Compounds > 4-cresol

4-cresol and 4-hydroxybenzaldehyde

4-cresol has been researched along with 4-hydroxybenzaldehyde in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's0 (0.00)18.2507
2000's3 (42.86)29.6817
2010's2 (28.57)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fujita, T; Nakajima, M; Nishioka, T1
Hachisuka, Y; Ikeda, K; Tochikubo, K; Tomida, H; Yasuda, Y1
Kapur, S; Rosario, M; Selassie, CD; Verma, RP1
Abellán Guillén, A; Cordeiro, MN; Garrido Escudero, A; Morales Helguera, A; Pérez-Garrido, A1
Cuervo-López, FM; Gómez, J; Houbron, E; Silva, CD; Texier, AC1
Beristain-Cardoso, R; Gómez, J; Silva, CD1
Harper, WJ; Kocaoglu-Vurma, NA; Langford, V; Rodriguez-Saona, LE; Sharp, MD1

Other Studies

7 other study(ies) available for 4-cresol and 4-hydroxybenzaldehyde

ArticleYear
Hydrogen-bonding parameter and its significance in quantitative structure--activity studies.
    Journal of medicinal chemistry, 1977, Volume: 20, Issue:8

    Topics: Acetylcholinesterase; Anesthetics; Benzene Derivatives; Benzenesulfonates; Carbamates; Chemical Phenomena; Chemistry; Chemistry, Physical; Hydrogen Bonding; Models, Biological; Models, Chemical; Phenoxyacetates; Solubility; Structure-Activity Relationship

1977
Quantitative structure-inhibitory activity relationships of phenols and fatty acids for Bacillus subtilis spore germination.
    Journal of medicinal chemistry, 1982, Volume: 25, Issue:3

    Topics: Alanine; Bacillus subtilis; Fatty Acids; Hydrogen-Ion Concentration; Kinetics; Phenols; Spores, Bacterial; Structure-Activity Relationship

1982
Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.
    Journal of medicinal chemistry, 2005, Nov-17, Volume: 48, Issue:23

    Topics: Animals; Antineoplastic Agents; Apoptosis; Caspases; Cell Line, Tumor; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Enzyme Activation; Mice; Molecular Conformation; Phenols; Quantitative Structure-Activity Relationship; Vinblastine

2005
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
p-Cresol biotransformation by a nitrifying consortium.
    Chemosphere, 2009, Volume: 75, Issue:10

    Topics: Benzaldehydes; Bioreactors; Biotransformation; Cresols; Nitrates; Oxidoreductases; Sewage; Thiourea; Waste Disposal, Fluid

2009
Simultaneous removal of 2-chlorophenol, phenol, p-cresol and p-hydroxybenzaldehyde under nitrifying conditions: kinetic study.
    Bioresource technology, 2011, Volume: 102, Issue:11

    Topics: Benzaldehydes; Biodegradation, Environmental; Biological Assay; Chlorophenols; Cresols; Kinetics; Nitrification; Oxidation-Reduction; Phenols; Quaternary Ammonium Compounds; Sewage; Time Factors

2011
Rapid discrimination and characterization of vanilla bean extracts by attenuated total reflection infrared spectroscopy and selected ion flow tube mass spectrometry.
    Journal of food science, 2012, Volume: 77, Issue:3

    Topics: Acetic Acid; Benzaldehydes; Cluster Analysis; Cresols; Flavoring Agents; Food Analysis; Guaiacol; Hemiterpenes; India; Indonesia; Madagascar; Multivariate Analysis; Odorants; Papua New Guinea; Pentanoic Acids; Plant Extracts; Spectrometry, Mass, Electrospray Ionization; Spectroscopy, Fourier Transform Infrared; Uganda; Vanilla

2012