glyburide has been researched along with amphotericin b in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (20.00) | 18.2507 |
| 2000's | 4 (40.00) | 29.6817 |
| 2010's | 3 (30.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Benz, RD; Contrera, JF; Kruhlak, NL; Matthews, EJ; Weaver, JL | 1 |
| González-Díaz, H; Orallo, F; Quezada, E; Santana, L; Uriarte, E; Viña, D; Yáñez, M | 1 |
| Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A | 1 |
| Chang, G; El-Kattan, A; Miller, HR; Obach, RS; Rotter, C; Steyn, SJ; Troutman, MD; Varma, MV | 1 |
| Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K | 1 |
| Delabio, LC; Dutra, JP; Hembecker, M; Kita, DH; Moure, VR; Pereira, GDS; Scheiffer, G; Valdameri, G; Zattoni, IF | 1 |
| Dart, C; Standen, NB | 1 |
| Deachapunya, C; O'Grady, SM | 1 |
| Gomes, P; Soares-Da-Silva, P | 1 |
| Díaz, E; Machuca, C; Padrón-Nieves, M; Ponte Sucre, A; Romero, A | 1 |
2 review(s) available for glyburide and amphotericin b
| 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 |
Targeting breast cancer resistance protein (BCRP/ABCG2): Functional inhibitors and expression modulators.
Topics: Antineoplastic Agents; ATP Binding Cassette Transporter, Subfamily G, Member 2; Breast Neoplasms; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Female; Humans; Neoplasm Proteins; Neoplastic Stem Cells | 2022 |
8 other study(ies) available for glyburide and amphotericin b
| Article | Year |
|---|---|
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
Topics: Adverse Drug Reaction Reporting Systems; Artificial Intelligence; Computers; Databases, Factual; Drug Prescriptions; Drug-Related Side Effects and Adverse Reactions; Endpoint Determination; Models, Molecular; Quantitative Structure-Activity Relationship; Software; United States; United States Food and Drug Administration | 2004 |
Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.
Topics: Computational Biology; Drug Design; Humans; Isoenzymes; Molecular Structure; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Quantitative Structure-Activity Relationship | 2008 |
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship | 2010 |
Physicochemical space for optimum oral bioavailability: contribution of human intestinal absorption and first-pass elimination.
Topics: Administration, Oral; Biological Availability; Humans; Intestinal Absorption; Pharmaceutical Preparations | 2010 |
Activation of ATP-dependent K+ channels by hypoxia in smooth muscle cells isolated from the pig coronary artery.
Topics: Adenosine Triphosphate; Amphotericin B; Animals; Cell Hypoxia; Cell Separation; Charybdotoxin; Coronary Vessels; Glyburide; Membrane Potentials; Muscle, Smooth, Vascular; Patch-Clamp Techniques; Potassium; Potassium Channels; Scorpion Venoms; Swine; Vasodilation | 1995 |
Regulation of chloride secretion across porcine endometrial epithelial cells by prostaglandin E2.
Topics: Amino Acid Sequence; Amphotericin B; Animals; Anions; Antibodies; Bumetanide; Carrier Proteins; Cell Membrane; Cell Membrane Permeability; Cells, Cultured; Chloride Channels; Chlorides; Cyclic AMP; Cystic Fibrosis Transmembrane Conductance Regulator; Dinoprostone; Endometrium; Epithelial Cells; Female; Furosemide; Glyburide; Kinetics; Membrane Potentials; Models, Biological; Nitrobenzoates; Peptide Fragments; Sodium-Potassium-Chloride Symporters; Swine; Thionucleotides; Time Factors | 1998 |
D2-like receptor-mediated inhibition of Na+-K+-ATPase activity is dependent on the opening of K+ channels.
Topics: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Amphotericin B; Animals; Antifungal Agents; Cardiotonic Agents; Cell Line; Dopamine; Dopamine Agonists; Dopamine Antagonists; Female; Glyburide; GTP-Binding Protein alpha Subunits, Gi-Go; Hypoglycemic Agents; Ion Channel Gating; Kidney; Opossums; Pertussis Toxin; Pinacidil; Potassium Channels; Quinolines; Receptors, Dopamine D2; Sodium; Sodium-Potassium-Exchanging ATPase; Sulpiride; Vasodilator Agents; Virulence Factors, Bordetella | 2002 |
Glibenclamide modulates glucantime activity and disposition in Leishmania major.
Topics: Amphotericin B; Animals; Antiprotozoal Agents; ATP-Binding Cassette Transporters; Cells, Cultured; Drug Synergism; Glyburide; Leishmania major; Macrophages, Peritoneal; Meglumine; Meglumine Antimoniate; Mice; Mice, Inbred BALB C; Microscopy, Electron; Organometallic Compounds | 2009 |