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EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2―activating mutations

Nature (London), 2012-12, Vol.492 (7427), p.108-112

2012

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Yangqing Chenfei formula (养清尘肺方) alleviates crystalline silica induced pulmonary inflammation and fibrosis by suppressing macrophage polarization

Journal of traditional Chinese medicine, 2023-12, Vol.43 (6), p.1126-1139

2023

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Integration of serum pharmacochemistry with network pharmacology to reveal the potential mechanism of Yangqing Chenfei formula (养清尘肺方) for the treatment of silicosis

Journal of traditional Chinese medicine, 2024-08, Vol.44 (4), p.784-793

2024

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Synthesis of (±)- and (+)-perovskone

Tetrahedron, 2011-12, Vol.67 (52), p.10129-10146

2011

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Electronically Engineering Water Resistance in Methane Combustion with an Atomically Dispersed Tungsten on PdO Catalyst

Angewandte Chemie International Edition, 2022-07, Vol.61 (27), p.e202201655-n/a

International ed. in English, 2022

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Diels-Alder reactions of 12-hydroxy-9(10®20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione

Molecules, 2013-06, Vol.18 (6), p.6969-6989

2013

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Fluorogenic Chemical Probe Strategy for Precise Tracking of Mitochondrial Polarity

Analytical chemistry (Washington), 2024-09, Vol.96 (37), p.14800-14808

2024

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Inhibition Of LSD1 As a Therapeutic Strategy For The Treatment Of Acute Myeloid Leukemia

Blood, 2013-11, Vol.122 (21), p.3964-3964

2013

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A simple fluorescent probe for glutathione detection and its bioimaging application in living cells

Microchemical journal, 2021-07, Vol.166, p.106135, Article 106135

2021

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Regulating catalytic stability of PtSnM/CeO2 (M = Mn, W, Nb) catalysts via the closely coupled multi-active sites to promote multicomponent VOCs oxidation

Chemical engineering journal (Lausanne, Switzerland : 1996), 2023-09, Vol.471, p.144456, Article 144456

2023

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A General Dual-Metal Nanocrystal Dissociation Strategy to Generate Robust High-Temperature-Stable Alumina-Supported Single-Atom Catalysts

Journal of the American Chemical Society, 2023-07, Vol.145 (29), p.15869-15878

2023

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Discovery of Orally Bioavailable 1,3,4-Trisubstituted 2-Oxopiperazine-Based Melanocortin-4 Receptor Agonists as Potential Antiobesity Agents

Journal of medicinal chemistry, 2008-10, Vol.51 (19), p.6055-6066

2008

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A highly water-soluble rhodol-based fluorescent probe for the organic-solvent independent sensing of biological hypochlorous acid

Dyes and pigments, 2022-08, Vol.204, p.110435, Article 110435

2022

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Synthesis and Pharmacological Evaluation of 3-(3,4-Dichlorophenyl)-1-indanamine Derivatives as Nonselective Ligands for Biogenic Amine Transporters

Journal of medicinal chemistry, 2004-05, Vol.47 (10), p.2624-2634

2004

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In vivo precision imaging of vicinal-dithiol-containing proteins by a FRET molecular probe sensitive to protein environment

Chinese chemical letters, 2023-12, Vol.34 (12), p.108329, Article 108329

2023

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A spiropyran with low pKa for tracking DNA G-quadruplexes and revealing the dissipation of ΔΨm with senescence using an in-situ switching strategy

Sensors and actuators. B, Chemical, 2022-05, Vol.359, p.131618, Article 131618

2022

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Discovery of Proline-Based p300/CBP Inhibitors Using DNA-Encoded Library Technology in Combination with High-Throughput Screening

Journal of medicinal chemistry, 2022-11, Vol.65 (21), p.14391-14408

2022

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Design and synthesis of potent and selective 1,3,4-trisubstituted-2-oxopiperazine based melanocortin-4 receptor agonists

Bioorganic & medicinal chemistry letters, 2006-09, Vol.16 (17), p.4668-4673

2006

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Design and synthesis of aminopyridine containing biaryls reducing c-MYC protein levels in cells

Bioorganic & medicinal chemistry letters, 2023-08, Vol.92, p.129385-129385, Article 129385

2023

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An efficient and practical synthesis of 2,4-substituted pyrido[4,3-d]pyrimidin-5(6H)-ones

Tetrahedron letters, 2019-12, Vol.60 (49), p.151312, Article 151312

2019

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Digoxin alleviates pulmonary fibrosis by regulating phosphatidylinositol-3-kinase/Akt signaling through inhibiting the activation of fibroblast: an in vivo and in vitro experiment

