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Silver(I)‐Catalyzed Widely Applicable Aerobic 1,2‐Diol Oxidative Cleavage

Angewandte Chemie International Edition, 2018-03, Vol.57 (10), p.2616-2620

International ed. in English, 2018

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Comprehensive scientometrics and visualization study profiles lymphoma metabolism and identifies its significant research signatures

Frontiers in endocrinology (Lausanne), 2023-09, Vol.14, p.1266721-1266721

2023

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Global research hotspots, development trends and prospect discoveries of phase separation in cancer: a decade-long informatics investigation

Biomarker research, 2024-04, Vol.12 (1), p.39-39, Article 39

2024

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An overview of phosphodiesterase 9 inhibitors: Insights from skeletal structure, pharmacophores, and therapeutic potential

European journal of medicinal chemistry, 2023-11, Vol.259, p.115682-115682, Article 115682

2023

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Discovery of 2‐(3,4‐dialkoxyphenyl)‐2‐(substituted pyridazin‐3‐yl)acetonitriles as phosphodiesterase 4 inhibitors with anti‐neuroinflammation potential based on three‐dimensional quantitative structure–activity relationship study

Chemical biology & drug design, 2019-04, Vol.93 (4), p.484-502

2019

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Discovery of 4‑Ethoxy-6-chloro-5-azaindazoles as Novel PDE4 Inhibitors for the Treatment of Alcohol Use Disorder and Alcoholic Liver Diseases

Journal of medicinal chemistry, 2024-01, Vol.67 (1), p.728-753

2024

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Simple and Clean Photo-induced Methylation of Heteroarenes with MeOH

Chem, 2017-05, Vol.2 (5), p.688-702

2017

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One-pot synthesis and antiproliferative activity of novel 2,4-diaminopyrimidine derivatives bearing piperidine and piperazine moieties

European journal of medicinal chemistry, 2014-09, Vol.84, p.127-134

2014

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Discovery of Dihydropyrrol-2-ones as Novel G0/G1-Phase Arresting Agents Inducing Apoptosis

ACS omega, 2019-10, Vol.4 (17), p.17556-17560

2019

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Selective Copper–N-Heterocyclic Carbene (Copper-NHC)-Catalyzed Aerobic Cleavage of β‑1 Lignin Models to Aldehydes

ACS catalysis, 2017-05, Vol.7 (5), p.3344-3348

2017

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Microwave-Assisted Efficient Synthesis of 2-Hydroxydeoxybenzoins from the Alkali Degradation of Readily Prepared 3-Aryl-4-hydroxycoumarins in Water

Chemical and Pharmaceutical Bulletin, 2013/11/01, Vol.61(11), pp.1166-1172

2013

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Advances in the development of phosphodiesterase 7 inhibitors

European journal of medicinal chemistry, 2023-03, Vol.250, p.115194-115194, Article 115194

2023

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Discovery of novel 2,3-dihydro-1H-inden-1-ones as dual PDE4/AChE inhibitors with more potency against neuroinflammation for the treatment of Alzheimer's disease

European journal of medicinal chemistry, 2022-08, Vol.238, p.114503-114503, Article 114503

2022

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Discovery of novel trimethoxyphenylbenzo[d]oxazoles as dual tubulin/PDE4 inhibitors capable of inducing apoptosis at G2/M phase arrest in glioma and lung cancer cells

European journal of medicinal chemistry, 2021-11, Vol.224, p.113700-113700, Article 113700

2021

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Microwave-Assisted Dieckmann Reaction: Efficient One-Step Synthesis of 2-Aroylbenzofuran-3-ols

Advanced synthesis & catalysis, 2010-10, Vol.352 (11-12), p.1909-1913

2010

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Synthesis, Cytotoxicities and DNA-Binding Affinities of Benzofuran-3-ols and Their Fused Analogs

Chemical and Pharmaceutical Bulletin, 2011/08/01, Vol.59(8), pp.1057-1061

2011

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Novel Phosphodiesterase 4 Inhibitor FCPR03 Alleviates Lipopolysaccharide-Induced Neuroinflammation by Regulation of the cAMP/PKA/CREB Signaling Pathway and NF- κ B Inhibition

The Journal of pharmacology and experimental therapeutics, 2017-07, Vol.362 (1), p.67

2017

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An Efficient Intramolecular Stetter Reaction in Room Temperature Ionic Liquids Promoted By Microwave Irradiation

Advanced synthesis & catalysis, 2006-09, Vol.348 (14), p.1826-1830

2006

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Discovery of Novel 3‑Amino-4-alkoxyphenylketones as PDE4 Inhibitors with Improved Oral Bioavailability and Safety against Spatial Memory Impairments

ACS chemical neuroscience, 2022-02, Vol.13 (3), p.390-405

2022

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Synthesis, Biological Evaluation, and Molecular Docking of Arylpyridines as Antiproliferative Agent Targeting Tubulin

