Page last updated: 2024-08-21

4-cyanophenol and phenol

4-cyanophenol has been researched along with phenol in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (11.11)18.2507
2000's7 (77.78)29.6817
2010's1 (11.11)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Caron, G; Ermondi, G1
Kapur, S; Rosario, M; Selassie, CD; Verma, RP1
Akamatsu, M; Fujikawa, M; Nakao, K; Shimizu, R1
Chilloux, A; Colucci, MA; Moody, CJ; Reigan, P; Ross, D; Siegel, D1
Hilvo, M; Innocenti, A; Parkkila, S; Scozzafava, A; Supuran, CT1
Innocenti, A; Scozzafava, A; Supuran, CT; Vullo, D1
Bua, S; Capasso, C; Del Prete, S; Entezari Heravi, Y; Gratteri, P; Nocentini, A; Saboury, AA; Sereshti, H; Supuran, CT1
Casella, L; Gaspard, S; Gullotti, M; Marchesini, A; Maritano, S; Monzani, E1
Ascenzi, P; Casella, L; Ciaccio, C; Moens, L; Monzani, E; Nicolis, S1

Other Studies

9 other study(ies) available for 4-cyanophenol and phenol

ArticleYear
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).
    Journal of medicinal chemistry, 2005, May-05, Volume: 48, Issue:9

    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.
    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
QSAR study on permeability of hydrophobic compounds with artificial membranes.
    Bioorganic & medicinal chemistry, 2007, Jun-01, Volume: 15, Issue:11

    Topics: Biological Transport; Caco-2 Cells; Drug Evaluation, Preclinical; Humans; Hydrophobic and Hydrophilic Interactions; Membranes, Artificial; Permeability; Pharmaceutical Preparations; Quantitative Structure-Activity Relationship

2007
Synthesis and evaluation of 3-aryloxymethyl-1,2-dimethylindole-4,7-diones as mechanism-based inhibitors of NAD(P)H:quinone oxidoreductase 1 (NQO1) activity.
    Journal of medicinal chemistry, 2007, Nov-15, Volume: 50, Issue:23

    Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Drug Screening Assays, Antitumor; Humans; Indoles; NAD(P)H Dehydrogenase (Quinone); Pancreatic Neoplasms; Quinones; Structure-Activity Relationship

2007
Carbonic anhydrase inhibitors: Inhibition of the new membrane-associated isoform XV with phenols.
    Bioorganic & medicinal chemistry letters, 2008, Jun-15, Volume: 18, Issue:12

    Topics: Animals; Binding Sites; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Humans; Hydrogen Bonding; Isoenzymes; Mice; Molecular Structure; Phenols; Stereoisomerism; Structure-Activity Relationship

2008
Carbonic anhydrase inhibitors: inhibition of mammalian isoforms I-XIV with a series of substituted phenols including paracetamol and salicylic acid.
    Bioorganic & medicinal chemistry, 2008, Aug-01, Volume: 16, Issue:15

    Topics: Acetaminophen; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Molecular Structure; Protein Isoforms; Salicylic Acid; Structure-Activity Relationship

2008
Inhibition of Malassezia globosa carbonic anhydrase with phenols.
    Bioorganic & medicinal chemistry, 2017, 05-01, Volume: 25, Issue:9

    Topics: Acetazolamide; Carbonic Anhydrase I; Carbonic Anhydrase Inhibitors; Dandruff; Humans; Hydrogen Bonding; Malassezia; Molecular Docking Simulation; Phenols; Structure-Activity Relationship

2017
Inhibition of ascorbate oxidase by phenolic compounds. Enzymatic and spectroscopic studies.
    Biochemistry, 1997, Apr-22, Volume: 36, Issue:16

    Topics: Ascorbate Oxidase; Binding, Competitive; Chlorophenols; Cresols; Electron Spin Resonance Spectroscopy; Enzyme Inhibitors; Hydrogen-Ion Concentration; Nitrophenols; Phenol; Phenols; Spectrophotometry, Ultraviolet

1997
Reactivity and endogenous modification by nitrite and hydrogen peroxide: does human neuroglobin act only as a scavenger?
    The Biochemical journal, 2007, Oct-01, Volume: 407, Issue:1

    Topics: Amino Acid Sequence; Binding Sites; Catalysis; Cysteine; Disulfides; Globins; Humans; Hydrogen Peroxide; Kinetics; Models, Molecular; Molecular Sequence Data; Myoglobin; Nerve Tissue Proteins; Neuroglobin; Nitrites; Oxidation-Reduction; Phenol; Phenols; Phenylacetates; Protein Conformation; Tandem Mass Spectrometry

2007