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407125

Sigma-Aldrich

D-myo-Inositol 1,2,3,4,5,6-Hexakisphosphate, Dodecasodium Salt

≥85% (HPLC), di- and trivalent cation chelator, solid

Synonym(s):

D-myo-Inositol 1,2,3,4,5,6-Hexakisphosphate, Dodecasodium Salt, Zea mays, D-Ins(1,2,3,4,5,6)P₆, 12Na, Phytic Acid, 12Na

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About This Item

Empirical Formula (Hill Notation):
C6H6O24P6 · 12Na
CAS Number:
14306-25-3
Molecular Weight:
923.82
MDL number:
MFCD00065350
UNSPSC Code:
12352211
NACRES:
NA.77

Product Name

D-myo-Inositol 1,2,3,4,5,6-Hexakisphosphate, Dodecasodium Salt, Zea mays, Major phosphorus compound in plants that chelates with a variety of di- and trivalent cations.

Quality Level

100

Assay

≥85% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
desiccated (hygroscopic)

color

white to off-white

solubility

water: 1 mg/mL

shipped in

ambient

storage temp.

−20°C

SMILES string

[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[P](=O)([O-])([O-])OC1C(C(C(C(C1O[P](=O)([O-])[O-])O[P](=O)([O-])[O-])O[P](=O)([O-])[O-])O[P](=O)([O-])[O-])O[P](=O)([O-])[O-]

InChI

1S/C6H18O24P6.12Na/c7-31(8,9)25-1-2(26-32(10,11)12)4(28-34(16,17)18)6(30-36(22,23)24)5(29-35(19,20)21)3(1)27-33(13,14)15;;;;;;;;;;;;/h1-6H,(H2,7,8,9)(H2,10,11,12)(H2,13,14,15)(H2,16,17,18)(H2,19,20,21)(H2,22,23,24);;;;;;;;;;;;/q;12*+1/p-12

InChI key

KETSPIPODMGOEJ-UHFFFAOYSA-B

Related Categories

General description

Major phosphorus compound in plants that chelates with a variety of di- and trivalent cations. Reported to suppress damaging iron-catalyzed redox reactions.
Major phosphorus compound in plants. Chelates with a variety of di- and trivalent cations. Inhibits growth and induces differentiation of PC-3 human prostate cancer cells. Also reported to suppress damaging iron-catalyzed redox reactions.

Biochem/physiol Actions

Cell permeable: no
Primary Target
Chelates with a variety of di- and trivalent cations
Product does not compete with ATP.
Reversible: no

Preparation Note

Following recosntitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

Shamsuddin, A.M., and Yang, G.Y. 1995. Carcinogenesis 16, 1975.
Graf, E., and Eaton, J.W. 1993. Nutr. Cancer19, 11.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Hayley Whitfield et al.
The Biochemical journal, 477(14), 2621-2638 (2020-07-25)
Inositol polyphosphates are ubiquitous molecular signals in metazoans, as are their pyrophosphorylated derivatives that bear a so-called 'high-energy' phosphoanhydride bond. A structural rationale is provided for the ability of Arabidopsis inositol tris/tetrakisphosphate kinase 1 to discriminate between symmetric and enantiomeric
Jone Paesmans et al.
eLife, 9 (2020-12-23)
Synaptojanin1 (Synj1) is a phosphoinositide phosphatase, important in clathrin uncoating during endocytosis of presynaptic vesicles. It was identified as a potential drug target for Alzheimer's disease, Down syndrome, and TBC1D24-associated epilepsy, while also loss-of-function mutations in Synj1 are associated with
Yann Desfougères et al.
Methods in molecular biology (Clifton, N.J.), 2091, 59-71 (2019-11-28)
The yeast Saccharomyces cerevisiae has given us much information on the metabolism and function of inositol polyphosphates and inorganic polyphosphate. To expand our knowledge of the metabolic as well as functional connections between inositol polyphosphates and inorganic polyphosphate, we have

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