ACS medicinal chemistry letters, 2020-08, Vol.11 (8), p.1611-1619

2020

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Development of highly potent phosphodiesterase 4 inhibitors with anti-neuroinflammation potential: Design, synthesis, and structure-activity relationship study of catecholamides bearing aromatic rings

European journal of medicinal chemistry, 2016-11, Vol.124, p.372-379

2016

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Discovery of 9H-purins as potential tubulin polymerization inhibitors: Synthesis, biological evaluation and structure−activity relationships

European journal of medicinal chemistry, 2017-09, Vol.138, p.1126-1134

2017

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Catecholic amides as potential selective phosphodiesterase 4D inhibitors: Design, synthesis, pharmacological evaluation and structure–activity relationships

Bioorganic & medicinal chemistry, 2015-11, Vol.23 (22), p.7332-7339

2015

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Design, synthesis and biological evaluation of substituted aminopyridazin-3(2H)-ones as G0/G1-phase arresting agents with apoptosis-inducing activities

European journal of medicinal chemistry, 2017-12, Vol.141, p.440-445

2017

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Synthesis and anticancer activities of 3-arylflavone-8-acetic acid derivatives

European journal of medicinal chemistry, 2015-01, Vol.90, p.251-257

2015

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Silver(I)‐Catalyzed Widely Applicable Aerobic 1,2‐Diol Oxidative Cleavage

Comprehensive scientometrics and visualization study profiles lymphoma metabolism and identifies its significant research signatures

Global research hotspots, development trends and prospect discoveries of phase separation in cancer: a decade-long informatics investigation

An overview of phosphodiesterase 9 inhibitors: Insights from skeletal structure, pharmacophores, and therapeutic potential

Discovery of 2‐(3,4‐dialkoxyphenyl)‐2‐(substituted pyridazin‐3‐yl)acetonitriles as phosphodiesterase 4 inhibitors with anti‐neuroinflammation potential based on three‐dimensional quantitative structure–activity relationship study

Discovery of 4‑Ethoxy-6-chloro-5-azaindazoles as Novel PDE4 Inhibitors for the Treatment of Alcohol Use Disorder and Alcoholic Liver Diseases

Simple and Clean Photo-induced Methylation of Heteroarenes with MeOH

One-pot synthesis and antiproliferative activity of novel 2,4-diaminopyrimidine derivatives bearing piperidine and piperazine moieties

Discovery of Dihydropyrrol-2-ones as Novel G0/G1-Phase Arresting Agents Inducing Apoptosis

Selective Copper–N-Heterocyclic Carbene (Copper-NHC)-Catalyzed Aerobic Cleavage of β‑1 Lignin Models to Aldehydes

Microwave-Assisted Efficient Synthesis of 2-Hydroxydeoxybenzoins from the Alkali Degradation of Readily Prepared 3-Aryl-4-hydroxycoumarins in Water

Advances in the development of phosphodiesterase 7 inhibitors

Discovery of novel 2,3-dihydro-1H-inden-1-ones as dual PDE4/AChE inhibitors with more potency against neuroinflammation for the treatment of Alzheimer's disease

Discovery of novel trimethoxyphenylbenzo[d]oxazoles as dual tubulin/PDE4 inhibitors capable of inducing apoptosis at G2/M phase arrest in glioma and lung cancer cells

Microwave-Assisted Dieckmann Reaction: Efficient One-Step Synthesis of 2-Aroylbenzofuran-3-ols

Synthesis, Cytotoxicities and DNA-Binding Affinities of Benzofuran-3-ols and Their Fused Analogs

Novel Phosphodiesterase 4 Inhibitor FCPR03 Alleviates Lipopolysaccharide-Induced Neuroinflammation by Regulation of the cAMP/PKA/CREB Signaling Pathway and NF- κ B Inhibition

An Efficient Intramolecular Stetter Reaction in Room Temperature Ionic Liquids Promoted By Microwave Irradiation

Discovery of Novel 3‑Amino-4-alkoxyphenylketones as PDE4 Inhibitors with Improved Oral Bioavailability and Safety against Spatial Memory Impairments

Synthesis, Biological Evaluation, and Molecular Docking of Arylpyridines as Antiproliferative Agent Targeting Tubulin

Development of highly potent phosphodiesterase 4 inhibitors with anti-neuroinflammation potential: Design, synthesis, and structure-activity relationship study of catecholamides bearing aromatic rings

Discovery of 9H-purins as potential tubulin polymerization inhibitors: Synthesis, biological evaluation and structure−activity relationships

Catecholic amides as potential selective phosphodiesterase 4D inhibitors: Design, synthesis, pharmacological evaluation and structure–activity relationships

Design, synthesis and biological evaluation of substituted aminopyridazin-3(2H)-ones as G0/G1-phase arresting agents with apoptosis-inducing activities

Synthesis and anticancer activities of 3-arylflavone-8-acetic acid derivatives

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