Phytochemical Constituents from the Aerial Part of Ducrosia ismaelis Asch
Phytochemical investigation of the aerial components of Ducrosia ismaelis Asch. led to the isolation of six known compounds, psoralen (1), isopsoralen (2), cnidioside A (3), (-)-syringaresinol-O-${\beta}$-D-glucopyranoside (4), (E)-plicatin B (5), trilinolein (6). The chemical structures of these co...
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Veröffentlicht in: | Natural product sciences 2015, Vol.21 (1), p.6-13 |
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description | Phytochemical investigation of the aerial components of Ducrosia ismaelis Asch. led to the isolation of six known compounds, psoralen (1), isopsoralen (2), cnidioside A (3), (-)-syringaresinol-O-${\beta}$-D-glucopyranoside (4), (E)-plicatin B (5), trilinolein (6). The chemical structures of these compounds were elucidated from spectroscopic data and by comparison of these data with previously published results. The antioxidant, anti-osteoporotic and cardiovascular related activities of the isolated compounds were assessed using oxygen radical absorbance capacity (ORAC), reducing capacity, tartrate-resistant acid phosphatase (TRAP), and soluble epoxide hydrolase (sEH) inhibitory activity assays. Compounds (3-5) showed potent peroxyl radical-scavenging capacities with ORAC values of $11.06{\pm}0.39$, $7.98{\pm}0.10$, and $13.99{\pm}0.06$ Trolox equivalent (TE) at concentrations of $10{\mu}M$, respectively. Only compounds 4 and 5 was able to significantly reduce $Cu^{2+}$ ions, with a reduction value of $9.06{\pm}0.32$ and $4.61{\pm}0.00{\mu}M$ Trolox Equivalent (TE) at a concentration of $10{\mu}M$. Compound 5 at $10{\mu}M$ exhibited a potent inhibitory effect on osteoclastic TRAP activity with a TRAP value of $86.05{\pm}6.55%$ of the control. Compounds 1, 3 and 5 potently inhibited sEH activity with $IC_{50}$ values of 41.6 4.9, 16.0 1.1, and 49.0 $5.7{\mu}M$, respectively. |
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The chemical structures of these compounds were elucidated from spectroscopic data and by comparison of these data with previously published results. The antioxidant, anti-osteoporotic and cardiovascular related activities of the isolated compounds were assessed using oxygen radical absorbance capacity (ORAC), reducing capacity, tartrate-resistant acid phosphatase (TRAP), and soluble epoxide hydrolase (sEH) inhibitory activity assays. Compounds (3-5) showed potent peroxyl radical-scavenging capacities with ORAC values of $11.06{\pm}0.39$, $7.98{\pm}0.10$, and $13.99{\pm}0.06$ Trolox equivalent (TE) at concentrations of $10{\mu}M$, respectively. Only compounds 4 and 5 was able to significantly reduce $Cu^{2+}$ ions, with a reduction value of $9.06{\pm}0.32$ and $4.61{\pm}0.00{\mu}M$ Trolox Equivalent (TE) at a concentration of $10{\mu}M$. Compound 5 at $10{\mu}M$ exhibited a potent inhibitory effect on osteoclastic TRAP activity with a TRAP value of $86.05{\pm}6.55%$ of the control. Compounds 1, 3 and 5 potently inhibited sEH activity with $IC_{50}$ values of 41.6 4.9, 16.0 1.1, and 49.0 $5.7{\mu}M$, respectively.</description><identifier>ISSN: 1226-3907</identifier><language>kor</language><ispartof>Natural product sciences, 2015, Vol.21 (1), p.6-13</ispartof><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024</link.rule.ids></links><search><creatorcontrib>Morgan, Abubaker M.A</creatorcontrib><creatorcontrib>Kim, Jang Hoon</creatorcontrib><creatorcontrib>Lee, Hyun Woo</creatorcontrib><creatorcontrib>Lee, Sang-Hyun</creatorcontrib><creatorcontrib>Lim, Chi-Hwan</creatorcontrib><creatorcontrib>Jang, Hae-Dong</creatorcontrib><creatorcontrib>Kim, Young Ho</creatorcontrib><title>Phytochemical Constituents from the Aerial Part of Ducrosia ismaelis Asch</title><title>Natural product sciences</title><addtitle>Natural product sciences</addtitle><description>Phytochemical investigation of the aerial components of Ducrosia ismaelis Asch. led to the isolation of six known compounds, psoralen (1), isopsoralen (2), cnidioside A (3), (-)-syringaresinol-O-${\beta}$-D-glucopyranoside (4), (E)-plicatin B (5), trilinolein (6). The chemical structures of these compounds were elucidated from spectroscopic data and by comparison of these data with previously published results. The antioxidant, anti-osteoporotic and cardiovascular related activities of