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Molecular docking reveals the potential of Salvadora persica flavonoids to inhibit COVID-19 virus main protease

RSC advances, 2020-05, Vol.10 (33), p.19570-19575

2020

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Nitroxyl (HNO): A Possible Strategy for Fighting Cancer

Current topics in medicinal chemistry, 2016-09, Vol.16 (22), p.2464-2470

2016

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OMA1520 and OMA1774, novel 1,2,4-triazole bearing analogs of combretastatin A-4, inhibit hepatocellular carcinoma: Histological and immunohistochemical studies

Biomedicine & pharmacotherapy, 2021-06, Vol.138, p.111417-111417, Article 111417

2021

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Combination of an Oxindole Derivative with (-)-β-Elemene Alters Cell Death Pathways in FLT3/ITD + Acute Myeloid Leukemia Cells

Molecules (Basel, Switzerland), 2023-07, Vol.28 (13), p.5253

2023

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Flavonoids of Salvadora persica L. (meswak) and its liposomal formulation as a potential inhibitor of SARS-CoV-2

RSC advances, 2021-04, Vol.11 (22), p.13537-13544

2021

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In silico identification of SARS-CoV-2 spike (S) protein-ACE2 complex inhibitors from eight Tecoma species and cultivars analyzed by LC-MS

RSC advances, 2020-11, Vol.10 (70), p.43103-43108

2020

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Twelve month outcome of manual small-incision cataract surgery in Assiut, Egypt: A retrospective study with a large sample size

Oman journal of ophthalmology, 2022-09, Vol.15 (3), p.326-330

2022

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Discovery and Anticancer Screening of Novel Oxindole-Based Derivative Bearing Pyridyl Group as Potent and Selective Dual FLT3/CDK2 Kinase Inhibitor

Pharmaceuticals (Basel, Switzerland), 2024-05, Vol.17 (5), p.659

2024

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Assessing the Antiproliferative Potential of a Novel Combretastatin A4 Derivative via Modulating Apoptosis, MAPK/ERK and PI3K/AKT Pathways in Human Breast Cancer Cells

Frontiers in bioscience (Landmark. Print), 2023-08, Vol.28 (8), p.185-185

2023

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Design and Synthesis of New Hydantoin Acetanilide Derivatives as Anti-NSCLC Targeting EGFRL858R/T790M Mutations

Pharmaceuticals (Basel, Switzerland), 2022-07, Vol.15 (7), p.857

2022

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Inhibition of SARS-CoV-2 main protease by phenolic compounds from Manilkara hexandra (Roxb.) Dubard assisted by metabolite profiling and in silico virtual screening

RSC advances, 2020-08, Vol.10 (53), p.32148-32155

2020

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1,3,4-oxadiazole-2-thione Derivatives; Novel Approach for Anticancer and Tubulin Polymerization Inhibitory Activities

Anti-cancer agents in medicinal chemistry, 2015, Vol.16 (2), p.269-277

2015

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Examination of the Validity of Skin Ultrasound to Quantitate Skin Involvement for Multicenter Clinical Trials in Patients with Systemic Sclerosis (SSc): A Systematic Literature Review (SLR)

ACR open rheumatology, 2022-03, Vol.4 (3), p.247-253

2022

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Potent combretastatin A-4 analogs containing 1,2,4-triazole: Synthesis, antiproliferative, anti-tubulin activity, and docking study

European journal of medicinal chemistry, 2019-12, Vol.183, p.111697-111697, Article 111697

2019

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Lossen Rearrangements under Heck Reaction Conditions

Advanced synthesis & catalysis, 2014-11, Vol.356 (16), p.3456-3464

2014

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Synthesis and investigation of anti-inflammatory activity and gastric ulcerogenicity of novel nitric oxide-donating pyrazoline derivatives

European journal of medicinal chemistry, 2009-07, Vol.44 (7), p.3068-3076

2009

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Chemical Composition of the Red Sea Green Algae Ulva lactuca : Isolation and In Silico Studies of New Anti-COVID-19 Ceramides

Metabolites, 2021-11, Vol.11 (12), p.816

2021

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Correlation between multifocal electroretinogram and optical coherence tomography findings with visual acuity after vitrectomy surgery for retinal detachment: an observational study

International journal of retina and vitreous, 2024-01, Vol.10 (1), p.10-10, Article 10

2024

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Twelve-month outcomes of single-step transepithelial photorefractive keratectomy for moderate hyperopia and hyperopic astigmatism

Eye and vision (Novato, Calif.), 2023-03, Vol.10 (1), p.7-7, Article 7

2023

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Synthesis, antiproliferative, anti-tubulin activity, and docking study of new 1,2,4-triazoles as potential combretastatin analogues

