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Multi-epitope peptide vaccines targeting dengue virus serotype 2 created via immunoinformatic analysis

Scientific reports, 2024-07, Vol.14 (1), p.17645-22, Article 17645

2024

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Alkaloids: Therapeutic Potential against Human Coronaviruses

Molecules (Basel, Switzerland), 2020-11, Vol.25 (23), p.5496

2020

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Discovery of pyrazolo[3,4-]pyrimidine and pyrazolo[4,3-][1,2,4]triazolo[1,5-]pyrimidine derivatives as novel CDK2 inhibitors: synthesis, biological and molecular modeling investigations

RSC advances, 2022-05, Vol.12 (23), p.14865-14882

2022

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Synthesis and QSAR study of novel cytotoxic spiro[3 H-indole-3,2′(1′ H)-pyrrolo[3,4- c]pyrrole]-2,3′,5′(1 H,2′ aH,4′ H)-triones

European journal of medicinal chemistry, 2012, Vol.47 (1), p.312-322

2012

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Design and Synthesis of New Quinoxaline Derivatives as Anticancer Agents and Apoptotic Inducers

Molecules (Basel, Switzerland), 2019-03, Vol.24 (6), p.1175

2019

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Medicinal attributes of pyridine scaffold as anticancer targeting agents

Future journal of pharmaceutical sciences, 2021-01, Vol.7 (1), p.24-17, Article 24

2021

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Synthesis, biological evaluation, and in silico studies of new CDK2 inhibitors based on pyrazolo[3,4-d]pyrimidine and pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine scaffold with apoptotic activity

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.1957-1973

2022

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Design, synthesis and biological study of novel pyrido[2,3-d]pyrimidine as anti-proliferative CDK2 inhibitors

European journal of medicinal chemistry, 2011-12, Vol.46 (12), p.5825-5832

2011

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Discovery of pyrano[2,3-]pyrimidine-2,4-dione derivatives as novel PARP-1 inhibitors: design, synthesis and antitumor activity

RSC advances, 2021-01, Vol.11 (8), p.4454-4464

2021

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Discovery of New Pyrazolopyridine, Furopyridine, and Pyridine Derivatives as CDK2 Inhibitors: Design, Synthesis, Docking Studies, and Anti-Proliferative Activity

Molecules (Basel, Switzerland), 2021-06, Vol.26 (13), p.3923

2021

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Design and Synthesis of New CDK2 Inhibitors Containing Thiazolone and Thiazolthione Scafold with Apoptotic Activity

Chemical and Pharmaceutical Bulletin, 2021/01/01, Vol.69(1), pp.106-117

2021

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Design, synthesis, docking study and anticancer evaluation of new trimethoxyphenyl pyridine derivatives as tubulin inhibitors and apoptosis inducers

RSC advances, 2021-12, Vol.11 (63), p.39728-39741

2021

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A molecular docking study repurposes FDA approved iron oxide nanoparticles to treat and control COVID-19 infection

European journal of pharmaceutical sciences, 2020-10, Vol.153, p.105465-105465, Article 105465

2020

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Synthesis, hypnotic properties and molecular modeling studies of 1,2,7,9-tetraaza-spiro[4.5]dec-2-ene-6,8,10-triones

European journal of medicinal chemistry, 2011-10, Vol.46 (10), p.4964-4969

2011

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A convenient synthesis and molecular modeling study of novel purine and pyrimidine derivatives as CDK2/cyclin A3 inhibitors

Bioorganic & medicinal chemistry, 2010-11, Vol.18 (21), p.7639-7650

2010

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Potential Role of Colchicine in Combating COVID-19 Cytokine Storm and Its Ability to Inhibit Protease Enzyme of SARS-CoV-2 as Conferred by Molecular Docking Analysis

Medicina (Kaunas, Lithuania), 2021-12, Vol.58 (1), p.20

2021

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Rational design, synthesis and molecular modeling studies of novel anti-oncological alkaloids against melanoma

Organic & biomolecular chemistry, 2015-06, Vol.13 (23), p.6619-6633

2015

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Facile synthesis, vasorelaxant properties and molecular modeling studies of 2-amino-8a-methoxy-4H-pyrano[3,2-c]pyridine-3-carbonitriles

European journal of medicinal chemistry, 2011-06, Vol.46 (6), p.2397-2407

2011

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Medicinal Attributes of Thienopyrimidine Based Scaffold Targeting Tyrosine Kinases and Their Potential Anticancer Activities

Archiv der Pharmazie (Weinheim), 2017-11, Vol.350 (11), p.n/a

2017

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Design, synthesis and anticancer evaluation of novel pyrazole, pyrazolo[3,4-d]pyrimidine and their glycoside derivatives

Nucleosides, nucleotides & nucleic acids, 2017-04, Vol.36 (4), p.275-291

2017

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In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms

Infection and drug resistance, 2022-07, Vol.15, p.3459-3475

2022

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Regioselective synthesis and molecular modeling study of vasorelaxant active 7,9-dioxa-1,2-diaza-spiro[4.5]dec-2-ene-6,10-diones

European journal of medicinal chemistry, 2010-09, Vol.45 (9), p.4229-4238

2010

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Molecular modeling based approach, synthesis and in vitro assay to new indole inhibitors of hepatitis C NS3/4A serine protease

Bioorganic & medicinal chemistry, 2011-01, Vol.19 (1), p.374-383

2011

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Design and Synthesis of New CDK2 Inhibitors Containing Thiazolone and Thiazolthione Scafold with Apoptotic Activity

Chemical and Pharmaceutical Bulletin, 2021-01, Vol.69 (1), p.106-117

2021

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Novel series of 6-(2-substitutedacetamido)-4-anilinoquinazolines as EGFR-ERK signal transduction inhibitors in MCF-7 breast cancer cells

European journal of medicinal chemistry, 2018-07, Vol.155, p.782-796

2018

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Multi-epitope peptide vaccines targeting dengue virus serotype 2 created via immunoinformatic analysis

Alkaloids: Therapeutic Potential against Human Coronaviruses

Discovery of pyrazolo[3,4-]pyrimidine and pyrazolo[4,3-][1,2,4]triazolo[1,5-]pyrimidine derivatives as novel CDK2 inhibitors: synthesis, biological and molecular modeling investigations

Synthesis and QSAR study of novel cytotoxic spiro[3 H-indole-3,2′(1′ H)-pyrrolo[3,4- c]pyrrole]-2,3′,5′(1 H,2′ aH,4′ H)-triones

Design and Synthesis of New Quinoxaline Derivatives as Anticancer Agents and Apoptotic Inducers

Medicinal attributes of pyridine scaffold as anticancer targeting agents

Synthesis, biological evaluation, and in silico studies of new CDK2 inhibitors based on pyrazolo[3,4-d]pyrimidine and pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine scaffold with apoptotic activity

Design, synthesis and biological study of novel pyrido[2,3-d]pyrimidine as anti-proliferative CDK2 inhibitors

Discovery of pyrano[2,3-]pyrimidine-2,4-dione derivatives as novel PARP-1 inhibitors: design, synthesis and antitumor activity

Discovery of New Pyrazolopyridine, Furopyridine, and Pyridine Derivatives as CDK2 Inhibitors: Design, Synthesis, Docking Studies, and Anti-Proliferative Activity

Design and Synthesis of New CDK2 Inhibitors Containing Thiazolone and Thiazolthione Scafold with Apoptotic Activity

Design, synthesis, docking study and anticancer evaluation of new trimethoxyphenyl pyridine derivatives as tubulin inhibitors and apoptosis inducers

A molecular docking study repurposes FDA approved iron oxide nanoparticles to treat and control COVID-19 infection

Synthesis, hypnotic properties and molecular modeling studies of 1,2,7,9-tetraaza-spiro[4.5]dec-2-ene-6,8,10-triones

A convenient synthesis and molecular modeling study of novel purine and pyrimidine derivatives as CDK2/cyclin A3 inhibitors

Potential Role of Colchicine in Combating COVID-19 Cytokine Storm and Its Ability to Inhibit Protease Enzyme of SARS-CoV-2 as Conferred by Molecular Docking Analysis

Rational design, synthesis and molecular modeling studies of novel anti-oncological alkaloids against melanoma

Facile synthesis, vasorelaxant properties and molecular modeling studies of 2-amino-8a-methoxy-4H-pyrano[3,2-c]pyridine-3-carbonitriles

Medicinal Attributes of Thienopyrimidine Based Scaffold Targeting Tyrosine Kinases and Their Potential Anticancer Activities

Design, synthesis and anticancer evaluation of novel pyrazole, pyrazolo[3,4-d]pyrimidine and their glycoside derivatives

In vitro Anti SARS-CoV-2 Activity and Docking Analysis of Pleurotus ostreatus, Lentinula edodes and Agaricus bisporus Edible Mushrooms

Regioselective synthesis and molecular modeling study of vasorelaxant active 7,9-dioxa-1,2-diaza-spiro[4.5]dec-2-ene-6,10-diones

Molecular modeling based approach, synthesis and in vitro assay to new indole inhibitors of hepatitis C NS3/4A serine protease

Design and Synthesis of New CDK2 Inhibitors Containing Thiazolone and Thiazolthione Scafold with Apoptotic Activity

Novel series of 6-(2-substitutedacetamido)-4-anilinoquinazolines as EGFR-ERK signal transduction inhibitors in MCF-7 breast cancer cells

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