Page last updated: 2024-08-16

vorinostat and urea

vorinostat has been researched along with urea in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A1
Choy, ML; Lee, JH; Marks, PA; Ngo, L; Venta-Perez, G1
Chao, YS; Chen, CH; Chen, CP; Chen, CT; Chiu, CH; Chou, LH; Hsieh, SY; Hsu, JT; Huang, CT; Jiaang, WT; Kao, LC; Lin, WH; Yeh, TK; Yen, KJ; Yen, SC1
Choi, SA; Kim, SK; Kwak, PA; Lee, CS; Lee, JH; Lee, JY; Park, CK; Phi, JH; Wang, KC1

Other Studies

4 other study(ies) available for vorinostat and urea

ArticleYear
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
    Chemical research in toxicology, 2010, Volume: 23, Issue:1

    Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship

2010
Role of checkpoint kinase 1 (Chk1) in the mechanisms of resistance to histone deacetylase inhibitors.
    Proceedings of the National Academy of Sciences of the United States of America, 2011, Dec-06, Volume: 108, Issue:49

    Topics: Animals; Cell Line, Tumor; Cell Survival; Cells, Cultured; Checkpoint Kinase 1; DNA Damage; Drug Resistance; Fibroblasts; Foreskin; Histone Deacetylase Inhibitors; Histones; Humans; Hydroxamic Acids; Immunoblotting; Male; Mice; Protein Kinases; Quinolines; Quinuclidines; RNA Interference; Spleen; Staurosporine; Thiophenes; Urea; Vorinostat

2011
Evaluation of the antitumor effects of BPR1J-340, a potent and selective FLT3 inhibitor, alone or in combination with an HDAC inhibitor, vorinostat, in AML cancer.
    PloS one, 2014, Volume: 9, Issue:1

    Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Benzamides; Cell Line, Tumor; Cell Proliferation; fms-Like Tyrosine Kinase 3; Histone Deacetylase Inhibitors; Hydroxamic Acids; Leukemia, Myeloid, Acute; Male; Mice; Mice, Nude; Protein Kinase Inhibitors; Rats; Signal Transduction; Urea; Vorinostat

2014
A novel histone deacetylase inhibitor, CKD5, has potent anti-cancer effects in glioblastoma.
    Oncotarget, 2017, Feb-07, Volume: 8, Issue:6

    Topics: Animals; Apoptosis; Brain Neoplasms; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Female; G2 Phase Cell Cycle Checkpoints; Glioblastoma; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Mice, Inbred BALB C; Mice, Nude; Time Factors; Tumor Burden; Urea; Vorinostat; Xenograft Model Antitumor Assays

2017
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