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P7115 Sigma-Aldrich

1,2-Dipalmitoylphosphatidylinositol 4,5-diphosphate triammonium salt

≥98%, solid

Synonym: 1,2-Dipalmitoyl-L-α-phosphatidyl-D-myo-inositol 4,5-bisphosphate triammonium salt, L-α-Phosphatidyl-(1,2-dipalmitoyl)-D-myo-inositol 4,5-bisphosphate triammonium salt, PI(4,5)P2 (dipalmitoyl) triammonium salt, Phosphatidylinositol-4,5-diphosphate C-16 triammonium salt, PtdIns(4,5)P2 (dipalmitoyl) triammonium salt

  • Linear Formula (C41H78O19P3)-3(NH4+)3

  • Molecular Weight 1022.08

  •  MDL number MFCD18074407

  •  PubChem Substance ID 24898820

  •  NACRES NA.77

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Properties

Related Categories Bioactive Small Molecule Alphabetical Index, Bioactive Small Molecules, Biochemicals and Reagents, Cell Biology, Cell Signaling and Neuroscience,
Quality Level   200
assay   ≥98%
form   solid
solubility   DMSO: soluble >10 mg/mL
shipped in   wet ice
storage temp.   −20°C
SMILES string   O[C@@H]1[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H](O)[C@@H](O)[C@H]1OP(OC[C@H](OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O)(O)=O.N.N.N
InChI   1S/C41H81O19P3.3H3N/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-34(42)55-31-33(57-35(43)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)32-56-63(53,54)60-39-36(44)37(45)40(58-61(47,48)49)41(38(39)46)59-62(50,51)52;;;/h33,36-41,44-46H,3-32H2,1-2H3,(H,53,54)(H2,47,48,49)(H2,50,51,52);3*1H3/t33-,36-,37+,38+,39-,40-,41-;;;/m1.../s1
InChI key   VYFVZCYVYQYDCN-QNYQTKJTSA-N

Description

Biochem/physiol Actions

Diphosphorylated phosphatidylinositol that may be hydrolyzed by PI-specific phospholipase C to generate IP3 and DAG.

Features and Benefits

This compound is featured on the Potassium Channels page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Protocols & Articles
Peer-Reviewed Papers
15

References

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