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I0510

Sigma-Aldrich

D-myo-Inositol 1,4-bisphosphate potassium salt

from bovine brain, ≥98% (TLC)

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About This Item

Empirical Formula (Hill Notation):
C6H12K2O12P2
CAS Number:
103476-30-8
Molecular Weight:
416.30
MDL number:
MFCD00144214
UNSPSC Code:
12352207
PubChem Substance ID:
24895904

biological source

bovine brain

Assay

≥98% (TLC)

storage temp.

−20°C

SMILES string

[K+].O[C@@H]1[C@@H](O)[C@H](OP(O)([O-])=O)[C@H](O)[C@H](O)[C@H]1OP(O)(O)=O

InChI

1S/C6H14O12P2.K/c7-1-2(8)6(18-20(14,15)16)4(10)3(9)5(1)17-19(11,12)13;/h1-10H,(H2,11,12,13)(H2,14,15,16);/q;+1/p-1/t1-,2-,3-,4+,5+,6+;/m1./s1

InChI key

UEZPJWQBOCTMMK-HTBPUPAMSA-M

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Biochem/physiol Actions

Phosphoinostol broken down from glycerophosphoinositols

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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I M Bird et al.
Molecular and cellular endocrinology, 66(2), 215-229 (1989-10-01)
The optimisation of a reaction for the conversion of glycerophosphoinositols to phosphoinositols is described. This reaction has been used in a scheme, described in detail, for the formation of D-myo-inositol 1,4-bisphosphate and D-myo-inositol 1,4,5-trisphosphate in mg quantities from a readily
A Emilsson et al.
The Journal of biological chemistry, 259(5), 3111-3116 (1984-03-10)
The inositol phospholipids of peritoneal macrophages were prelabeled with [3H]inositol to enable studies on the enzymatic mechanisms of stimulus-induced phosphatidylinositol breakdown. Ionophore A23187 induced a rapid breakdown of phosphatidylinositol in the presence of Ca2+ with 25% loss occurring within 5

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