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1. Full Text Synthesis, characterization and biological studies of Schiff bases derived from heterocyclic moiety
by Shanty, Angamaly Antony and Philip, Jessica Elizabeth and Sneha, Eeettinilkunnathil Jose and Prathapachandra Kurup, Maliyeckal R and Balachandran, Sreedharannair and Mohanan, Puzhavoorparambil Velayudhan
Bioorganic chemistry, ISSN 0045-2068, 02/2017, Volume 70, pp. 67 - 73
Schiff bases | Spectral studies | Antibacterial activity | Amines | Antioxidant activity | Heterocyclic aldehydes | Antioxidants - chemistry | Aminophenols - chemistry | Humans | Bacteria - drug effects | Crystallography, X-Ray | Aminophenols - pharmacology | Nitrophenols - chemistry | Schiff Bases - pharmacology | Microbial Sensitivity Tests | Nitrophenols - pharmacology | Aldehydes - pharmacology | Anti-Bacterial Agents - chemistry | Cresols - pharmacology | Bacterial Infections - drug therapy | Models, Molecular | Thiophenes - pharmacology | Antioxidants - pharmacology | Drug Discovery | Cresols - chemistry | Pyrroles - pharmacology | Schiff Bases - chemistry | Pyrroles - chemistry | Anti-Bacterial Agents - pharmacology | Thiophenes - chemistry | Aldehydes - chemistry | Heterocyclic compounds | Antioxidants | Analysis | Escherichia coli | Thiophene | Aldehydes | Antibacterial agents | Index Medicus
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2. Full Text Some new nano-sized Fe(II), Cd(II) and Zn(II) Schiff base complexes as precursor for metal oxides: Sonochemical synthesis, characterization, DNA interaction, in vitro antimicrobial and anticancer activities
by Abdel-Rahman, Laila H and Abu-Dief, Ahmed M and El-Khatib, Rafat M and Abdel-Fatah, Shimaa Mahdy
Bioorganic chemistry, ISSN 0045-2068, 12/2016, Volume 69, pp. 140 - 152
Nanoparticles | Metal oxides | Antimicrobial activity | DNA interaction | Cytotoxic activity | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Chemistry, Organic | Life Sciences & Biomedicine | Science & Technology | Nanoparticles - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Oxides - chemistry | Bacteria - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Structure-Activity Relationship | Zinc - chemistry | Schiff Bases - pharmacology | Dose-Response Relationship, Drug | Microbial Sensitivity Tests | Anti-Bacterial Agents - chemistry | Antineoplastic Agents - pharmacology | Iron - pharmacology | DNA - drug effects | Antifungal Agents - pharmacology | Fungi - drug effects | HCT116 Cells | Iron - chemistry | Cadmium - pharmacology | Antineoplastic Agents - chemistry | Hep G2 Cells | Anti-Bacterial Agents - chemical synthesis | Oxides - pharmacology | Organometallic Compounds - chemical synthesis | Schiff Bases - chemistry | Organometallic Compounds - chemistry | Anti-Bacterial Agents - pharmacology | Cell Proliferation - drug effects | Zinc - pharmacology | Organometallic Compounds - pharmacology | Cadmium - chemistry | Drug Screening Assays, Antitumor | Index Medicus
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3. Full Text Synthesis, spectral characterization and antioxidant activity studies of a bidentate Schiff base, 5-methyl thiophene-2-carboxaldehyde-carbohydrazone and its Cd(II), Cu(II), Ni(II) and Zn(II) complexes
by Harinath, Y and Harikishore Kumar Reddy, D and Naresh Kumar, B and Apparao, Ch and Seshaiah, K
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, ISSN 1386-1425, 01/2013, Volume 101, pp. 264 - 272
