barbital and cyclobarbital

barbital has been researched along with cyclobarbital in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19903 (42.86)18.7374
1990's0 (0.00)18.2507
2000's3 (42.86)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baker, JK; Borne, RF; Rauls, DO1
Brent, DA; Henry, DW; Minick, DJ; Sabatka, JJ1
Baert, B; Beetens, J; Bodé, S; De Spiegeleer, B; Deconinck, E; Lambert, J; Slegers, G; Slodicka, M; Stoppie, P; Van Gele, M; Vander Heyden, Y1
Abellán Guillén, A; Cordeiro, MN; Garrido Escudero, A; Morales Helguera, A; Pérez-Garrido, A1
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
POE, CF; SNODGRASS, AS; WITT, NF1

Other Studies

7 other study(ies) available for barbital and cyclobarbital

ArticleYear
Correlation of biological activity and high-pressure liquid chromatographic retention index for a series of propranolol, barbiturate, and anthranilic acid analogues.
    Journal of medicinal chemistry, 1979, Volume: 22, Issue:11

    Topics: Animals; Anti-Arrhythmia Agents; Anti-Inflammatory Agents; Barbiturates; Cell Division; Chromatography, High Pressure Liquid; In Vitro Techniques; Myocardial Contraction; ortho-Aminobenzoates; Propranolol; Rabbits; Rats; Sleep; Solubility

1979
A simplified high-pressure liquid chromatography method for determining lipophilicity for structure-activity relationships.
    Journal of medicinal chemistry, 1983, Volume: 26, Issue:7

    Topics: Animals; Bacteria; Barbiturates; Biological Assay; Cell Division; Chromatography, High Pressure Liquid; Female; Ovum; Oxygen Consumption; Rabbits; Solubility; Structure-Activity Relationship; Sulfanilamides

1983
Transdermal penetration behaviour of drugs: CART-clustering, QSPR and selection of model compounds.
    Bioorganic & medicinal chemistry, 2007, Nov-15, Volume: 15, Issue:22

    Topics: Anti-Inflammatory Agents; Cell Membrane Permeability; Cluster Analysis; Drug Evaluation, Preclinical; Humans; Models, Biological; Predictive Value of Tests; Quantitative Structure-Activity Relationship; Regression Analysis; Skin; Skin Absorption

2007
Convenient QSAR model for predicting the complexation of structurally diverse compounds with beta-cyclodextrins.
    Bioorganic & medicinal chemistry, 2009, Jan-15, Volume: 17, Issue:2

    Topics: beta-Cyclodextrins; Hydrophobic and Hydrophilic Interactions; Organic Chemicals; 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
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
Derivatives of evipal, alurate, and phanodorn.
    Mikrochemie, 1949, Volume: 34, Issue:3

    Topics: Barbital; Barbiturates; Hexobarbital

1949