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File:Fig5 Cicaloni Separ22 9-4.png - Revision history
2026-09-26T22:25:05Z
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Shawndouglas: Shawndouglas uploaded File:Fig5 Cicaloni Separ22 9-4.png
2023-12-26T22:53:05Z
<p>Shawndouglas uploaded <a href="/index.php/File:Fig5_Cicaloni_Separ22_9-4.png" title="File:Fig5 Cicaloni Separ22 9-4.png">File:Fig5 Cicaloni Separ22 9-4.png</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 22:53, 26 December 2023</td>
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Shawndouglas
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Shawndouglas: 3 revisions imported
2023-12-20T22:47:48Z
<p>3 revisions imported</p>
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Shawndouglas
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Shawndouglas: /* Summary */ Formatting
2022-08-22T21:28:24Z
<p><span class="autocomment">Summary: </span> Formatting</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 21:28, 22 August 2022</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1">Line 1:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>==Summary==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>==Summary==</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Information</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Information</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Description='''Fig. 5''' Analysis of the top 25 correlated compounds based on Pearson correlation coefficient for δ-9-cis-tetrahydrocannabinol, α-pinene, β-caryophyllene, and β-myrcene. The numbers in the figure represent: 1: (1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]hept-2-yl (6ar,10ar)-1-hydroxy-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromene-2-carboxylate<del style="font-weight: bold; text-decoration: none;">; </del>2: 4-(6-hydroxy-1,2,3,9a-tetrahydro-3ah-spiro[cyclopenta[b]chromene-9,1′-cyclopentan]-3a-yl)-1,3-benzenediol<del style="font-weight: bold; text-decoration: none;">; </del>3:(2R,3R,4R,5R)-2-{(1R)-5-[(5R,7R)-1,6-dioxaspiro[4.5]dec-7-yl]-1-hydroxypentyl}-5-(hydroxymethyl)-3,4-pyrrolidinediol<del style="font-weight: bold; text-decoration: none;">; </del>4: (5Z,8Z,11Z,14Z)-N-(2-furylmethyl)-5,8,11,14-icosatetraenamide<del style="font-weight: bold; text-decoration: none;">; </del>5: 3,19-diacetoxy-5,14-dihydroxycard-20(22)-enolide<del style="font-weight: bold; text-decoration: none;">; </del>6: 5,7,4′-trihydroxy-3,6-dimethoxy-3′,5′-diprenylflavone<del style="font-weight: bold; text-decoration: none;">; </del>7: 1,5-anhydro-2,4,6-tris-O-(3,4,5-trihydroxybenzoyl)-D-glucitol<del style="font-weight: bold; text-decoration: none;">; </del>8: methyl (1R,2R,3S,3ar,8bs)-2,3,3a,8b-tetrahydro-1,6,8b-trihydroxy-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-1H-cyclopenta[b]benzofuran-2-carboxylate<del style="font-weight: bold; text-decoration: none;">.</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Description='''Fig. 5''' Analysis of the top 25 correlated compounds based on Pearson correlation coefficient for δ-9-cis-tetrahydrocannabinol, α-pinene, β-caryophyllene, and β-myrcene. The numbers in the figure represent:<ins style="font-weight: bold; text-decoration: none;"><br /></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>1: (1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]hept-2-yl (6ar,10ar)-1-hydroxy-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromene-2-carboxylate<ins style="font-weight: bold; text-decoration: none;"><br /></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>2: 4-(6-hydroxy-1,2,3,9a-tetrahydro-3ah-spiro[cyclopenta[b]chromene-9,1′-cyclopentan]-3a-yl)-1,3-benzenediol<ins style="font-weight: bold; text-decoration: none;"><br /></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>3:(2R,3R,4R,5R)-2-{(1R)-5-[(5R,7R)-1,6-dioxaspiro[4.5]dec-7-yl]-1-hydroxypentyl}-5-(hydroxymethyl)-3,4-pyrrolidinediol<ins style="font-weight: bold; text-decoration: none;"><br /></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>4: (5Z,8Z,11Z,14Z)-N-(2-furylmethyl)-5,8,11,14-icosatetraenamide<ins style="font-weight: bold; text-decoration: none;"><br /></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>5: 3,19-diacetoxy-5,14-dihydroxycard-20(22)-enolide<ins style="font-weight: bold; text-decoration: none;"><br /></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>6: 