Hydrazones | Transition metal complexes | Antioxidant activity | Microbial assay | Spectroscopy | Technology | Science & Technology | Antioxidants - chemistry | Anti-Infective Agents - pharmacology | Humans | Bacteria - drug effects | Zinc - chemistry | Schiff Bases - pharmacology | Microbial Sensitivity Tests | Copper - chemistry | Aldehydes - pharmacology | Anti-Infective Agents - chemistry | Coordination Complexes - pharmacology | Schiff Bases - chemical synthesis | Nickel - pharmacology | Fungi - drug effects | Nickel - chemistry | Aldehydes - chemical synthesis | Bacterial Infections - drug therapy | Copper - pharmacology | Cadmium - pharmacology | Thiophenes - pharmacology | Hydrazones - chemical synthesis | Antioxidants - chemical synthesis | Antioxidants - pharmacology | Coordination Complexes - chemistry | Anti-Infective Agents - chemical synthesis | Hydrazones - chemistry | Hydrazones - pharmacology | Thiophenes - chemical synthesis | Schiff Bases - chemistry | Mycoses - drug therapy | Coordination Complexes - chemical synthesis | Zinc - pharmacology | Thiophenes - chemistry | Aldehydes - chemistry | Cadmium - chemistry
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4. Full Text Sulfadiazine salicylaldehyde-based schiff bases: Synthesis, antimicrobial activity and cytotoxicity
by Krátký, Martin and Dzurková, Magdaléna and Janoušek, Jiří and Konečná, Klára and Trejtnar, František and Stolaříková, Jiřina and VinŠová, Jarmila
Molecules (Basel, Switzerland), ISSN 1420-3049, 09/2017, Volume 22, Issue 9, p. 1573
Antifungal activity | Schiff bases | Sulfadiazine | Sulfonamides | Antibacterial activity | Cytotoxicity | Antimycobacterial activity | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Multidisciplinary | Science & Technology | Antifungal Agents - pharmacology | Cell Survival - drug effects | Aldehydes - chemical synthesis | Pyrimidines - chemical synthesis | Anti-Infective Agents - pharmacology | Humans | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Structure-Activity Relationship | Pyrimidines - pharmacology | Sulfadiazine - pharmacology | Anti-Infective Agents - chemical synthesis | Schiff Bases - pharmacology | Hep G2 Cells | Sulfadiazine - chemical synthesis | Anti-Bacterial Agents - chemical synthesis | Microbial Sensitivity Tests | Aldehydes - pharmacology | Anti-Bacterial Agents - chemistry | Sulfadiazine - analogs & derivatives | Schiff Bases - chemical synthesis | Anti-Bacterial Agents - pharmacology | Drugs | Yeasts | Antimicrobial activity | Fungicides | Toxicity | Molds | Atomic properties | Antimicrobial agents | Selectivity | Drug resistance | Drug development | Methicillin | Tuberculosis | Imines | Benzene | Minimum inhibitory concentration | Bacteria | Gram-negative bacteria | Inhibition | Index Medicus | antibacterial activity | antimycobacterial activity | sulfonamides | antifungal activity | sulfadiazine | cytotoxicity
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5. Full Text New insight into the structural, electrochemical and biological aspects of macroacyclic Cu(II) complexes derived from S-substituted dithiocarbazate schiff bases
by Low, May Lee and Maigre, Laure and Tahir, Mohamed Ibrahim M and Tiekink, Edward R.T and Dorlet, Pierre and Guillot, Régis and Ravoof, Thahira Begum and Rosli, Rozita and Pagès, Jean-Marie and Policar, Clotilde and Delsuc, Nicolas and Crouse, Karen A
European journal of medicinal chemistry, ISSN 0223-5234, 09/2016, Volume 120, pp. 1 - 12
Schiff base | Dithiocarbazate | NNSS ligand | MCF-7 | Gram-positive | Gram-negative | Macroacyclic ligand | Tetradendate ligand | Bioactivity | MDA-MB-231 | Copper complexes | Hydrazines - pharmacology | Macrocyclic Compounds - chemistry | Humans | Bacteria - drug effects | Copper - pharmacology | Coordination Complexes - chemistry | Schiff Bases - pharmacology | Macrocyclic Compounds - pharmacology | Hydrazines - chemistry | Copper - chemistry | Anti-Bacterial Agents - chemistry | Schiff Bases - chemistry | Cell Line, Tumor | Coordination Complexes - pharmacology | Anti-Bacterial Agents - pharmacology | Copper compounds | Schiff bases | Thiophene | Antibacterial agents | Analysis | Electric properties | Index Medicus | Life Sciences | Chemical Sciences
