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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
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ChemBase ID:
133721
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Molecular Formular:
C25H49O19P3
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Molecular Mass:
746.566443
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Monoisotopic Mass:
746.20808924
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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
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Cite this record
CBID:133721 http://www.chembase.cn/molecule-133721.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
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IUPAC name
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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
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IUPAC Traditional name
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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]oxyphosphonic acid
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Synonyms
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L-α-Phosphatidyl-D-myo-inositol 3,4-diphosphate, dioctanoyl
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MDL Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
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Acid pKa
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0.62676716
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H Acceptors
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13
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H Donor
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8
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LogD (pH = 5.5)
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-5.695914
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LogD (pH = 7.4)
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-8.189437
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Log P
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1.6338252
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Molar Refractivity
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158.6976 cm3
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Polarizability
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65.17116 Å3
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Polar Surface Area
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302.57 Å2
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Rotatable Bonds
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26
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Lipinski's Rule of Five
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false
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DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
P4725
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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. |
PATENTS
PATENTS
PubChem Patent
Google Patent