4-chlorophenol has been researched along with 3-cresol in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kubinyi, H | 1 |
| Fujita, T; Nakajima, M; Nishioka, T | 1 |
| Hachisuka, Y; Ikeda, K; Tochikubo, K; Tomida, H; Yasuda, Y | 1 |
| Caron, G; Ermondi, G | 1 |
| Kapur, S; Rosario, M; Selassie, CD; Verma, RP | 1 |
| Abellán Guillén, A; Cordeiro, MN; Garrido Escudero, A; Morales Helguera, A; Pérez-Garrido, A | 1 |
| Pfaender, FK; Shimp, RJ | 1 |
| Aronson, J; Bufler, J; Dengler, R; Haeseler, G; Hecker, H; Leuwer, M; Piepenbrink, A; Piepenbrock, S | 1 |
8 other study(ies) available for 4-chlorophenol and 3-cresol
| Article | Year |
|---|---|
Quantitative structure-activity relationships. 2. A mixed approach, based on Hansch and Free-Wilson Analysis.
Topics: Animals; Aspergillus niger; Bacillus cereus; Bacillus subtilis; Enterococcus faecalis; Haemophilus; Hydrazines; Methacrylates; Microbial Sensitivity Tests; Models, Chemical; Molecular Conformation; Mycobacterium tuberculosis; Phenols; Quaternary Ammonium Compounds; Rats; Regression Analysis; Rifamycins; Sarcina; Staphylococcus aureus; Structure-Activity Relationship; Thyronines; Thyroxine | 1976 |
Hydrogen-bonding parameter and its significance in quantitative structure--activity studies.
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.
Topics: Alanine; Bacillus subtilis; Fatty Acids; Hydrogen-Ion Concentration; Kinetics; Phenols; Spores, Bacterial; Structure-Activity Relationship | 1982 |
Calculating virtual log P in the alkane/water system (log P(N)(alk)) and its derived parameters deltalog P(N)(oct-alk) and log D(pH)(alk).
Topics: 1-Octanol; Alkanes; Hydrogen-Ion Concentration; Least-Squares Analysis; Mathematics; Models, Chemical; Models, Molecular; Solvents; Water | 2005 |
Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.
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.
Topics: beta-Cyclodextrins; Hydrophobic and Hydrophilic Interactions; Organic Chemicals; Quantitative Structure-Activity Relationship | 2009 |
Effect of adaptation to phenol on biodegradation of monosubstituted phenols by aquatic microbial communities.
Topics: Adaptation, Physiological; Aminophenols; Biodegradation, Environmental; Chlorophenols; Cresols; Kinetics; Phenol; Phenols; Water Microbiology | 1987 |
Phenol derivatives accelerate inactivation kinetics in one inactivation-deficient mutant human skeletal muscle Na(+) channel.
Topics: Cell Line; Chlorophenols; Cresols; Dose-Response Relationship, Drug; Humans; Kinetics; Membrane Potentials; Muscle, Skeletal; Mutation; Phenols; Sodium Channels; Xylenes | 2001 |