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6. Full Text Regioselective reaction: Synthesis, characterization and pharmacological studies of some new Mannich bases derived from 1,2,4-triazoles
by Isloor, Arun M and Kalluraya, Balakrishna and Shetty, Prashanth
European journal of medicinal chemistry, ISSN 0223-5234, 2009, Volume 44, Issue 9, pp. 3784 - 3787
Schiff bases | Antifungal activity | Antibacterial activity | Mannich bases | 1,2,4-Triazoles | Biological and medical sciences | Medical sciences | Antibacterial agents | Pharmacology. Drug treatments | Antifungal agents | Antibiotics. Antiinfectious agents. Antiparasitic agents | Antifungal Agents - pharmacology | Triazoles - chemistry | Anti-Infective Agents - pharmacology | Bacteria - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Structure-Activity Relationship | Anti-Infective Agents - chemical synthesis | Mannich Bases - chemistry | Mannich Bases - chemical synthesis | Anti-Bacterial Agents - chemical synthesis | Microbial Sensitivity Tests | Triazoles - pharmacology | Candida albicans - drug effects | Anti-Bacterial Agents - chemistry | Anti-Infective Agents - chemistry | Mannich Bases - pharmacology | Triazoles - chemical synthesis | Anti-Bacterial Agents - pharmacology | Formaldehyde | Chemical properties | Nuclear magnetic resonance | Index Medicus
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7. Full Text Structure and biological properties of mixed-ligand Cu(II) Schiff base complexes as potential anticancer agents
by Gou, Yi and Li, Jinlong and Fan, Boyi and Xu, Bohui and Zhou, Min and Yang, Feng
European journal of medicinal chemistry, ISSN 0223-5234, 07/2017, Volume 134, pp. 207 - 217
Anticancer mechanism | Aroylhydrazone Cu(II) complexes | Anti-metastatic activity | Anticancer activity | Pharmacology & Pharmacy | Life Sciences & Biomedicine | Chemistry, Medicinal | Science & Technology | Neoplasms - metabolism | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Antineoplastic Agents - chemical synthesis | Humans | Crystallography, X-Ray | Schiff Bases - pharmacology | Copper - chemistry | Neoplasms - genetics | Cattle | Coordination Complexes - pharmacology | Schiff Bases - chemical synthesis | Antineoplastic Agents - pharmacology | Copper - pharmacology | Models, Molecular | Hydrazones - chemical synthesis | Antineoplastic Agents - chemistry | Coordination Complexes - chemistry | DNA Cleavage - drug effects | Hydrazones - chemistry | Hydrazones - pharmacology | Neoplasms - drug therapy | DNA - genetics | DNA - chemistry | Animals | Cell Cycle Checkpoints - drug effects | Schiff Bases - chemistry | Cell Line, Tumor | Coordination Complexes - chemical synthesis | Antimitotic agents | Schiff bases | Care and treatment | Pyridine | Analysis | Lung cancer | Metastasis | Antineoplastic agents | Cancer | Index Medicus
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8. Full Text Synthesis, characterization, and biological evaluation of Schiff base–platinum(II) complexes
by Shiju, C and Arish, D and Bhuvanesh, N and Kumaresan, S
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, ISSN 1386-1425, 06/2015, Volume 145, pp. 213 - 222
