maprotiline and lofepramine

maprotiline has been researched along with lofepramine in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's2 (28.57)18.2507
2000's2 (28.57)29.6817
2010's2 (28.57)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Topliss, JG; Yoshida, F1
Bleich, S; Gulbins, E; Kornhuber, J; Reichel, M; Terfloth, L; Tripal, P; Wiltfang, J1
García-Mera, X; González-Díaz, H; Prado-Prado, FJ1
Afshari, CA; Chen, Y; Dunn, RT; Hamadeh, HK; Kalanzi, J; Kalyanaraman, N; Morgan, RE; van Staden, CJ1
Finke, G; Wegener, G1
Graf, U; van Schaik, N1
Kodama, Y; Nomura, S; Shimizu, K; Watanabe, M1

Trials

1 trial(s) available for maprotiline and lofepramine

ArticleYear
[Comparison of the therapeutic effects of lofepramine and maprotiline in depression].
    MMW, Munchener medizinische Wochenschrift, 1982, Mar-26, Volume: 124, Issue:12

    Topics: Anthracenes; Clinical Trials as Topic; Depressive Disorder; Dibenzazepines; Humans; Lofepramine; Maprotiline

1982

Other Studies

6 other study(ies) available for maprotiline and lofepramine

ArticleYear
QSAR model for drug human oral bioavailability.
    Journal of medicinal chemistry, 2000, Jun-29, Volume: 43, Issue:13

    Topics: Administration, Oral; Biological Availability; Humans; Models, Biological; Models, Molecular; Pharmaceutical Preparations; Pharmacokinetics; Structure-Activity Relationship

2000
Identification of new functional inhibitors of acid sphingomyelinase using a structure-property-activity relation model.
    Journal of medicinal chemistry, 2008, Jan-24, Volume: 51, Issue:2

    Topics: Algorithms; Animals; Cell Line; Cell Line, Tumor; Chemical Phenomena; Chemistry, Physical; Enzyme Inhibitors; Humans; Hydrogen-Ion Concentration; Molecular Conformation; Quantitative Structure-Activity Relationship; Rats; Sphingomyelin Phosphodiesterase

2008
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
    Bioorganic & medicinal chemistry, 2010, Mar-15, Volume: 18, Issue:6

    Topics: Antiparasitic Agents; Molecular Structure; Neural Networks, Computer; Parasitic Diseases; Quantitative Structure-Activity Relationship; Species Specificity; Thermodynamics

2010
A multifactorial approach to hepatobiliary transporter assessment enables improved therapeutic compound development.
    Toxicological sciences : an official journal of the Society of Toxicology, 2013, Volume: 136, Issue:1

    Topics: Animals; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters; Biological Transport; Chemical and Drug Induced Liver Injury; Cluster Analysis; Drug-Related Side Effects and Adverse Reactions; Humans; Liver; Male; Multidrug Resistance-Associated Proteins; Pharmacokinetics; Rats; Rats, Sprague-Dawley; Recombinant Proteins; Risk Assessment; Risk Factors; Toxicity Tests

2013
Structure-activity relationships of tricyclic antidepressants and related compounds in the wing somatic mutation and recombination test of Drosophila melanogaster.
    Mutation research, 1993, Volume: 286, Issue:2

    Topics: Animals; Antidepressive Agents, Tricyclic; Chlorpromazine; CHO Cells; Clomipramine; Cricetinae; Drosophila melanogaster; Female; Lofepramine; Male; Maprotiline; Mianserin; Mutagenicity Tests; Mutagens; Recombination, Genetic; Structure-Activity Relationship

1993
[A case of allergic cross reaction between tricyclic antidepressants and maprotiline].
    Nihon shinkei seishin yakurigaku zasshi = Japanese journal of psychopharmacology, 1998, Volume: 18, Issue:4

    Topics: Aged; Amoxapine; Antidepressive Agents, Second-Generation; Antidepressive Agents, Tricyclic; Cross Reactions; Depression; Drug Eruptions; Female; Humans; Lofepramine; Maprotiline

1998