European journal of medicinal chemistry, 2017-12, Vol.141, p.293-305

2017

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Synthesis, Cytotoxic Properties and Tubulin Polymerization Inhibitory Activity of Novel 2-Pyrazoline Derivatives

Archiv der Pharmazie (Weinheim), 2012-07, Vol.345 (7), p.535-548

2012

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Spirohydantoins and 1,2,4-triazole-3-carboxamide derivatives as inhibitors of histone deacetylase: Design, synthesis, and biological evaluation

European journal of medicinal chemistry, 2018-02, Vol.146, p.79-92

2018

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Design, synthesis and anticonvulsant activity of new imidazolidindione and imidazole derivatives

Bioorganic chemistry, 2020-08, Vol.101, p.104020, Article 104020

2020

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Potential of Ficus microcarpa metabolites against SARS-CoV-2 main protease supported by docking studies

Natural product research, 2022-02, Vol.36 (4), p.994-998

2022

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Discovery of oxindole‐based FLT3 inhibitors as a promising therapeutic lead for acute myeloid leukemia carrying the oncogenic ITD mutation

Archiv der Pharmazie (Weinheim), 2023-02, Vol.356 (2), p.e2200407-n/a

2023

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Molecular docking reveals the potential of Salvadora persica flavonoids to inhibit COVID-19 virus main protease

Nitroxyl (HNO): A Possible Strategy for Fighting Cancer

OMA1520 and OMA1774, novel 1,2,4-triazole bearing analogs of combretastatin A-4, inhibit hepatocellular carcinoma: Histological and immunohistochemical studies

Combination of an Oxindole Derivative with (-)-β-Elemene Alters Cell Death Pathways in FLT3/ITD + Acute Myeloid Leukemia Cells

Flavonoids of Salvadora persica L. (meswak) and its liposomal formulation as a potential inhibitor of SARS-CoV-2

In silico identification of SARS-CoV-2 spike (S) protein-ACE2 complex inhibitors from eight Tecoma species and cultivars analyzed by LC-MS

Twelve month outcome of manual small-incision cataract surgery in Assiut, Egypt: A retrospective study with a large sample size

Discovery and Anticancer Screening of Novel Oxindole-Based Derivative Bearing Pyridyl Group as Potent and Selective Dual FLT3/CDK2 Kinase Inhibitor

Assessing the Antiproliferative Potential of a Novel Combretastatin A4 Derivative via Modulating Apoptosis, MAPK/ERK and PI3K/AKT Pathways in Human Breast Cancer Cells

Design and Synthesis of New Hydantoin Acetanilide Derivatives as Anti-NSCLC Targeting EGFRL858R/T790M Mutations

Inhibition of SARS-CoV-2 main protease by phenolic compounds from Manilkara hexandra (Roxb.) Dubard assisted by metabolite profiling and in silico virtual screening

1,3,4-oxadiazole-2-thione Derivatives; Novel Approach for Anticancer and Tubulin Polymerization Inhibitory Activities

Examination of the Validity of Skin Ultrasound to Quantitate Skin Involvement for Multicenter Clinical Trials in Patients with Systemic Sclerosis (SSc): A Systematic Literature Review (SLR)

Potent combretastatin A-4 analogs containing 1,2,4-triazole: Synthesis, antiproliferative, anti-tubulin activity, and docking study

Lossen Rearrangements under Heck Reaction Conditions

Synthesis and investigation of anti-inflammatory activity and gastric ulcerogenicity of novel nitric oxide-donating pyrazoline derivatives

Chemical Composition of the Red Sea Green Algae Ulva lactuca : Isolation and In Silico Studies of New Anti-COVID-19 Ceramides

Correlation between multifocal electroretinogram and optical coherence tomography findings with visual acuity after vitrectomy surgery for retinal detachment: an observational study

Twelve-month outcomes of single-step transepithelial photorefractive keratectomy for moderate hyperopia and hyperopic astigmatism

Synthesis, antiproliferative, anti-tubulin activity, and docking study of new 1,2,4-triazoles as potential combretastatin analogues

Synthesis, Cytotoxic Properties and Tubulin Polymerization Inhibitory Activity of Novel 2-Pyrazoline Derivatives

Spirohydantoins and 1,2,4-triazole-3-carboxamide derivatives as inhibitors of histone deacetylase: Design, synthesis, and biological evaluation

Design, synthesis and anticonvulsant activity of new imidazolidindione and imidazole derivatives

Potential of Ficus microcarpa metabolites against SARS-CoV-2 main protease supported by docking studies

Discovery of oxindole‐based FLT3 inhibitors as a promising therapeutic lead for acute myeloid leukemia carrying the oncogenic ITD mutation

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