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De‐epimerization of Monosaccharides by Dynamic Kinetic Resolution: Ligand‐Controlled Synthesis of O‐Aryl‐Glycosides through Copper‐Catalyzed Cross‐Coupling

Advanced synthesis & catalysis, 2024-03, Vol.366 (5), p.1144-1151

2024

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CDK2-mediated site-specific phosphorylation of EZH2 drives and maintains triple-negative breast cancer

Nature communications, 2019-11, Vol.10 (1), p.5114-5114, Article 5114

2019

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Biomarkers beyond BRCA: promising combinatorial treatment strategies in overcoming resistance to PARP inhibitors

Journal of biomedical science, 2022-10, Vol.29 (1), p.1-86, Article 86

2022

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EGFR and c-MET Cooperate to Enhance Resistance to PARP Inhibitors in Hepatocellular Carcinoma

Cancer research (Chicago, Ill.), 2019-02, Vol.79 (4), p.819-829

2019

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Iminosugars as therapeutic agents: recent advances and promising trends

Future medicinal chemistry, 2011-09, Vol.3 (12), p.1513-1521

2011

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Synthesis and glycosidase inhibition of N-substituted derivatives of 1,4-dideoxy-1,4-imino-d-mannitol (DIM)

Organic & biomolecular chemistry, 2020-02, Vol.18 (5), p.999-1011

2020

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Diastereoselective Synthesis, Glycosidase Inhibition, and Docking Study of C‑7-Fluorinated Casuarine and Australine Derivatives

Journal of organic chemistry, 2022-06, Vol.87 (11), p.7291-7307

2022

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Inhibition of the EGFR/STAT3/CEBPD Axis Reverses Cisplatin Cross-resistance with Paclitaxel in the Urothelial Carcinoma of the Urinary Bladder

Clinical cancer research, 2017-01, Vol.23 (2), p.503-513

2017

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Synthesis and glycosidase inhibition of 5-C-alkyl-DNJ and 5-C-alkyl-l-ido-DNJ derivatives

European journal of medicinal chemistry, 2021-11, Vol.224, p.113716-113716, Article 113716

2021

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De Novo Synthesis of Orthogonally-Protected C2-Fluoro Digitoxoses and Cymaroses: Development and Application for the Synthesis of Fluorinated Digoxin

Journal of organic chemistry, 2022-01, Vol.87 (2), p.1272-1284

2022

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C-6 fluorinated casuarines as highly potent and selective amyloglucosidase inhibitors: Synthesis and structure-activity relationship study

European journal of medicinal chemistry, 2022-12, Vol.244, p.114852-114852, Article 114852

2022

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Design and synthesis of iso- allo -DNJ and L-isoDALDP derivatives: pursuit of potent and selective inhibitors of α-glucosidase

Organic & biomolecular chemistry, 2023-04, Vol.21 (16), p.3453-3464

2023

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Introduction of C -alkyl branches to l -iminosugars changes their active site binding orientation

Organic & biomolecular chemistry, 2022-09, Vol.20 (36), p.7250-7260

2022

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Design, synthesis and glycosidase inhibition of DAB derivatives with C-4 peptide and dipeptide branches

Organic & biomolecular chemistry, 2023-03, Vol.21 (13), p.2729-2741

2023

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Synthesis and Glycosidase Inhibition of Broussonetine M and Its Analogues

Molecules (Basel, Switzerland), 2019-10, Vol.24 (20), p.3712

2019

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Stereocomplementary synthesis of casuarine and its 6-epi-, 7-epi-, and 6,7-diepi-stereoisomers

Organic & biomolecular chemistry, 2021-11, Vol.19 (43), p.9410-9420

2021

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Fluorinated Radicamine A and B: Synthesis and Glycosidase Inhibition

European journal of organic chemistry, 2016-03, Vol.2016 (7), p.1429-1438

2016

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Synthesis and Glycosidase Inhibition of Australine and Its Fluorinated Derivatives

Organic letters, 2015-02, Vol.17 (3), p.716-719

2015

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Activated but not resting regulatory T cells accumulated in tumor microenvironment and correlated with tumor progression in patients with colorectal cancer

International journal of cancer, 2013-03, Vol.132 (6), p.1341-1350

2013

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First total synthesis of (+)-broussonetine W: glycosidase inhibition of natural product & analogs

