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Increased risk of reflux esophagitis in non-obese individuals with nonalcoholic fatty liver disease: a cross-sectional study

Annals of medicine (Helsinki), 2023, Vol.55 (2), p.2294933-2294933

2023

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Design, synthesis and biological evaluation of chalcone analogues with novel dual antioxidant mechanisms as potential anti-ischemic stroke agents

Acta pharmaceutica Sinica. B, 2019-03, Vol.9 (2), p.335-350

2019

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Colloidal silver nanoparticles modified electrode and its application to the electroanalysis of Cytochrome c

Electrochimica acta, 2008-06, Vol.53 (16), p.5368-5372

2008

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Design and Synthesis of Novel Nordihydroguaiaretic Acid (NDGA) Analogues as Potential FGFR1 Kinase Inhibitors With Anti-Gastric Activity and Chemosensitizing Effect

Frontiers in pharmacology, 2020-09, Vol.11, p.518068-518068

2020

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Author correction to ‘Design, synthesis and biological evaluation of chalcone analogues with novel dual antioxidant mechanisms as potential anti-ischemic stroke agents’ [Acta Pharmaceutica Sinica B 9 (2019) 335–350]

Acta pharmaceutica Sinica. B, 2022-08, Vol.12 (8), p.3451-3452

2022

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Simultaneous determination of five toxic alkaloids in body fluids by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2008-11, Vol.875 (2), p.471-477

2008

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Synthesis of 2-substituted quinazolines by CsOH-mediated direct aerobic oxidative cyclocondensation of 2-aminoarylmethanols with nitriles in air

Green chemistry : an international journal and green chemistry resource : GC, 2017, Vol.19 (13), p.2945-2951

2017

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Design, synthesis, and evaluation of chalcone analogues incorporate α,β-Unsaturated ketone functionality as anti-lung cancer agents via evoking ROS to induce pyroptosis

European journal of medicinal chemistry, 2018-09, Vol.157, p.1395-1405

2018

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Design, synthesis, anti-lung cancer activity, and chemosensitization of tumor-selective MCACs based on ROS-mediated JNK pathway activation and NF-κB pathway inhibition

European journal of medicinal chemistry, 2018-05, Vol.151, p.508-519

2018

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Simultaneous determination of selenium and arsenic contents in different extracts of Radix Astragali by enhancement effect of ethanol in hydride generation-inductively coupled plasma-atomic emission spectrometry

Microchemical journal, 2007-10, Vol.87 (1), p.1-5

2007

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Design, synthesis and QSAR study of novel isatin analogues inspired Michael acceptor as potential anticancer compounds

European journal of medicinal chemistry, 2018-01, Vol.144, p.493-503

2018

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Synthesis and evaluation of asymmetric curcuminoid analogs as potential anticancer agents that downregulate NF-κB activation and enhance the sensitivity of gastric cancer cell lines to irinotecan chemotherapy

European journal of medicinal chemistry, 2017-10, Vol.139, p.917-925

2017

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A Steroid-Type Antioxidant Targeting the Keap1/Nrf2/ARE Signaling Pathway from the Soft Coral Dendronephthya gigantea

Journal of natural products (Washington, D.C.), 2018-11, Vol.81 (11), p.2567-2575

2018

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Design, synthesis, and evaluation of NDGA analogues as potential anti-ischemic stroke agents

European journal of medicinal chemistry, 2018-01, Vol.143, p.1165-1173

2018

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Design, synthesis, and evaluation of asymmetric EF24 analogues as potential anti-cancer agents for lung cancer

European journal of medicinal chemistry, 2017-01, Vol.125, p.1321-1331

2017

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Hydroazulene Diterpenes from a Dictyota Brown Alga and Their Antioxidant and Neuroprotective Effects Against Cerebral Ischemia-Reperfusion Injury

Journal of natural products (Washington, D.C.), 2021-04, Vol.84 (4), p.1306-1315

2021

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Synthesis of 2-substituted quinazolines by CsOH-mediated direct aerobic oxidative cyclocondensation of 2-aminoarylmethanols with nitriles in airElectronic supplementary information (ESI) available: Experimental details, condition screening tables, and characterization and copies of the 1H and 13C NMR spectra of the products. See DOI: 10.1039/c7gc00977a

2017-07

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Synthesis and anti-tumor activity of EF24 analogues as IKKβ inhibitors

European journal of medicinal chemistry, 2018-01, Vol.144, p.218-228

2018

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Novel antioxidants’ synthesis and their anti-oxidative activity through activating Nrf2 signaling pathway

Bioorganic & medicinal chemistry letters, 2017-04, Vol.27 (7), p.1616-1619

2017

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A novel non-ATP competitive FGFR1 inhibitor with therapeutic potential on gastric cancer through inhibition of cell proliferation, survival and migration