Schiff base | Antimicrobial | Anticancer | Antitubercular | Platinum complexes | Spectroscopy | Technology | Science & Technology | Powders | Fungi - drug effects | Anti-Infective Agents - pharmacology | HCT116 Cells | Humans | Molecular Conformation | Antitubercular Agents - pharmacology | Bacteria - drug effects | Crystallography, X-Ray | Coordination Complexes - chemistry | Schiff Bases - pharmacology | Microbial Sensitivity Tests | Spectrophotometry, Infrared | Proton Magnetic Resonance Spectroscopy | Schiff Bases - chemistry | Coordination Complexes - chemical synthesis | Coordination Complexes - pharmacology | Inhibitory Concentration 50 | Schiff Bases - chemical synthesis | Ligands | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | HeLa Cells | Platinum - pharmacology | Schiff bases | Analysis | Colon cancer
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9. Full Text Schiff bases of indoline-2,3-dione (isatin) derivatives and nalidixic acid carbohydrazide, synthesis, antitubercular activity and pharmacophoric model building
by Aboul-Fadl, Tarek and Bin-Jubair, Fayzah A.S and Aboul-Wafa, Omima
European journal of medicinal chemistry, ISSN 0223-5234, 2010, Volume 45, Issue 10, pp. 4578 - 4586
Nalidixic acid carbohydrazide | Schiff bases | MOE | Pharmacophore | Antitubercular activity | Isatin derivatives | Biological and medical sciences | Medical sciences | Antibacterial agents | Pharmacology. Drug treatments | Antibiotics. Antiinfectious agents. Antiparasitic agents | Antitubercular Agents - chemical synthesis | Hydrazines - pharmacology | Nalidixic Acid - chemical synthesis | Antitubercular Agents - chemistry | Humans | Antitubercular Agents - pharmacology | Isatin - pharmacology | Models, Molecular | Isatin - chemistry | Schiff Bases - pharmacology | Mycobacterium - drug effects | Hydrazines - chemistry | Hydrazines - chemical synthesis | Isatin - chemical synthesis | Nalidixic Acid - chemistry | Schiff Bases - chemistry | Tuberculosis - drug therapy | Drug Design | Nalidixic Acid - pharmacology | Schiff Bases - chemical synthesis | Antitubercular agents | Tuberculosis | Bacterial infections | Health aspects | Public health | Index Medicus
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10. Full Text Antiaflatoxigenic and Antimicrobial Activities of Schiff Bases of 2‑Hydroxy-4-methoxybenzaldehyde, Cinnamaldehyde, and Similar Aldehydes
by Harohally, Nanishankar V and Cherita, Chris and Bhatt, Praveena and Anu Appaiah, K. A
Journal of agricultural and food chemistry, ISSN 0021-8561, 10/2017, Volume 65, Issue 40, pp. 8773 - 8778
Schiff base | 2-hydroxy-4-methoxybenzaldehyde | foodborne pathogen | aflatoxin | cinnamaldehyde | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Applied | Food Science & Technology | Agriculture, Multidisciplinary | Agriculture | Science & Technology | Antifungal Agents - pharmacology | Acrolein - analogs & derivatives | Acrolein - pharmacology | Plant Extracts - chemistry | Benzaldehydes - chemistry | Hemidesmus - chemistry | Apocynaceae - chemistry | Aspergillus flavus - drug effects | Aspergillus flavus - metabolism | Cinnamomum zeylanicum - chemistry | Plant Extracts - pharmacology | Benzaldehydes - pharmacology | Antifungal Agents - chemistry | Schiff Bases - pharmacology | Aspergillus flavus - growth & development | Aldehydes - pharmacology | Schiff Bases - chemistry | Aflatoxin B1 - metabolism | Molecular Structure | Acrolein - chemistry | Aldehydes - chemistry | Index Medicus
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11. Full Text Curcumin-I Knoevenagel’s condensates and their Schiff’s bases as anticancer agents: Synthesis, pharmacological and simulation studies
by Ali, Imran and Haque, Ashanul and Saleem, Kishwar and Hsieh, Ming Fa
Bioorganic & medicinal chemistry, ISSN 0968-0896, 07/2013, Volume 21, Issue 13, pp. 3808 - 3820
