Two- and three-directional synthesis by 3–7CRs of novel (imidazolidine/thiazolidine)-2,4-diones: preparation, antibacterial, anticonvulsant, and molecular docking investigation

[1]  Haiyang Liu,et al.  Acylphloroglucinol trimers from Callistemon salignus seeds: Isolation, configurational assignment, hAChE inhibitory effects, and molecular docking studies. , 2021, Bioorganic chemistry.

[2]  Runling Wang,et al.  Design, synthesis, biological evaluation and molecular dynamics simulation studies of imidazolidine-2,4-dione derivatives as novel PTP1B inhibitors. , 2021, Biochemical and biophysical research communications.

[3]  Nosrat O. Mahmoodi,et al.  Synthesis and characterization of derivatives including thiazolidine-2,4-dione/1-H- imidazole and evaluation of antimicrobial, antioxidant, and cytotoxic properties of new synthetic heterocyclic compounds , 2021, Research on Chemical Intermediates.

[4]  R. Liu,et al.  sCharacterization of Anoectochilus roxburghii polysaccharide and its therapeutic effect on type 2 diabetic mice. , 2021, International journal of biological macromolecules.

[5]  M. Bakherad,et al.  Synthesis of hydantoin alkynes through palladium‐catalyzed reaction, antibacterial evaluation, and molecular docking studies , 2021 .

[6]  Nosrat O. Mahmoodi,et al.  Design and synthesis of a new tripod-chromogenic sensor based on a s-triazine and thiazolidine-2,4-dione ring (TCST) for naked-eye detection of Li+ , 2021 .

[7]  S. Alarifi,et al.  Antimicrobial activity of novel 5-benzylidene-3-(3-phenylallylideneamino)imidazolidine-2,4-dione derivatives causing clinical pathogens: Synthesis and molecular docking studies. , 2020, Journal of infection and public health.

[8]  N. Mahmoodi,et al.  Synthesis and antibacterial evaluation of diaminomaleonitrile-based azo-Schiff bases and 8,9-dihydro-7H-purine-6-carboxamides , 2020, Research on Chemical Intermediates.

[9]  R. Karamian,et al.  New nickel, palladium and platinum complexes of hydantoin derivative: Synthesis, characterization, theoretical study and biological activity , 2020 .

[10]  F. Ren,et al.  FGF19 alleviates palmitate-induced atrophy in C2C12 cells by inhibiting mitochondrial overload and insulin resistance. , 2020, International journal of biological macromolecules.

[11]  G. Ginalska,et al.  Design, synthesis and antimycobacterial activity of thiazolidine-2,4-dione-based thiosemicarbazone derivatives. , 2020, Bioorganic chemistry.

[12]  K. Ramesh,et al.  Molecular docking studies of phytochemicals against trehalose–6–phosphate phosphatases of pathogenic microbes , 2020, Beni-Suef University Journal of Basic and Applied Sciences.

[13]  Shahrzad Javanshir,et al.  Magnetic γFe2O3@Sh@Cu2O: an efficient solid-phase catalyst for reducing agent and base-free click synthesis of 1,4-disubstituted-1,2,3-triazoles , 2020, BMC chemistry.

[14]  Yu-Han Su,et al.  Exopolysaccharides of Bacillus amyloliquefaciens modulate glycemic level in mice and promote glucose uptake of cells through the activation of Akt. , 2019, International journal of biological macromolecules.

[15]  R. J. Kshirsagar,et al.  Plasmon-Induced Dimerization of Thiazolidine-2, 4-Dione on Silver Nanoparticles - Revealed by Surface-Enhanced Raman Scattering Study. , 2019, The journal of physical chemistry. A.

[16]  Fateme Ghanbari Pirbasti,et al.  One pot multicomponent synthesis of Novel Bis‐ N ‐(1,2,3‐ triazolylacetyl) as Potent Antioxidant and Antibacterial Agents , 2019, ChemistrySelect.

[17]  A. Mahn,et al.  Molecular Docking of Potential Inhibitors of Broccoli Myrosinase , 2018, Molecules.

[18]  Y. Suneetha,et al.  Design, synthesis, neuroprotective, antibacterial activities and docking studies of novel thieno[2,3-d]pyrimidine-alkyne Mannich base and oxadiazole hybrids. , 2018, Bioorganic & medicinal chemistry letters.

[19]  N. Mahmoodi,et al.  Recent Advances in the Synthesis of Biscoumarin Derivatives , 2018 .

[20]  N. Mahmoodi,et al.  Recent synthetic routes for the synthesis of symmetrical tris-compound , 2018, Journal of the Iranian Chemical Society.

[21]  Kapil Kumar,et al.  Synthetic and medicinal perspective of thiazolidinones: A review. , 2017, Bioorganic chemistry.

[22]  Jean Martínez,et al.  Recent Advances in the Synthesis of Hydantoins: The State of the Art of a Valuable Scaffold. , 2017, Chemical reviews.

[23]  N. Mahmoodi,et al.  Thiazolyl-pyrazole-biscoumarin synthesis and evaluation of their antibacterial and antioxidant activities , 2017, Research on Chemical Intermediates.

[24]  R. Reed,et al.  Effects of Levetiracetam, Carbamazepine, Phenytoin, Valproate, Lamotrigine, Oxcarbazepine, Topiramate, Vinpocetine and Sertraline on Presynaptic Hippocampal Na+ and Ca2+ Channels Permeability , 2016, Neurochemical Research.

