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ファイル | 記述 | サイズ | フォーマット | |
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j.bmcl.2013.04.094.pdf | 414.11 kB | Adobe PDF | 見る/開く |
タイトル: | Affinity-based screening of MDM2/MDMX-p53 interaction inhibitors by chemical array: Identification of novel peptidic inhibitors. |
著者: | Noguchi, Taro ![]() ![]() Oishi, Shinya ![]() ![]() Honda, Kaori Kondoh, Yasumitsu Saito, Tamio Kubo, Tatsuhiko Kaneda, Masato Ohno, Hiroaki ![]() ![]() ![]() Osada, Hiroyuki Fujii, Nobutaka ![]() |
著者名の別形: | 大石, 真也 |
キーワード: | MDM2 MDMX p53 Protein HTS Microarray technology |
発行日: | 1-Jul-2013 |
出版者: | Elsevier BV |
誌名: | Bioorganic & medicinal chemistry letters |
巻: | 23 |
号: | 13 |
開始ページ: | 3802 |
終了ページ: | 3805 |
抄録: | MDM2 and MDMX are oncoproteins that negatively regulate the activity and stability of the tumor suppressor protein p53. The inhibitors of protein-protein interactions (PPIs) of MDM2-p53 and MDMX-p53 represent potential anticancer agents. In this study, a novel approach for identifying MDM2-p53 and MDMX-p53 PPI inhibitor candidates by affinity-based screening using a chemical array has been established. A number of compounds from an in-house compound library, which were immobilized onto a chemical array, were screened for interaction with fluorescence-labeled MDM2 and MDMX proteins. The subsequent fluorescent polarization assay identified several compounds that inhibited MDM2-p53 and MDMX-p53 interactions. |
著作権等: | © 2013 Elsevier Ltd. This is not the published version. Please cite only the published version. この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。 |
URI: | http://hdl.handle.net/2433/176375 |
DOI(出版社版): | 10.1016/j.bmcl.2013.04.094 |
PubMed ID: | 23726030 |
出現コレクション: | 学術雑誌掲載論文等 |

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