Solvent-Free Synthesis of Acridone Based Dihydropyrazine Derivatives Using CuFe_2O_4 Nanoparticles as Heterogeneous Catalyst: Molecular Docking and In-vitro Studies as Anticancer Agents

[1]  Lakhwinder Singh,et al.  Chemistry of Quinoline Based Heterocycle Scaffolds: A Comprehensive Review , 2022, ChemistrySelect.

[2]  D. Tripathy,et al.  Acridine and Its Derivatives: Synthesis, Biological, and Anticorrosion Properties , 2022, Materials.

[3]  R. Madhu,et al.  One pot, three component synthesis of fluoro and trifluoromethyl substituted unsymmetrical dihydropyrazine fused acridine-3-carboxamide using renewable 2-MeTHF solvent and their DFT studies , 2022, Journal of Fluorine Chemistry.

[4]  M. Murahari,et al.  A comprehensive review on acridone based derivatives as future anti-cancer agents and their structure activity relationships. , 2022, European journal of medicinal chemistry.

[5]  Lakhwinder Singh,et al.  Solvent‐Free Synthesis of Glycoside Annulated 1,2,3‐Triazole Based Dihydropyrimidinones using Copper Ferrite Nanomaterials as Heterogeneous Catalyst and DFT Studies , 2022, ChemistrySelect.

[6]  Nancy,et al.  Synthesis and DFT studies of 1,2-disubstituted benzimidazoles using expeditious and magnetically recoverable CoFe2O4/Cu(OH)2 nanocomposite under solvent-free condition , 2021, Journal of Saudi Chemical Society.

[7]  Anjaneyulu Bendi,et al.  Ultrasound-Accelerated, Concise, and Highly Efficient Synthesis of 2-Oxazoline Derivatives Using Heterogenous Calcium Ferrite Nanoparticles and Their DFT Studies , 2021, Journal of Chemistry.

[8]  P. L. Praveen Nematic and smectic bithiophenes for UV sensing mechanism: Comparative calculations on different homologues , 2021 .

[9]  Sangeeta,et al.  A Study on Camphor Derivatives and Its Applications: A Review , 2021, Current organic chemistry.

[10]  A. S. Burange,et al.  Green synthesis of xanthene and acridine-based heterocycles of pharmaceutical importance: a review , 2021, Environmental Chemistry Letters.

[11]  H. Naeimi,et al.  A Brønsted acidic ionic liquid anchored to magnetite nanoparticles as a novel recoverable heterogeneous catalyst for the Biginelli reaction , 2021, RSC advances.

[12]  Anjaneyulu Bendi,et al.  CoFe2O4/Cu(OH)2 Nanocomposite: Expeditious and magnetically recoverable heterogeneous catalyst for the four component Biginelli/transesterification reaction and their DFT studies , 2021, Results in Chemistry.

[13]  G. Rao,et al.  Click chemistry: In vitro evaluation of glycosyl hybrid phosphorylated/thiophosphorylated 1,2,3-triazole derivatives as irreversible acetyl cholinesterase (AChE) inhibitors , 2021, Results in Chemistry.

[14]  Visweswara Rao Pasupuleti,et al.  Synthesis of novel cytotoxic tetracyclic acridone derivatives and study of their molecular docking, ADMET, QSAR, bioactivity and protein binding properties , 2020, Scientific Reports.

[15]  M. Nasseri,et al.  Cu-Mn Bimetallic Complex Immobilized on Magnetic NPs as an Efficient Catalyst for Domino One-Pot Preparation of Benzimidazole and Biginelli Reactions from Alcohols , 2020, Catalysis Letters.

[16]  Joong-Hoon Ahn,et al.  Synthesis of acridone derivatives via heterologous expression of a plant type III polyketide synthase in Escherichia coli , 2020, Microbial Cell Factories.

[17]  D M Parkin,et al.  Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods , 2018, International journal of cancer.

[18]  Rajendra Prasad Reddy Bhoomireddy,et al.  Green synthesis of 1,2,3-triazoles via Cu2 O NPs on hydrogen trititanate nanotubes promoted 1,3-dipolar cycloadditions , 2019, Applied Organometallic Chemistry.

[19]  F. Saadati,et al.  Copper ferrite nanoparticle modified starch as a highly recoverable catalyst for room temperature click chemistry: multicomponent synthesis of 1,2,3-triazoles in water , 2018 .

[20]  B. Akhlaghinia,et al.  Cu(II) immobilized on Fe$_{3}$O$_{4}$ @Agarose nanomagnetic catalyst functionalized with ethanolamine phosphate-salicylaldehyde Schiff base: a magnetically reusable nanocatalyst for preparation of 2-substituted imidazolines, oxazolines, and thiazolines , 2018 .

[21]  B. Narasimhan,et al.  2-Mercaptobenzimidazole Schiff Bases: Design, Synthesis, Antimicrobial Studies and Anticancer Activity on HCT-116 Cell Line. , 2018, Mini reviews in medicinal chemistry.

[22]  S. Bhushan,et al.  Green synthesis and anticancer potential of chalcone linked-1,2,3-triazoles. , 2017, European journal of medicinal chemistry.

[23]  D. P. Ojha,et al.  UV spectral characterization of a smectic-C liquid crystal: Theoretical support to the experiment , 2017 .

[24]  C. Mathers,et al.  Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012 , 2015, International journal of cancer.

[25]  M. P. Kaushik,et al.  A facile one-pot five-component synthesis of glycoside annulated dihydropyrimidinone derivatives with 1,2,3-triazol linkage via transesterification/Biginelli/click reactions in aqueous medium , 2014 .

[26]  Anuj Jain,et al.  CuFe2O4 nanoparticles as a highly efficient and magnetically recoverable catalyst for the synthesis of medicinally privileged spiropyrimidine scaffolds , 2013 .

[27]  Arthur J. Olson,et al.  AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading , 2009, J. Comput. Chem..

[28]  David S. Goodsell,et al.  AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility , 2009, J. Comput. Chem..

[29]  T. Godet,et al.  Acridine and acridone derivatives, anticancer properties and synthetic methods: where are we now? , 2007, Anti-cancer agents in medicinal chemistry.

[30]  Gerbrand Ceder,et al.  Toward Computational Materials Design: The Impact of Density Functional Theory on Materials Research , 2006 .

[31]  W. Denny,et al.  Acridine derivatives as chemotherapeutic agents. , 2002, Current medicinal chemistry.

[32]  F. Charmantray,et al.  Interest of acridine derivatives in the anticancer chemotherapy. , 2001, Current pharmaceutical design.