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Dynamic Perception of Jasmonates by the F-Box Protein COI1

Molecular plant, 2018-10, Vol.11 (10), p.1237-1247

2018

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Construction of the Hexacyclic Core of Dispirocochlearoids A—C via a Diels−Alder Reaction

Chinese journal of chemistry, 2022-07, Vol.40 (13), p.1566-1570

2022

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Structural basis of GPBAR activation and bile acid recognition

Nature (London), 2020-11, Vol.587 (7834), p.499-504

2020

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Arabidopsis CORONATINE INSENSITIVE1 Protein Is a Jasmonate Receptor

The Plant cell, 2009-08, Vol.21 (8), p.2220-2236

2009

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Strigolactone mimic 2‐nitrodebranone is highly active in Arabidopsis growth and development

The Plant journal : for cell and molecular biology, 2021-07, Vol.107 (1), p.67-76

2021

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Endogenous Bioactive Jasmonate Is Composed of a Set of (+)-7-iso-JA-Amino Acid Conjugates

Plant physiology (Bethesda), 2016-12, Vol.172 (4), p.2154-2164

2016

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Protecting‐Group‐Free One‐Step Palladium‐Catalyzed Coupling on C25 of Cucurbitacin B Expands Chemical Diversity with Improved Cytotoxicity against A549 Cells

Chinese journal of chemistry, 2022-07, Vol.40 (14), p.1662-1666

2022

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Epilepsy phenotype and response to KCNQ openers in mice harboring the Kcnq2 R207W voltage-sensor mutation

Neurobiology of disease, 2022-11, Vol.174, p.105860-105860, Article 105860

2022

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Ligand activation mechanisms of human KCNQ2 channel

Nature communications, 2023-10, Vol.14 (1), p.6632-6632, Article 6632

2023

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Effect of GR24 Stereoisomers on Plant Development in Arabidopsis

Molecular plant, 2016-10, Vol.9 (10), p.1432-1435

2016

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Polyphenol Compound 18a Modulates UCP1-Dependent Thermogenesis to Counteract Obesity

Biomolecules (Basel, Switzerland), 2024-06, Vol.14 (6), p.618

2024

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Development of the novel ACLY inhibitor 326E as a promising treatment for hypercholesterolemia

Acta pharmaceutica Sinica. B, 2023-02, Vol.13 (2), p.739-753

2023

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The HDAC inhibitor GCJ-490A suppresses c-Met expression through IKKα and overcomes gefitinib resistance in non-small cell lung cancer

Cancer biology & medicine, 2022-02, Vol.19 (8), p.1172-1192

2022

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Modulation of hERG potassium channel gating normalizes action potential duration prolonged by dysfunctional KCNQ1 potassium channel

Proceedings of the National Academy of Sciences - PNAS, 2012-07, Vol.109 (29), p.11866-11871

2012

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nonpeptidic agonist of glucagon-like peptide 1 receptors with efficacy in diabetic db/db mice

Proceedings of the National Academy of Sciences - PNAS, 2007-01, Vol.104 (3), p.943-948

2007

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Combinatorial augmentation of voltage-gated KCNQ potassium channels by chemical openers

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (8), p.3128-3133

2008

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Synthesis of Urea-Based Inhibitors as Active Site Probes of Glutamate Carboxypeptidase II: Efficacy as Analgesic Agents

Journal of medicinal chemistry, 2004-03, Vol.47 (7), p.1729-1738

2004

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Disruption of the unfolded protein response (UPR) by lead compound selectively suppresses cancer cell growth

Cancer letters, 2015-05, Vol.360 (2), p.257-268

2015

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An activity-based probe reveals dynamic protein–protein interactions mediating IGF-1R transactivation by the GABAB receptor

Biochemical journal, 2012-05, Vol.443 (3), p.627-634

2012

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Determination of Saikosaponin Derivatives in Radix bupleuri and in Pharmaceuticals of the Chinese Multiherb Remedy Xiaochaihu-tang Using Liquid Chromatographic Tandem Mass Spectrometry

