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16-hydroxycleroda-3,13(14)-dien-15,16-olide and imatinib mesylate

16-hydroxycleroda-3,13(14)-dien-15,16-olide has been researched along with imatinib mesylate in 1 studies

*Imatinib Mesylate: A tyrosine kinase inhibitor and ANTINEOPLASTIC AGENT that inhibits the BCR-ABL kinase created by chromosome rearrangements in CHRONIC MYELOID LEUKEMIA and ACUTE LYMPHOBLASTIC LEUKEMIA, as well as PDG-derived tyrosine kinases that are overexpressed in gastrointestinal stromal tumors. [MeSH]

*Imatinib Mesylate: A tyrosine kinase inhibitor and ANTINEOPLASTIC AGENT that inhibits the BCR-ABL kinase created by chromosome rearrangements in CHRONIC MYELOID LEUKEMIA and ACUTE LYMPHOBLASTIC LEUKEMIA, as well as PDG-derived tyrosine kinases that are overexpressed in gastrointestinal stromal tumors. [MeSH]

Compound Research Comparison

Studies
(16-hydroxycleroda-3,13(14)-dien-15,16-olide)
Trials
(16-hydroxycleroda-3,13(14)-dien-15,16-olide)
Recent Studies (post-2010)
(16-hydroxycleroda-3,13(14)-dien-15,16-olide)
Studies
(imatinib mesylate)
Trials
(imatinib mesylate)
Recent Studies (post-2010) (imatinib mesylate)
130811,4779605,773

Protein Interaction Comparison

ProteinTaxonomy16-hydroxycleroda-3,13(14)-dien-15,16-olide (IC50)imatinib mesylate (IC50)
Tyrosine-protein kinase ABL1Homo sapiens (human)0.31
Mast/stem cell growth factor receptor KitHomo sapiens (human)0.1

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chan, WL; Chang, JG; Chang, WH; Lee, CC; Lin, YH; Wu, YC1

Other Studies

1 other study(ies) available for 16-hydroxycleroda-3,13(14)-dien-15,16-olide and imatinib mesylate

ArticleYear
16-Hydroxycleroda-3,13-dien-15,16-olide deregulates PI3K and Aurora B activities that involve in cancer cell apoptosis.
    Toxicology, 2011, Jul-11, Volume: 285, Issue:1-2

    Topics: Antineoplastic Agents; Apoptosis; Aurora Kinase B; Aurora Kinases; Benzamides; Cell Cycle; Cell Line, Tumor; Cell Survival; Diterpenes; DNA Damage; Drug Resistance, Neoplasm; Gene Expression Regulation, Neoplastic; Gene Silencing; Humans; Imatinib Mesylate; Neoplasms; Phosphoinositide-3 Kinase Inhibitors; Piperazines; Protein Serine-Threonine Kinases; Pyrimidines; Signal Transduction

2011