المراجع (Citations)
1 publicationsمنشورات الباحثين الذين استخدموا هذا المنتجالوصف (Description)
Hesperadin is an ATP competitive indolinone inhibitor of Aurora B with an IC50 of 250nM[1]. Aurora B kinase is a key serine/threonine kinase that regulates chromosome segregation and cytokinesis during cell mitosis[2]. Hesperadin inhibits kinase activity through the ATP competition mechanism and is usually used in the research of cancer, malaria and influenza virus infections by inhibiting[3].
In vitro, treatment of HeLa cells with Hesperadin (50 or 100nM; 20h) inhibits Aurora B kinase activity, abolishes histone H3 Ser10 phosphorylation, prevents chromosome alignment, permits anaphase entry with monooriented chromosomes, stalls cytokinesis, generates polyploid nuclei, overrides taxol- and monastrol-induced mitotic arrest within 1h, and reduces BubR1 kinetochore recruitment[4]. Treatment of Miapaca-2 and BxPC-3 cells with Hesperadin (50-100nM; 48–72h) inhibits cell proliferation, abolishes DNA synthesis, blocks colony formation, arrests cells in G2/M, induces polyploidy, collapses mitochondrial membrane potential and ATP content, elevates intracellular ROS, and drives caspase-3/PARP cleavage and apoptosis in Miapaca-2 and BxPC-3 cells[5].
In vivo, Hesperadin (2.5μg/kg/day; i.p.; 4 weeks) reduced cardiac infarct size, decreased serum LDH concentration, and attenuated cardiac cell death and DNA damage in a mouse model of acute ischemia/reperfusion injury[6]. Hesperadin (0.5μg/μl; 12h; intracerebroventricular injection) decreased brain edema, improved neurobehavioral function, reduced MST4 expression, increased pAKT levels, and attenuated autophagy in the perihematoma brain tissue of intracerebral hemorrhage mice[7].
References:
[1] Jetton N, Rothberg KG, Hubbard JG, et al. The cell cycle as a therapeutic target against Trypanosoma brucei: Hesperadin inhibits Aurora kinase-1 and blocks mitotic progression in bloodstream forms. Mol Microbiol. 2009;72(2):442-458.
[2] Krenn V, Musacchio A. The Aurora B Kinase in Chromosome Bi-Orientation and Spindle Checkpoint Signaling. Front Oncol. 2015;5:225.
[3] Hu Y, Zhang J, Musharrafieh R, Hau R, Ma C, Wang J. Chemical Genomics Approach Leads to the Identification of Hesperadin, an Aurora B Kinase Inhibitor, as a Broad-Spectrum Influenza Antiviral. Int J Mol Sci. 2017;18(9):1929.
[4] Hauf S, Cole RW, LaTerra S, et al. The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpoint. J Cell Biol. 2003;161(2):281-294.
[5] Zhang Y, Wu J, Fu Y, et al. Hesperadin suppresses pancreatic cancer through ATF4/GADD45A axis at nanomolar concentrations. Oncogene. 2022;41(25):3394-3408.
[6] Zhang J, Liang R, Wang K, et al. Novel CaMKII-δ Inhibitor Hesperadin Exerts Dual Functions to Ameliorate Cardiac Ischemia/Reperfusion Injury and Inhibit Tumor Growth. Circulation. 2022;145(15):1154-1168.
[7] Wu X, Wu J, Hu W, et al. MST4 Kinase Inhibitor Hesperadin Attenuates Autophagy and Behavioral Disorder via the MST4/AKT Pathway in Intracerebral Hemorrhage Mice. Behav Neurol. 2020;2020:2476861.
البروتوكول (Protocol)
| Cell experiment [1]: | |
Cell lines | HeLa cells |
Preparation Method | HeLa cells were grown in DMEM medium supplemented with 10% FCS, 0.2mM L-glutamine, 100U/ml penicillin, and 100μg/ml streptomycin. Hesperadin was used at 50 or 100nM for 20h. Then cells were collected and lysed. Proteins were extracted and resolved by SDS-PAGE and transferred to Immobilon-P membrane. Blocking and antibody incubations were in 4% low-fat milk in TBS-T (150mM NaCl, 20mM Tris, pH8.0, 0.05% Tween 20), washings were in TBS-T. Blots were developed by ECL. |
Reaction Conditions | 50 or 100nM; 20h |
Applications | Hesperadin inhibits Aurora B kinase activity, abolishes histone H3 Ser10 phosphorylation in HeLa cells. |
| Animal experiment [2]: | |
Animal models | Male C57BL/6 mic |
Preparation Method | Male C57BL/6 mice (7-8 weeks old) were kept in separate cages and given free access to standard laboratory feed and water. Intracerebral hemorrhage (ICH) model was inducted by injection of collagenase IV. Hesperadin(0.5μg/μl) was injected intraventricularly 1h before ICH. 12 hours after cerebral hemorrhage was determined as the time point. Mice were randomly divided into four groups: sham group, sham+Hesperadin group, ICH group, and ICH +Hesperadin group (n=13 in each group). In each group, mice were selected randomly for western blot (n=6), immunofluorescence (n=3), and brain edema (n=4). A total of 52 mice were used, and all mice in the four groups were examined for behavior before euthanasia. |
Dosage form | 0.5μg/μl; 12h; intracerebroventricular injection |
Applications | Hesperadin decreased brain edema, improved neurobehavioral function, reduced MST4 expression, increased pAKT levels, and attenuated autophagy in the perihematoma brain tissue of intracerebral hemorrhage mice. |
References: | |
وثائق المنتج (Product Documents)
الخصائص الكيميائية (Chemical Properties)
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية
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