Correction: Novel (E)-3-(1-substituted-1H-indazol-5-yl)-N-hydroxypropenamides as histone deacetylase inhibitors: design, synthesis and structure–activity relationships

Minh Sang Doan; Eun Jae Park; Duong Tien Anh; Do Thi Mai Dung; Le Quang-Bao; Pham-The Hai; Dao Thi Kim Oanh; Truong Thanh Tung; Ik Ho Na; Joo Hee Kwon; Jong Soon Kang; Sang-Bae Han; Dinh Thi Thanh Hai; Nguyen-Hai Nam

doi:10.1039/D3NJ90190D

Correction: Novel (E)-3-(1-substituted-1H-indazol-5-yl)-N-hydroxypropenamides as histone deacetylase inhibitors: design, synthesis and structure–activity relationships

Minh Sang Doan,^a Eun Jae Park,^b Duong Tien Anh,^a Do Thi Mai Dung,^a Le Quang-Bao,^a Pham-The Hai,^a Dao Thi Kim Oanh,^a Truong Thanh Tung,^cd Ik Ho Na,^b Joo Hee Kwon,^e Jong Soon Kang,^e Sang-Bae Han,*^b Dinh Thi Thanh Hai^a and Nguyen-Hai Nam*^a

Author affiliations

* Corresponding authors

^a Department of Pharmaceutical Chemistry, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi, Vietnam
E-mail: namnh@hup.edu.vn

^b College of Pharmacy, Chungbuk National University, 194-31, Osongsaengmyung-1, Heungdeok, Cheongju, Chungbuk, Republic of Korea
E-mail: shan@chungbuk.ac.kr

^c PHENIKAA Institute for Advanced Study (PIAS), Phenikaa University, Hanoi 12116, Vietnam

^d Faculty of Pharmacy, PHENIKAA University, Hanoi 12116, Vietnam

^e Korea Research Institute of Bioscience and Biotechnology, Cheongju, Chungbuk, Republic of Korea

Abstract

Correction for ‘Novel (E)-3-(1-substituted-1H-indazol-5-yl)-N-hydroxypropenamides as histone deacetylase inhibitors: design, synthesis and structure–activity relationships’ by Minh Sang Doan et al., New J. Chem., 2023, 47, 4478–4490, https://doi.org/10.1039/D2NJ04894A.

New Journal of Chemistry

Correction: Novel (E)-3-(1-substituted-1H-indazol-5-yl)-N-hydroxypropenamides as histone deacetylase inhibitors: design, synthesis and structure–activity relationships

Abstract

Associated articles

Article information

Download Citation

Permissions

Correction: Novel (E)-3-(1-substituted-1H-indazol-5-yl)-N-hydroxypropenamides as histone deacetylase inhibitors: design, synthesis and structure–activity relationships

Social activity

Search articles by author

Spotlight

Advertisements