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Mining expression and prognosis of topoisomerase isoforms in non-small-cell lung cancer by using Oncomine and Kaplan-Meier plotter

PloS one, 2017-03, Vol.12 (3), p.e0174515-e0174515

2017

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Discovery of a novel rhein-SAHA hybrid as a multi-targeted anti-glioblastoma drug

Investigational new drugs, 2020-06, Vol.38 (3), p.755-764

2020

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Wild-type IDH2 protects nuclear DNA from oxidative damage and is a potential therapeutic target in colorectal cancer

Oncogene, 2021-09, Vol.40 (39), p.5880-5892

2021

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Mild Cu(I)-Catalyzed Cascade Reaction of Cyclic Diaryliodoniums, Sodium Azide, and Alkynes: Efficient Synthesis of Triazolophenanthridines

Organic letters, 2014-11, Vol.16 (21), p.5600-5603

2014

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Copper‐Catalyzed One‐Pot Synthesis of Dibenzofurans, Xanthenes, and Xanthones from Cyclic Diphenyl Iodoniums

European journal of organic chemistry, 2019-07, Vol.2019 (28), p.4566-4571

2019

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N-Benzyldithiocarbamate Salts as Sulfur Sources to Access Tricyclic Thioheterocycles Mediated by Copper Species

Advanced synthesis & catalysis, 2016-09, Vol.358 (17), p.2733-2738

2016

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Reductive TCA cycle catalyzed by wild-type IDH2 promotes acute myeloid leukemia and is a metabolic vulnerability for potential targeted therapy

Journal of hematology and oncology, 2022-03, Vol.15 (1), p.30-30, Article 30

2022

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Wild-type IDH2 is a therapeutic target for triple-negative breast cancer

Nature communications, 2024-04, Vol.15 (1), p.3445-3445, Article 3445

2024

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Heterocyclic iodoniums as versatile synthons to approach diversified polycyclic heteroarenes

RSC advances, 2019-10, Vol.9 (57), p.3317-33179

2019

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Developing Bi-Gold Compound BGC2a to Target Mitochondria for the Elimination of Cancer Cells

International journal of molecular sciences, 2022-10, Vol.23 (20), p.12169

2022

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Micro-RNA-155 is induced by K-Ras oncogenic signal and promotes ROS stress in pancreatic cancer

Oncotarget, 2015-08, Vol.6 (25), p.21148-21158

2015

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Synergy between Auranofin and Celecoxib against Colon Cancer In Vitro and In Vivo through a Novel Redox-Mediated Mechanism

Cancers, 2019-07, Vol.11 (7), p.931

2019

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Advances in the studies of roles of Rho/Rho-kinase in diseases and the development of its inhibitors

European journal of medicinal chemistry, 2013-12, Vol.70, p.613-622

2013

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The rheumatoid arthritis drug auranofin exerts potent anti-lymphoma effect by stimulating TXNRD-mediated ROS generation and inhibition of energy metabolism

Redox biology, 2024-09, Vol.75, p.103245, Article 103245

2024

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Three-Component Pd/Cu-Catalyzed Cascade Reactions of Cyclic Iodoniums, Alkynes, and Boronic Acids: An Approach to Methylidenefluorenes

Organic letters, 2014-05, Vol.16 (9), p.2350-2353

2014

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EZH2 mediated metabolic rewiring promotes tumor growth independently of histone methyltransferase activity in ovarian cancer

Molecular cancer, 2023-05, Vol.22 (1), p.85-85, Article 85

2023

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Design, Synthesis, and Evaluation of VHL-Based EZH2 Degraders to Enhance Therapeutic Activity against Lymphoma

Journal of medicinal chemistry, 2021-07, Vol.64 (14), p.10167-10184

2021

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Application of Fragment Growing and Fragment Linking to the Discovery of Inhibitors of Mycobacterium tuberculosis Pantothenate Synthetase

Angewandte Chemie (International ed.), 2009-10, Vol.48 (45), p.8452-8456

2009

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Mitochondrial TXNRD3 confers drug resistance via redox-mediated mechanism and is a potential therapeutic target in vivo

Redox biology, 2020-09, Vol.36, p.101652-101652, Article 101652

2020

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Relayed Regioselective Alkynylation/Olefination of Unsymmetrical Cyclic Diaryliodonium Species Catalyzed by Cu and Pd: Affording Fluorescent Cytotoxic Benzoxazoles

