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MFCD02259149 molecular structure
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{[(1S,2S,3S,4S,5R,6R)-4-({[(2R)-2,3-bis(octanoyloxy)propoxy](hydroxy)phosphoryl}oxy)-3,5,6-trihydroxy-2-(phosphonooxy)cyclohexyl]oxy}phosphonic acid

ChemBase ID: 133721
Molecular Formular: C25H49O19P3
Molecular Mass: 746.566443
Monoisotopic Mass: 746.20808924
SMILES and InChIs

SMILES:
CCCCCCCC(=O)OC[C@H](COP(=O)(O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H]([C@H]1O)OP(=O)(O)O)OP(=O)(O)O)O)O)OC(=O)CCCCCCC
Canonical SMILES:
CCCCCCCC(=O)O[C@@H](COP(=O)(O[C@H]1[C@H](O)[C@@H](O)[C@@H]([C@H]([C@H]1O)OP(=O)(O)O)OP(=O)(O)O)O)COC(=O)CCCCCCC
InChI:
InChI=1S/C25H49O19P3/c1-3-5-7-9-11-13-18(26)39-15-17(41-19(27)14-12-10-8-6-4-2)16-40-47(37,38)44-23-20(28)21(29)24(42-45(31,32)33)25(22(23)30)43-46(34,35)36/h17,20-25,28-30H,3-16H2,1-2H3,(H,37,38)(H2,31,32,33)(H2,34,35,36)/t17-,20-,21-,22+,23+,24+,25+/m1/s1
InChIKey:
XLNCEHRXXWQMPK-AWGZLWLLSA-N

Cite this record

CBID:133721 http://www.chembase.cn/molecule-133721.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
{[(1S,2S,3S,4S,5R,6R)-4-({[(2R)-2,3-bis(octanoyloxy)propoxy](hydroxy)phosphoryl}oxy)-3,5,6-trihydroxy-2-(phosphonooxy)cyclohexyl]oxy}phosphonic acid
IUPAC Traditional name
[(1S,2S,3S,4S,5R,6R)-4-{[(2R)-2,3-bis(octanoyloxy)propoxy(hydroxy)phosphoryl]oxy}-3,5,6-trihydroxy-2-(phosphonooxy)cyclohexyl]oxyphosphonic acid
Synonyms
L-α-Phosphatidyl-D-myo-inositol 3,4-diphosphate, dioctanoyl
MDL Number
MFCD02259149
PubChem SID
162227998
24898494
PubChem CID
16219852

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
P4725 external link Add to cart Please log in.
Data Source Data ID
PubChem 16219852 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 0.62676716  H Acceptors 13 
H Donor LogD (pH = 5.5) -5.695914 
LogD (pH = 7.4) -8.189437  Log P 1.6338252 
Molar Refractivity 158.6976 cm3 Polarizability 65.17116 Å3
Polar Surface Area 302.57 Å2 Rotatable Bonds 26 
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Physical Property Safety Information Bioassay(PubChem)
Solubility
H2O: soluble expand Show data source
German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Storage Temperature
-20°C expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - P4725 external link
Biochem/physiol Actions
Activates Ca2+-insensitive PKC isotypes δ, ε, and η, activates Akt (a serine-threonine kinase also known as PKBα) by direct interaction with the Akt pleckstrin homology domain.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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