Discovery and biological activity of computer-assisted drug designed Akt pathway inhibitors
[Display omitted] •Based on solenopsin A an iterative pharmacophore modeling strategy was used.•In silico conformational studies and alignments were carried out.•The commercially compounds were purchased and tested for Akt inhibition.•One of the top three hits had promising inhibition and verified o...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2018-10, Vol.28 (19), p.3247-3250 |
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creator | Uko, Nne E. Güner, Osman F. Barnett, Lillie M.A. Matesic, Diane F. Bowen, J. Phillip |
description | [Display omitted]
•Based on solenopsin A an iterative pharmacophore modeling strategy was used.•In silico conformational studies and alignments were carried out.•The commercially compounds were purchased and tested for Akt inhibition.•One of the top three hits had promising inhibition and verified our approach.
The P13K/Akt pathway is a growth-regulating cellular signaling pathway that is over-activated in numerous human cancers. A novel series of Akt pathway inhibitors were identified using iterative pharmacophore modeling, energy-based calculations, and property predictions of known Akt inhibitors. Inhibitory effects on activation of Akt and growth of human neoplastic cells are reported. Results show variable inhibitory effects of three selected compounds on Akt phosphorylation at a key activation site, and on proliferation of tumorigenic cells. We identify one lead compound with potent inhibitory activity on both human carcinoma cell proliferation and Akt activation. |
doi_str_mv | 10.1016/j.bmcl.2018.08.006 |
format | Article |
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•Based on solenopsin A an iterative pharmacophore modeling strategy was used.•In silico conformational studies and alignments were carried out.•The commercially compounds were purchased and tested for Akt inhibition.•One of the top three hits had promising inhibition and verified our approach.
The P13K/Akt pathway is a growth-regulating cellular signaling pathway that is over-activated in numerous human cancers. A novel series of Akt pathway inhibitors were identified using iterative pharmacophore modeling, energy-based calculations, and property predictions of known Akt inhibitors. Inhibitory effects on activation of Akt and growth of human neoplastic cells are reported. Results show variable inhibitory effects of three selected compounds on Akt phosphorylation at a key activation site, and on proliferation of tumorigenic cells. We identify one lead compound with potent inhibitory activity on both human carcinoma cell proliferation and Akt activation.</description><identifier>ISSN: 0960-894X</identifier><identifier>EISSN: 1464-3405</identifier><identifier>DOI: 10.1016/j.bmcl.2018.08.006</identifier><identifier>PMID: 30143420</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Akt kinase ; Alkaloids - chemistry ; Alkaloids - pharmacology ; Anti-tumor ; Cell Line, Tumor ; Drug Design ; Enzyme Activation ; Humans ; Lung Neoplasms - enzymology ; Lung Neoplasms - pathology ; Models, Molecular ; Molecular modeling ; Pharmacophore ; Phosphorylation ; Protein Kinase Inhibitors - pharmacology ; Proto-Oncogene Proteins c-akt - antagonists & inhibitors ; Proto-Oncogene Proteins c-akt - metabolism ; Signal Transduction ; Solenopsin</subject><ispartof>Bioorganic & medicinal chemistry letters, 2018-10, Vol.28 (19), p.3247-3250</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-cb9f91f5e264961c3295882e6973cf48077f99bf75fc5db94302fd88d40189c3</citedby><cites>FETCH-LOGICAL-c356t-cb9f91f5e264961c3295882e6973cf48077f99bf75fc5db94302fd88d40189c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bmcl.2018.08.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30143420$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uko, Nne E.</creatorcontrib><creatorcontrib>Güner, Osman F.</creatorcontrib><creatorcontrib>Barnett, Lillie M.A.</creatorcontrib><creatorcontrib>Matesic, Diane F.</creatorcontrib><creatorcontrib>Bowen, J. Phillip</creatorcontrib><title>Discovery and biological activity of computer-assisted drug designed Akt pathway inhibitors</title><title>Bioorganic & medicinal chemistry letters</title><addtitle>Bioorg Med Chem Lett</addtitle><description>[Display omitted]
•Based on solenopsin A an iterative pharmacophore modeling strategy was used.•In silico conformational studies and alignments were carried out.•The commercially compounds were purchased and tested for Akt inhibition.•One of the top three hits had promising inhibition and verified our approach.