Zhonghua wei zhong bing ji jiu yi xue, 2022-11, Vol.34 (11), p.1161

2022

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Probes for Narcotic Receptor-Mediated Phenomena. 33. Construction of a Strained trans-5,6-Ring System by Displacement of a Nitro-Activated Aromatic Fluorine. Synthesis of the Penultimate Oxide-Bridged Phenylmorphans

Journal of organic chemistry, 2004-08, Vol.69 (16), p.5322-5327

2004

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Design, Synthesis, and Evaluation of Proline and Pyrrolidine Based Melanocortin Receptor Agonists. A Conformationally Restricted Dipeptide Mimic Approach

Journal of medicinal chemistry, 2006-07, Vol.49 (15), p.4745-4761

2006

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Cell-Based Drug Discovery: Identification and Optimization of Small Molecules that Reduce c‑MYC Protein Levels in Cells

Journal of medicinal chemistry, 2021-11, Vol.64 (21), p.16056-16087

2021

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Identification of Potent, Selective, Cell-Active Inhibitors of the Histone Lysine Methyltransferase EZH2

ACS medicinal chemistry letters, 2012-12, Vol.3 (12), p.1091-1096

2012

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EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2―activating mutations

Yangqing Chenfei formula (养清尘肺方) alleviates crystalline silica induced pulmonary inflammation and fibrosis by suppressing macrophage polarization

Integration of serum pharmacochemistry with network pharmacology to reveal the potential mechanism of Yangqing Chenfei formula (养清尘肺方) for the treatment of silicosis

Synthesis of (±)- and (+)-perovskone

Electronically Engineering Water Resistance in Methane Combustion with an Atomically Dispersed Tungsten on PdO Catalyst

Diels-Alder reactions of 12-hydroxy-9(10®20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione

Fluorogenic Chemical Probe Strategy for Precise Tracking of Mitochondrial Polarity

Inhibition Of LSD1 As a Therapeutic Strategy For The Treatment Of Acute Myeloid Leukemia

A simple fluorescent probe for glutathione detection and its bioimaging application in living cells

Regulating catalytic stability of PtSnM/CeO2 (M = Mn, W, Nb) catalysts via the closely coupled multi-active sites to promote multicomponent VOCs oxidation

A General Dual-Metal Nanocrystal Dissociation Strategy to Generate Robust High-Temperature-Stable Alumina-Supported Single-Atom Catalysts

Discovery of Orally Bioavailable 1,3,4-Trisubstituted 2-Oxopiperazine-Based Melanocortin-4 Receptor Agonists as Potential Antiobesity Agents

A highly water-soluble rhodol-based fluorescent probe for the organic-solvent independent sensing of biological hypochlorous acid

Synthesis and Pharmacological Evaluation of 3-(3,4-Dichlorophenyl)-1-indanamine Derivatives as Nonselective Ligands for Biogenic Amine Transporters

In vivo precision imaging of vicinal-dithiol-containing proteins by a FRET molecular probe sensitive to protein environment

A spiropyran with low pKa for tracking DNA G-quadruplexes and revealing the dissipation of ΔΨm with senescence using an in-situ switching strategy

Discovery of Proline-Based p300/CBP Inhibitors Using DNA-Encoded Library Technology in Combination with High-Throughput Screening

Design and synthesis of potent and selective 1,3,4-trisubstituted-2-oxopiperazine based melanocortin-4 receptor agonists

Design and synthesis of aminopyridine containing biaryls reducing c-MYC protein levels in cells

An efficient and practical synthesis of 2,4-substituted pyrido[4,3-d]pyrimidin-5(6H)-ones

Digoxin alleviates pulmonary fibrosis by regulating phosphatidylinositol-3-kinase/Akt signaling through inhibiting the activation of fibroblast: an in vivo and in vitro experiment

Probes for Narcotic Receptor-Mediated Phenomena. 33. Construction of a Strained trans-5,6-Ring System by Displacement of a Nitro-Activated Aromatic Fluorine. Synthesis of the Penultimate Oxide-Bridged Phenylmorphans

Design, Synthesis, and Evaluation of Proline and Pyrrolidine Based Melanocortin Receptor Agonists. A Conformationally Restricted Dipeptide Mimic Approach

Cell-Based Drug Discovery: Identification and Optimization of Small Molecules that Reduce c‑MYC Protein Levels in Cells

Identification of Potent, Selective, Cell-Active Inhibitors of the Histone Lysine Methyltransferase EZH2

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