caged-Ins(145)P3 / PM

D-23-O-Isopropylidene-6-O-(2-nitro-4.5-dimethoxy)benzyl-myo-Inositol 145-trisphosphate-Hexakis(propionoxymethyl) Ester

photoactivatable AND membrane-permenat IP3 derivative 

In stock
Catalogue
cag-iso-2-145-100
Size: 100 µg
€650.00
More Information
Catalogue cag-iso-2-145-100
Formula C42H64NO31P3
CAS 1009832-82-9
MW 1171.87
Appearance oil
Purity > 98%
Solubility in DMSO. CH2Cl2. Me
Size 100 µg
Storage Keep cool and dry. Protect from light and moisture.
<p><strong>Membrane-permeant derivatives of inositol phosphates </strong>require the intracellular enzymatic hydrolysis of several protecting groups in order to generate the biologically active compound.  The photolysis of membrane-permeant caged derivatives of Ins(145)P3 might mimic fast intracellular responses. In an initial step <strong>cells are loaded with the caged Ins(145)P3 derivative</strong>.</p> <p>Within 30 to 180 minutes all bioactivatable protecting groups remove generating <strong>caged inositol phosphate</strong>. The cage is known to prevent biological activity. The photochemical destruction of the cage (360-400nm) releases active Ins(145)P3 within a few seconds. Since this approach does not (directly) trigger other signaling events, membrane-permeant derivatives of signaling molecules are able to help dissecting <strong>signaling pathways</strong>.</p>
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