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Thymoquinone Inhibition of Chemokines in TNF-α-Induced Inflammatory and Metastatic Effects in Triple-Negative Breast Cancer Cells

International journal of molecular sciences, 2023-06, Vol.24 (12), p.9878

2023

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Design and Synthesis of Tetrahydroisoquinoline Derivatives as Anti-Angiogenesis and Anti-Cancer Agents

Anti-cancer agents in medicinal chemistry, 2021-01, Vol.21 (18), p.2505-2511

2021

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Transcriptome Profile Analysis of Triple-Negative Breast Cancer Cells in Response to a Novel Cytostatic Tetrahydroisoquinoline Compared to Paclitaxel

International journal of molecular sciences, 2021-07, Vol.22 (14), p.7694

2021

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The Antiproliferative Effects of Flavonoid MAO Inhibitors on Prostate Cancer Cells

Molecules (Basel, Switzerland), 2020-05, Vol.25 (9), p.2257

2020

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In-Vitro Antiproliferative Activity of New Tetrahydroisoquinolines (THIQs) on Ishikawa Cells and their 3D Pharmacophore Models

Letters in drug design & discovery, 2014-05, Vol.11 (4), p.428-436

2014

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Functional evaluation of synthetic flavonoids and chalcones for potential antiviral and anticancer properties

Bioorganic & medicinal chemistry letters, 2017-06, Vol.27 (11), p.2350-2356

2017

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Mentoring Minority Cancer Researchers of Tomorrow: Comparison of the Face-to-Face, Virtual, and Hybrid Training Methods of the CaRE2 Summer Cancer Research Education and Training Program

Journal of cancer education, 2024-08, Vol.39 (4), p.405-412

2024

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Synthesis of new analogs of N-substituted(benzoylamino)-1,2,3,6-tetrahydropyridines

Open Chemistry, 2024-04, Vol.22 (1), p.4367-58

2024

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Research Infrastructure Core Facilities at Research Centers in Minority Institutions: Part I-Research Resources Management, Operation, and Best Practices

International journal of environmental research and public health, 2022-12, Vol.19 (24), p.16979

2022

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Substituted Tetrahydroisoquinolines as Microtubule-destabilizing Agents in Triple Negative Human Breast Cancer Cells

Anticancer research, 2016-10, Vol.36 (10), p.5043-5052

2016

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Developing a Novel Framework for an Undergraduate Cancer Research Education and Engagement Program for Underrepresented Minority Students: the Florida-California CaRE2 Research Education Core (REC) Training Program

Journal of cancer education, 2021-10, Vol.36 (5), p.914-919

2021

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Synthesis and Cytotoxic Evaluation of Pyrrole Hetarylazoles Containing Benzimidazole/Pyrazolone/1,3,4-Oxadiazole Motifs

Journal of heterocyclic chemistry, 2016-11, Vol.53 (6), p.1871-1877

2016

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Biological evaluation of synthetic chalcone and flavone derivatives as anti-inflammatory agents

Medicinal chemistry research, 2015-04, Vol.24 (4), p.1672-1680

2015

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Synthesis and Pharmacological Evolution of Tetrahydroisoquinolines as Anti Breast Cancer Agents

Journal of cancer science & therapy, 2014-04, Vol.6 (5)

Gangapuram, Madhavi

2014

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Synthesis and Biological Evaluation of Substituted N-[3-(1H-Pyrrol-1-yl)methyl]-1,2,5,6-tetrahydropyridin-1-yl]benzamide/benzene Sulfonamides as Anti-Inflammatory Agents

Archiv der Pharmazie (Weinheim), 2014-05, Vol.347 (5), p.360-369

2014

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Synthesis of substituted N-[4(5-methyl/phenyl-1,3,4-oxadiazol-2-yl)-3,6-dihydropyridin-1(2H)-yl]benzamide/benzene sulfonamides as anti-inflammatory and anti-cancer agents

Journal of heterocyclic chemistry, 2009-03, Vol.46 (2), p.309-316

2009

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Synthesis of 2-(N-benzylpyrrolyl)-benzimidazoles using polyphosphoric acid prompted cyclocondensation

Journal of heterocyclic chemistry, 2010-11, Vol.47 (6), p.1367-1371

2010

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Synthesis of N-Substituted Carbonylamino-1,2,3,6-tetrahydropyridines as Potential Anti-Inflammatory Agents

Synthetic communications, 2011-01, Vol.41 (17), p.2615-2623

2011

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Synthesis of 1-(substituted phenylcarbonyl/sulfonylamino)-1,2,3,6-tetrahydropyridine-5-carboxylic acid diethylamides as potential anti-inflammatory agents

Journal of heterocyclic chemistry, 2006-05, Vol.43 (3), p.709-718

2006

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N-(4-amino-7-nitrobenzaoxa-1,3-diazole)-substituted aza crown ethers: complexation with alkali, alkaline earth metal ions and ammonium

Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2010-12, Vol.68 (3-4), p.305-312

2010

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Abstract 3102: Synthesis of N-benzoylamino-tetrahydropyridine analogues as selective COX-2 inhibitors and anti-breast cancer agents

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.3102-3102

2023

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Abstract D076: Florida-California Cancer Health Disparity Research, Education & Engagement (CaRE2) Center: Research education overview and preliminary results

Cancer epidemiology, biomarkers & prevention, 2020-06, Vol.29 (6_Supplement_2), p.D076-D076

2020

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Mentoring Minority Cancer Researchers of Tomorrow: Comparison of the Face-to-Face, Virtual, and Hybrid Training Methods of the CaRE 2 Summer Cancer Research Education and Training Program

Journal of cancer education, 2024-08, Vol.39 (4), p.405

2024

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Substituted Chalcones and Flavones as Human Monoamine Oxidase A (hMAO‐A) Inhibitors with Prostate Cancer Antiproliferative Effects

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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Synthesis of novel flavonoid derivatives as potential HIV- Integrase inhibitors

Journal of heterocyclic chemistry, 2002-11, Vol.39 (6), p.1251-1258

2002

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Thymoquinone Inhibition of Chemokines in TNF-α-Induced Inflammatory and Metastatic Effects in Triple-Negative Breast Cancer Cells

Design and Synthesis of Tetrahydroisoquinoline Derivatives as Anti-Angiogenesis and Anti-Cancer Agents

Transcriptome Profile Analysis of Triple-Negative Breast Cancer Cells in Response to a Novel Cytostatic Tetrahydroisoquinoline Compared to Paclitaxel

The Antiproliferative Effects of Flavonoid MAO Inhibitors on Prostate Cancer Cells

In-Vitro Antiproliferative Activity of New Tetrahydroisoquinolines (THIQs) on Ishikawa Cells and their 3D Pharmacophore Models

Functional evaluation of synthetic flavonoids and chalcones for potential antiviral and anticancer properties

Mentoring Minority Cancer Researchers of Tomorrow: Comparison of the Face-to-Face, Virtual, and Hybrid Training Methods of the CaRE2 Summer Cancer Research Education and Training Program

Synthesis of new analogs of N-substituted(benzoylamino)-1,2,3,6-tetrahydropyridines

Research Infrastructure Core Facilities at Research Centers in Minority Institutions: Part I-Research Resources Management, Operation, and Best Practices

Substituted Tetrahydroisoquinolines as Microtubule-destabilizing Agents in Triple Negative Human Breast Cancer Cells

Developing a Novel Framework for an Undergraduate Cancer Research Education and Engagement Program for Underrepresented Minority Students: the Florida-California CaRE2 Research Education Core (REC) Training Program

Synthesis and Cytotoxic Evaluation of Pyrrole Hetarylazoles Containing Benzimidazole/Pyrazolone/1,3,4-Oxadiazole Motifs

Biological evaluation of synthetic chalcone and flavone derivatives as anti-inflammatory agents

Synthesis and Pharmacological Evolution of Tetrahydroisoquinolines as Anti Breast Cancer Agents

Synthesis and Biological Evaluation of Substituted N-[3-(1H-Pyrrol-1-yl)methyl]-1,2,5,6-tetrahydropyridin-1-yl]benzamide/benzene Sulfonamides as Anti-Inflammatory Agents

Synthesis of substituted N-[4(5-methyl/phenyl-1,3,4-oxadiazol-2-yl)-3,6-dihydropyridin-1(2H)-yl]benzamide/benzene sulfonamides as anti-inflammatory and anti-cancer agents

Synthesis of 2-(N-benzylpyrrolyl)-benzimidazoles using polyphosphoric acid prompted cyclocondensation

Synthesis of N-Substituted Carbonylamino-1,2,3,6-tetrahydropyridines as Potential Anti-Inflammatory Agents

Synthesis of 1-(substituted phenylcarbonyl/sulfonylamino)-1,2,3,6-tetrahydropyridine-5-carboxylic acid diethylamides as potential anti-inflammatory agents

N-(4-amino-7-nitrobenzaoxa-1,3-diazole)-substituted aza crown ethers: complexation with alkali, alkaline earth metal ions and ammonium

Abstract 3102: Synthesis of N-benzoylamino-tetrahydropyridine analogues as selective COX-2 inhibitors and anti-breast cancer agents

Abstract D076: Florida-California Cancer Health Disparity Research, Education & Engagement (CaRE2) Center: Research education overview and preliminary results

Mentoring Minority Cancer Researchers of Tomorrow: Comparison of the Face-to-Face, Virtual, and Hybrid Training Methods of the CaRE 2 Summer Cancer Research Education and Training Program

Substituted Chalcones and Flavones as Human Monoamine Oxidase A (hMAO‐A) Inhibitors with Prostate Cancer Antiproliferative Effects

Synthesis of novel flavonoid derivatives as potential HIV- Integrase inhibitors

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