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Physalins V-IX, 16,24-cyclo-13,14-seco withanolides from Physalis angulata and their antiproliferative and anti-inflammatory activities

Scientific reports, 2017-06, Vol.7 (1), p.4057-10, Article 4057

2017

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Comprehensive transcriptome and proteome analyses reveal a novel sodium chloride responsive gene network in maize seed tissues during germination

Plant, cell and environment, 2021-01, Vol.44 (1), p.88-101

2021

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Alisma genus: Phytochemical constituents, biosynthesis, and biological activities

Phytotherapy research, 2021-04, Vol.35 (4), p.1872-1886

2021

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Preliminary enrichment and separation of chlorogenic acid from Helianthus tuberosus L. leaves extract by macroporous resins

Food chemistry, 2015-02, Vol.168, p.55-62

2015

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Unprecedented diterpenoid dimers with soluble epoxide hydrolase inhibitory effect from Euphorbia fischeriana

Organic & biomolecular chemistry, 2022-03, Vol.20 (12), p.2508-2517

2022

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Uncaria rhynchophylla Ameliorates Parkinson’s Disease by Inhibiting HSP90 Expression: Insights from Quantitative Proteomics

Cellular physiology and biochemistry, 2018-01, Vol.47 (4), p.1453-1464

2018

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Macrophage Inactivation by Small Molecule Wedelolactone via Targeting sEH for the Treatment of LPS-Induced Acute Lung Injury

ACS central science, 2023-03, Vol.9 (3), p.440-456

2023

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Association of SOX11 Polymorphisms in distal 3′UTR with Susceptibility for Schizophrenia

Journal of clinical laboratory analysis, 2020-08, Vol.34 (8), p.n/a

2020

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Editorial: Isolation, structural elucidation, and biological evaluation of bioactive products from traditional medicine

Frontiers in chemistry, 2022-08, Vol.10, p.984399-984399

2022

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Tetracyclic triterpenoids as inhibitors of cytochrome P450 3A4 and their quantitative structure activity relationship analysis

Arabian journal of chemistry, 2023-10, Vol.16 (10), p.105156, Article 105156

2023

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Uncarialins J—M from Uncaria rhynchophylla and Their Anti‐depression Mechanism in Unpredictable Chronic Mild Stress‐Induced Mice via Activating 5‐HT1A Receptor

Chinese journal of chemistry, 2021-05, Vol.39 (5), p.1331-1343

2021

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Discovery of New Iridoids as Farnesoid X Receptor Agonists from Morinda officinalis: Agonistic Potentials and Molecular Stimulation

Chinese journal of chemistry, 2021-05, Vol.39 (5), p.1288-1296

2021

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Isolation and identification of two new sargentodoxosides from Sargentodoxa cuneata and their agonistic effects against FXR

Natural product research, 2022-07, Vol.36 (14), p.3665-3672

2022

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Novel protostane-type triterpenoids with inhibitory human carboxylesterase 2 activities

RSC advances, 2017, Vol.7 (46), p.28702-28710

2017

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A highly selective near infrared fluorescent probe for carboxylesterase 2 and its biological applications

Journal of materials chemistry. B, Materials for biology and medicine, 2021-03, Vol.9 (1), p.2457-2461

2021

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Kurarinone alleviated Parkinson's disease via stabilization of epoxyeicosatrienoic acids in animal model

Proceedings of the National Academy of Sciences - PNAS, 2022-03, Vol.119 (9), p.1

2022

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Discovery of Soluble Epoxide Hydrolase Inhibitors from Chemical Synthesis and Natural Products

Journal of medicinal chemistry, 2021-01, Vol.64 (1), p.184-215

2021

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Inhibition of gut bacterial β-glucuronidase by chemical components from black tea: Inhibition interactions and molecular mechanism

Arabian journal of chemistry, 2021-12, Vol.14 (12), p.103457, Article 103457

2021

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Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity

Phytochemistry (Oxford), 2022-01, Vol.193, p.113011-113011, Article 113011

2022

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Identification of Escherichia coli β-glucuronidase inhibitors from Polygonum cuspidatum Siebold & Zucc

