Jasplakinolide

Jasplakinolide

Catalog Number:
FC01366083APE
Mfr. No.:
APE-B7189
Price:
$420
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      • Overview
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          Background

          Jasplakinolide, a cyclodepsipeptide originally isolated from the marine sponge, Jaspis johnstoni, is a potent inducer of actin polymerization, which also stabilizes pre-formed actin filaments. Jasplakinolide may exert its cytotoxic effect by binding to F-actin. Compared with Ca2+-actin, jasplakinolide shows a much greater effect on Mg2+-actin, and binds to F-actin competitively with phalloidin with a Kd value of ~ 15 nM. Jasplakinolide exhibits both fungicidal and antiproliferative activity. In addition, jasplakinolide is membrane-permeable, which makes it a commonly used tool in cell biology, when actin polymerization or actin filament stabilization has to be achieved.

          1. Bubb MR, Senderowicz AM, Sausville EA, et al. Jasplakinolide, a cytotoxic natural product, induces actin polymerization and competitively inhibits the binding of phalloidin to F-actin. Journal of Biological Chemistry, 1994, 269(21): 14869-14871.
          2. Holzinger A. Jasplakinolide: an actin-specific reagent that promotes actin polymerization. Methods in Molecular Biology, 2009, 586: 71-87.

      • Properties
        • Categories
          A potent actin polymerization inducer, which also stabilizes pre-existing actin filaments
          Alternative Name
          (4R,7R,10S,13R,17R,19S,E)-7-((2-bromo-1H-indol-3-yl)methyl)-4-(4-hydroxyphenyl)-8,10,13,15,17,19-hexamethyl-1-oxa-5,8,11-triazacyclononadec-15-ene-2,6,9,12-tetraone
          CAS Number
          102396-24-7
          Molecular Formula
          C36H45BrN4O6
          Molecular Weight
          709.67
          Appearance
          An off-white solid
          Purity
          98.00%
          Solubility
          Soluble in DMSO
          Storage
          Store at -20°C
          SMILES
          BrC(NC1=CC=CC=C21)=C2C[[email protected]](C(N[[email protected]@H](C(C=C3)=CC=C3O)CC(O[[email protected]@H](C)C[[email protected]@H](C)C=C(C)C[[email protected]@H](C)C(N[[email protected]]4C)=O)=O)=O)N(C)C4=O

          * For Research Use Only

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