the isolated compounds were assessed using oxygen radical absorbance capacity (ORAC), reducing capacity, tartrate-resistant acid phosphatase (TRAP), and soluble epoxide hydrolase (sEH) inhibitory activity assays. Compounds (3-5) showed potent peroxyl radical-scavenging capacities with ORAC values of $11.06{\pm}0.39$, $7.98{\pm}0.10$, and $13.99{\pm}0.06$ Trolox equivalent (TE) at concentrations of $10{\mu}M$, respectively. Only compounds 4 and 5 was able to significantly reduce $Cu^{2+}$ ions, with a reduction value of $9.06{\pm}0.32$ and $4.61{\pm}0.00{\mu}M$ Trolox Equivalent (TE) at a concentration of $10{\mu}M$. Compound 5 at $10{\mu}M$ exhibited a potent inhibitory effect on osteoclastic TRAP activity with a TRAP value of $86.05{\pm}6.55%$ of the control. Compounds 1, 3 and 5 potently inhibited sEH activity with $IC_{50}$ values of 41.6 4.9, 16.0 1.1, and 49.0 $5.7{\mu}M$, respectively.</description><issn>1226-3907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNqNjL0OgjAYADtoIlHeoYsjSVso4EhQ488ggzuptaRfLDTpVwbfXgcfwOmGu9yCJFyIMst3rFqRFBEeTOZ5VdayTsi5s-_otTUjaOVo6yeMEGczRaRD8CON1tDGBPjKToVI_UD3sw4eQVHAURkHSBvUdkOWg3Jo0h_XZHs83NtT9oLvsp-e6PpLc70JxiVnUjLJCymK_N_uA0l5Opc</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>Morgan, Abubaker M.A</creator><creator>Kim, Jang Hoon</creator><creator>Lee, Hyun Woo</creator><creator>Lee, Sang-Hyun</creator><creator>Lim, Chi-Hwan</creator><creator>Jang, Hae-Dong</creator><creator>Kim, Young Ho</creator><scope>JDI</scope></search><sort><creationdate>2015</creationdate><title>Phytochemical Constituents from the Aerial Part of Ducrosia ismaelis Asch</title><author>Morgan, Abubaker M.A ; Kim, Jang Hoon ; Lee, Hyun Woo ; Lee, Sang-Hyun ; Lim, Chi-Hwan ; Jang, Hae-Dong ; Kim, Young Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO2015105505145243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2015</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Morgan, Abubaker M.A</creatorcontrib><creatorcontrib>Kim, Jang Hoon</creatorcontrib><creatorcontrib>Lee, Hyun Woo</creatorcontrib><creatorcontrib>Lee, Sang-Hyun</creatorcontrib><creatorcontrib>Lim, Chi-Hwan</creatorcontrib><creatorcontrib>Jang, Hae-Dong</creatorcontrib><creatorcontrib>Kim, Young Ho</creatorcontrib><collection>KoreaScience</collection><jtitle>Natural product sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morgan, Abubaker M.A</au><au>Kim, Jang Hoon</au><au>Lee, Hyun Woo</au><au>Lee, Sang-Hyun</au><au>Lim, Chi-Hwan</au><au>Jang, Hae-Dong</au><au>Kim, Young Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phytochemical Constituents from the Aerial Part of Ducrosia ismaelis Asch</atitle><jtitle>Natural product sciences</jtitle><addtitle>Natural product sciences</addtitle><date>2015</date><risdate>2015</risdate><volume>21</volume><issue>1</issue><spage>6</spage><epage>13</epage><pages>6-13</pages><issn>1226-3907</issn><abstract>Phytochemical investigation of the aerial components of Ducrosia ismaelis Asch. led to the isolation of six known compounds, psoralen (1), isopsoralen (2), cnidioside A (3), (-)-syringaresinol-O-${\beta}$-D-glucopyranoside (4), (E)-plicatin B (5), trilinolein (6). The chemical structures of these compounds were elucidated from spectroscopic data and by comparison of these data with previously published results. The antioxidant, anti-osteoporotic and cardiovascular related activities of the isolated compounds were assessed using oxygen radical absorbance capacity (ORAC), reducing capacity, tartrate-resistant acid phosphatase (TRAP), and soluble epoxide hydrolase (sEH) inhibitory activity assays. Compounds (3-5) showed potent peroxyl radical-scavenging capacities with ORAC values of $11.06{\pm}0.39$, $7.98{\pm}0.10$, and $13.99{\pm}0.06$ Trolox equivalent (TE) at concentrations of $10{\mu}M$, respectively. Only compounds 4 and 5 was able to significantly reduce $Cu^{2+}$ ions, with a reduction value of $9.06{\pm}0.32$ and $4.61{\pm}0.00{\mu}M$ Trolox Equivalent (TE) at a concentration of $10{\mu}M$. Compound 5 at $10{\mu}M$ exhibited a potent inhibitory effect on osteoclastic TRAP activity with a TRAP value of $86.05{\pm}6.55%$ of the control. Compounds 1, 3 and 5 potently inhibited sEH activity with $IC_{50}$ values of 41.6 4.9, 16.0 1.1, and 49.0 $5.7{\mu}M$, respectively.</abstract><oa>free_for_read</oa></addata></record> |
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