Development of axially chiral urazole scaffolds for antiplant virus applications againstpotato virus Y

Author:

Jin Jiamiao1ORCID,Mou Chengli2,Zou Juan2,Xie Xin3ORCID,Wang Chen1,Shen Tingwei1,Deng Youlin1,Li Benpeng1,Jin Zhichao1ORCID,Li Xiangyang1ORCID,Chi Yonggui Robin14ORCID

Affiliation:

1. National Key Laboratory of Green Pesticide, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education Guizhou University Guiyang China

2. School of Pharmacy Guizhou University of Traditional Chinese Medicine Guiyang China

3. Department of Plant Pathology College of Agriculture, Guizhou University Guiyang China

4. School of Chemistry, Chemical Engineering, and Biotechnology Nanyang Technological University Singapore Singapore

Abstract

AbstractBACKGROUNDPotato virus Y(PVY) was first discovered by Smith in 1931 and is currently ranked as the fifth most significant plant virus. It can cause severe damage to plants from the familySolanaceae, which results in billions of dollars of economic loss worldwide every year. To discover new antiviral drugs, a class of multifunctional urazole derivatives bearing a stereogenic CN axis were synthesized with excellent optical purities for antiviral evaluations against PVY.RESULTSThe absolute configurations of the axially chiral compounds exhibited obvious distinctions in antiviral bioactivities, with several of these enantio‐enriched axially chiral molecules showing excellent anti‐PVY activities. In particular, compound (R)‐9fexhibited remarkable curative activities against PVY with a 50% maximal effective concentration (EC50) of 224.9 μg mL−1, which was better than that of ningnanmycin (NNM), which had an EC50of 234.0 μg mL−1. And the EC50value of the protective activities of compound (R)‐9f was 462.2 μg mL−1, which was comparable to that of NNM (442.0 μg mL−1). The mechanisms of two enantiomer of the axially chiral compounds9f were studied by both molecule docking and defensive enzyme activity tests.CONCLUSIONMechanistic studies demonstrated that the axially chiral configurations of the compounds played significant roles in the molecule PVY‐CP (PVY Coat Protein) interactions and could enhance the activities of the defense enzymes. The (S)‐9f showed only one carbon–hydrogen bond and one π–cation interaction between the chiral molecule and the PVY‐CP amino acid sites. In contrast, the (R)‐enantiomer of 9f exhibited three hydrogen bonding interactions between the carbonyl groups and the PVY‐CP active sites of ARG157 and GLN158. The current study provides significant information on the roles that axial chiralities play in plant protection against viruses, which will facilitate the development of novel green pesticides bearing axial chiralities with excellent optical purities. © 2023 Society of Chemical Industry.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Insect Science,Agronomy and Crop Science,General Medicine

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