The P13K/Akt pathway is a growth-regulating cellular signaling pathway that is over-activated in numerous human cancers. A novel series of Akt pathway inhibitors were identified using iterative pharmacophore modeling, energy-based calculations, and property predictions of known Akt inhibitors. Inhibitory effects on activation of Akt and growth of human neoplastic cells are reported. Results show variable inhibitory effects of three selected compounds on Akt phosphorylation at a key activation site, and on proliferation of tumorigenic cells. We identify one lead compound with potent inhibitory activity on both human carcinoma cell proliferation and Akt activation.</description><subject>Akt kinase</subject><subject>Alkaloids - chemistry</subject><subject>Alkaloids - pharmacology</subject><subject>Anti-tumor</subject><subject>Cell Line, Tumor</subject><subject>Drug Design</subject><subject>Enzyme Activation</subject><subject>Humans</subject><subject>Lung Neoplasms - enzymology</subject><subject>Lung Neoplasms - pathology</subject><subject>Models, Molecular</subject><subject>Molecular modeling</subject><subject>Pharmacophore</subject><subject>Phosphorylation</subject><subject>Protein Kinase Inhibitors - pharmacology</subject><subject>Proto-Oncogene Proteins c-akt - antagonists & inhibitors</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Signal Transduction</subject><subject>Solenopsin</subject><issn>0960-894X</issn><issn>1464-3405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE-LFDEQxYMo7rj6BTxIjl56rHTS6Q54Wda_sOBlD4KHkE4qsxm7O2OSHplvb4ZZPQoFVQW_9-A9Ql4z2DJg8t1-O8522rbAhi3UAfmEbJiQouECuqdkA0pCMyjx_Yq8yHkPwAQI8Zxc8Xpx0cKG_PgQso1HTCdqFkfHEKe4C9ZM1NgSjqGcaPTUxvmwFkyNyTnkgo66tO6owxx2S_1ufhZ6MOXhtznRsDyEMZSY8kvyzJsp46vHfU3uP328v_3S3H37_PX25q6xvJOlsaPyivkOWymUZJa3qhuGFqXqufVigL73So2-77zt3KgEh9a7YXCiBleWX5O3F9tDir9WzEXPNRNOk1kwrlm3oDhXfa-GirYX1KaYc0KvDynMJp00A33uVO_1uVN97lRDHZBV9ObRfx1ndP8kf0uswPsLgDXkMWDS2QZcLLqQ0BbtYvif_x91kojO</recordid><startdate>20181015</startdate><enddate>20181015</enddate><creator>Uko, Nne E.</creator><creator>Güner, Osman F.</creator><creator>Barnett, Lillie M.A.</creator><creator>Matesic, Diane F.</creator><creator>Bowen, J. Phillip</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20181015</creationdate><title>Discovery and biological activity of computer-assisted drug designed Akt pathway inhibitors</title><author>Uko, Nne E. ; Güner, Osman F. ; Barnett, Lillie M.A. ; Matesic, Diane F. ; Bowen, J. Phillip</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-cb9f91f5e264961c3295882e6973cf48077f99bf75fc5db94302fd88d40189c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Akt kinase</topic><topic>Alkaloids - chemistry</topic><topic>Alkaloids - pharmacology</topic><topic>Anti-tumor</topic><topic>Cell Line, Tumor</topic><topic>Drug Design</topic><topic>Enzyme Activation</topic><topic>Humans</topic><topic>Lung Neoplasms - enzymology</topic><topic>Lung Neoplasms - pathology</topic><topic>Models, Molecular</topic><topic>Molecular modeling</topic><topic>Pharmacophore</topic><topic>Phosphorylation</topic><topic>Protein Kinase Inhibitors - pharmacology</topic><topic>Proto-Oncogene Proteins c-akt - antagonists & inhibitors</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Signal Transduction</topic><topic>Solenopsin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uko, Nne E.</creatorcontrib><creatorcontrib>Güner, Osman F.</creatorcontrib><creatorcontrib>Barnett, Lillie M.A.</creatorcontrib><creatorcontrib>Matesic, Diane F.</creatorcontrib><creatorcontrib>Bowen, J. Phillip</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioorganic & medicinal chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uko, Nne E.</au><au>Güner, Osman F.</au><au>Barnett, Lillie M.A.</au><au>Matesic, Diane F.</au><au>Bowen, J. Phillip</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Discovery and biological activity of computer-assisted drug designed Akt pathway inhibitors</atitle><jtitle>Bioorganic & medicinal chemistry letters</jtitle><addtitle>Bioorg Med Chem Lett</addtitle><date>2018-10-15</date><risdate>2018</risdate><volume>28</volume><issue>19</issue><spage>3247</spage><epage>3250</epage><pages>3247-3250</pages><issn>0960-894X</issn><eissn>1464-3405</eissn><abstract>[Display omitted]
•Based on solenopsin A an iterative pharmacophore modeling strategy was used.•In silico conformational studies and alignments were carried out.•The commercially compounds were purchased and tested for Akt inhibition.•One of the top three hits had promising inhibition and verified our approach.
The P13K/Akt pathway is a growth-regulating cellular signaling pathway that is over-activated in numerous human cancers. A novel series of Akt pathway inhibitors were identified using iterative pharmacophore modeling, energy-based calculations, and property predictions of known Akt inhibitors. Inhibitory effects on activation of Akt and growth of human neoplastic cells are reported. Results show variable inhibitory effects of three selected compounds on Akt phosphorylation at a key activation site, and on proliferation of tumorigenic cells. We identify one lead compound with potent inhibitory activity on both human carcinoma cell proliferation and Akt activation.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>30143420</pmid><doi>10.1016/j.bmcl.2018.08.006</doi><tpages>4</tpages></addata></record> |
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subjects | Akt kinase Alkaloids - chemistry Alkaloids - pharmacology Anti-tumor Cell Line, Tumor Drug Design Enzyme Activation Humans Lung Neoplasms - enzymology Lung Neoplasms - pathology Models, Molecular Molecular modeling Pharmacophore Phosphorylation Protein Kinase Inhibitors - pharmacology Proto-Oncogene Proteins c-akt - antagonists & inhibitors Proto-Oncogene Proteins c-akt - metabolism Signal Transduction Solenopsin |
title | Discovery and biological activity of computer-assisted drug designed Akt pathway inhibitors |
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