Docking studies | Anticancer agents | Curcumin-I derivatives | DNA binding and hemolysis and cell line profiles | Hemolysis - drug effects | Cell Survival - drug effects | Curcumin - analogs & derivatives | Pyrazoles - chemical synthesis | Antineoplastic Agents - chemical synthesis | Humans | Curcumin - pharmacology | DNA - metabolism | Antineoplastic Agents - chemistry | Curcumin - chemical synthesis | Schiff Bases - pharmacology | Neoplasms - drug therapy | Pyrazoles - chemistry | MCF-7 Cells | Schiff Bases - chemistry | Schiff Bases - chemical synthesis | Antineoplastic Agents - pharmacology | Molecular Docking Simulation | Pyrazoles - pharmacology | Antimitotic agents | Care and treatment | Antineoplastic agents | Cancer | Index Medicus
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12. Full Text Synthesis and biological evaluation of benzo[ d]isothiazole, benzothiazole and thiazole Schiff bases
by Vicini, Paola and Geronikaki, Athina and Incerti, Matteo and Busonera, Bernadetta and Poni, Graziella and Cabras, Carla Alba and La Colla, Paolo
Bioorganic & medicinal chemistry, ISSN 0968-0896, 2003, Volume 11, Issue 22, pp. 4785 - 4789
Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Chemistry, Organic | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Chemistry, Medicinal | Science & Technology | Biological and medical sciences | General aspects | Medical sciences | Antineoplastic agents | Pharmacology. Drug treatments | Anti-HIV Agents - pharmacology | Anti-Infective Agents - pharmacology | Antineoplastic Agents - chemical synthesis | Humans | Anti-HIV Agents - chemical synthesis | Schiff Bases - pharmacology | T-Lymphocytes - virology | Microbial Sensitivity Tests | Cattle | T-Lymphocytes - drug effects | Inhibitory Concentration 50 | Schiff Bases - chemical synthesis | Antineoplastic Agents - pharmacology | Molecular Structure | Drug Evaluation, Preclinical | HIV-1 - drug effects | Anti-Infective Agents - chemical synthesis | Cell Division - drug effects | Mycobacterium - drug effects | Animals | Thiazoles - chemical synthesis | Cell Line, Tumor | Thiazoles - chemistry | Thiazoles - pharmacology | Benzothiazoles | Index Medicus
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13. Full Text Spectroscopic studies and biological evaluation of some transition metal complexes of azo Schiff-base ligand derived from (1-phenyl-2,3-dimethyl-4-aminopyrazol-5-one) and 5-((4-chlorophenyl)diazenyl)-2-hydroxybenzaldehyde
by Anitha, C and Sheela, C.D and Tharmaraj, P and Sumathi, S
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, ISSN 1386-1425, 10/2012, Volume 96, pp. 493 - 500
Spectroscopy | Antimicrobial activity | DNA study | Salicylaldehyde | Azo Schiff base | SEM | Metal complexes | Technology | Science & Technology | Pyrazoles - chemical synthesis | Bacteria - drug effects | Crystallography, X-Ray | Electric Conductivity | Schiff Bases - pharmacology | Azo Compounds - chemistry | Microbial Sensitivity Tests | Pyrazoles - chemistry | Spectrophotometry, Infrared | Electrophoresis, Agar Gel | Magnetic Phenomena | Mass Spectrometry | Oxidation-Reduction - drug effects | Coordination Complexes - pharmacology | Schiff Bases - chemical synthesis | Azo Compounds - pharmacology | Pyrazoles - pharmacology | Antifungal Agents - pharmacology | Microscopy, Electron, Scanning | Benzaldehydes - chemistry | Transition Elements - pharmacology | Electrochemical Techniques | Electron Spin Resonance Spectroscopy | Fungi - drug effects | Magnetic Resonance Spectroscopy | Azo Compounds - chemical synthesis | Benzaldehydes - pharmacology | Schiff Bases - chemistry | Ligands | Anti-Bacterial Agents - pharmacology | Benzaldehydes - chemical synthesis | Electrons
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