Dynasore

Dynasore

Catalog Number:
L002368313APE
Mfr. No.:
APE-A1605
Price:
$220
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      • Overview
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          Background

          Dynasore is a noncompetitive inhibitor of GTPases with the IC50 value of 15 μM[1] [2].GTPases (singular GTPase) are hydrolase enzymes that play an important role in GTP binding and hydrolyzing. GTPases involve in many processes, like, transduction signal, protein biosynthesis, translocation proteins through membranes, and transporting vesicles within the cell. It has been reported that dynasore could inhibit the GTPase activity of dynamin1, dynamin2 and Drp1 [3] [4].Dynasore is a potent GTPases inhibitor and functions on the sites of dynamin1, dynamin2 or Drp1. When tested with HL-1 cells, treated cells with dynasore blocked the endocytic process via inhibiting the activity of dynamin [1]. Using genetically encoded pH-sensitive fluorescent probe synaptopHluorin to study the role of dynasore in the synapses expressing spH, and the results showed that dyansore treatment resulted in the normal stimulus-triggered increase in fluorescence intensity via reducing the GTPase activity of dynamin which in turn blocked the synaptic endocytosis[4]. Dynasore worked as inhibitor of dynamin GTPase activity which blocks dynamin-dependent endocytosis not only in cells, but also including neurons [3].

          [1].Zheng, J., et al., Chymase mediates injury and mitochondrial damage in cardiomyocytes during acute ischemia/reperfusion in the dog. PLoS One, 2014. 9(4): p. e94732.
          [2].McCluskey, A., et al., Building a better dynasore: the dyngo compounds potently inhibit dynamin and endocytosis. Traffic, 2013. 14(12): p. 1272-89.
          [3].Kirchhausen, T., E. Macia, and H.E. Pelish, Use of dynasore, the small molecule inhibitor of dynamin, in the regulation of endocytosis. Methods Enzymol, 2008. 438: p. 77-93.
          [4].Newton, A.J., T. Kirchhausen, and V.N. Murthy, Inhibition of dynamin completely blocks compensatory synaptic vesicle endocytosis. Proc Natl Acad Sci U S A, 2006. 103(47): p. 17955-60.

      • Properties
        • Alternative Name
          (E)-N'-(3,4-dihydroxybenzylidene)-3-hydroxy-2-naphthohydrazide
          CAS Number
          304448-55-3
          Molecular Formula
          C18H14N2O4
          Molecular Weight
          322.31
          Appearance
          A solid
          Purity
          98.00%
          Solubility
          insoluble in H2O; insoluble in EtOH; ≥16.12 mg/mL in DMSO
          Storage
          Store at -20°C

          * For Research Use Only

      • Reference
        • 1. Wei P, Ning M, et al. "Spiroplasma eriocheiris entered Drosophila Schneider 2 cells and relied on clathrin-mediated endocytosis and macropinocytosis." Infect Immun. 2019 Aug 26. pii: IAI.00233-19. PMID:31451616
          2. Ying Wen, Shouwen Chen, et al."Dysregulated haemolysin promotes bacterial outer membrane vesicles‐induced pyroptotic‐like cell death in zebrafish."Cellular Microbiology. 31 January 2019.
          3. Wang H, Liu W, et al. "Inhibitor analysis revealed that clathrin-mediated endocytosis is involed in cellular entry of type III grass carp reovirus." Virol J. 2018 May 24;15(1):92. PMID:29793525
          4. Mai J, Li X, et al. "A DNA Thioaptamer with Homing Specificity to Lymphoma Bone Marrow Involvement." Mol Pharm. 2018 May 7;15(5):1814-1825. PMID:29537266
          5. Schappe MS, Szteyn K, et al."Chanzyme TRPM7 Mediates the Ca(2+) Influx Essential for
          Lipopolysaccharide-Induced Toll-Like Receptor 4 Endocytosis and Macrophage Activation." Immunity. 2018 Jan 16;48(1):59-74.e5. PMID:29343440

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