Enhanced Bioactivity of Natural Products by Halogenation: A Database Survey and Quantum Chemistry Calculation Study

Natural products (NPs) have long been the cornerstone of drug discovery. Halogenated organic NPs are limited, while around one-fourth of approved chemical drugs are organohalogens. This suggests that the introduction of halogens into NPs may enhance their potential for transformation into drugs. In this study, we utilized a matched molecular pair (MMP) approach alongside a database survey to investigate the impact of halogenation on this transformation. The study revealed that halogenation increased the bioactivity of 70.3% of NPs, with 50.3% exhibiting at least a 2-fold enhancement. Halogen bonds (XBs) are prevalent between organohalogens and their targets. To explore whether halogenated NPs could form XBs with their targets, computational studies were performed and demonstrated that halogenated NPs or NP-derived drugs formed strong XBs with their targets, resulting in improved binding affinities. This study highlights the considerable potential of introducing halogens into NPs as a strategic approach for enhancing bioactivity and facilitating the development of drugs.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-05-07
DOI
https://doi.org/10.1021/acs.jmedchem.5c00944
Citations
6
Primary Topic
Bioactive Compounds and Antitumor Agents
Type
article
Field-Weighted Citation Impact
7.84

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article

Enhanced Bioactivity of Natural Products by Halogenation: A Database Survey and Quantum Chemistry Calculation Study

Qingyi Liao, Weiliang Zhu, Yong Zhang, Zhijian Xu et al.
6 citations
Journal of Medicinal Chemistry
Bioactive Compounds and Antitumor Agents
7.84
article

Enhanced Bioactivity of Natural Products by Halogenation: A Database Survey and Quantum Chemistry Calculation Study

Qingyi Liao, Weiliang Zhu, Yong Zhang, Zhijian Xu, Jintian Li, Qian Zhang, Mei Shao, Tingting Cai, Renting Cao
article en
6 citations

Abstract

Natural products (NPs) have long been the cornerstone of drug discovery. Halogenated organic NPs are limited, while around one-fourth of approved chemical drugs are organohalogens. This suggests that the introduction of halogens into NPs may enhance their potential for transformation into drugs. In this study, we utilized a matched molecular pair (MMP) approach alongside a database survey to investigate the impact of halogenation on this transformation. The study revealed that halogenation increased the bioactivity of 70.3% of NPs, with 50.3% exhibiting at least a 2-fold enhancement. Halogen bonds (XBs) are prevalent between organohalogens and their targets. To explore whether halogenated NPs could form XBs with their targets, computational studies were performed and demonstrated that halogenated NPs or NP-derived drugs formed strong XBs with their targets, resulting in improved binding affinities. This study highlights the considerable potential of introducing halogens into NPs as a strategic approach for enhancing bioactivity and facilitating the development of drugs.

Journal of Medicinal ChemistryVol. 68(10)
Nanjing University of Chinese Medicine (CN), Henan University (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Materia Medica (CN), Drug Discovery Laboratory (Norway) (NO), University of Chinese Academy of Sciences (CN), State Key Laboratory of Drug Research, East China Normal University (CN)
National Natural Science Foundation of China, Shanghai Municipal Education Commission, National Key Research and Development Program of China
Openalex Percentile: Top 2%
Bioactive Compounds and Antitumor Agents
7.84
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