Compounds > benzohydroxamic acid
Page last updated: 2024-08-21

benzohydroxamic acid and vorinostat

benzohydroxamic acid has been researched along with vorinostat in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's4 (80.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Charton, J; Dassonneville, S; Deprez, B; Deprez-Poulain, R; Flipo, M; Hocine, A1
Amici, R; Bigogno, C; Boggio, R; Cappa, A; Carrara, S; Cataudella, T; Colombo, A; di Ventimiglia, SJ; Dondio, G; Fusar, F; Gagliardi, S; Gianti, E; Mai, A; Mercurio, C; Minucci, S; Moroni, M; Munari, D; Pain, G; Regalia, N; Sartori, L; Thaler, F; Varasi, M; Vultaggio, S1
Aidoud, N; Davoine, EL; Gale, JP; Holson, EB; Kaya, T; Lemercier, BC; Olson, DE; Thomas, M; Wagner, FF; Weïwer, M; Zhang, YL1
D'hooghe, M; De Vreese, R; De Wever, O; Depetter, Y; Desmet, T; Franceus, J; Geurs, S; Vanden Bussche, F1
Kochetkov, SN; Konduktorov, KA; Kozlov, MV; Shcherbakova, AS1

Other Studies

5 other study(ies) available for benzohydroxamic acid and vorinostat

ArticleYear
Hydroxamates: relationships between structure and plasma stability.
    Journal of medicinal chemistry, 2009, Nov-12, Volume: 52, Issue:21

    Topics: Animals; Drug Evaluation, Preclinical; Drug Stability; Esterases; Half-Life; Humans; Hydrolysis; Hydrophobic and Hydrophilic Interactions; Hydroxamic Acids; Plasma; Prodrugs; Rats; Rats, Sprague-Dawley; Stereoisomerism; Structure-Activity Relationship

2009
Synthesis and biological evaluation of N-hydroxyphenylacrylamides and N-hydroxypyridin-2-ylacrylamides as novel histone deacetylase inhibitors.
    Journal of medicinal chemistry, 2010, Jan-28, Volume: 53, Issue:2

    Topics: Acrylamides; Antineoplastic Agents; Benzene Derivatives; Cell Proliferation; Colonic Neoplasms; Drug Stability; Enzyme Inhibitors; HeLa Cells; Histone Deacetylase Inhibitors; Humans; Pyridines; Structure-Activity Relationship; Xenograft Model Antitumor Assays

2010
Potent and selective inhibition of histone deacetylase 6 (HDAC6) does not require a surface-binding motif.
    Journal of medicinal chemistry, 2013, Feb-28, Volume: 56, Issue:4

    Topics: HeLa Cells; Histone Deacetylase 6; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Hydroxamic Acids; Isoenzymes; Molecular Mimicry; Protein Interaction Domains and Motifs; Structure-Activity Relationship

2013
Assessment of the trifluoromethyl ketone functionality as an alternative zinc-binding group for selective HDAC6 inhibition.
    MedChemComm, 2018, Jun-01, Volume: 9, Issue:6

    Topics:

2018
Synthesis of N'-propylhydrazide analogs of hydroxamic inhibitors of histone deacetylases (HDACs) and evaluation of their impact on activities of HDACs and replication of hepatitis C virus (HCV).
    Bioorganic & medicinal chemistry letters, 2019, 08-15, Volume: 29, Issue:16

    Topics: Antiviral Agents; Dose-Response Relationship, Drug; Hepacivirus; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Hydrazines; Microbial Sensitivity Tests; Molecular Structure; Repressor Proteins; Structure-Activity Relationship; Virus Replication

2019