Discovery of Structural Diversity Guided N‐S Heterocyclic Derivatives Based on Natural Benzothiazole Alkaloids as Potential Cytotoxic Agents

ABSTRACT Benzothiazole alkaloids are a class of rare heterocyclic alkaloids with unique structures and exhibit a wide range of biological activities. So, the aim of this work is to investigate structural diversity‐guided N‐S heterocyclic derivatives based on natural benzothiazole alkaloids as potential cytotoxic agents. Three series of novel benzothiazole derivatives, including 22 compounds, were designed and synthesized using pharmacophore hybridization, and their in vitro cytotoxic activities against Huh‐7 and A875 were fully evaluated. The results indicated that some of these benzothiazole derivatives had significantly good cytotoxic activities against two tested cell lines compared with the positive control 5‐fluorouracil, and other compounds 3f–3i displayed good selectivity between A875 and Huh‐7 cell lines, which might be used as promising lead molecule for discovery of novel benzothiazole‐type cytotoxic agents.

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Publication Details

Journal
Journal of Heterocyclic Chemistry
Published
2024-09-16
DOI
https://doi.org/10.1002/jhet.4886
Citations
6
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
1.50

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article

Discovery of Structural Diversity Guided N‐S Heterocyclic Derivatives Based on Natural Benzothiazole Alkaloids as Potential Cytotoxic Agents

Xiufang Cao, Kaimei Wang, Shaoyong Ke, Yingwu Shi et al.
6 citations
Journal of Heterocyclic Chemistry
Synthesis and biological activity
1.50
article

Discovery of Structural Diversity Guided N‐S Heterocyclic Derivatives Based on Natural Benzothiazole Alkaloids as Potential Cytotoxic Agents

Xiufang Cao, Kaimei Wang, Shaoyong Ke, Yingwu Shi, Manli Liu, Longzhu Bao, Lirong Guo, Yafei Wan, Fuqiang Zheng
article en
6 citations

Abstract

ABSTRACT Benzothiazole alkaloids are a class of rare heterocyclic alkaloids with unique structures and exhibit a wide range of biological activities. So, the aim of this work is to investigate structural diversity‐guided N‐S heterocyclic derivatives based on natural benzothiazole alkaloids as potential cytotoxic agents. Three series of novel benzothiazole derivatives, including 22 compounds, were designed and synthesized using pharmacophore hybridization, and their in vitro cytotoxic activities against Huh‐7 and A875 were fully evaluated. The results indicated that some of these benzothiazole derivatives had significantly good cytotoxic activities against two tested cell lines compared with the positive control 5‐fluorouracil, and other compounds 3f–3i displayed good selectivity between A875 and Huh‐7 cell lines, which might be used as promising lead molecule for discovery of novel benzothiazole‐type cytotoxic agents.

Journal of Heterocyclic ChemistryVol. 61(11)
Huazhong Agricultural University (CN), Xinjiang Academy of Agricultural Sciences (CN), Ministry of Agriculture and Rural Affairs (CN), Hubei Academy of Agricultural Sciences (CN), Hubei University of Technology (CN)
Natural Science Foundation of Hubei Province, National Key Research and Development Program of China
Openalex Percentile: Top 19%
Synthesis and biological activity
1.50
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Discovery of Structural Diversity Guided N‐S Heterocyclic Derivatives Based on Natural Benzothiazole Alkaloids as Potential Cytotoxic Agents — Xiufang Cao, Kaimei Wang, et al. · Journal of Heterocyclic Chemistry (2024) | TGRS Research Map | TGRS