Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation
Two series of novel 4-oxoquinazoline-based N-hydroxypropenamides (9a–m and 10a–m) were designed, synthesized, and evaluated for their inhibitory and cytotoxicity activities against histone deacetylase (HDAC). The compounds showed good to potent HDAC inhib
Lưu vào:
Tác giả chính: | , , , , , , , , , , , , |
---|---|
Định dạng: | Bài trích |
Ngôn ngữ: | eng |
Nhà xuất bản: |
American Chemical Society
2021
|
Truy cập trực tuyến: | https://pubs.acs.org/doi/abs/10.1021/acsomega.0c05870 https://dlib.phenikaa-uni.edu.vn/handle/PNK/2748 https://doi.org/10.1021/acsomega.0c05870 |
Từ khóa: |
Thêm từ khóa
Không có từ khóa, Hãy là người đầu tiên đánh dấu biểu ghi này!
|
id |
oai:localhost:PNK-2748 |
---|---|
record_format |
dspace |
spelling |
oai:localhost:PNK-27482022-08-17T05:54:47Z Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation Duong T. Anh Pham-The Hai Le D. Huy Hoang B. Ngoc Trinh T. M. Ngoc Do T. M. Dung Eun J. Park In K. Song Jong S. Kang Joo-Hee Kwon Truong T. Tung Sang-Bae Han Nguyen-Hai Nam Two series of novel 4-oxoquinazoline-based N-hydroxypropenamides (9a–m and 10a–m) were designed, synthesized, and evaluated for their inhibitory and cytotoxicity activities against histone deacetylase (HDAC). The compounds showed good to potent HDAC inhib 2021-09-10T04:46:53Z 2021-09-10T04:46:53Z 2021 Bài trích https://pubs.acs.org/doi/abs/10.1021/acsomega.0c05870 https://dlib.phenikaa-uni.edu.vn/handle/PNK/2748 https://doi.org/10.1021/acsomega.0c05870 eng application/pdf American Chemical Society |
institution |
Digital Phenikaa |
collection |
Digital Phenikaa |
language |
eng |
description |
Two series of novel 4-oxoquinazoline-based N-hydroxypropenamides (9a–m and 10a–m) were designed, synthesized, and evaluated for their inhibitory and cytotoxicity activities against histone deacetylase (HDAC). The compounds showed good to potent HDAC inhib |
format |
Bài trích |
author |
Duong T. Anh Pham-The Hai Le D. Huy Hoang B. Ngoc Trinh T. M. Ngoc Do T. M. Dung Eun J. Park In K. Song Jong S. Kang Joo-Hee Kwon Truong T. Tung Sang-Bae Han Nguyen-Hai Nam |
spellingShingle |
Duong T. Anh Pham-The Hai Le D. Huy Hoang B. Ngoc Trinh T. M. Ngoc Do T. M. Dung Eun J. Park In K. Song Jong S. Kang Joo-Hee Kwon Truong T. Tung Sang-Bae Han Nguyen-Hai Nam Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation |
author_facet |
Duong T. Anh Pham-The Hai Le D. Huy Hoang B. Ngoc Trinh T. M. Ngoc Do T. M. Dung Eun J. Park In K. Song Jong S. Kang Joo-Hee Kwon Truong T. Tung Sang-Bae Han Nguyen-Hai Nam |
author_sort |
Duong T. Anh |
title |
Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation |
title_short |
Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation |
title_full |
Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation |
title_fullStr |
Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation |
title_full_unstemmed |
Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation |
title_sort |
novel 4-oxoquinazoline-based n-hydroxypropenamides as histone deacetylase inhibitors: design, synthesis, and biological evaluation |
publisher |
American Chemical Society |
publishDate |
2021 |
url |
https://pubs.acs.org/doi/abs/10.1021/acsomega.0c05870 https://dlib.phenikaa-uni.edu.vn/handle/PNK/2748 https://doi.org/10.1021/acsomega.0c05870 |
_version_ |
1751856263012024320 |
score |
8.891787 |