barbital has been researched along with cyclobarbital in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (42.86) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 1 (14.29) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Baker, JK; Borne, RF; Rauls, DO | 1 |
Brent, DA; Henry, DW; Minick, DJ; Sabatka, JJ | 1 |
Baert, B; Beetens, J; Bodé, S; De Spiegeleer, B; Deconinck, E; Lambert, J; Slegers, G; Slodicka, M; Stoppie, P; Van Gele, M; Vander Heyden, Y | 1 |
Abellán Guillén, A; Cordeiro, MN; Garrido Escudero, A; Morales Helguera, A; Pérez-Garrido, A | 1 |
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A | 1 |
Choi, SS; Contrera, JF; Hastings, KL; Kruhlak, NL; Sancilio, LF; Weaver, JL; Willard, JM | 1 |
POE, CF; SNODGRASS, AS; WITT, NF | 1 |
7 other study(ies) available for barbital and cyclobarbital
Article | Year |
---|---|
Correlation of biological activity and high-pressure liquid chromatographic retention index for a series of propranolol, barbiturate, and anthranilic acid analogues.
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.
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.
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.
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.
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.
Topics: | 2008 |
Derivatives of evipal, alurate, and phanodorn.
Topics: Barbital; Barbiturates; Hexobarbital | 1949 |