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Design, synthesis and biological evaluation of thienopyrimidine hydroxamic acid based derivatives as structurally novel histone deacetylase (HDAC) inhibitors

European journal of medicinal chemistry, 2017-03, Vol.128, p.293-299

2017

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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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Inhibition of B-cell receptor signaling disrupts cell adhesion in mantle cell lymphoma via RAC2

Blood advances, 2021-01, Vol.5 (1), p.185-197

2021

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Selective Late‐Stage Oxygenation of Sulfides with Ground‐State Oxygen by Uranyl Photocatalysis

Angewandte Chemie International Edition, 2019-09, Vol.58 (38), p.13499-13506

International ed. in English, 2019

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High-throughput screening using pseudotyped lentiviral particles: A strategy for the identification of HIV-1 inhibitors in a cell-based assay

Antiviral research, 2009-03, Vol.81 (3), p.239-247

2009

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Interfacial properties of friction stir lap welded 430/304 stainless steels using Cu interlayer

Materials letters, 2021-02, Vol.284, p.129027, Article 129027

2021

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Discovery of HZ-L105, a Next Generation of Bcl-2 Inhibitor, Overcomes Bcl-2 Mutation and Exhibits Superior Antitumor Activity

Blood, 2022-11, Vol.140 (Supplement 1), p.7798-7799

2022

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Synthesis and biological evaluation of 3-aryl-4-indolyl-maleimides as potent mutant isocitrate dehydrogenase-1 inhibitors

Bioorganic & medicinal chemistry, 2019-02, Vol.27 (4), p.589-603

2019

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Discovery of (R)-5-((5-(1-methyl-1H-pyrazol-4-yl)-4-(methylamino)pyrimidin-2-yl)amino)-3-(piperidin-3-yloxy)picolinonitrile, a novel CHK1 inhibitor for hematologic malignancies

European journal of medicinal chemistry, 2019-07, Vol.173, p.44-62

2019

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Mitochondrial Uncoupling Coordinated With PDH Activation Safely Ameliorates Hyperglycemia via Promoting Glucose Oxidation

Diabetes (New York, N.Y.), 2019-12, Vol.68 (12), p.2197-2209

2019

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Discovery of novel indoleaminopyrimidine NIK inhibitors based on molecular docking-based support vector regression (SVR) model

Chemical physics letters, 2019-03, Vol.718, p.38-45

2019

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Synthesis and Evaluation of 3--Maleimides as Potent Mutant Isocitrate Dehydrogenase-1 Inhibitors

Pharmaceutical chemistry journal, 2021-10, Vol.55 (7), p.655

2021

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Structure-based design, synthesis and bioactivity evaluation of macrocyclic inhibitors of mutant isocitrate dehydrogenase 2 (IDH2) displaying activity in acute myeloid leukemia cells

European journal of medicinal chemistry, 2020-10, Vol.203, p.112491-112491, Article 112491

2020

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Synthesis and Evaluation of 3-(Indol-3-yl)-4-(pyrazolo[3,4- c ]pyridazin-3-yl)maleimides as Potent Mutant Isocitrate Dehydrogenase-1 Inhibitors

Yŏujī huàxué, 2021-05, p.1991

2021

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Abstract 1621: L105, a next generation of Bcl-2 inhibitor, overcomes Bcl-2 mutation and exhibits superior antitumor activity

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.1621-1621

2023

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Synthesis and biological evaluation of novel 4,5-bisindolyl-1,2,4-triazol-3-ones as glycogen synthase kinase-3β inhibitors and neuroprotective agents

Pharmazie, 2017-12, Vol.72 (12), p.707-713

2017

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Synthesis and Evaluation of 3-(Indol-3-yl)-4-(Pyrazolo[3,4-c]Pyridazin-3-yl)-Maleimides as Potent Mutant Isocitrate Dehydrogenase-1 Inhibitors

Pharmaceutical chemistry journal, 2021-10, Vol.55 (7), p.655-664

2021

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3‐(7‐Azaindolyl)‐4‐indolylmaleimides as a novel class of mutant isocitrate dehydrogenase‐1 inhibitors: Design, synthesis, and biological evaluation

Archiv der Pharmazie (Weinheim), 2018-10, Vol.351 (10), p.e1800039-n/a

2018

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RAC2 Links B-Cell Receptor Signaling and Cell Adhesion in Mantle Cell Lymphoma

Blood, 2017-12, Vol.130, p.2752-2752

2017

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Inhibition of B-Cell Receptor Signaling Disrupts Cell Adhesion in Mantle Cell Lymphoma Via RAC2

