Synthesis and biological evaluation of a novel class of β-carboline derivatives
In this study, several novel β-carboline derivatives, 1-(4-hydroxy-3-methoxyphenyl)-β-carboline-3-carboxyl-Trp-Trp-AA-OBzl compounds, were designed and synthesized as potential anticancer agents. Their in vitro cytotoxic activities were evaluated using methylthiazoltetrazolium (MTT) assay. The in vi...
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Veröffentlicht in: | New journal of chemistry 2014, Vol.38 (9), p.4155-4166 |
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container_title | New journal of chemistry |
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creator | Chen, Hao Gao, Pengchao Zhang, Meng Liao, Wei Zhang, Jianwei |
description | In this study, several novel β-carboline derivatives, 1-(4-hydroxy-3-methoxyphenyl)-β-carboline-3-carboxyl-Trp-Trp-AA-OBzl compounds, were designed and synthesized as potential anticancer agents. Their
in vitro
cytotoxic activities were evaluated using methylthiazoltetrazolium (MTT) assay. The
in vivo
anti-tumor activity of the newly synthesized β-carboline derivatives was determined in a S180 bearing mouse model and some of the compounds demonstrated tumor growth inhibition similar to the positive control, doxorubicin. The intercalation of the β-carboline derivatives synthesized with calf thymus (CT) DNA was also studied. |
doi_str_mv | 10.1039/C4NJ00262H |
format | Article |
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in vitro
cytotoxic activities were evaluated using methylthiazoltetrazolium (MTT) assay. The
in vivo
anti-tumor activity of the newly synthesized β-carboline derivatives was determined in a S180 bearing mouse model and some of the compounds demonstrated tumor growth inhibition similar to the positive control, doxorubicin. The intercalation of the β-carboline derivatives synthesized with calf thymus (CT) DNA was also studied.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/C4NJ00262H</identifier><language>eng</language><ispartof>New journal of chemistry, 2014, Vol.38 (9), p.4155-4166</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c231t-7d7799280d361901fd73c07712a296badcd62300c4c17e11d199059e1a7fbc293</citedby><cites>FETCH-LOGICAL-c231t-7d7799280d361901fd73c07712a296badcd62300c4c17e11d199059e1a7fbc293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,4025,27925,27926,27927</link.rule.ids></links><search><creatorcontrib>Chen, Hao</creatorcontrib><creatorcontrib>Gao, Pengchao</creatorcontrib><creatorcontrib>Zhang, Meng</creatorcontrib><creatorcontrib>Liao, Wei</creatorcontrib><creatorcontrib>Zhang, Jianwei</creatorcontrib><title>Synthesis and biological evaluation of a novel class of β-carboline derivatives</title><title>New journal of chemistry</title><description>In this study, several novel β-carboline derivatives, 1-(4-hydroxy-3-methoxyphenyl)-β-carboline-3-carboxyl-Trp-Trp-AA-OBzl compounds, were designed and synthesized as potential anticancer agents. Their
in vitro
cytotoxic activities were evaluated using methylthiazoltetrazolium (MTT) assay. The
in vivo
anti-tumor activity of the newly synthesized β-carboline derivatives was determined in a S180 bearing mouse model and some of the compounds demonstrated tumor growth inhibition similar to the positive control, doxorubicin. The intercalation of the β-carboline derivatives synthesized with calf thymus (CT) DNA was also studied.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpFkMFKxDAURYMoOI5u_IKshep7SScxSynqKIMK6rq8JqlGYiNJLcxv-SF-kzMouLqXy-EuDmPHCKcI0pw19d0tgFBiucNmKJWpjFC4u-lY1xUsarXPDkp5A0DUCmfs4XE9jK--hMJpcLwLKaaXYClyP1H8pDGkgaeeEx_S5CO3kUrZDt9flaXcpRgGz53PYdqwky-HbK-nWPzRX87Z89XlU7OsVvfXN83FqrJC4lhpp7Ux4hycVGgAe6elBa1RkDCqI2edEhLA1ha1R3RoDCyMR9J9Z4WRc3by-2tzKiX7vv3I4Z3yukVoty7afxfyB_9AUdc</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Chen, Hao</creator><creator>Gao, Pengchao</creator><creator>Zhang, Meng</creator><creator>Liao, Wei</creator><creator>Zhang, Jianwei</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2014</creationdate><title>Synthesis and biological evaluation of a novel class of β-carboline derivatives</title><author>Chen, Hao ; Gao, Pengchao ; Zhang, Meng ; Liao, Wei ; Zhang, Jianwei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c231t-7d7799280d361901fd73c07712a296badcd62300c4c17e11d199059e1a7fbc293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Hao</creatorcontrib><creatorcontrib>Gao, Pengchao</creatorcontrib><creatorcontrib>Zhang, Meng</creatorcontrib><creatorcontrib>Liao, Wei</creatorcontrib><creatorcontrib>Zhang, Jianwei</creatorcontrib><collection>CrossRef</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Hao</au><au>Gao, Pengchao</au><au>Zhang, Meng</au><au>Liao, Wei</au><au>Zhang, Jianwei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and biological evaluation of a novel class of β-carboline derivatives</atitle><jtitle>New journal of chemistry</jtitle><date>2014</date><risdate>2014</risdate><volume>38</volume><issue>9</issue><spage>4155</spage><epage>4166</epage><pages>4155-4166</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>In this study, several novel β-carboline derivatives, 1-(4-hydroxy-3-methoxyphenyl)-β-carboline-3-carboxyl-Trp-Trp-AA-OBzl compounds, were designed and synthesized as potential anticancer agents. Their
in vitro
cytotoxic activities were evaluated using methylthiazoltetrazolium (MTT) assay. The
in vivo
anti-tumor activity of the newly synthesized β-carboline derivatives was determined in a S180 bearing mouse model and some of the compounds demonstrated tumor growth inhibition similar to the positive control, doxorubicin. The intercalation of the β-carboline derivatives synthesized with calf thymus (CT) DNA was also studied.</abstract><doi>10.1039/C4NJ00262H</doi><tpages>12</tpages></addata></record> |
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title | Synthesis and biological evaluation of a novel class of β-carboline derivatives |
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