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Andrographolide sodium bisulfate attenuates UV‑induced photo‑damage by activating the keap1/Nrf2 pathway and downregulating the NF‑κB pathway in HaCaT keratinocytes

International journal of molecular medicine, 2020-02, Vol.45 (2), p.343-352

2020

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Total synthesis of natural (+)- [corrected] and ent-(-)-4-desacetoxy-6,7-dihydrovindorosine [corrected] and natural and ent-minovine: oxadiazole tandem intramolecular Diels-Alder/1,3-dipolar cycloaddition reaction

Organic letters, 2005-02, Vol.7 (4), p.741-744

2005

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Improved antitumor activity of epirubicin-loaded CXCR4-targeted polymeric nanoparticles in liver cancers

International journal of pharmaceutics, 2016-03, Vol.500 (1-2), p.54-61

2016

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Protective effects of andrographolide sodium bisulfate on UV-induced skin carcinogenesis in mice model

European journal of pharmaceutical sciences, 2022-09, Vol.176, p.106232-106232, Article 106232

2022

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Gender differences in UV-induced skin inflammation, skin carcinogenesis and systemic damage

Environmental toxicology and pharmacology, 2021-01, Vol.81, p.103512, Article 103512

2021

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Novel Chemical Series of 5‑Lipoxygenase-Activating Protein Inhibitors for Treatment of Coronary Artery Disease

Journal of medicinal chemistry, 2019-05, Vol.62 (9), p.4325-4349

2019

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Enhancement of cisplatin sensitivity in Lewis Lung carcinoma by liposome-mediated delivery of a survivin mutant

Journal of experimental & clinical cancer research, 2010-05, Vol.29 (1), p.46-46, Article 46

2010

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Identification of Mineralocorticoid Receptor Modulators with Low Impact on Electrolyte Homeostasis but Maintained Organ Protection

Journal of medicinal chemistry, 2019-02, Vol.62 (3), p.1385-1406

2019

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Isoindolinone compounds active as Kv1.5 blockers identified using a multicomponent reaction approach

Bioorganic & medicinal chemistry letters, 2016-04, Vol.26 (8), p.2023-2029

2016

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GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3‑c]pyridines That Mimic the C‑Terminal Arg-Phe Motif of QRFP26

Journal of medicinal chemistry, 2014-07, Vol.57 (14), p.5935-5948

2014

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Discovery of 4-morpholino-pyrimidin-6-one and 4-morpholino-pyrimidin-2-one-containing Phosphoinositide 3-kinase (PI3K) p110β isoform inhibitors through structure-based fragment optimisation

Bioorganic & medicinal chemistry letters, 2012-11, Vol.22 (21), p.6665-6670

2012

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Observation and analysis of clinical efficacy of breast-conserving therapy integrated with neoadjuvant chemotherapy on Breast Cancer

Pakistan journal of pharmaceutical sciences, 2018-11, Vol.31 (6(Special)), p.2869-2872

2018

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Identification and design of a novel series of MGAT2 inhibitors

Bioorganic & medicinal chemistry letters, 2013-05, Vol.23 (9), p.2721-2726

2013

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Discovery of phosphoinositide 3-kinases (PI3K) p110β isoform inhibitor 4-[2-hydroxyethyl(1-naphthylmethyl)amino]-6-[(2S)-2-methylmorpholin-4-yl]-1H-pyrimidin-2-one, an effective antithrombotic agent without associated bleeding and insulin resistance

Bioorganic & medicinal chemistry letters, 2012-11, Vol.22 (21), p.6671-6676

2012

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MicroRNA-26a inhibits proliferation by targeting high mobility group AT-hook 1 in breast cancer

International journal of clinical and experimental pathology, 2015, Vol.8 (1), p.368-373

2015

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Lactam sulfonamides as potent inhibitors of the Kv1.5 potassium ion channel

Bioorganic & medicinal chemistry letters, 2014-03, Vol.24 (5), p.1269-1273

2014

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Inhibition of lymphatic metastases by a survivin dominant-negative mutant

Oncology research, 2012-01, Vol.20 (12), p.579

2012

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Therapeutic effects of survivin dominant negative mutant in a mouse model of prostate cancer

Journal of cancer research and clinical oncology, 2011, Vol.137 (1), p.19-28

2011

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Formalin irrigation for hemorrhagic chronic radiation proctitis

World journal of gastroenterology : WJG, 2015-03, Vol.21 (12), p.3593-3598

2015

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Anti-prostate cancer activity of Survivin-T34A mutant in vitro and in vivo

