Crystal Structure, Biological and Docking Studies of Solvothermally Isolated Novel Schiff Base
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[1] G. Thilagavathi,et al. Synthesis, structural, spectral, computational, docking and biological activities of Schiff base (E)-4-bromo-2-hydroxybenzylidene) amino)-N-(pyrimidin-2-yl) benzenesulfonamide from 5-bromosalicylaldehyde and sulfadiazine , 2023, Journal of the Indian Chemical Society.
[2] D. Golemi-Kotra,et al. Drug-Repurposing Approach To Combat Staphylococcus aureus: Biomolecular and Binding Interaction Study , 2022, ACS omega.
[3] V. Dalal,et al. Promising antivirals for PLpro of SARS-CoV-2 using virtual screening, molecular docking, dynamics, and MMPBSA , 2022, Journal of biomolecular structure & dynamics.
[4] S. N. Dhuri,et al. Construction of Pyrazine-Appended 1D and 3D Cobalt(II) Succinate Coordination Polymers: Influence of Solvent on Architectures and Applications in Gas Adsorption and NAC Detection , 2022, ACS omega.
[5] N. Dege,et al. Crystal structure and Hirshfeld surface analysis of 6,6′-((1E,1′E)-{[1,4-phenylenebis(methylene)]bis(azanylylidene)}bis(methaneylylidene))bis(2-methoxyphenol) , 2022, Acta crystallographica. Section E, Crystallographic communications.
[6] S. R. Pathak,et al. Structural-based virtual screening and identification of novel potent antimicrobial compounds against YsxC of Staphylococcus aureus , 2022, Journal of Molecular Structure.
[7] G. Viola,et al. Cinnamic acid derivatives linked to arylpiperazines as novel potent inhibitors of tyrosinase activity and melanin synthesis. , 2022, European journal of medicinal chemistry.
[8] M. Kosanić,et al. Synthesis, characterization, biological evaluation, BSA binding properties, density functional theory and molecular docking study of Schiff bases , 2021 .
[9] V. Dalal,et al. Identification of potential inhibitors for LLM of Staphylococcus aureus: structure-based pharmacophore modeling, molecular dynamics, and binding free energy studies , 2021, Journal of biomolecular structure & dynamics.
[10] Monsurat M. Lawal,et al. Design of New Schiff-Base Copper(II) Complexes: Synthesis, Crystal Structures, DFT Study, and Binding Potency toward Cytochrome P450 3A4 , 2021, ACS omega.
[11] B. Larijani,et al. Anti-melanogenesis and anti-tyrosinase properties of aryl-substituted acetamides of phenoxy methyl triazole conjugated with thiosemicarbazide: Design, synthesis and biological evaluations. , 2021, Bioorganic chemistry.
[12] S. N. Dhuri,et al. A Water‐Rich Cobalt(II) Compound: Hydrothermal Synthesis, Spectroscopic, Thermal, Crystal Structure Characterization and Antimicrobial Properties , 2021 .
[13] K. Bhat,et al. Triticum aestivum (wheat grass) Exhibited Anticancer Activity on Oral Cancer (KB) Cell Line , 2020 .
[14] Gangadhar C. Gouripur,et al. Preparation, characterization and antimicrobial activity of betel-leaf-extract-doped polysaccharide blend films , 2020, Green Materials.
[15] Patrick McCabe,et al. Mercury 4.0: from visualization to analysis, design and prediction , 2020, Journal of applied crystallography.
[16] M. Ghosh,et al. Synthesis of Two Mononuclear Schiff Base Metal (M = Fe, Cu) Complexes: MOF Structure, Dye Degradation, H2O2 Sensing, and DNA Binding Property , 2019, ACS omega.
[17] K. Bhat,et al. An in vitro evaluation of cytotoxicity of curcumin against human periodontal ligament fibroblasts , 2019, Ayu.
[18] K. Bhat,et al. In vitro evaluation of cytotoxicity of Emblica officinalis (amla) on cultured human primary dental pulp fibroblasts , 2019, Journal of the Indian Society of Pedodontics and Preventive Dentistry.
