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1. 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
In the present investigation, a series of new 4[(3-substituted-1 -pyrazol-4-yl)methyleneamino]-5-substituted-2-[(4-methylpiperzine-1-yl)methyl]-2... 
Schiff bases | Antifungal activity | Antibacterial activity | Mannich bases | 1,2,4-Triazoles | CHEMISTRY, MEDICINAL | ANTICANCER | BIOLOGICAL-ACTIVITY | DERIVATIVES | 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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2. Full Text RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency
by Song, Jun and Yang, Dongshan and Xu, Jie and Zhu, Tianqing and Chen, Y. Eugene and Zhang, Jifeng
Nature Communications, ISSN 2041-1723, 01/2016, Volume 7, Issue 1, pp. 10548 - 10548
Zinc-finger nuclease, transcription activator-like effector nuclease and CRISPR (clustered regularly interspaced short palindromic repeats)/Cas9... 
OVEREXPRESSION | REPAIR | RAD51 | CHROMATIN | MULTIDISCIPLINARY SCIENCES | CRISPR-CAS9 | HOMOLOGOUS RECOMBINATION | MUTATIONS | TARGETED MUTAGENESIS | GENOME | ONE-STEP GENERATION | DNA End-Joining Repair - drug effects | Gene Targeting | Rabbits | Animals | CRISPR-Cas Systems | Female | Benzamides - pharmacology | Pyrimidines - pharmacology | Sulfonamides - pharmacology | Recombinational DNA Repair - drug effects | Schiff Bases - pharmacology | Gene Knock-In Techniques | Index Medicus
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3. Full Text Fluorescent mixed ligand copper(ii) complexes of anthracene-appended Schiff bases: studies on DNA binding, nuclease activity and cytotoxicity
by Jaividhya, Paramasivam and Ganeshpandian, Mani and Dhivya, Rajkumar and Akbarsha, Mohammad Abdulkadher and Palaniandavar, Mallayan
Dalton Transactions, ISSN 1477-9226, 07/2015, Volume 44, Issue 26, pp. 11997 - 12010
A series of mixed ligand copper(II) complexes of the type [Cu(L)(phen)(ACN)](ClO4)(2) 1-5, where L is a bidentate Schiff base ligand... 
RUTHENIUM(II) COMPLEXES | CLEAVAGE PROPERTIES | APOPTOSIS | ANTICANCER | 1,10-PHENANTHROLINES | PROTEASE ACTIVITIES | DIIMINE CO-LIGANDS | CRYSTAL-STRUCTURE | DONOR LIGANDS | EFFICIENT CHEMICAL NUCLEASE | CHEMISTRY, INORGANIC & NUCLEAR | Anthracenes - chemistry | Humans | Copper - pharmacology | Models, Molecular | Crystallography, X-Ray | DNA - metabolism | Antineoplastic Agents - chemistry | Coordination Complexes - chemistry | Anthracenes - pharmacology | DNA Cleavage - drug effects | Schiff Bases - pharmacology | DNA - chemistry | Animals | Copper - chemistry | Phenanthrolines - pharmacology | MCF-7 Cells | Phenanthrolines - chemistry | Cattle | Schiff Bases - chemistry | Coordination Complexes - pharmacology | Ligands | Antineoplastic Agents - pharmacology | Index Medicus | Binding | Biotechnology | Deoxyribonucleic acid | Fluorescence | Affinity | Spectra | Coordination compounds
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4. 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
Tuberculosis (TB) remains among the world’s great public health challenges. Worldwide resurgence of TB is due to two major problems: the AIDS epidemic, which... 
Nalidixic acid carbohydrazide | Schiff bases | MOE | Pharmacophore | Antitubercular activity | Isatin derivatives | CHEMISTRY, MEDICINAL | TUBERCULOSIS | DNA GYRASE | DISCOVERY | 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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5. Full Text Mixed-ligand copper(II) Schiff base complexes: The role of the co-ligand in DNA binding, DNA cleavage, protein binding and cytotoxicity
by Lian, Wen-Jing and Wang, Xin-Tian and Xie, Cheng-Zhi and Tian, He and Song, Xue-Qing and Pan, He-Ting and Qiao, Xin and Xu, Jing-Yuan
Dalton Transactions, ISSN 1477-9226, 2016, Volume 45, Issue 22, pp. 9073 - 9087
Four novel mononuclear Schiff base copper(II) complexes, namely, [Cu(L)(OAc)] center dot H2O (1), [Cu(HL)(C2O4) (EtOH)] center dot EtOH (2), [Cu(L)(Bza)] (3)... 
