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Molecule
ID:133088
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₉NO₁₈P₄
Molecular Mass
517.106004
Exact Mass
516.95525929
Charge
0
InChI
InChI=1S/C6H16O18P4.H3N/c7-1-3(21-25(9,10)11)2(8)5(23-27(15,16)17)6(24-28(18,19)20)4(1)22-26(12,13)14;/h1-8H,(H2,9,10,11)(H2,12,13,14)(H2,15,16,17)(H2,18,19,20);1H3/t1-,2-,3-,4+,5-,6-;/m0./s1
InChIKey
LDRGGXGJARVUBP-SUBVTSALSA-N
Canonic Smiles
O[C@@H]1[C@H](OP(=O)(O)O)[C@@H](OP(=O)(O)O)[C@@H]([C@H]([C@@H]1OP(=O)(O)O)O)OP(=O)(O)O.N
Isomeric Smiles
[C@@H]1([C@@H]([C@@H]([C@@H]([C@H]([C@@H]1OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)O)OP(=O)(O)O)O.N
Calculated Properties
JChem
Acid pKa
0.32703635
H Acceptors
14
H Donor
10
LogD (pH = 5.5)
-14.237286
LogD (pH = 7.4)
-19.160568
Log P
-4.2762737
Molar Refractivity
79.2666
Polarizability
33.802597
Polar Surface Area
307.5
Rotatable Bonds
8
Lipinski's Rule of Five
false
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Data Source
Commercial Catalog
Sigma Aldrich
I8636
Academic Data
PubChem
16219534
Names and Identifiers
Synonyms
D-myo-Inositol 1,3,4,5-tetrakis(phosphate) ammonium salt
IP4
IUPAC Traditional name
[(1S,2S,3R,4S,5S,6S)-2,6-dihydroxy-3,4,5-tris(phosphonooxy)cyclohexyl]oxyphosphonic acid amine
IUPAC name
{[(1S,2S,3R,4S,5S,6S)-2,6-dihydroxy-3,4,5-tris(phosphonooxy)cyclohexyl]oxy}phosphonic acid amine
Registration numbers
CAS Number
102850-29-3
PubChem SID
24896142
162227365
MDL Number
MFCD00213747
PubChem CID
16219534
Properties
Safety Information
Storage Temperature
-20°C
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
Product Information
Purity
≥95%
Source
Molecule Details
Sigma Aldrich
I8636
Biochem/physiol Actions
Precursor of inositol 1,3,4-trisphosphate; increases entry of calcium across the plasma membrane; proposed regulator of intracellular calcium by control of plasma membrane transport of calcium ions.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay