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Stable Axially Chiral Isomers of Arylnaphthalene Lignan Glycosides with Antiviral Potential Discovered from Justicia procumbens

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471266949.bmc016.pub2openalex-snapshot
Chirality and Biological Activity
inferredcites →https://doi.org/10.1002/9780470147238.ch1openalex-snapshot
Recent Advances in Atropisomerism
inferredcites →https://doi.org/10.1002/anie.200902641openalex-snapshot
All‐Organic Discotic Radical with a Spin‐Carrying Rigid‐Core Showing Intracolumnar Interactions and Multifunctional Properties
inferredcites →https://doi.org/10.1002/ardp.200300841openalex-snapshot
Two New Arylnaphthalide Lignans and Antiplatelet Constituents from Justicia procumbens
inferredcites →https://doi.org/10.1002/cbic.200300906openalex-snapshot
Atropisomerism, Biphenyls, and Fluorine: A Comparison of Rotational Barriers and Twist Angles
inferredcites →https://doi.org/10.1002/chir.22138openalex-snapshot
SpecDis: Quantifying the Comparison of Calculated and Experimental Electronic Circular Dichroism Spectra
inferredcites →https://doi.org/10.1002/chir.22600openalex-snapshot
Good Computational Practice in the Assignment of Absolute Configurations by TDDFT Calculations of ECD Spectra
inferredcites →https://doi.org/10.1002/cmdc.201000485openalex-snapshot
Revealing Atropisomer Axial Chirality in Drug Discovery
inferredcites →https://doi.org/10.1002/ejoc.201901918openalex-snapshot
Stereochemistry and Recent Applications of Axially Chiral Organic Molecules
inferredcites →https://doi.org/10.1002/mrc.1830openalex-snapshot
Complete assignments of 1H and 13C NMR data for seven arylnaphthalide lignans from Justicia procumbens
inferredcites →https://doi.org/10.1016/0031-9422(84)83096-4openalex-snapshot
Lignans of haplophyllum tuberculatum
inferredcites →https://doi.org/10.1016/0031-9422(96)00024-6openalex-snapshot
Antiviral activity of lignans and their glycosides from Justicia procumbens
inferredcites →https://doi.org/10.1016/0031-9422(96)00061-1openalex-snapshot
Minor lignans from haplophyllum cappadocicum
inferredcites →https://doi.org/10.1016/b978-0-12-417185-5.00010-7openalex-snapshot
Studies in the Synthesis of Biaryl Natural Products
inferredcites →https://doi.org/10.1016/j.ebiom.2019.08.060openalex-snapshot
Glycosylated diphyllin as a broad-spectrum antiviral agent against Zika virus
inferredcites →https://doi.org/10.1016/j.phytochem.2009.05.016openalex-snapshot
Glycosides of arylnaphthalene lignans from Acanthus mollis having axial chirality
inferredcites →https://doi.org/10.1016/j.phytochem.2017.01.005openalex-snapshot
Anti-HIV diphyllin glycosides from Justicia gendarussa
inferredcites →https://doi.org/10.1016/j.tetasy.2017.09.006openalex-snapshot
Thermal racemization of biaryl atropisomers
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00004openalex-snapshot
Potent Inhibitor of Drug-Resistant HIV-1 Strains Identified from the Medicinal Plant Justicia gendarussa
inferredcites →https://doi.org/10.1021/jm200584gopenalex-snapshot
Assessing Atropisomer Axial Chirality in Drug Discovery and Development
inferredcites →https://doi.org/10.1021/jo952048eopenalex-snapshot
Hindered Rotation in Arylnaphthalene Lignans
inferredcites →https://doi.org/10.1021/jo9623705openalex-snapshot
Determination of the Enantiomerization Barrier of Arylnaphthalene Lignans by Cryogenic Subcritical Fluid Chromatography and Computer Simulation
inferredcites →https://doi.org/10.1021/np000191jopenalex-snapshot
New Lignan Glycosides with Potent Antiinflammatory Effect, Isolated from Justicia ciliata
inferredcites →https://doi.org/10.1021/np0101651openalex-snapshot
Potent Cytotoxic Lignans from Justicia procumbens and Their Effects on Nitric Oxide and Tumor Necrosis Factor-α Production in Mouse Macrophages
inferredcites →https://doi.org/10.1039/c4np00121dopenalex-snapshot
A twist of nature – the significance of atropisomers in biological systems
inferredcites →https://doi.org/10.1039/c6np00021eopenalex-snapshot
Recent advances in research on lignans and neolignans
inferredcites →https://doi.org/10.1039/c7ra13754kopenalex-snapshot
Arylnaphthalene lactone analogues: synthesis and development as excellent biological candidates for future drug discovery
inferredcites →https://doi.org/10.1039/c9ra03526eopenalex-snapshot