ANTIVIRAL AGENTS | CANCER CELLS | ZN(II) COMPLEXES | CRYSTAL-STRUCTURE | SERUM-ALBUMIN | ANTICANCER AGENTS | DONOR LIGANDS | DOUBLE HELIX | IN-VITRO CYTOTOXICITY | APOPTOSIS INDUCTION | CHEMISTRY, INORGANIC & NUCLEAR | Antineoplastic Agents - chemical synthesis | Humans | Molecular Conformation | Crystallography, X-Ray | Schiff Bases - pharmacology | Salicylic Acid - chemistry | Salicylic Acid - pharmacology | Copper - chemistry | Spectrophotometry, Infrared | Protein Binding - drug effects | Schiff Bases - chemical synthesis | Antineoplastic Agents - pharmacology | Intercalating Agents - chemical synthesis | Serum Albumin, Human - chemistry | DNA - drug effects | Benzoic Acid - pharmacology | Copper - pharmacology | Spectrometry, Fluorescence | Intercalating Agents - pharmacology | Antineoplastic Agents - chemistry | Intercalating Agents - chemistry | Hep G2 Cells | DNA - chemistry | Hydrogen Bonding | Benzoic Acid - chemistry | Cell Proliferation - drug effects | HeLa Cells | DNA Cleavage | Index Medicus | Binding | Schiff bases | Salicylic acid | Deoxyribonucleic acid | Fluorescence | Ligands | Assaying | Cancer
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6. 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
Copper (II) complexes synthesized from the products of condensation of S-methyl- and S-benzyldithiocarbazate with 2,5-hexanedione (SMHDH2 and SBHDH2... 
Schiff base | Dithiocarbazate | NNSS ligand | MCF-7 | Gram-positive | Gram-negative | Macroacyclic ligand | Tetradendate ligand | Bioactivity | MDA-MB-231 | Copper complexes | CHEMISTRY, MEDICINAL | TRANSITION-METAL-COMPLEXES | CRYSTAL-STRUCTURE | X-RAY-STRUCTURE | COPPER(II) COMPLEXES | QUADRIDENTATE SNNS LIGANDS | GRAM-NEGATIVE BACTERIA | EFFLUX PUMP | ANTIBACTERIAL ACTIVITY | BIFUNCTIONAL CHELATORS | DIMETHYL-SULFOXIDE | 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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7. 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 and Medicinal Chemistry, ISSN 0968-0896, 07/2013, Volume 21, Issue 13, pp. 3808 - 3820
Pyrazolealdehydes (4a-d), Knoevenagel's condensates (5a-d) and Schiff's bases (6a-d) of curcumin-I were synthesized, purified and characterized. Hemolysis... 
Docking studies | Anticancer agents | Curcumin-I derivatives | DNA binding and hemolysis and cell line profiles | DNA-BINDING | CHEMISTRY, MEDICINAL | PYRAZOLE DERIVATIVES | ANALOGS | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | DRUG DISCOVERY | COMPLEXES | CHEMISTRY, ORGANIC | SPECTRAL PROPERTIES | LIGANDS | PHOTOCLEAVAGE | BIOLOGICAL EVALUATION | 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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8. Full Text Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies
by Rahim, Fazal and Malik, Fazal and Ullah, Hayat and Wadood, Abdul and Khan, Fahad and Khan, Khalid Mohammed and Javid, Muhammad Tariq and Taha, Muhammad and Rehman, Wajid and Ur Rehman, Ashfaq
Bioorganic Chemistry, ISSN 0045-2068, 06/2015, Volume 60, pp. 42 - 48
Isatin base Schiff bases ( ) were synthesized, characterized by H NMR and EI/MS and evaluated for -glucosidase inhibitory potential. Out of these twenty ( )... 
Schiff bases | α-Glucosidase inhibition | Synthesis | Isatin | Molecular docking | VIRUS | ANALOGS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | SUGARS | SKELETON | REPLICATION | SUBSTRATE | BIOLOGICAL EVALUATION | alpha-Glucosidase inhibition | AGENTS | DERIVATIVES | Isatin - analogs & derivatives | Humans | Schiff Bases - chemistry | Isatin - pharmacology | Saccharomyces cerevisiae - enzymology | Molecular Docking Simulation | Structure-Activity Relationship | Glycoside Hydrolase Inhibitors - chemistry | Glycoside Hydrolase Inhibitors - pharmacology | Schiff Bases - pharmacology | alpha-Glucosidases - metabolism | Index Medicus
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9. 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
The complexes of Fe(II), Cd(II) and Zn(II) with Schiff base derived from 2-amino-3-hydroxypyridine and 3-methoxysalicylaldehyde have been prepared. Melting... 