Brazilian Journal of Pharmaceutical Sciences, 2022-01, Vol.58

2022

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Total terpenoids of Inula japonica activated the Nrf2 receptor to alleviate the inflammation and oxidative stress in LPS-induced acute lung injury

Phytomedicine (Stuttgart), 2022-12, Vol.107, p.154377-154377, Article 154377

2022

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Total flavonoids of Inula japonica alleviated the inflammatory response and oxidative stress in LPS-induced acute lung injury via inhibiting the sEH activity: Insights from lipid metabolomics

Phytomedicine (Stuttgart), 2022-12, Vol.107, p.154380-154380, Article 154380

2022

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Flavonoids as human carboxylesterase 2 inhibitors: Inhibition potentials and molecular docking simulations

International journal of biological macromolecules, 2019-06, Vol.131, p.201-208

2019

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Direct targeting of sEH with alisol B alleviated the apoptosis, inflammation, and oxidative stress in cisplatin-induced acute kidney injury

International journal of biological sciences, 2023, Vol.19 (1), p.294-310

2023

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Targeting Keap1 with Inulae Herba activated the Nrf2 receptor to alleviate LPS-mediated acute lung injury

Journal of ethnopharmacology, 2024-01, Vol.319 (Pt 3), p.117358-117358, Article 117358

2024

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Physalins V-IX, 16,24-cyclo-13,14-seco withanolides from Physalis angulata and their antiproliferative and anti-inflammatory activities

Comprehensive transcriptome and proteome analyses reveal a novel sodium chloride responsive gene network in maize seed tissues during germination

Alisma genus: Phytochemical constituents, biosynthesis, and biological activities

Preliminary enrichment and separation of chlorogenic acid from Helianthus tuberosus L. leaves extract by macroporous resins

Unprecedented diterpenoid dimers with soluble epoxide hydrolase inhibitory effect from Euphorbia fischeriana

Uncaria rhynchophylla Ameliorates Parkinson’s Disease by Inhibiting HSP90 Expression: Insights from Quantitative Proteomics

Macrophage Inactivation by Small Molecule Wedelolactone via Targeting sEH for the Treatment of LPS-Induced Acute Lung Injury

Association of SOX11 Polymorphisms in distal 3′UTR with Susceptibility for Schizophrenia

Editorial: Isolation, structural elucidation, and biological evaluation of bioactive products from traditional medicine

Tetracyclic triterpenoids as inhibitors of cytochrome P450 3A4 and their quantitative structure activity relationship analysis

Uncarialins J—M from Uncaria rhynchophylla and Their Anti‐depression Mechanism in Unpredictable Chronic Mild Stress‐Induced Mice via Activating 5‐HT1A Receptor

Discovery of New Iridoids as Farnesoid X Receptor Agonists from Morinda officinalis: Agonistic Potentials and Molecular Stimulation

Isolation and identification of two new sargentodoxosides from Sargentodoxa cuneata and their agonistic effects against FXR

Novel protostane-type triterpenoids with inhibitory human carboxylesterase 2 activities

A highly selective near infrared fluorescent probe for carboxylesterase 2 and its biological applications

Kurarinone alleviated Parkinson's disease via stabilization of epoxyeicosatrienoic acids in animal model

Discovery of Soluble Epoxide Hydrolase Inhibitors from Chemical Synthesis and Natural Products

Inhibition of gut bacterial β-glucuronidase by chemical components from black tea: Inhibition interactions and molecular mechanism

Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity

Identification of Escherichia coli β-glucuronidase inhibitors from Polygonum cuspidatum Siebold & Zucc

Total terpenoids of Inula japonica activated the Nrf2 receptor to alleviate the inflammation and oxidative stress in LPS-induced acute lung injury

Total flavonoids of Inula japonica alleviated the inflammatory response and oxidative stress in LPS-induced acute lung injury via inhibiting the sEH activity: Insights from lipid metabolomics

Flavonoids as human carboxylesterase 2 inhibitors: Inhibition potentials and molecular docking simulations

Direct targeting of sEH with alisol B alleviated the apoptosis, inflammation, and oxidative stress in cisplatin-induced acute kidney injury

Targeting Keap1 with Inulae Herba activated the Nrf2 receptor to alleviate LPS-mediated acute lung injury

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