Platanosides from Platanus x acerifolia: New molecules, SAR, and target validation of a strong lead for drug-resistant bacterial infections and the associated sepsis

Document Type

Article

Publication Date

2-1-2024

Abstract

Three undescribed (1-3) and nine known (4-12) platanosides were isolated and characterized from a bioactive extract of the May leaves of Platanus x acerifolia that initially showed inhibition against Staphylococcus aureus. Targeted compound mining was guided by an LC-MS/MS-based molecular ion networking (MoIN) strategy combined with conventional isolation procedures from a unique geographic location. The novel structures were mainly determined by 2D NMR and computational (NMR/ECD calculations) methods. Compound 1 is a rare acylated kaempferol rhamnoside possessing a truxinate unit. 6 (Z,E-platanoside) and 7 (E,E-platanoside) were confirmed to have remarkable inhibitory effects against both methicillin-resistant S. aureus (MIC: <= 16 mu g/mL) and glycopeptide-resistant Enterococcus faecium (MIC: <= 1 mu g/mL). These platanosides were subjected to docking analyses against FabI (enoyl-ACP reductase) and PBP1/2 (penicillin binding protein), both of which are pivotal enzymes governing bacterial growth but not found in the human host. The results showed that 6 and 7 displayed superior binding affinities towards FabI and PBP2. Moreover, surface plasmon resonance studies on the interaction of 1/7 and FabI revealed that 7 has a higher affinity (KD = 1.72 mu M), which further supports the above in vitro data and is thus expected to be a novel anti-antibacterial drug lead.

Keywords

Platanus x acerifolia, Platanosides, Molecular ion networking (MoIN), Antibacterial, Staphylococcus aureus, Enterococcus faecium, Structure -activity relationship (SAR), Molecular docking, Target validation

Divisions

CHEMISTRY

Funders

National Natural Science Foundation of China (NSFC) (21937002); (81773599); (82003659),NCCIH (RO1AT0072318-01)

Publication Title

Bioorganic Chemistry

Volume

143

Publisher

Elsevier

Publisher Location

525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA

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