Page last updated: 2024-08-23

danazol and griseofulvin

danazol has been researched along with griseofulvin in 15 studies

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's6 (40.00)29.6817
2010's9 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Benz, RD; Contrera, JF; Kruhlak, NL; Matthews, EJ; Weaver, JL1
Du-Cuny, L; Mash, EA; Meuillet, EJ; Moses, S; Powis, G; Song, Z; Zhang, S1
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A1
Fisk, L; Greene, N; Naven, RT; Note, RR; Patel, ML; Pelletier, DJ1
Ekins, S; Williams, AJ; Xu, JJ1
Annand, R; Gozalbes, R; Jacewicz, M; Pineda-Lucena, A; Tsaioun, K1
Chen, M; Fang, H; Liu, Z; Shi, Q; Tong, W; Vijay, V1
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K1
Boyd, BJ; Charman, WN; Porter, CJ1
Boyd, BJ; Charman, WN; Kaukonen, AM; Porter, CJ2
Aso, Y; Furumoto, K; Hayashi, Y; Shiraki, K; Takano, R; Takata, N; Yamashita, S1
Bogner, RH; Murdande, SB; Pikal, MJ; Shanker, RM1
Decker, H; Hellmann, N; Johnson, R; Khoshakhlagh, P; Langguth, P; Nawroth, T; Schmueser, L; Szekely, NK1
Chen, X; Kalantar, TH; Kuo, TC; Ladika, M; Stoneburner, K1

Reviews

1 review(s) available for danazol and griseofulvin

ArticleYear
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
    Drug discovery today, 2016, Volume: 21, Issue:4

    Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk

2016

Other Studies

14 other study(ies) available for danazol and griseofulvin

ArticleYear
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
    Current drug discovery technologies, 2004, Volume: 1, Issue:4

    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
Computational modeling of novel inhibitors targeting the Akt pleckstrin homology domain.
    Bioorganic & medicinal chemistry, 2009, Oct-01, Volume: 17, Issue:19

    Topics: Antineoplastic Agents; Blood Proteins; Caco-2 Cells; Cell Membrane Permeability; Computer Simulation; Drug Discovery; Drug Screening Assays, Antitumor; Humans; Models, Molecular; Phosphoproteins; Protein Binding; Protein Kinase Inhibitors; Protein Structure, Tertiary; Proto-Oncogene Proteins c-akt; Quantitative Structure-Activity Relationship

2009
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
    Chemical research in toxicology, 2010, Volume: 23, Issue:1

    Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship

2010
Developing structure-activity relationships for the prediction of hepatotoxicity.
    Chemical research in toxicology, 2010, Jul-19, Volume: 23, Issue:7

    Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Humans; Structure-Activity Relationship; Tetracyclines; Thiophenes

2010
A predictive ligand-based Bayesian model for human drug-induced liver injury.
    Drug metabolism and disposition: the biological fate of chemicals, 2010, Volume: 38, Issue:12

    Topics: Bayes Theorem; Chemical and Drug Induced Liver Injury; Humans; Ligands

2010
QSAR-based permeability model for drug-like compounds.
    Bioorganic & medicinal chemistry, 2011, Apr-15, Volume: 19, Issue:8

    Topics: Caco-2 Cells; Cell Membrane Permeability; Drug Discovery; Humans; Pharmaceutical Preparations; Pharmacokinetics; Quantitative Structure-Activity Relationship

2011
FDA-approved drug labeling for the study of drug-induced liver injury.
    Drug discovery today, 2011, Volume: 16, Issue:15-16

    Topics: Animals; Benchmarking; Biomarkers, Pharmacological; Chemical and Drug Induced Liver Injury; Drug Design; Drug Labeling; Drug-Related Side Effects and Adverse Reactions; Humans; Pharmaceutical Preparations; Reproducibility of Results; United States; United States Food and Drug Administration

2011
Using the polymer partitioning method to probe the thermodynamic activity of poorly water-soluble drugs solubilized in model lipid digestion products.
    Journal of pharmaceutical sciences, 2003, Volume: 92, Issue:6

    Topics: Bile Acids and Salts; Chemistry, Pharmaceutical; Chromatography, High Pressure Liquid; Danazol; Diazepam; Fatty Acids; Griseofulvin; Lipids; Micelles; Models, Biological; Pharmaceutical Preparations; Phosphatidylcholines; Polymers; Solubility; Thermodynamics; Water

2003
Drug solubilization behavior during in vitro digestion of simple triglyceride lipid solution formulations.
    Pharmaceutical research, 2004, Volume: 21, Issue:2

    Topics: Cinnarizine; Danazol; Diazepam; Digestion; Griseofulvin; Models, Biological; Pharmaceutical Preparations; Pharmaceutical Solutions; Phenanthrenes; Solubility; Triglycerides; Water

2004
Drug solubilization behavior during in vitro digestion of suspension formulations of poorly water-soluble drugs in triglyceride lipids.
    Pharmaceutical research, 2004, Volume: 21, Issue:2

    Topics: Cinnarizine; Danazol; Diazepam; Digestion; Griseofulvin; Pharmaceutical Preparations; Phenanthrenes; Solubility; Suspensions; Triglycerides; Water

2004
Rate-limiting steps of oral absorption for poorly water-soluble drugs in dogs; prediction from a miniscale dissolution test and a physiologically-based computer simulation.
    Pharmaceutical research, 2008, Volume: 25, Issue:10

    Topics: Administration, Oral; Animals; Aprepitant; Computer Simulation; Danazol; Dogs; Griseofulvin; Intestinal Absorption; Models, Biological; Morpholines; Nonlinear Dynamics; Particle Size; Permeability; Reproducibility of Results; Solubility; Technology, Pharmaceutical; Water

2008
Solubility advantage of amorphous pharmaceuticals, part 3: Is maximum solubility advantage experimentally attainable and sustainable?
    Journal of pharmaceutical sciences, 2011, Volume: 100, Issue:10

    Topics: Chemistry, Pharmaceutical; Colloids; Crystallization; Danazol; Griseofulvin; Hypromellose Derivatives; Iopanoic Acid; Kinetics; Light; Methylcellulose; Pharmaceutical Preparations; Povidone; Scattering, Radiation; Solubility; Technology, Pharmaceutical; Ultracentrifugation

2011
Fasted-state simulated intestinal fluid "FaSSIF-C", a cholesterol containing intestinal model medium for in vitro drug delivery development.
    Journal of pharmaceutical sciences, 2015, Volume: 104, Issue:7

    Topics: Body Fluids; Caco-2 Cells; Carbamazepine; Cholesterol; Danazol; Drug Delivery Systems; Fasting; Female; Fenofibrate; Griseofulvin; Humans; Intestinal Absorption; Intestinal Mucosa; Male; Models, Theoretical; Particle Size; Solubility

2015
High-Throughput Raman Spectroscopy Screening of Excipients for the Stabilization of Amorphous Drugs.
    Applied spectroscopy, 2015, Volume: 69, Issue:11

    Topics: Chemistry, Pharmaceutical; Danazol; Drug Stability; Excipients; Griseofulvin; Ketoprofen; Probucol; Spectrum Analysis, Raman

2015