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Salicylic acid directly binds to ribosomal protein S3 and suppresses CDK4 expression in colorectal cancer cells

Biochemical and biophysical research communications, 2022-11, Vol.628, p.110-115

2022

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Novel RAF/MEK inhibitor CH5126766/VS‐6766 has efficacy in combination with eribulin for the treatment of triple‐negative breast cancer

Cancer science, 2021-10, Vol.112 (10), p.4166-4175

2021

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Sulindac sulfone inhibits the mTORC1 pathway in colon cancer cells by directly targeting voltage-dependent anion channel 1 and 2

Biochemical and biophysical research communications, 2018-11, Vol.505 (4), p.1203-1210

2018

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PDK1 is a potential therapeutic target against angiosarcoma cells

Journal of dermatological science, 2015-04, Vol.78 (1), p.44-50

2015

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Discovery of cancer-preventive juices reactivating RB functions

Environmental health and preventive medicine, 2023-01, Vol.28, p.54-54, Article 23-00160

2023

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Cycloartenyl Ferulate and β-Sitosteryl Ferulate - Steryl Ferulates of γ-Oryzanol - Suppress Intracellular Reactive Oxygen Species in Cell-based System

Journal of Oleo Science, 2019, Vol.68(8), pp.765-768

2019

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Cucurbitacin B induces G2 arrest and apoptosis via a reactive oxygen species-dependent mechanism in human colon adenocarcinoma SW480 cells

Molecular nutrition & food research, 2010-04, Vol.54 (4), p.559-565

2010

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The Rationale for the Dual-Targeting Therapy for RSK2 and AKT in Multiple Myeloma

International journal of molecular sciences, 2022-03, Vol.23 (6), p.2919

2022

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Sulforaphane suppresses cell growth and collagen expression of keloid fibroblasts

Wound repair and regeneration, 2017-04, Vol.25 (2), p.224-233

2017

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C-H activation enables a rapid structure-activity relationship study of arylcyclopropyl amines for potent and selective LSD1 inhibitors

Organic & biomolecular chemistry, 2016-01, Vol.14 (36), p.8576-8585

2016

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Targeting the glyoxalase pathway enhances TRAIL efficacy in cancer cells by downregulating the expression of antiapoptotic molecules

Molecular cancer therapeutics, 2012-10, Vol.11 (10), p.2294-2300

2012

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FGFR inhibitor BGJ398 and HDAC inhibitor OBP-801 synergistically inhibit cell growth and induce apoptosis in bladder cancer cells

Oncology reports, 2018-02, Vol.39 (2), p.627-632

2018

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Retinoblastoma gene‐independent G1 phase arrest by flavone, phosphatidylinositol 3‐kinase inhibitor, and histone deacetylase inhibitor

Cancer science, 2012-12, Vol.103 (12), p.2139-2143

2012

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Oridonin inhibits SASP by blocking p38 and NF-κB pathways in senescent cells

Biochemical and biophysical research communications, 2022-01, Vol.590, p.55-62

2022

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Sulforaphane enhances apoptosis induced by Lactobacillus pentosus strain S‑PT84 via the TNFα pathway in human colon cancer cells

Oncology letters, 2019-10, Vol.18 (4), p.4253-4261

2019

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Sulforaphane enhances apoptosis induced by Lactobacillus pentosus strain S-PT84 via the TNF[alpha] pathway in human colon cancer cells

Oncology letters, 2019-10, Vol.18 (4), p.4253

2019

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Dehydrozingerone, a Structural Analogue of Curcumin, Induces Cell-Cycle Arrest at the G2/M Phase and Accumulates Intracellular ROS in HT-29 Human Colon Cancer Cells

Journal of natural products (Washington, D.C.), 2012-12, Vol.75 (12), p.2088-2093

2012

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Design, synthesis and evaluation of γ-turn mimetics as LSD1-selective inhibitors

Bioorganic & medicinal chemistry, 2018-02, Vol.26 (3), p.775-785

2018

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A Histone Deacetylase Inhibitor, OBP-801, and Celecoxib Synergistically Inhibit the Cell Growth with Apoptosis via a DR5-Dependent Pathway in Bladder Cancer Cells

Molecular cancer therapeutics, 2016-09, Vol.15 (9), p.2066-2075

2016

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Myeloid zinc finger 1 mediates sulindac sulfide-induced upregulation of death receptor 5 of human colon cancer cells

Scientific reports, 2014-08, Vol.4 (1), p.6000, Article 6000

2014

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The HDAC inhibitor OBP-801 suppresses the growth of myxofibrosarcoma cells

