Total synthesis of (+)-A83586C, (+)- kettapeptin and (+)-azinothricin: powerful new inhibitors of β-catenin/TCF4- and E2F-mediated gene transcription
dc.contributor.author | Hale, K. | |
dc.contributor.author | Manaviazar, S. | |
dc.contributor.author | George, J. | |
dc.date.issued | 2010 | |
dc.description.abstract | Herein we describe our asymmetric total syntheses of (+)-A83586C, (+)-kettapeptin and (+)-azinothricin. We also demonstrate that molecules of this class powerfully inhibit β-catenin/TCF4- and E2F-mediated gene transcription within malignant human colon cancer cells at low drug concentrations. | |
dc.description.statementofresponsibility | Karl J. Hale, Soraya Manaviazar and Jonathan George | |
dc.identifier.citation | Chemical Communications, 2010; 46(23):4021-4042 | |
dc.identifier.doi | 10.1039/C000603C | |
dc.identifier.issn | 1359-7345 | |
dc.identifier.issn | 1364-548X | |
dc.identifier.orcid | George, J. [0000-0002-7330-2160] | |
dc.identifier.uri | http://hdl.handle.net/2440/68553 | |
dc.language.iso | en | |
dc.publisher | Royal Soc Chemistry | |
dc.rights | This journal is copyright The Royal Society of Chemistry 2010 | |
dc.source.uri | https://doi.org/10.1039/c000603c | |
dc.subject | Cell Line, Tumor | |
dc.subject | Humans | |
dc.subject | Colonic Neoplasms | |
dc.subject | Depsipeptides | |
dc.subject | Peptides | |
dc.subject | Transcription Factors | |
dc.subject | Transcription, Genetic | |
dc.subject | E2F Transcription Factors | |
dc.subject | beta Catenin | |
dc.subject | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors | |
dc.subject | Transcription Factor 4 | |
dc.title | Total synthesis of (+)-A83586C, (+)- kettapeptin and (+)-azinothricin: powerful new inhibitors of β-catenin/TCF4- and E2F-mediated gene transcription | |
dc.title.alternative | Total synthesis of (+) - A83586C, (+)- kettapeptin and (+)- azinothricin: powerful new inhibitors of beta-catenin/TCF4- and E2F-mediated gene transcription | |
dc.type | Journal article | |
pubs.publication-status | Published |