococcus aureus Staphylococcus aureus - drug effects |
title | Antimicrobial Dihydroflavonols and Isoflavans Isolated from the Root Bark of Dalbergia gloveri |
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