Compounds > ephedrine
Page last updated: 2024-08-21

ephedrine and nortriptyline

ephedrine has been researched along with nortriptyline in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19903 (37.50)18.7374
1990's0 (0.00)18.2507
2000's1 (12.50)29.6817
2010's4 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A1
Choi, SS; Contrera, JF; Hastings, KL; Kruhlak, NL; Sancilio, LF; Weaver, JL; Willard, JM1
Gozalbes, R; Pineda-Lucena, A1
Bellman, K; Knegtel, RM; Settimo, L1
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K1
Agren, A; Brodin, A1
Brodin, A1
Brodin, A; Nilsson, MI1

Reviews

1 review(s) available for ephedrine and nortriptyline

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

7 other study(ies) available for ephedrine and nortriptyline

ArticleYear
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
Development of a phospholipidosis database and predictive quantitative structure-activity relationship (QSAR) models.
    Toxicology mechanisms and methods, 2008, Volume: 18, Issue:2-3

    Topics:

2008
QSAR-based solubility model for drug-like compounds.
    Bioorganic & medicinal chemistry, 2010, Oct-01, Volume: 18, Issue:19

    Topics: Databases, Factual; Models, Molecular; Pharmaceutical Preparations; Quantitative Structure-Activity Relationship; Solubility; Water

2010
Comparison of the accuracy of experimental and predicted pKa values of basic and acidic compounds.
    Pharmaceutical research, 2014, Volume: 31, Issue:4

    Topics: Chemistry, Pharmaceutical; Forecasting; Hydrogen-Ion Concentration; Pharmaceutical Preparations; Random Allocation

2014
Rates of transfer of organic protolytic solutes between an aqueous and an organic phase. I. A study of the transfer dependency of pH and the absolute rate of resolvation.
    Acta pharmaceutica Suecica, 1971, Volume: 8, Issue:6

    Topics: Alprenolol; Cyclohexanes; Ephedrine; Hydrogen-Ion Concentration; Kinetics; Nortriptyline; Phenothiazines; Phenylbutazone; Procaine; Promazine; Solubility; Spectrophotometry; Water

1971
Rates of transfer of organic protolytic solutes between an aqueous and an organic phase. 3. Mass transfer between water and some polar organic liquids.
    Acta pharmaceutica Suecica, 1974, Volume: 11, Issue:2

    Topics: Acetates; Alprenolol; Ephedrine; Fatty Alcohols; Hexobarbital; Hydrogen-Ion Concentration; Ketones; Methods; Nortriptyline; Solubility; Solvents; Spectrophotometry, Ultraviolet; Water

1974
Rates of transfer of organic protolytic solutes between an aqueous and an organic phase. II. Rates of mass transfer between water and different organic liquids.
    Acta pharmaceutica Suecica, 1973, Volume: 10, Issue:3

    Topics: Alprenolol; Benzene; Chloroform; Cyclohexanes; Ephedrine; Hydrogen-Ion Concentration; Methods; Nortriptyline; Pentobarbital; Phenobarbital; Phenylbutazone; Promazine; Solubility; Solvents; Water

1973