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{[(2S,3R,4E)-3-hydroxy-2-octanamidooctadec-4-en-1-yl]oxy}phosphonic acid
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ChemBase ID:
90890
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Molecular Formular:
C26H52NO6P
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Molecular Mass:
505.667941
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Monoisotopic Mass:
505.35322502
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SMILES and InChIs
SMILES:
CCCCCCCCCCCCC/C=C/[C@@H](O)[C@H](COP(=O)(O)O)NC(=O)CCCCCCC
Canonical SMILES:
CCCCCCCCCCCCC/C=C/[C@H]([C@@H](NC(=O)CCCCCCC)COP(=O)(O)O)O
InChI:
InChI=1S/C26H52NO6P/c1-3-5-7-9-10-11-12-13-14-15-16-18-19-21-25(28)24(23-33-34(30,31)32)27-26(29)22-20-17-8-6-4-2/h19,21,24-25,28H,3-18,20,22-23H2,1-2H3,(H,27,29)(H2,30,31,32)/b21-19+/t24-,25+/m0/s1
InChIKey:
VSSNYUXSRXINIP-WRBRXSDHSA-N
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Cite this record
CBID:90890 http://www.chembase.cn/molecule-90890.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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{[(2S,3R,4E)-3-hydroxy-2-octanamidooctadec-4-en-1-yl]oxy}phosphonic acid
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IUPAC Traditional name
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[(2S,3R,4E)-3-hydroxy-2-octanamidooctadec-4-en-1-yl]oxyphosphonic acid
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Synonyms
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N-Octanoylsphingosine-1-phosphate
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C8 Ceramide-1-phosphate
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D-erythro-Ceramide C8 1-phosphate
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CAS Number
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MDL Number
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MFCD00270853
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MFCD00270917
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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
Acid pKa
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1.528374
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H Acceptors
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5
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H Donor
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4
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LogD (pH = 5.5)
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4.781171
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LogD (pH = 7.4)
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3.902242
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Log P
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7.0234156
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Molar Refractivity
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139.8406 cm3
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Polarizability
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55.07053 Å3
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Polar Surface Area
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116.09 Å2
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Rotatable Bonds
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24
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Lipinski's Rule of Five
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false
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DETAILS
DETAILS
Apollo Scientific
Sigma Aldrich
Apollo Scientific Ltd -
OR6272T
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Stimulates DNA synthesis when added exogenously to cultured fibroblasts at 5uM. Mitogenic activity is antagonized by cell permeable ceramides. |
Sigma Aldrich -
C8355
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Biochem/physiol Actions Cell permeable stimulator of DNA synthesis in cultured fibroblasts; antagonizes mitogenic activity. |
PATENTS
PATENTS
PubChem Patent
Google Patent