[19] Vinko Nemec,et al. Halogen bonding of the aldehyde oxygen atom in cocrystals of aromatic aldehydes and 1,4-diiodotetrafluorobenzene , 2019, CrystEngComm.
[20] R. Gaur. Selective anionic dye adsorption, topology and luminescence study of structurally diverse cadmium(ii) coordination polymers , 2019, Inorganic Chemistry Frontiers.
[21] M. Kurian,et al. Synthesis and catalytic applications of metal–organic frameworks: a review on recent literature , 2018, International Nano Letters.
[22] D. Velmurugan,et al. Bis(thiosemicarbazone)copper(I) Complexes as Prospective Therapeutic Agents: Interaction with DNA/BSA Molecules, and In Vitro and In Vivo Anti-Proliferative Activities , 2018, ChemistrySelect.
[23] J. Ellena,et al. A vanillin-based copper(ii) metal complex with a DNA-mediated apoptotic activity , 2018, RSC advances.
[24] A. Kulandaisamy,et al. DNA, in vitro antimicrobial/anticancer activities and biocidal based statistical analysis of Schiff base metal complexes derived from salicylalidene-4-imino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one and 2-aminothiazole , 2018 .
[25] V. McKee,et al. Synthesis, Characterization and Biological Assay of Salicylaldehyde Schiff Base Cu(II) Complexes and their Precursors , 2018 .
[26] L. Teh,et al. Synthesis of azomethines derived from cinnamaldehyde and vanillin: in vitro aetylcholinesterase inhibitory, antioxidant and insilico molecular docking studies , 2018, Medicinal Chemistry Research.
[27] Xiang Liu,et al. Multidentate unsymmetrically-substituted Schiff bases and their metal complexes: Synthesis, functional materials properties, and applications to catalysis , 2018 .
[28] Francoise M. Amombo Noa,et al. Co-crystals and salts of vanillic acid and vanillin with amines , 2018 .
[29] Y. Ko,et al. Synthesis, characterization, and biological activity of Schiff bases metal complexes , 2018 .
[30] S. Thakur,et al. Studies on the DNA binding and anticancer activity of Ru(II) polypyridyl complexes by using a (2-(4-(diethoxymethyl)-1H-imidazo[4,5-f][1,10] phenanthroline)) intercalative ligand , 2018 .
[31] A. Ghorbani‐Choghamarani,et al. Synthesis and Characterization of Pd Schiff Base Complex Immobilized onto Functionalized Nanoporous MCM-41 and its Catalytic Efficacy in the Suzuki, Heck and Stille Coupling Reactions , 2017, Catalysis Letters.
[32] Olivier Michielin,et al. SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules , 2017, Scientific Reports.
[33] Y. Ko,et al. Schiff base complexes and their versatile applications as catalysts in oxidation of organic compounds: part I , 2017 .
[34] H. Fun,et al. Synthesis, characterization, antimicrobial screening and computational studies of 4-[3-(4-methoxy-phenyl)-allylideneamino]-1,5-dimethyl-2-phenyl-1,2-dihydro-pyrazol-3-one , 2016 .
[35] P. Arya,et al. Dependence of solvents, pH, molar ratio and temperature in tuning metal organic framework architecture , 2016, Arabian Journal of Chemistry.
[36] M. Andruh. The exceptionally rich coordination chemistry generated by Schiff-base ligands derived from o-vanillin. , 2015, Dalton transactions.
[37] J. Steed,et al. Packing problems: high Z' crystal structures and their relationship to cocrystals, inclusion compounds, and polymorphism. , 2015, Chemical reviews.
[38] G. Sheldrick. Crystal structure refinement with SHELXL , 2015, Acta crystallographica. Section C, Structural chemistry.
[39] Adriano Bof de Oliveira,et al. Crystal structure of (E)-2-[4-(4-hydroxyphenyl)butan-2-ylidene]hydrazine-1-carbothioamide , 2015, Acta crystallographica. Section E, Crystallographic communications.