5,7,4′-trihydroxy-3,6-dimethoxy-3′,5′-diprenylflavone<ins style="font-weight: bold; text-decoration: none;"><br /></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>7: 1,5-anhydro-2,4,6-tris-O-(3,4,5-trihydroxybenzoyl)-D-glucitol<ins style="font-weight: bold; text-decoration: none;"><br /></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>8: methyl (1R,2R,3S,3ar,8bs)-2,3,3a,8b-tetrahydro-1,6,8b-trihydroxy-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-1H-cyclopenta[b]benzofuran-2-carboxylate<ins style="font-weight: bold; text-decoration: none;"></blockquote></ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source={{cite journal |title=Chemical profiling and characterization of different cultivars of ''Cannabis sativa'' L. inflorescences by SPME-GC-MS and UPLC-MS |journal=Separations |author=Cicaloni, V.; Salvini, L.; Vitalini, S.; Garzoli, S. |volume=9 |issue=4 |at=90 |year=2022 |doi=10.3390/separations9040090}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source={{cite journal |title=Chemical profiling and characterization of different cultivars of ''Cannabis sativa'' L. inflorescences by SPME-GC-MS and UPLC-MS |journal=Separations |author=Cicaloni, V.; Salvini, L.; Vitalini, S.; Garzoli, S. |volume=9 |issue=4 |at=90 |year=2022 |doi=10.3390/separations9040090}}</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Author=Cicaloni, V.; Salvini, L.; Vitalini, S.; Garzoli, S.</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Author=Cicaloni, V.; Salvini, L.; Vitalini, S.; Garzoli, S.</div></td></tr>
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Shawndouglas
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Shawndouglas: Added summary
2022-08-22T21:23:12Z
<p>Added summary</p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 21:23, 22 August 2022</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1">Line 1:</td>
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<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">==Summary==</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">{{Information</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Description='''Fig. 5''' Analysis of the top 25 correlated compounds based on Pearson correlation coefficient for δ-9-cis-tetrahydrocannabinol, α-pinene, β-caryophyllene, and β-myrcene. The numbers in the figure represent: 1: (1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]hept-2-yl (6ar,10ar)-1-hydroxy-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromene-2-carboxylate; 2: 4-(6-hydroxy-1,2,3,9a-tetrahydro-3ah-spiro[cyclopenta[b]chromene-9,1′-cyclopentan]-3a-yl)-1,3-benzenediol; 3:(2R,3R,4R,5R)-2-{(1R)-5-[(5R,7R)-1,6-dioxaspiro[4.5]dec-7-yl]-1-hydroxypentyl}-5-(hydroxymethyl)-3,4-pyrrolidinediol; 4: (5Z,8Z,11Z,14Z)-N-(2-furylmethyl)-5,8,11,14-icosatetraenamide; 5: 3,19-diacetoxy-5,14-dihydroxycard-20(22)-enolide; 6: 5,7,4′-trihydroxy-3,6-dimethoxy-3′,5′-diprenylflavone; 7: 1,5-anhydro-2,4,6-tris-O-(3,4,5-trihydroxybenzoyl)-D-glucitol; 8: methyl (1R,2R,3S,3ar,8bs)-2,3,3a,8b-tetrahydro-1,6,8b-trihydroxy-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-1H-cyclopenta[b]benzofuran-2-carboxylate.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Source={{cite journal |title=Chemical profiling and characterization of different cultivars of ''Cannabis sativa'' L. inflorescences by SPME-GC-MS and UPLC-MS |journal=Separations |author=Cicaloni, V.; Salvini, L.; Vitalini, S.; Garzoli, S. |volume=9 |issue=4 |at=90 |year=2022 |doi=10.3390/separations9040090}}</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Author=Cicaloni, V.; Salvini, L.; Vitalini, S.; Garzoli, S.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Date=2022</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Permission=[http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International]</ins></div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Licensing ==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Licensing ==</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{cc-by-4.0}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{cc-by-4.0}}</div></td></tr>
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Shawndouglas
https://www.limswiki.org/index.php?title=File:Fig5_Cicaloni_Separ22_9-4.png&diff=54921&oldid=prev
Shawndouglas at 21:20, 22 August 2022
2022-08-22T21:20:56Z
<p></p>
<p><b>New page</b></p><div><br />
== Licensing ==<br />
{{cc-by-4.0}}</div>
Shawndouglas