{"id":{"repo_id":"etsu","oai_identifier":"oai:dc.etsu.edu:etd-3342"},"canonical_url":"https://search.dev.ndltd.org/etd/etsu/oai:dc.etsu.edu:etd-3342","repository":{"repo_id":"etsu","name":"East Tennessee State University","base_url":"https://dc.etsu.edu/do/oai/"},"display":{"title":"Synthesis of Marine Chemicals and Derivatives as Potential Anti-Cancer Drugs.","abstract":"<p>Two natural marine compounds, 3-bromo-4,5-dihydroxybenzaldehyde <b>2</b> and 2,3-dibromo-4,5-dihydroxybenzaldehyde <b>5</b> together with two novel derivatives, 3-bromo-5-(tert-butyl-dimethyl-silanyloxy)-4-hydroxybenzaldehyde <b>3</b> and 1-bromo-2,3-dimethoxy-5-nitrooxy-methylbenzene <b>9</b>, were synthesized. Compounds <b>2</b>, <b>3</b>, and <b>5</b> were evaluated for their biological activity towards the inhibition of prostate cancer cell growth using staurosporine a a positive control. All three compounds have shown significant inhibition of prostate cancer cell growth. Compound <b>9</b> is yet to be evaluated.</p>","abstract_html":"&lt;p&gt;Two natural marine compounds, 3-bromo-4,5-dihydroxybenzaldehyde &lt;b&gt;2&lt;/b&gt; and 2,3-dibromo-4,5-dihydroxybenzaldehyde &lt;b&gt;5&lt;/b&gt; together with two novel derivatives, 3-bromo-5-(tert-butyl-dimethyl-silanyloxy)-4-hydroxybenzaldehyde &lt;b&gt;3&lt;/b&gt; and 1-bromo-2,3-dimethoxy-5-nitrooxy-methylbenzene &lt;b&gt;9&lt;/b&gt;, were synthesized. Compounds &lt;b&gt;2&lt;/b&gt;, &lt;b&gt;3&lt;/b&gt;, and &lt;b&gt;5&lt;/b&gt; were evaluated for their biological activity towards the inhibition of prostate cancer cell growth using staurosporine a a positive control. All three compounds have shown significant inhibition of prostate cancer cell growth. Compound &lt;b&gt;9&lt;/b&gt; is yet to be evaluated.&lt;/p&gt;","abstract_has_math":false,"creators":["Bannerman-Akwei, Laude"],"institution":null,"degree_name":"MS (Master of Science)","degree_level":"Thesis - unrestricted","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2008,"date_issued":"2008-12-13T08:00:00Z","date_published":"2008-12-13T08:00:00Z","updated_at":"2026-07-24T02:21:11Z","subjects":["Marine","Cancer","Drugs","Natural Products","Synthesis","Medicine and Health Sciences","Natural Products Chemistry and Pharmacognosy","Pharmacy and Pharmaceutical Sciences"],"languages":[],"rights":["Copyright by the authors."],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://dc.etsu.edu/etd/1990","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Bannerman-Akwei, Laude"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.issued","label":"Date","values":["2008-12-13T08:00:00Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis - unrestricted"]},{"key":"thesis:degree_name","label":"Degree Name","values":["MS (Master of Science)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Marine","Cancer","Drugs","Natural Products","Synthesis","Medicine and Health Sciences","Natural Products Chemistry and Pharmacognosy","Pharmacy and Pharmaceutical Sciences"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["Copyright by the authors."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://dc.etsu.edu/context/etd/article/3342/viewcontent/Bannerman_AkweiL082708f.pdf","https://dc.etsu.edu/etd/1990"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["<p>Two natural marine compounds, 3-bromo-4,5-dihydroxybenzaldehyde <b>2</b> and 2,3-dibromo-4,5-dihydroxybenzaldehyde <b>5</b> together with two novel derivatives, 3-bromo-5-(tert-butyl-dimethyl-silanyloxy)-4-hydroxybenzaldehyde <b>3</b> and 1-bromo-2,3-dimethoxy-5-nitrooxy-methylbenzene <b>9</b>, were synthesized. Compounds <b>2</b>, <b>3</b>, and <b>5</b> were evaluated for their biological activity towards the inhibition of prostate cancer cell growth using staurosporine a a positive control. All three compounds have shown significant inhibition of prostate cancer cell growth. Compound <b>9</b> is yet to be evaluated.</p>"]},{"key":"dc:title","label":"Title","values":["Synthesis of Marine Chemicals and Derivatives as Potential Anti-Cancer Drugs."]}]}],"canonical_facts":{"dc:creator":["Bannerman-Akwei, Laude"],"dc:date.issued":["2008-12-13T08:00:00Z"],"dc:description.abstract":["<p>Two natural marine compounds, 3-bromo-4,5-dihydroxybenzaldehyde <b>2</b> and 2,3-dibromo-4,5-dihydroxybenzaldehyde <b>5</b> together with two novel derivatives, 3-bromo-5-(tert-butyl-dimethyl-silanyloxy)-4-hydroxybenzaldehyde <b>3</b> and 1-bromo-2,3-dimethoxy-5-nitrooxy-methylbenzene <b>9</b>, were synthesized. Compounds <b>2</b>, <b>3</b>, and <b>5</b> were evaluated for their biological activity towards the inhibition of prostate cancer cell growth using staurosporine a a positive control. All three compounds have shown significant inhibition of prostate cancer cell growth. Compound <b>9</b> is yet to be evaluated.</p>"],"dc:identifier":["https://dc.etsu.edu/context/etd/article/3342/viewcontent/Bannerman_AkweiL082708f.pdf","https://dc.etsu.edu/etd/1990"],"dc:rights":["Copyright by the authors."],"dc:subject":["Marine","Cancer","Drugs","Natural Products","Synthesis","Medicine and Health Sciences","Natural Products Chemistry and Pharmacognosy","Pharmacy and Pharmaceutical Sciences"],"dc:title":["Synthesis of Marine Chemicals and Derivatives as Potential Anti-Cancer Drugs."],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Thesis - unrestricted"],"thesis:degree_name":["MS (Master of Science)"]},"updated_at":"2026-07-24T02:21:11Z"}