Determination of the absolute configuration of conformationally flexible molecules by simulation of chiro-optical spectra: a case study
inferredcites →https://doi.org/10.1063/1.1626543openalex-snapshot
Comparative assessment of a new nonempirical density functional: Molecules and hydrogen-bonded complexes
inferredcites →https://doi.org/10.1063/1.478522openalex-snapshot
Toward reliable density functional methods without adjustable parameters: The PBE0 model
inferredcites →https://doi.org/10.1080/10286020.2011.653561openalex-snapshot
Total synthesis of 6′-hydroxyjusticidin A
inferredcites →https://doi.org/10.1080/10286020.2013.805208openalex-snapshot
The synthesis of justicidinoside B and its atropisomer
inferredcites →https://doi.org/10.1103/physrevlett.77.3865openalex-snapshot
Generalized Gradient Approximation Made Simple
inferredcites →https://doi.org/10.1146/annurev-physchem-052516-044827openalex-snapshot
Calculating Natural Optical Activity of Molecules from First Principles
inferredcites →https://doi.org/10.2174/0929867324666170310112009openalex-snapshot
Absolute Configuration Determination by Quantum Mechanical Calculation of Chiroptical Spectra: Basics and Applications to Fungal Metabolites
inferredcites →https://doi.org/10.4172/jaa.1000027openalex-snapshot
Development of an Antiviral Screening Protocol: One-Stone-Two-birds

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113199zenodo-depositor-declared
Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
inferred← citeshttps://doi.org/10.1002/ajoc.202200267openalex-snapshot
Axial Chirality and Antiviral Activity Evaluation of Arylnaphthalene Lignan Glycosides from Justicia procumbens
inferred← citeshttps://doi.org/10.1002/med.22037openalex-snapshot
Bioactive atropisomers: Unraveling design strategies and synthetic routes for drug discovery
inferred← citeshttps://doi.org/10.1016/b978-0-323-85542-6.00028-7openalex-snapshot
Bioprospecting and bioassay-guided isolation of medicinal plants—A tool for drug discovery
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107570openalex-snapshot
Axially chiral dihydrophenanthrene dimers from Pholidota yunnanensis with anti-neuroinflammatory activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118398openalex-snapshot
Effect of stereochemistry at position C14 on the antiproliferative activity and selectivity of simplified oridonin O-acylated derivatives
inferred← citeshttps://doi.org/10.1016/j.jep.2023.116819openalex-snapshot
Ethnomedicinal uses, phytochemistry, and pharmacological relevance of Justicia procumbens (Oriental Water Willow) - A promising traditional plant
inferred← citeshttps://doi.org/10.1016/j.polymdegradstab.2023.110536openalex-snapshot
A quantum chemical and molecular dynamics simulation study on photo-oxidative aging of polyethylene: Mechanism and differences between crystalline and amorphous phases
inferred← citeshttps://doi.org/10.1021/acs.chemrev.2c00591openalex-snapshot
Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00589openalex-snapshot
Goyangamins A–C, Three Pairs of Enantiomeric 2(1 H )-Quinolinone Alkaloid Dimers with Antisenescent Activity from Tetradium daniellii
inferred← citeshttps://doi.org/10.1080/10286020.2022.2117169openalex-snapshot
Survey of natural products reported by Asian research groups in 2021
inferred← citeshttps://doi.org/10.1080/14786419.2021.1948843openalex-snapshot
The efficient synthesis and biological evaluation of justicidin B
inferred← citeshttps://doi.org/10.1186/s12906-023-04079-5openalex-snapshot
Mechanisms of Rostellularia procumbens (L.) Nees on treating chronic glomerulonephritis explored by network pharmacology, RNA-seq, and in vitro experiments
inferred← citeshttps://doi.org/10.3390/molecules28010302openalex-snapshot
Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins
inferred← citeshttps://doi.org/10.3390/molecules30173554openalex-snapshot
In-Depth Exploration of Chemical Constituents from Justicia procumbens L. Through UHPLC-Q-Exactive Orbitrap Mass Spectrometry
inferred← citeshttps://doi.org/10.6084/m9.figshare.23740724openalex-snapshot
Additional file 1 of Mechanisms of Rostellularia procumbens (L.) Nees on treating chronic glomerulonephritis explored by network pharmacology, RNA-seq, and in vitro experiments
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