Nanoparticles | Metal oxides | Antimicrobial activity | DNA interaction | Cytotoxic activity | PHARMACOLOGICALLY ACTIVE AGENTS | CU(II) | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANTIBACTERIAL | CHEMISTRY, ORGANIC | STRUCTURAL-CHARACTERIZATION | CO(II) | NI(II) | LIGANDS | AMINO-ACID COMPLEXES | HYDROXIDE ION ATTACK | BINDING | 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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10. 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, ISSN 1420-3049, 09/2017, Volume 22, Issue 9, p. 1573
The resistance among microbes has brought an urgent need for new drugs. Thus, we synthesized a series of Schiff bases derived from the sulfa drug sulfadiazine... 
Antifungal activity | Schiff bases | Sulfadiazine | Sulfonamides | Antibacterial activity | Cytotoxicity | Antimycobacterial activity | antibacterial activity | MYCOBACTERIUM-TUBERCULOSIS | ACID | antimycobacterial activity | COMPLEXES | ANTIBACTERIAL | CHEMISTRY, ORGANIC | sulfonamides | IN-VITRO SUSCEPTIBILITY | antifungal activity | sulfadiazine | INHIBITION | TRIMETHOPRIM | DERIVATIVES | cytotoxicity | 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
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11. Full Text Synthesis, in vitro and in vivo antitumor activity of symmetrical bis-Schiff base derivatives of isatin
by Liang, Chengyuan and Xia, Juan and Lei, Dong and Li, Xiang and Yao, Qizheng and Gao, Jing
European Journal of Medicinal Chemistry, ISSN 0223-5234, 03/2014, Volume 74, pp. 742 - 750
Eighteen symmetrical bis-Schiff base derivatives of isatin were synthesized by condensation of the natural or synthetic isatins with hydrazine and were... 
Schiff base | Cytotoxicity | Isatin | Mitosis interference | Antitumor | Apoptosis | CHEMISTRY, MEDICINAL | COMPLEXES | ANTIBACTERIAL | KINASE INHIBITORS | CANCER | PROTEIN-KINASES | ANTIFUNGAL | INDIRUBIN | MANNICH-BASES | Magnetic Resonance Spectroscopy | Humans | Isatin - pharmacology | Isatin - chemistry | Antineoplastic Agents - chemistry | Schiff Bases - pharmacology | Xenograft Model Antitumor Assays | Animals | Mass Spectrometry | Schiff Bases - chemistry | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Mice | In Vitro Techniques | Neoplasms - pathology | Drugstores | Schiff bases | Index Medicus
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12. Full Text Synthesis and antimicrobial activities of Schiff bases derived from 5-chloro-salicylaldehyde
by Shi, Lei and Ge, Hui-Ming and Tan, Ren-Xiang and Tan, Shu-Hua and Li, Huan-Qiu and Song, Yong-Chun and Zhu, Hai-Liang
European Journal of Medicinal Chemistry, ISSN 0223-5234, 2007, Volume 42, Issue 4, pp. 558 - 564
A series of Schiff bases (compounds – ) were synthesized by reacting 5-chloro-salicylaldehyde and primary amines, 15 (compounds – , , , , – , , and ) of which... 
Schiff base | Antifungal activity | Antibacterial activity | Aldehyde | Primary amine | Structure–activity relationship | Structure-activity relationship | antibacterial activity | CHEMISTRY, MEDICINAL | ANTIBACTERIAL | aldehyde | ISATIN DERIVATIVES | ANTITUMOR-ACTIVITY | antifungal activity | primary amine | SALICYLALDEHYDE | ANTIFUNGAL | structure-activity relationship | MANNICH-BASES | Antifungal Agents - pharmacology | Fungi - drug effects | Bacteria - drug effects | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Schiff Bases - pharmacology | Anti-Bacterial Agents - chemical synthesis | Microbial Sensitivity Tests | Anti-Bacterial Agents - chemistry | Schiff Bases - chemistry | Schiff Bases - chemical synthesis | Anti-Bacterial Agents - pharmacology | Molecular Structure | Aldehydes - chemistry | Index Medicus
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13. Full Text Synthesis and antioxidant activity of thymol and carvacrol based Schiff bases
by Beena and Kumar, Deepak and Rawat, Diwan S
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 02/2013, Volume 23, Issue 3, pp. 641 - 645
Thymol and carvacrol are well known antioxidants found in the extract of the plants of thyme species. The Schiff bases of 2- -propyl-5-methyl-phenol (thymol/... 
