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Quinazoline‐Based Hydroxamic Acids: Design, Synthesis, and Evaluation of Histone Deacetylase Inhibitory Effects and Cytotoxicity
Author(s) -
Hieu Doan Thanh,
Anh Duong Tien,
Hai PhamThe,
Huong LeThiThu,
Park Eun Jae,
Choi Jeong Eun,
Kang Jong Soon,
Dung Phan Thi Phuong,
Han SangBae,
Nam NguyenHai
Publication year - 2018
Publication title -
chemistry and biodiversity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 70
eISSN - 1612-1880
pISSN - 1612-1872
DOI - 10.1002/cbdv.201800027
Subject(s) - chemistry , cytotoxicity , vorinostat , quinazoline , histone deacetylase , hydroxamic acid , hela , stereochemistry , docking (animal) , biochemistry , pharmacology , in vitro , histone , medicine , nursing , gene
In our search for novel histone deacetylases inhibitors, we have designed and synthesized a series of novel hydroxamic acids and N ‐hydroxybenzamides incorporating quinazoline heterocycles ( 4a  –  4i , 6a  –  6i ). Bioevaluation showed that these quinazoline‐based hydroxamic acids and N ‐hydroxybenzamides were potently cytotoxic against three human cancer cell lines ( SW 620, colon; PC ‐3, prostate; NCI ‐H23, lung). In term of cytotoxicity, several compounds, e.g ., 4g , 4c , 4g  –  4i , 6c , and 6h , displayed from 5‐ up to 10‐fold higher potency than SAHA (suberoylanilidehydroxamic acid, vorinostat). The compounds were also generally comparable to SAHA in inhibiting HDAC s with IC 50 values in sub‐micromolar range. Some compounds, e.g ., 4g , 6c , 6e , and 6h , were even more potent HDAC inhibitors compared to SAHA in HeLa extract assay. Docking studies demonstrated that the compounds tightly bound to HDAC 2 at the active binding site with binding affinities higher than that of SAHA . Detailed investigation on the estimation of absorption, distribution, metabolism, excretion, and toxicity ( ADMET ) suggested that compounds 4g , 6c , and 6g , while showing potent HDAC 2 inhibitory activity and cytotoxicity, also potentially displayed ADMET characteristics desirable to be expected as promising anticancer drug candidates.

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