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407125

Sigma-Aldrich

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.

Synonyme(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

Formule empirique (notation de Hill):
C6H6O24P6 · 12Na
Numéro CAS:
14306-25-3
Poids moléculaire :
923.82
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.77

Niveau de qualité

100

Pureté

≥85% (HPLC)

Forme

solid

Fabricant/nom de marque

Calbiochem®

Conditions de stockage

OK to freeze
desiccated (hygroscopic)

Couleur

white to off-white

Solubilité

water: 1 mg/mL

Conditions d'expédition

ambient

Température de stockage

−20°C

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

Clé InChI

KETSPIPODMGOEJ-UHFFFAOYSA-B

Catégories apparentées

Description générale

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.

Actions biochimiques/physiologiques

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

Avertissement

Toxicity: Standard Handling (A)

Reconstitution

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

Autres remarques

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

Informations légales

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

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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