Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors
HDAC inhibitors have been developed very rapidly in clinical trials and even in approvals for treating several cancers. However, there are few reported HDAC inhibitors designed from Nɛ-acetyl lysine. In the current study, we raised a novel design, which concerns Nɛ-acetyl lysine derivatives containi...
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The Royal Society
2019-06-01
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Series: | Royal Society Open Science |
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Online Access: | https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.190338 |
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doaj-f493a2bb0afd4a09b70b28c7cfe57dbb2020-11-25T04:02:57ZengThe Royal SocietyRoyal Society Open Science2054-57032019-06-016610.1098/rsos.190338190338Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitorsFang WangChun WangJie WangYefang ZouXiaoxue ChenTing LiuYan LiYonglong ZhaoYongjun LiBin HeHDAC inhibitors have been developed very rapidly in clinical trials and even in approvals for treating several cancers. However, there are few reported HDAC inhibitors designed from Nɛ-acetyl lysine. In the current study, we raised a novel design, which concerns Nɛ-acetyl lysine derivatives containing amide acetyl groups with the hybridization of ZBG groups as novel HDAC inhibitors.https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.190338nɛ-acetyl lysinezbg groupanalogueshybridizationhdac inhibitor |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fang Wang Chun Wang Jie Wang Yefang Zou Xiaoxue Chen Ting Liu Yan Li Yonglong Zhao Yongjun Li Bin He |
spellingShingle |
Fang Wang Chun Wang Jie Wang Yefang Zou Xiaoxue Chen Ting Liu Yan Li Yonglong Zhao Yongjun Li Bin He Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors Royal Society Open Science nɛ-acetyl lysine zbg group analogues hybridization hdac inhibitor |
author_facet |
Fang Wang Chun Wang Jie Wang Yefang Zou Xiaoxue Chen Ting Liu Yan Li Yonglong Zhao Yongjun Li Bin He |
author_sort |
Fang Wang |
title |
Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors |
title_short |
Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors |
title_full |
Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors |
title_fullStr |
Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors |
title_full_unstemmed |
Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors |
title_sort |
nɛ-acetyl lysine derivatives with zinc binding groups as novel hdac inhibitors |
publisher |
The Royal Society |
series |
Royal Society Open Science |
issn |
2054-5703 |
publishDate |
2019-06-01 |
description |
HDAC inhibitors have been developed very rapidly in clinical trials and even in approvals for treating several cancers. However, there are few reported HDAC inhibitors designed from Nɛ-acetyl lysine. In the current study, we raised a novel design, which concerns Nɛ-acetyl lysine derivatives containing amide acetyl groups with the hybridization of ZBG groups as novel HDAC inhibitors. |
topic |
nɛ-acetyl lysine zbg group analogues hybridization hdac inhibitor |
url |
https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.190338 |
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