Analytical chemistry (Washington), 2004-07, Vol.76 (14), p.4208-4216

2004

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Synthetic Analogues of Betulinic Acid as Potent Inhibitors of PS1/BACE1 Interaction to Reduce Aβ Generation

Chinese journal of chemistry, 2017, Vol.35 (1), p.103-112

2017

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Design of Remarkably Simple, Yet Potent Urea-Based Inhibitors of Glutamate Carboxypeptidase II (NAALADase)

Journal of medicinal chemistry, 2001-02, Vol.44 (3), p.298-301

2001

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DWARF14 is a non-canonical hormone receptor for strigolactone

Nature (London), 2016-08, Vol.536 (7617), p.469-473

2016

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The metabolic ER stress sensor IRE1α suppresses alternative activation of macrophages and impairs energy expenditure in obesity

Nature immunology, 2017-05, Vol.18 (5), p.519

2017

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First Total Synthesis of Leucamide A

Journal of organic chemistry, 2003-02, Vol.68 (4), p.1636-1639

2003

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Dynamic Perception of Jasmonates by the F-Box Protein COI1

Construction of the Hexacyclic Core of Dispirocochlearoids A—C via a Diels−Alder Reaction

Structural basis of GPBAR activation and bile acid recognition

Arabidopsis CORONATINE INSENSITIVE1 Protein Is a Jasmonate Receptor

Strigolactone mimic 2‐nitrodebranone is highly active in Arabidopsis growth and development

Endogenous Bioactive Jasmonate Is Composed of a Set of (+)-7-iso-JA-Amino Acid Conjugates

Protecting‐Group‐Free One‐Step Palladium‐Catalyzed Coupling on C25 of Cucurbitacin B Expands Chemical Diversity with Improved Cytotoxicity against A549 Cells

Epilepsy phenotype and response to KCNQ openers in mice harboring the Kcnq2 R207W voltage-sensor mutation

Ligand activation mechanisms of human KCNQ2 channel

Effect of GR24 Stereoisomers on Plant Development in Arabidopsis

Polyphenol Compound 18a Modulates UCP1-Dependent Thermogenesis to Counteract Obesity

Development of the novel ACLY inhibitor 326E as a promising treatment for hypercholesterolemia

The HDAC inhibitor GCJ-490A suppresses c-Met expression through IKKα and overcomes gefitinib resistance in non-small cell lung cancer

Modulation of hERG potassium channel gating normalizes action potential duration prolonged by dysfunctional KCNQ1 potassium channel

nonpeptidic agonist of glucagon-like peptide 1 receptors with efficacy in diabetic db/db mice

Combinatorial augmentation of voltage-gated KCNQ potassium channels by chemical openers

Synthesis of Urea-Based Inhibitors as Active Site Probes of Glutamate Carboxypeptidase II: Efficacy as Analgesic Agents

Disruption of the unfolded protein response (UPR) by lead compound selectively suppresses cancer cell growth

An activity-based probe reveals dynamic protein–protein interactions mediating IGF-1R transactivation by the GABAB receptor

Determination of Saikosaponin Derivatives in Radix bupleuri and in Pharmaceuticals of the Chinese Multiherb Remedy Xiaochaihu-tang Using Liquid Chromatographic Tandem Mass Spectrometry

Synthetic Analogues of Betulinic Acid as Potent Inhibitors of PS1/BACE1 Interaction to Reduce Aβ Generation

Design of Remarkably Simple, Yet Potent Urea-Based Inhibitors of Glutamate Carboxypeptidase II (NAALADase)

DWARF14 is a non-canonical hormone receptor for strigolactone

The metabolic ER stress sensor IRE1α suppresses alternative activation of macrophages and impairs energy expenditure in obesity

First Total Synthesis of Leucamide A

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