Journal of B.U.ON. : official journal of the Balkan Union of Oncology, 2020-01, Vol.25 (1), p.464

2020

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Cycloartenyl Ferulate and β-Sitosteryl Ferulate - Steryl Ferulates of γ-Oryzanol - Suppress Intracellular Reactive Oxygen Species in Cell-based System

Journal of Oleo Science, 2019-08, Vol.68 (8), p.765-768

2019

Volltextzugriff (PDF)

Cycloartenyl Ferulate and β-Sitosteryl Ferulate - Steryl Ferulates of γ-Oryzanol - Suppress Intracellular Reactive Oxygen Species in Cell-based System

Journal of Oleo Science, 2019, pp.ess19054

2019

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C-H activation enables a rapid structure-activity relationship study of arylcyclopropyl amines for potent and selective LSD1 inhibitorsElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ob01483f

2016-09

Volltextzugriff (PDF)

Retinoblastoma gene‐independent G 1 phase arrest by flavone, phosphatidylinositol 3‐kinase inhibitor, and histone deacetylase inhibitor

Cancer science, 2012-12, Vol.103 (12), p.2139-2143

2012

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Salicylic acid directly binds to ribosomal protein S3 and suppresses CDK4 expression in colorectal cancer cells

Novel RAF/MEK inhibitor CH5126766/VS‐6766 has efficacy in combination with eribulin for the treatment of triple‐negative breast cancer

Sulindac sulfone inhibits the mTORC1 pathway in colon cancer cells by directly targeting voltage-dependent anion channel 1 and 2

PDK1 is a potential therapeutic target against angiosarcoma cells

Discovery of cancer-preventive juices reactivating RB functions

Cycloartenyl Ferulate and β-Sitosteryl Ferulate - Steryl Ferulates of γ-Oryzanol - Suppress Intracellular Reactive Oxygen Species in Cell-based System

Cucurbitacin B induces G2 arrest and apoptosis via a reactive oxygen species-dependent mechanism in human colon adenocarcinoma SW480 cells

The Rationale for the Dual-Targeting Therapy for RSK2 and AKT in Multiple Myeloma

Sulforaphane suppresses cell growth and collagen expression of keloid fibroblasts

C-H activation enables a rapid structure-activity relationship study of arylcyclopropyl amines for potent and selective LSD1 inhibitors

Targeting the glyoxalase pathway enhances TRAIL efficacy in cancer cells by downregulating the expression of antiapoptotic molecules

FGFR inhibitor BGJ398 and HDAC inhibitor OBP-801 synergistically inhibit cell growth and induce apoptosis in bladder cancer cells

Retinoblastoma gene‐independent G1 phase arrest by flavone, phosphatidylinositol 3‐kinase inhibitor, and histone deacetylase inhibitor

Oridonin inhibits SASP by blocking p38 and NF-κB pathways in senescent cells

Sulforaphane enhances apoptosis induced by Lactobacillus pentosus strain S‑PT84 via the TNFα pathway in human colon cancer cells

Sulforaphane enhances apoptosis induced by Lactobacillus pentosus strain S-PT84 via the TNF[alpha] pathway in human colon cancer cells

Dehydrozingerone, a Structural Analogue of Curcumin, Induces Cell-Cycle Arrest at the G2/M Phase and Accumulates Intracellular ROS in HT-29 Human Colon Cancer Cells

Design, synthesis and evaluation of γ-turn mimetics as LSD1-selective inhibitors

A Histone Deacetylase Inhibitor, OBP-801, and Celecoxib Synergistically Inhibit the Cell Growth with Apoptosis via a DR5-Dependent Pathway in Bladder Cancer Cells

Myeloid zinc finger 1 mediates sulindac sulfide-induced upregulation of death receptor 5 of human colon cancer cells

The HDAC inhibitor OBP-801 suppresses the growth of myxofibrosarcoma cells

Cycloartenyl Ferulate and β-Sitosteryl Ferulate - Steryl Ferulates of γ-Oryzanol - Suppress Intracellular Reactive Oxygen Species in Cell-based System

Cycloartenyl Ferulate and β-Sitosteryl Ferulate - Steryl Ferulates of γ-Oryzanol - Suppress Intracellular Reactive Oxygen Species in Cell-based System

C-H activation enables a rapid structure-activity relationship study of arylcyclopropyl amines for potent and selective LSD1 inhibitorsElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ob01483f

Retinoblastoma gene‐independent G 1 phase arrest by flavone, phosphatidylinositol 3‐kinase inhibitor, and histone deacetylase inhibitor

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