Blood, 2018-11, Vol.132 (Supplement 1), p.1369-1369

2018

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Cyclopeptide RA-V Inhibits Organ Enlargement and Tumorigenesis Induced by YAP Activation

Cancers, 2018-11, Vol.10 (11), p.449

2018

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Selective Late‐Stage Oxygenation of Sulfides with Ground‐State Oxygen by Uranyl Photocatalysis

Angewandte Chemie, 2019-09, Vol.131 (38), p.13633-13640

2019

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Comparison of Quality of Pulping and Paper-Making between Normal Wood and Tension Wood of Poplar Clone 107 （ Populus x euramericana Neva） Tree

Linye kexue (1979), 2012-05, Vol.48 (5)

2012

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Cobalt phthalocyanine-graphene complex for electro-catalytic oxidation of dopamine

Journal of natural gas chemistry, 2012-05, Vol.21 (3), p.265-269

2012

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Inhibitive activity of the extracts of plants in Artemisia against Fusarium oxysporum f. sp. vasinfectum and Fusarium momiliforme

Hunan agricultural science & technology newsletter : HASTN, 2010-04, Vol.11 (2)

2010

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Design, synthesis and biological evaluation of thienopyrimidine hydroxamic acid based derivatives as structurally novel histone deacetylase (HDAC) inhibitors

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

Inhibition of B-cell receptor signaling disrupts cell adhesion in mantle cell lymphoma via RAC2

Selective Late‐Stage Oxygenation of Sulfides with Ground‐State Oxygen by Uranyl Photocatalysis

High-throughput screening using pseudotyped lentiviral particles: A strategy for the identification of HIV-1 inhibitors in a cell-based assay

Interfacial properties of friction stir lap welded 430/304 stainless steels using Cu interlayer

Discovery of HZ-L105, a Next Generation of Bcl-2 Inhibitor, Overcomes Bcl-2 Mutation and Exhibits Superior Antitumor Activity

Synthesis and biological evaluation of 3-aryl-4-indolyl-maleimides as potent mutant isocitrate dehydrogenase-1 inhibitors

Discovery of (R)-5-((5-(1-methyl-1H-pyrazol-4-yl)-4-(methylamino)pyrimidin-2-yl)amino)-3-(piperidin-3-yloxy)picolinonitrile, a novel CHK1 inhibitor for hematologic malignancies

Mitochondrial Uncoupling Coordinated With PDH Activation Safely Ameliorates Hyperglycemia via Promoting Glucose Oxidation

Discovery of novel indoleaminopyrimidine NIK inhibitors based on molecular docking-based support vector regression (SVR) model

Synthesis and Evaluation of 3--Maleimides as Potent Mutant Isocitrate Dehydrogenase-1 Inhibitors

Structure-based design, synthesis and bioactivity evaluation of macrocyclic inhibitors of mutant isocitrate dehydrogenase 2 (IDH2) displaying activity in acute myeloid leukemia cells

Synthesis and Evaluation of 3-(Indol-3-yl)-4-(pyrazolo[3,4- c ]pyridazin-3-yl)maleimides as Potent Mutant Isocitrate Dehydrogenase-1 Inhibitors

Abstract 1621: L105, a next generation of Bcl-2 inhibitor, overcomes Bcl-2 mutation and exhibits superior antitumor activity

Synthesis and biological evaluation of novel 4,5-bisindolyl-1,2,4-triazol-3-ones as glycogen synthase kinase-3β inhibitors and neuroprotective agents

Synthesis and Evaluation of 3-(Indol-3-yl)-4-(Pyrazolo[3,4-c]Pyridazin-3-yl)-Maleimides as Potent Mutant Isocitrate Dehydrogenase-1 Inhibitors

3‐(7‐Azaindolyl)‐4‐indolylmaleimides as a novel class of mutant isocitrate dehydrogenase‐1 inhibitors: Design, synthesis, and biological evaluation

RAC2 Links B-Cell Receptor Signaling and Cell Adhesion in Mantle Cell Lymphoma

Inhibition of B-Cell Receptor Signaling Disrupts Cell Adhesion in Mantle Cell Lymphoma Via RAC2

Cyclopeptide RA-V Inhibits Organ Enlargement and Tumorigenesis Induced by YAP Activation

Selective Late‐Stage Oxygenation of Sulfides with Ground‐State Oxygen by Uranyl Photocatalysis

Comparison of Quality of Pulping and Paper-Making between Normal Wood and Tension Wood of Poplar Clone 107 （ Populus x euramericana Neva） Tree

Cobalt phthalocyanine-graphene complex for electro-catalytic oxidation of dopamine

Inhibitive activity of the extracts of plants in Artemisia against Fusarium oxysporum f. sp. vasinfectum and Fusarium momiliforme

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