Chemistry : a European journal, 2015-12, Vol.21 (52), p.18915-18920

2015

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Macrolactamization versus Macrolactonization: Total Synthesis of FK228, the Depsipeptide Histone Deacetylase Inhibitor

Journal of organic chemistry, 2008-12, Vol.73 (23), p.9353-9361

2008

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Synthesis of N‑Acyl‑N,O‑acetals Mediated by Titanium Ethoxide

Organic letters, 2014-01, Vol.16 (1), p.10-13

2014

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New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents

Molecules (Basel, Switzerland), 2017-06, Vol.22 (6), p.773

2017

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Loss of mitochondrial aconitase promotes colorectal cancer progression via SCD1-mediated lipid remodeling

Molecular metabolism (Germany), 2021-06, Vol.48, p.101203, Article 101203

2021

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Synthesis and biological evaluation of novel bi-gold mitocans in lung cancer cells

Frontiers in chemistry, 2023-12, Vol.11, p.1292115-1292115

2023

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Mining expression and prognosis of topoisomerase isoforms in non-small-cell lung cancer by using Oncomine and Kaplan-Meier plotter

Discovery of a novel rhein-SAHA hybrid as a multi-targeted anti-glioblastoma drug

Wild-type IDH2 protects nuclear DNA from oxidative damage and is a potential therapeutic target in colorectal cancer

Mild Cu(I)-Catalyzed Cascade Reaction of Cyclic Diaryliodoniums, Sodium Azide, and Alkynes: Efficient Synthesis of Triazolophenanthridines

Copper‐Catalyzed One‐Pot Synthesis of Dibenzofurans, Xanthenes, and Xanthones from Cyclic Diphenyl Iodoniums

N-Benzyldithiocarbamate Salts as Sulfur Sources to Access Tricyclic Thioheterocycles Mediated by Copper Species

Reductive TCA cycle catalyzed by wild-type IDH2 promotes acute myeloid leukemia and is a metabolic vulnerability for potential targeted therapy

Wild-type IDH2 is a therapeutic target for triple-negative breast cancer

Heterocyclic iodoniums as versatile synthons to approach diversified polycyclic heteroarenes

Developing Bi-Gold Compound BGC2a to Target Mitochondria for the Elimination of Cancer Cells

Micro-RNA-155 is induced by K-Ras oncogenic signal and promotes ROS stress in pancreatic cancer

Synergy between Auranofin and Celecoxib against Colon Cancer In Vitro and In Vivo through a Novel Redox-Mediated Mechanism

Advances in the studies of roles of Rho/Rho-kinase in diseases and the development of its inhibitors

The rheumatoid arthritis drug auranofin exerts potent anti-lymphoma effect by stimulating TXNRD-mediated ROS generation and inhibition of energy metabolism

Three-Component Pd/Cu-Catalyzed Cascade Reactions of Cyclic Iodoniums, Alkynes, and Boronic Acids: An Approach to Methylidenefluorenes

EZH2 mediated metabolic rewiring promotes tumor growth independently of histone methyltransferase activity in ovarian cancer

Design, Synthesis, and Evaluation of VHL-Based EZH2 Degraders to Enhance Therapeutic Activity against Lymphoma

Application of Fragment Growing and Fragment Linking to the Discovery of Inhibitors of Mycobacterium tuberculosis Pantothenate Synthetase

Mitochondrial TXNRD3 confers drug resistance via redox-mediated mechanism and is a potential therapeutic target in vivo

Relayed Regioselective Alkynylation/Olefination of Unsymmetrical Cyclic Diaryliodonium Species Catalyzed by Cu and Pd: Affording Fluorescent Cytotoxic Benzoxazoles

Macrolactamization versus Macrolactonization: Total Synthesis of FK228, the Depsipeptide Histone Deacetylase Inhibitor

Synthesis of N‑Acyl‑N,O‑acetals Mediated by Titanium Ethoxide

New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents

Loss of mitochondrial aconitase promotes colorectal cancer progression via SCD1-mediated lipid remodeling

Synthesis and biological evaluation of novel bi-gold mitocans in lung cancer cells

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