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Actinomycetes for marine drug discovery isolated from mangrove soils and plants in China

Marine drugs, 2009-03, Vol.7 (1), p.24-44

2009

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Downregulation of c-Myc expression confers sensitivity to CHK1 inhibitors in hematologic malignancies

Acta pharmacologica Sinica, 2022-01, Vol.43 (1), p.220-228

2022

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Pharmacodynamic, pharmacokinetic, and phase 1a study of bisthianostat, a novel histone deacetylase inhibitor, for the treatment of relapsed or refractory multiple myeloma

Acta pharmacologica Sinica, 2022-04, Vol.43 (4), p.1091-1099

2022

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Berberine-stimulated glucose uptake in L6 myotubes involves both AMPK and p38 MAPK

Biochimica et biophysica acta, 2006-11, Vol.1760 (11), p.1682-1689

2006

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Activation of unfolded protein response overcomes Ibrutinib resistance in diffuse large B-cell lymphoma

Acta pharmacologica Sinica, 2021-05, Vol.42 (5), p.814-823

2021

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Synthesis and Biological Evaluation of C7-Demethyl Largazole Analogues

ChemMedChem, 2009-08, Vol.4 (8), p.1269-1272

2009

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Novel CHOP activator LGH00168 induces necroptosis in A549 human lung cancer cells via ROS-mediated ER stress and NF-κB inhibition

Acta pharmacologica Sinica, 2016-09, Vol.37 (10), p.1381-1390

2016

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Berberine combined with 2-deoxy-d-glucose synergistically enhances cancer cell proliferation inhibition via energy depletion and unfolded protein response disruption

Biochimica et biophysica acta, 2013-11, Vol.1830 (11), p.5175-5183

2013

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Discovery of toxoflavin, a potent IRE1α inhibitor acting through structure-dependent oxidative inhibition

Acta pharmacologica Sinica, 2023-01, Vol.44 (1), p.234-243

2023

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Diterpenoids from the Hainan Soft Coral Sinularia parva

Helvetica chimica acta, 2009-07, Vol.92 (7), p.1341-1348

2009

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Design, synthesis and biological evaluation of bisthiazole-based trifluoromethyl ketone derivatives as potent HDAC inhibitors with improved cellular efficacy

European journal of medicinal chemistry, 2016-04, Vol.112, p.81-90

2016

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Fluevirosines A–C: A Biogenesis Inspired Example in the Discovery of New Bioactive Scaffolds from Flueggea virosa

Organic letters, 2013-01, Vol.15 (1), p.120-123

2013

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Covalent docking modelling-based discovery of tripeptidyl epoxyketone proteasome inhibitors composed of aliphatic-heterocycles

European journal of medicinal chemistry, 2019-02, Vol.164, p.602-614

2019

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Curcusone D, a novel ubiquitin-proteasome pathway inhibitor via ROS-induced DUB inhibition, is synergistic with bortezomib against multiple myeloma cell growth

Biochimica et biophysica acta, 2014-06, Vol.1840 (6), p.2004-2013

2014

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Azoxystrobin, a mitochondrial complex III Qo site inhibitor, exerts beneficial metabolic effects in vivo and in vitro

Biochimica et biophysica acta, 2014-07, Vol.1840 (7), p.2212-2221

2014

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Discovery and Optimization of 2,4-Diaminoquinazoline Derivatives as a New Class of Potent Dengue Virus Inhibitors

Journal of medicinal chemistry, 2012-04, Vol.55 (7), p.3135-3143

2012

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Synthesis and Biological Evaluation of C7-Demethyl Largazole Analogues

ChemMedChem, 2009-08, Vol.4 (8), p.1217-1217

2009

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Correction: Hong, K. et al. Actinomycetes for Marine Drug Discovery Isolated from Mangrove Soils and Plants in China. Mar. Drugs 2009, 7, 24–44

Marine drugs, 2009-10, Vol.7 (4), p.495-496

2009

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Author Correction: Discovery of toxoflavin, a potent IRE1α inhibitor acting through structure-dependent oxidative inhibition

Acta pharmacologica Sinica, 2023-08, Vol.44 (12), p.2550-2550

2023

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Diffuse large B-cell lymphoma with low 18 F-fluorodeoxyglucose avidity features silent B-cell receptor signaling