[40] Adriano Bof de Oliveira,et al. 4-Hydroxy-3-methoxybenzaldehyde 4-ethylthiosemicarbazone , 2014, Acta crystallographica. Section E, Structure reports online.
[41] Ming-hui Li,et al. Vanillin derivatives as the selective small molecule inhibitors of FtsZ , 2014, Medicinal Chemistry Research.
[42] Adriano Bof de Oliveira,et al. 4-Hydroxy-3-methoxybenzaldehyde thiosemicarbazone , 2013, Acta crystallographica. Section E, Structure reports online.
[43] Shyam Biswas,et al. Synthesis of metal-organic frameworks (MOFs): routes to various MOF topologies, morphologies, and composites. , 2012, Chemical reviews.
[44] N. Zeghal,et al. Evaluation of the antioxidant, anti-inflammatory and hepatoprotective properties of vanillin in carbon tetrachloride-treated rats. , 2011, European journal of pharmacology.
[45] A. Pandey,et al. Synthesis, Characterization and Antibacterial Activity of Biologically Important Vanillin Related Hydrazone Derivatives , 2011 .
[46] H. Khavasi,et al. Synthesis and characterization of some new Co(II) and Cd(II) macroacyclic Schiff-base complexes containing piperazine moiety , 2009 .
[47] T. Konno,et al. Synthesis and characterization of luminescent zinc(II) and cadmium(II) complexes with N,S-chelating Schiff base ligands. , 2008, Inorganic chemistry.
[48] Mingjie Zhang,et al. 4-Hydroxy-3-methoxybenzaldehyde (pyrazin-2-yl)hydrazone , 2007 .
[49] Yang Qu,et al. (E,E)‐4‐Hydroxy‐3‐methoxybenzaldehyde azine , 2005 .
[50] B. Ziyadanoğulları,et al. Synthesis, spectroscopic and thermodynamic studies of new transition metal complexes with N,N′-bis(2-hydroxynaphthalin-1-carbaldehydene)-1,2-bis(m-aminophenoxy)ethane and their determination by spectrophotometric methods , 2005 .
[51] H. Sakurai,et al. Vanillin suppresses in vitro invasion and in vivo metastasis of mouse breast cancer cells. , 2005, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[52] P. Cozzi. Metal-Salen Schiff base complexes in catalysis: practical aspects. , 2004, Chemical Society reviews.
[53] R. Moezelaar,et al. The Phenolic Hydroxyl Group of Carvacrol Is Essential for Action against the Food-Borne Pathogen Bacillus cereus , 2002, Applied and Environmental Microbiology.
[54] R. Setzer,et al. The antimutagenic effect of vanillin and cinnamaldehyde on spontaneous mutation in Salmonella TA104 is due to a reduction in mutations at GC but not AT sites. , 2001, Mutation research.
[55] Yuji Hamada,et al. White-Light-Emitting Material for Organic Electroluminescent Devices , 1996 .
[56] S. De Flora,et al. Inhibition of the 'spontaneous' mutagenicity in Salmonella typhimurium TA102 and TA104. , 1994, Mutation research.
[57] Y. Sasaki,et al. Suppression of 6-TG-resistant mutations in V79 cells and recessive spot formations in mice by vanillin. , 1990, Mutation research.
[58] K. Aravindakshan,et al. Synthesis, Characterization, Cytotoxic, Anticancer and Antimicrobial Studies of Novel Schiff Base Ligand Derived From Vanillin and Its Transition Metal Complexes , 2017 .
[59] B. Brzeziński,et al. Biological Properties of Schiff Bases and Azo Derivatives of Phenols , 2009 .
[60] Gautam R. Desiraju,et al. On the presence of multiple molecules in the crystal asymmetric unit ( Z ′ > 1) , 2007 .
[61] K. Watanabe,et al. Inhibitory effects of flavourings on mutagenesis induced by chemicals in bacteria. , 1986, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.