Schiff base | Carvacrol | DPPH | Antioxidant | Thymol | ABTS | CHEMISTRY, MEDICINAL | ESSENTIAL OIL | CHEMISTRY, ORGANIC | IN-VITRO | ANTIBACTERIAL ACTIVITY | ANTIMALARIAL ACTIVITY | EXTRACTS | DERIVATIVES | ANTIMICROBIAL ACTIVITY | Antioxidants - chemistry | Schiff Bases - chemistry | Thymus Plant - chemistry | Ascorbic Acid - pharmacology | Inhibitory Concentration 50 | Monoterpenes - chemistry | Schiff Bases - chemical synthesis | Antioxidants - chemical synthesis | Antioxidants - pharmacology | Thymol - chemistry | Schiff Bases - pharmacology | Antioxidants | Phenols | Schiff bases | Index Medicus | thymol | Ascorbic acid | Plant extracts
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14. Full Text Synthesis, antibacterial, antifungal and antiviral activity evaluation of some new bis-Schiff bases of isatin and their derivatives
by Jarrahpour, Aliasghar and Khalili, Dariush and De Clercq, Erik and Salmi, Chanaz and Brunel, Jean Michel
Molecules, ISSN 1420-3049, 08/2007, Volume 12, Issue 8, pp. 1720 - 1730
Twelve new bis-Schiff bases of isatin, benzylisatin and 5-fluoroisatin 3a-31 were prepared by condensation of isatin, benzylisatin and 5-fluoroisatin with... 
Bis-Schiff base | Antiviral | Antifungal | Antibacterial | Isatin | ANTI-HIV ACTIVITIES | COPPER(II) COMPLEXES | antifungal | bis-Schiff base | VIRUS | N-MANNICH BASES | BIOCHEMISTRY & MOLECULAR BIOLOGY | antiviral | antibacterial | isatin | CHEMISTRY, MULTIDISCIPLINARY | ANTIMICROBIAL ACTIVITY | Anti-Infective Agents - pharmacology | Humans | Bacteria - drug effects | Isatin - pharmacology | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Isatin - chemistry | Schiff Bases - pharmacology | Isatin - analogs & derivatives | Antiviral Agents - chemistry | Anti-Bacterial Agents - chemistry | Anti-Infective Agents - chemistry | Schiff Bases - chemical synthesis | Antifungal Agents - pharmacology | Cell Line | Antiviral Agents - pharmacology | Fungi - drug effects | Viruses - drug effects | Anti-Infective Agents - chemical synthesis | Anti-Bacterial Agents - chemical synthesis | Animals | Isatin - chemical synthesis | Schiff Bases - chemistry | Antiviral Agents - chemical synthesis | Anti-Bacterial Agents - pharmacology | Index Medicus
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15. Full Text Synthesis and antitumor activities of novel hybrid molecules containing 1,3,4-oxadiazole and 1,3,4-thiadiazole bearing Schiff base moiety
by Zhang, Kai and Wang, Peng and Xuan, Li-Na and Fu, Xiao-Yun and Jing, Fen and Li, Sha and Liu, Yu-Ming and Chen, Bao-Quan
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 11/2014, Volume 24, Issue 22, pp. 5154 - 5156
A series of novel hybrid molecules containing 1,3,4-oxadiazole and 1,3,4-thiadiazole bearing Schiff base moiety were synthesized. The newly synthesized... 
Schiff base | 1,3,4-Thiadiazole | Antitumor agents | 1,3,4-Oxadiazole | 1 3 4-Oxadiazole | 1 3 4-Thiadiazole | ANTIOXIDANT ACTIVITY | DESIGN | CHEMISTRY, MEDICINAL | ANGIOGENESIS | SULFONE DERIVATIVES | CHEMISTRY, ORGANIC | THIADIAZOLE DERIVATIVES | 1,2,4-TRIAZOLE | POTENT | INHIBITION | ANTICANCER | BIOLOGICAL EVALUATION | Drug Screening Assays, Antitumor - methods | Oxadiazoles - chemical synthesis | Antineoplastic Agents - chemical synthesis | Humans | Cell Proliferation - physiology | Schiff Bases - pharmacology | Thiadiazoles - chemical synthesis | MCF-7 Cells | Oxadiazoles - pharmacology | Schiff Bases - chemical synthesis | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Thiadiazoles - pharmacology | Schiff bases | Index Medicus
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