Organic & biomolecular chemistry, 2016-06, Vol.14 (22), p.5157-5174

2016

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Synthesis of Pyrrolidine Monocyclic Analogues of Pochonicine and Its Stereoisomers: Pursuit of Simplified Structures and Potent β-N-Acetylhexosaminidase Inhibition

Molecules (Basel, Switzerland), 2020-03, Vol.25 (7), p.1498

2020

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CD4⁺ T cells expressing latency-associated peptide and Foxp3 are an activated subgroup of regulatory T cells enriched in patients with colorectal cancer

PloS one, 2014-09, Vol.9 (9), p.e108554

2014

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Quinazoline-directed selective ortho-iodination for the synthesis of 2-(2-iodoaryl)-4-arylquinazolines

Journal of organometallic chemistry, 2017-08, Vol.843, p.20-25

2017

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Radiation-induced senescence in securin-deficient cancer cells promotes cell invasion involving the IL-6/STAT3 and PDGF-BB/PDGFR pathways

Scientific reports, 2013-04, Vol.3 (1), p.1675-1675, Article 1675

2013

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Radicamines A and B: Synthesis and Revision of the Absolute Configuration

Organic letters, 2006-07, Vol.8 (14), p.3021-3024

2006

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De‐epimerization of Monosaccharides by Dynamic Kinetic Resolution: Ligand‐Controlled Synthesis of O‐Aryl‐Glycosides through Copper‐Catalyzed Cross‐Coupling

CDK2-mediated site-specific phosphorylation of EZH2 drives and maintains triple-negative breast cancer

Biomarkers beyond BRCA: promising combinatorial treatment strategies in overcoming resistance to PARP inhibitors

EGFR and c-MET Cooperate to Enhance Resistance to PARP Inhibitors in Hepatocellular Carcinoma

Iminosugars as therapeutic agents: recent advances and promising trends

Synthesis and glycosidase inhibition of N-substituted derivatives of 1,4-dideoxy-1,4-imino-d-mannitol (DIM)

Diastereoselective Synthesis, Glycosidase Inhibition, and Docking Study of C‑7-Fluorinated Casuarine and Australine Derivatives

Inhibition of the EGFR/STAT3/CEBPD Axis Reverses Cisplatin Cross-resistance with Paclitaxel in the Urothelial Carcinoma of the Urinary Bladder

Synthesis and glycosidase inhibition of 5-C-alkyl-DNJ and 5-C-alkyl-l-ido-DNJ derivatives

De Novo Synthesis of Orthogonally-Protected C2-Fluoro Digitoxoses and Cymaroses: Development and Application for the Synthesis of Fluorinated Digoxin

C-6 fluorinated casuarines as highly potent and selective amyloglucosidase inhibitors: Synthesis and structure-activity relationship study

Design and synthesis of iso- allo -DNJ and L-isoDALDP derivatives: pursuit of potent and selective inhibitors of α-glucosidase

Introduction of C -alkyl branches to l -iminosugars changes their active site binding orientation

Design, synthesis and glycosidase inhibition of DAB derivatives with C-4 peptide and dipeptide branches

Synthesis and Glycosidase Inhibition of Broussonetine M and Its Analogues

Stereocomplementary synthesis of casuarine and its 6-epi-, 7-epi-, and 6,7-diepi-stereoisomers

Fluorinated Radicamine A and B: Synthesis and Glycosidase Inhibition

Synthesis and Glycosidase Inhibition of Australine and Its Fluorinated Derivatives

Activated but not resting regulatory T cells accumulated in tumor microenvironment and correlated with tumor progression in patients with colorectal cancer

First total synthesis of (+)-broussonetine W: glycosidase inhibition of natural product & analogs

Synthesis of Pyrrolidine Monocyclic Analogues of Pochonicine and Its Stereoisomers: Pursuit of Simplified Structures and Potent β-N-Acetylhexosaminidase Inhibition

CD4⁺ T cells expressing latency-associated peptide and Foxp3 are an activated subgroup of regulatory T cells enriched in patients with colorectal cancer

Quinazoline-directed selective ortho-iodination for the synthesis of 2-(2-iodoaryl)-4-arylquinazolines

Radiation-induced senescence in securin-deficient cancer cells promotes cell invasion involving the IL-6/STAT3 and PDGF-BB/PDGFR pathways

Radicamines A and B: Synthesis and Revision of the Absolute Configuration

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