4-hydroxybenzaldehyde and hydroquinone

4-hydroxybenzaldehyde has been researched along with hydroquinone in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dunn, WJ; Grigoras, S; Koehler, MG1
Kapur, S; Rosario, M; Selassie, CD; Verma, RP1
Abellán Guillén, A; Cordeiro, MN; Garrido Escudero, A; Morales Helguera, A; Pérez-Garrido, A1
Kim, KH; Lee, SK; Oh, DC; Oh, KB; Oh, WK; Shin, J; Song, IH; Won, TH; Yang, WY1
Alam, MA; Alam, MI; Alam, O; Koul, S; Nargotra, A; Taneja, SC1

Other Studies

5 other study(ies) available for 4-hydroxybenzaldehyde and hydroquinone

ArticleYear
The role of solvent-accessible surface area in determining partition coefficients.
    Journal of medicinal chemistry, 1987, Volume: 30, Issue:7

    Topics: Diffusion; Solubility; Solvents; Structure-Activity Relationship

1987
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
Bioactive Metabolites from the Fruits of Psoralea corylifolia.
    Journal of natural products, 2015, Apr-24, Volume: 78, Issue:4

    Topics: Aminoacyltransferases; Bacterial Proteins; Cysteine Endopeptidases; Flavonoids; Fruit; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Psoralea; Republic of Korea; Staphylococcus; Terpenes

2015
Molecular modeling and snake venom phospholipase A2 inhibition by phenolic compounds: Structure-activity relationship.
    European journal of medicinal chemistry, 2016, May-23, Volume: 114

    Topics: Antivenins; Biological Products; Dose-Response Relationship, Drug; Models, Molecular; Molecular Structure; Phenols; Phospholipase A2 Inhibitors; Phospholipases A2; Plant Extracts; Plant Roots; Snake Venoms; Structure-Activity Relationship

2016