Leukemia & lymphoma, 2020-06, Vol.61 (6), p.1364-1371

2020

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Diffuse large B-cell lymphoma with low 18F-fluorodeoxyglucose avidity features silent B-cell receptor signaling

Leukemia & lymphoma, 2020-06, Vol.61 (6), p.1364-1371

2020

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Novel CHOP activator LGH00168 induces necroptosis in A549 human lung cancer cells via ROS-mediated ER stress and NF-[kappa]B inhibition

Acta pharmacologica Sinica, 2016-10, Vol.37 (10), p.1381

2016

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Novel CHOP activator LGHO0168 induces necroptosis in A549 human lung cancer cells via ROS-mediated ER stress and NF-κB inhibition

中国药理学报：英文版, 2016 (10), p.1381-1390

Yi-ming MA Yan-min PENG Qiong-hua ZHU An-hui GAO Bo CHAO Qiao-jun HE Jia LI You-hong HU Yu-bo ZHOU

2016

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ChemInform Abstract: Diterpenoids from the Hainan Soft Coral Sinularia parva

ChemInform, 2009-12, Vol.40 (50), p.no-no

2009

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Significance of Lateral Pillar in Osteonecrosis of Femoral Head： A Finite Element Analysis

Chinese medical journal, 2017-11, Vol.130 (21), p.2569-2574

2017

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Actinomycetes for marine drug discovery isolated from mangrove soils and plants in China

Downregulation of c-Myc expression confers sensitivity to CHK1 inhibitors in hematologic malignancies

Pharmacodynamic, pharmacokinetic, and phase 1a study of bisthianostat, a novel histone deacetylase inhibitor, for the treatment of relapsed or refractory multiple myeloma

Berberine-stimulated glucose uptake in L6 myotubes involves both AMPK and p38 MAPK

Activation of unfolded protein response overcomes Ibrutinib resistance in diffuse large B-cell lymphoma

Synthesis and Biological Evaluation of C7-Demethyl Largazole Analogues

Novel CHOP activator LGH00168 induces necroptosis in A549 human lung cancer cells via ROS-mediated ER stress and NF-κB inhibition

Berberine combined with 2-deoxy-d-glucose synergistically enhances cancer cell proliferation inhibition via energy depletion and unfolded protein response disruption

Discovery of toxoflavin, a potent IRE1α inhibitor acting through structure-dependent oxidative inhibition

Diterpenoids from the Hainan Soft Coral Sinularia parva

Design, synthesis and biological evaluation of bisthiazole-based trifluoromethyl ketone derivatives as potent HDAC inhibitors with improved cellular efficacy

Fluevirosines A–C: A Biogenesis Inspired Example in the Discovery of New Bioactive Scaffolds from Flueggea virosa

Covalent docking modelling-based discovery of tripeptidyl epoxyketone proteasome inhibitors composed of aliphatic-heterocycles

Curcusone D, a novel ubiquitin-proteasome pathway inhibitor via ROS-induced DUB inhibition, is synergistic with bortezomib against multiple myeloma cell growth

Azoxystrobin, a mitochondrial complex III Qo site inhibitor, exerts beneficial metabolic effects in vivo and in vitro

Discovery and Optimization of 2,4-Diaminoquinazoline Derivatives as a New Class of Potent Dengue Virus Inhibitors

Synthesis and Biological Evaluation of C7-Demethyl Largazole Analogues

Correction: Hong, K. et al. Actinomycetes for Marine Drug Discovery Isolated from Mangrove Soils and Plants in China. Mar. Drugs 2009, 7, 24–44

Author Correction: Discovery of toxoflavin, a potent IRE1α inhibitor acting through structure-dependent oxidative inhibition

Diffuse large B-cell lymphoma with low 18 F-fluorodeoxyglucose avidity features silent B-cell receptor signaling

Diffuse large B-cell lymphoma with low 18F-fluorodeoxyglucose avidity features silent B-cell receptor signaling

Novel CHOP activator LGH00168 induces necroptosis in A549 human lung cancer cells via ROS-mediated ER stress and NF-[kappa]B inhibition

Novel CHOP activator LGHO0168 induces necroptosis in A549 human lung cancer cells via ROS-mediated ER stress and NF-κB inhibition

ChemInform Abstract: Diterpenoids from the Hainan Soft Coral Sinularia parva

Significance of Lateral Pillar in Osteonecrosis of Femoral Head： A Finite Element Analysis

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