[25]  Atefeh Ghavidast,et al.  One-pot multicomponent synthesis of indol-3-yl-hydrazinyl thiazoles as antimicrobial agents , 2016, Research on Chemical Intermediates.

[26]  N. Mahmoodi,et al.  Synthesis and evaluation of biological activities of 4-cyclopropyl-5-(2-fluorophenyl) arylhydrazono-2,3-dihydrothiazoles as potent antioxidant agents , 2016 .

[27]  A. Tosetto,et al.  Comparison between different D‐Dimer cutoff values to assess the individual risk of recurrent venous thromboembolism: analysis of results obtained in the DULCIS study , 2016, International journal of laboratory hematology.

[28]  M. S. Bahia,et al.  Thiazolidine-2,4-dione derivatives: programmed chemical weapons for key protein targets of various pathological conditions. , 2015, Bioorganic & medicinal chemistry.

[29]  N. Desai,et al.  Thiazolidinedione compounds: a patent review (2010 – present) , 2015, Expert opinion on therapeutic patents.

[30]  Vivek Asati,et al.  Thiazolidine-2,4-diones as multi-targeted scaffold in medicinal chemistry: Potential anticancer agents. , 2014, European journal of medicinal chemistry.

[31]  Jean Martínez,et al.  Mechanochemical preparation of hydantoins from amino esters: application to the synthesis of the antiepileptic drug phenytoin. , 2014, The Journal of organic chemistry.

[32]  M. Vallet‐Regí,et al.  A molecular model to explain the controlled release from SBA-15 functionalized with APTES , 2014 .

[33]  N. Mahmoodi,et al.  Facile Regioselective Synthesis of Novel bis‐Thiazole Derivatives and Their Antimicrobial Activity , 2013, Archiv der Pharmazie.

[34]  M. Hill,et al.  A magnesium-mediated cascade assembly for the atom-economical synthesis of bis(imidazolidine-2,4-dione)s. , 2013, Angewandte Chemie.

[35]  N. Mahmoodi,et al.  One‐Pot Synthesis and Characterization of Some New Types of 5,5′‐Disubstituted Bis(imidazolidine‐2,4‐diones) , 2013 .

[36]  N. Khalil,et al.  Synthesis and anticonvulsant activity of new phenytoin derivatives. , 2013, European journal of medicinal chemistry.

[37]  V. Avupati,et al.  Synthesis, characterization and biological evaluation of some novel 2,4-thiazolidinediones as potential cytotoxic, antimicrobial and antihyperglycemic agents. , 2012, Bioorganic & medicinal chemistry letters.

[38]  C. H. Suresh,et al.  1,3-Phenyl linked urea-based receptors for anions and the facile cyclization to imidazolidinedione , 2012 .

[39]  K. Alagawadi,et al.  New thiazolidinedione-5-acetic acid amide derivatives: synthesis, characterization and investigation of antimicrobial and cytotoxic properties , 2012, Medicinal Chemistry Research.

[40]  N. Mahmoodi,et al.  Two 1,3‐Diazabicyclo[3.1.0]hex‐3‐enes with a ‘Tripod’ Core , 2012 .

[41]  N. Mahmoodi,et al.  An efficient one‐pot synthesis of pyridazinones and phthalazinones using HY‐zeolite , 2011 .

[42]  N. Mahmoodi,et al.  Convenient Ultrasound-Promoted Regioselective Synthesis of Fused 6-Amino-3-methyl-4-aryl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile , 2011 .

[43]  J. Dash,et al.  Synthesis of spirocyclic thiazolidinediones using ring-closing metathesis and one-pot sequential ring-closing/cross metathesis. , 2011, Organic & biomolecular chemistry.

[44]  F. Badria,et al.  Synthesis, antimicrobial, antioxidant, anti-hemolytic and cytotoxic evaluation of new imidazole-based heterocycles. , 2011, European journal of medicinal chemistry.

[45]  N. Mahmoodi,et al.  An efficient chemo- and regioselective three-component synthesis of pyridazinones and phthalazinones using activated KSF , 2010 .

[46]  A. Klegeris,et al.  Synthesis and biological evaluation of novel pyrazolyl-2,4-thiazolidinediones as anti-inflammatory and neuroprotective agents. , 2010, Bioorganic & medicinal chemistry.

[47]  Mohammad Reza Ganjali,et al.  Schiff's Bases and Crown Ethers as Supramolecular Sensing Materials in the Construction of Potentiometric Membrane Sensors , 2008, Sensors.

[48]  C. Stevens,et al.  Synthesis of N3,N'3-polymethylene-bis-hydantoins and their macrocyclic derivatives. , 2006, The Journal of organic chemistry.

[49]  P. Vogel,et al.  Deracemization of 5-(4-hydroxyphenyl)-5-phenylhydantoin (HPPH): practical synthesis of (−)-(S)-HPPH , 2004 .

[50]  A. Becke.  Density-functional thermochemistry. III. The role of exact exchange , 1993 .

[51]  Y. Yaari,et al.  Frequency-dependent effects of phenytoin on frog junctional transmission: Presynaptic mechanisms , 1985, Brain Research.

[52]  S. F. Boys,et al.  The calculation of small molecular interactions by the differences of separate total energies. Some procedures with reduced errors , 1970 .

[53]  R. Bader,et al.  Atoms in molecules , 1990 .