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2010-05, Vol.41 (3), p.390

2010

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Colostomy is a simple and effective procedure for severe chronic radiation proctitis

World journal of gastroenterology : WJG, 2016-06, Vol.22 (24), p.5598-5608

2016

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Andrographolide sodium bisulfate attenuates UV-induced photo-damage by activating the keapl/Nrf2 pathway and downregulating the NF-[kappa]B pathway in HaCaT keratinocytes

International journal of molecular medicine, 2020-02, Vol.45 (2), p.343

2020

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Dextran Gadolinium Complex Containing Folate Groups as a Potential Magnetic Resonance Imaging Contrast Agent

Chinese journal of polymer science, 2015-09, Vol.33 (9), p.1325-1333

2015

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Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3‑c]pyridines That Mimic the C‑Terminal Arg-Phe Motif of QRFP26

Journal of medicinal chemistry, 2015-05, Vol.58 (9), p.4086-4086

2015

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Discovery of 4-morpholino-pyrimidin-6-one and 4-morpholino-pyrimidin-2-one-containing Phosphoinositide 3-kinase (PI3K) p110[beta] isoform inhibitors through structure-based fragment optimisation

Bioorganic & medicinal chemistry letters, 2012-11, Vol.22 (21), p.6665-6670

2012

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Andrographolide sodium bisulfate attenuates UV‑induced photo‑damage by activating the keap1/Nrf2 pathway and downregulating the NF‑κB pathway in HaCaT keratinocytes

Total synthesis of natural (+)- [corrected] and ent-(-)-4-desacetoxy-6,7-dihydrovindorosine [corrected] and natural and ent-minovine: oxadiazole tandem intramolecular Diels-Alder/1,3-dipolar cycloaddition reaction

Improved antitumor activity of epirubicin-loaded CXCR4-targeted polymeric nanoparticles in liver cancers

Protective effects of andrographolide sodium bisulfate on UV-induced skin carcinogenesis in mice model

Gender differences in UV-induced skin inflammation, skin carcinogenesis and systemic damage

Novel Chemical Series of 5‑Lipoxygenase-Activating Protein Inhibitors for Treatment of Coronary Artery Disease

Enhancement of cisplatin sensitivity in Lewis Lung carcinoma by liposome-mediated delivery of a survivin mutant

Identification of Mineralocorticoid Receptor Modulators with Low Impact on Electrolyte Homeostasis but Maintained Organ Protection

Isoindolinone compounds active as Kv1.5 blockers identified using a multicomponent reaction approach

GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3‑c]pyridines That Mimic the C‑Terminal Arg-Phe Motif of QRFP26

Discovery of 4-morpholino-pyrimidin-6-one and 4-morpholino-pyrimidin-2-one-containing Phosphoinositide 3-kinase (PI3K) p110β isoform inhibitors through structure-based fragment optimisation

Observation and analysis of clinical efficacy of breast-conserving therapy integrated with neoadjuvant chemotherapy on Breast Cancer

Identification and design of a novel series of MGAT2 inhibitors

Discovery of phosphoinositide 3-kinases (PI3K) p110β isoform inhibitor 4-[2-hydroxyethyl(1-naphthylmethyl)amino]-6-[(2S)-2-methylmorpholin-4-yl]-1H-pyrimidin-2-one, an effective antithrombotic agent without associated bleeding and insulin resistance

MicroRNA-26a inhibits proliferation by targeting high mobility group AT-hook 1 in breast cancer

Lactam sulfonamides as potent inhibitors of the Kv1.5 potassium ion channel

Inhibition of lymphatic metastases by a survivin dominant-negative mutant

Therapeutic effects of survivin dominant negative mutant in a mouse model of prostate cancer

Formalin irrigation for hemorrhagic chronic radiation proctitis

Anti-prostate cancer activity of Survivin-T34A mutant in vitro and in vivo

Colostomy is a simple and effective procedure for severe chronic radiation proctitis

Andrographolide sodium bisulfate attenuates UV-induced photo-damage by activating the keapl/Nrf2 pathway and downregulating the NF-[kappa]B pathway in HaCaT keratinocytes

Dextran Gadolinium Complex Containing Folate Groups as a Potential Magnetic Resonance Imaging Contrast Agent

Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3‑c]pyridines That Mimic the C‑Terminal Arg-Phe Motif of QRFP26

Discovery of 4-morpholino-pyrimidin-6-one and 4-morpholino-pyrimidin-2-one-containing Phosphoinositide 3-kinase (PI3K) p110[beta] isoform inhibitors through structure-based fragment optimisation

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