amikacin has been researched along with nystatin a1 in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 6 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chaturvedi, AK; Shukla, PK; Singh, RV; Tandon, VK; Yadav, DB | 1 |
| Andelković, K; Godevac, D; Milenković, M; Milosavljević, S; Miodragović, D; Miodragović, Z; Mitić, D | 1 |
| Maurya, HK; Mishra, NN; Shukla, PK; Tandon, VK | 2 |
| Ali, M; Hussain, R; Jones, PG; Rashid, N; Saeed, S | 1 |
| Kumar, R; Maurya, HK; Shukla, PK; Tandon, VK; Verma, MK | 1 |
| Kljajić, Z; Matić, I; Novaković, I; Šegan, D; Sladić, D; Stanojković, T; Vilipić, J | 1 |
| Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K | 1 |
| Banković, J; Dinić, J; Jeremić, M; Novaković, I; Pešić, M; Šegan, D; Sladić, D | 1 |
1 review(s) available for amikacin and nystatin a1
| Article | Year |
|---|---|
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk | 2016 |
8 other study(ies) available for amikacin and nystatin a1
| Article | Year |
|---|---|
Synthesis and biological evaluation of novel (L)-alpha-amino acid methyl ester, heteroalkyl, and aryl substituted 1,4-naphthoquinone derivatives as antifungal and antibacterial agents.
Topics: Amino Acids; Anti-Bacterial Agents; Antifungal Agents; Bacteria; Fungi; Methyl Ethers; Molecular Structure; Naphthoquinones | 2005 |
Synthesis, characterization and antimicrobial activity of Co(II), Zn(II) and Cd(II) complexes with N-benzyloxycarbonyl-S-phenylalanine.
Topics: Absorption; Anti-Infective Agents; Bacteria; Cadmium; Candida; Cobalt; Electrons; Magnetic Resonance Spectroscopy; Metals, Heavy; Organometallic Compounds; Phenylalanine; Spectrophotometry, Infrared; Zinc | 2009 |
Design, synthesis and biological evaluation of novel nitrogen and sulfur containing hetero-1,4-naphthoquinones as potent antifungal and antibacterial agents.
Topics: Anti-Bacterial Agents; Antifungal Agents; Bacteria; Drug Design; Fungi; Microbial Sensitivity Tests; Naphthoquinones; Nitrogen; Sulfur | 2009 |
Synthesis, characterization and biological evaluation of some thiourea derivatives bearing benzothiazole moiety as potential antimicrobial and anticancer agents.
Topics: Anti-Infective Agents; Antineoplastic Agents; Benzothiazoles; Cell Line, Tumor; Humans; Microbial Sensitivity Tests; Structure-Activity Relationship; Thiourea | 2010 |
'On water' assisted synthesis and biological evaluation of nitrogen and sulfur containing hetero-1,4-naphthoquinones as potent antifungal and antibacterial agents.
Topics: Anti-Bacterial Agents; Antifungal Agents; Bacteria; Fungi; Green Chemistry Technology; Microbial Sensitivity Tests; Naphthoquinones; Nitrogen; Sulfur; Water | 2010 |
Micelles catalyzed chemoselective synthesis 'in water' and biological evaluation of oxygen containing hetero-1,4-naphthoquinones as potential antifungal agents.
Topics: Antifungal Agents; Candida; Catalysis; Drug Evaluation, Preclinical; Micelles; Microbial Sensitivity Tests; Naphthoquinones; Oxygen; Sporothrix; Trichophyton; Water | 2011 |
Synthesis and biological activity of amino acid derivatives of avarone and its model compound.
Topics: Amino Acids; Anti-Bacterial Agents; Antifungal Agents; Apoptosis; Cell Cycle Checkpoints; Cell Line, Tumor; Cyclohexenes; Drug Screening Assays, Antitumor; Fungi; Gram-Negative Bacteria; Gram-Positive Bacteria; HeLa Cells; Humans; K562 Cells; Microbial Sensitivity Tests; Quinones; Sesquiterpenes; Structure-Activity Relationship | 2015 |
Simple avarone mimetics as selective agents against multidrug resistant cancer cells.
Topics: Anti-Bacterial Agents; Antifungal Agents; Antineoplastic Agents; Apoptosis; Benzoquinones; Cell Line, Tumor; Cyclohexenes; Drug Design; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Humans; Hydroquinones; Membrane Potential, Mitochondrial; Sesquiterpenes | 2016 |