Apoptosis (London), 2017-06, Vol.22 (6), p.852-864

2017

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Erratum: Author correction to 'Design, synthesis and biological evaluation of chalcone analogues with novel dual antioxidant mechanisms as potential anti-ischemic stroke agents' [Acta Pharmaceutica Sinica B 9 (2019) 335-350]

Acta pharmaceutica Sinica. B, 2022-08, Vol.12 (8), p.3451-3452

2022

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Design and Green Synthesis of Piperlongumine Analogs and Their Antioxidant Activity against Cerebral Ischemia-Reperfusion Injury

ACS chemical neuroscience, 2019-11, Vol.10 (11), p.4545-4557

2019

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A novel double carbonyl analog of curcumin induces the apoptosis of human lung cancer H460 cells via the activation of the endoplasmic reticulum stress signaling pathway

Oncology reports, 2016-09, Vol.36 (3), p.1640-1648

2016

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The therapeutic potential of a novel non-ATP-competitive fibroblast growth factor receptor 1 inhibitor on gastric cancer

Anti-cancer drugs, 2015-04, Vol.26 (4), p.379-387

2015

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Inclusion Bodies are Formed in SFTSV-infected Human Macrophages

Bingdu xuebao, 2016-01, Vol.32 (1), p.19

2016

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Increased risk of reflux esophagitis in non-obese individuals with nonalcoholic fatty liver disease: a cross-sectional study

Design, synthesis and biological evaluation of chalcone analogues with novel dual antioxidant mechanisms as potential anti-ischemic stroke agents

Colloidal silver nanoparticles modified electrode and its application to the electroanalysis of Cytochrome c

Design and Synthesis of Novel Nordihydroguaiaretic Acid (NDGA) Analogues as Potential FGFR1 Kinase Inhibitors With Anti-Gastric Activity and Chemosensitizing Effect

Author correction to ‘Design, synthesis and biological evaluation of chalcone analogues with novel dual antioxidant mechanisms as potential anti-ischemic stroke agents’ [Acta Pharmaceutica Sinica B 9 (2019) 335–350]

Simultaneous determination of five toxic alkaloids in body fluids by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry

Synthesis of 2-substituted quinazolines by CsOH-mediated direct aerobic oxidative cyclocondensation of 2-aminoarylmethanols with nitriles in air

Design, synthesis, and evaluation of chalcone analogues incorporate α,β-Unsaturated ketone functionality as anti-lung cancer agents via evoking ROS to induce pyroptosis

Design, synthesis, anti-lung cancer activity, and chemosensitization of tumor-selective MCACs based on ROS-mediated JNK pathway activation and NF-κB pathway inhibition

Simultaneous determination of selenium and arsenic contents in different extracts of Radix Astragali by enhancement effect of ethanol in hydride generation-inductively coupled plasma-atomic emission spectrometry

Design, synthesis and QSAR study of novel isatin analogues inspired Michael acceptor as potential anticancer compounds

Synthesis and evaluation of asymmetric curcuminoid analogs as potential anticancer agents that downregulate NF-κB activation and enhance the sensitivity of gastric cancer cell lines to irinotecan chemotherapy

A Steroid-Type Antioxidant Targeting the Keap1/Nrf2/ARE Signaling Pathway from the Soft Coral Dendronephthya gigantea

Design, synthesis, and evaluation of NDGA analogues as potential anti-ischemic stroke agents

Design, synthesis, and evaluation of asymmetric EF24 analogues as potential anti-cancer agents for lung cancer

Hydroazulene Diterpenes from a Dictyota Brown Alga and Their Antioxidant and Neuroprotective Effects Against Cerebral Ischemia-Reperfusion Injury

Synthesis and anti-tumor activity of EF24 analogues as IKKβ inhibitors

Novel antioxidants’ synthesis and their anti-oxidative activity through activating Nrf2 signaling pathway

A novel non-ATP competitive FGFR1 inhibitor with therapeutic potential on gastric cancer through inhibition of cell proliferation, survival and migration

Erratum: Author correction to 'Design, synthesis and biological evaluation of chalcone analogues with novel dual antioxidant mechanisms as potential anti-ischemic stroke agents' [Acta Pharmaceutica Sinica B 9 (2019) 335-350]

Design and Green Synthesis of Piperlongumine Analogs and Their Antioxidant Activity against Cerebral Ischemia-Reperfusion Injury

A novel double carbonyl analog of curcumin induces the apoptosis of human lung cancer H460 cells via the activation of the endoplasmic reticulum stress signaling pathway

The therapeutic potential of a novel non-ATP-competitive fibroblast growth factor receptor 1 inhibitor on gastric cancer

Inclusion Bodies are Formed in SFTSV-infected Human Macrophages

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