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4682-48-8 molecular structure
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(2R,3S)-N-({[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}methyl)-3-(hexadec-3-en-1-yl)-2-hydroxytetracosanamide

ChemBase ID: 153318
Molecular Formular: C53H101NO13
Molecular Mass: 960.36794
Monoisotopic Mass: 959.7272923
SMILES and InChIs

SMILES:
CCCCCCCCCCCCCCCCCCCCC[C@@H](CC/C=C/CCCCCCCCCCCC)[C@H](C(=O)NCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O[C@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O)O)O)O
Canonical SMILES:
CCCCCCCCCCCCCCCCCCCCC[C@H]([C@H](C(=O)NCO[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O[C@@H]1O[C@H](CO)[C@@H]([C@@H]([C@H]1O)O)O)O)CC/C=C/CCCCCCCCCCCC
InChI:
InChI=1S/C53H101NO13/c1-3-5-7-9-11-13-15-17-19-20-21-22-23-25-27-29-31-33-35-37-41(36-34-32-30-28-26-24-18-16-14-12-10-8-6-4-2)44(57)51(63)54-40-64-52-49(62)47(60)50(43(39-56)66-52)67-53-48(61)46(59)45(58)42(38-55)65-53/h30,32,41-50,52-53,55-62H,3-29,31,33-40H2,1-2H3,(H,54,63)/t41-,42-,43-,44-,45+,46+,47-,48-,49-,50-,52-,53+/m1/s1
InChIKey:
DAMLYUHJAAMPKB-QYGOQDOTSA-N

Cite this record

CBID:153318 http://www.chembase.cn/molecule-153318.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2R,3S)-N-({[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}methyl)-3-(hexadec-3-en-1-yl)-2-hydroxytetracosanamide
IUPAC Traditional name
(2R,3S)-N-({[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}methyl)-3-(hexadec-3-en-1-yl)-2-hydroxytetracosanamide
Synonyms
CDH
Ceramide β-lactoside
Ceramide dihexoside
Ceramide-β-D-lactoside
Lactocerebrosides from bovine brain
CAS Number
4682-48-8
MDL Number
MFCD00133445
PubChem SID
162247457
24892591
PubChem CID
16219109

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
C3166 external link Add to cart Please log in.
Data Source Data ID
PubChem 16219109 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 11.556998  H Acceptors 13 
H Donor LogD (pH = 5.5) 10.908708 
LogD (pH = 7.4) 10.90868  Log P 10.908709 
Molar Refractivity 262.6343 cm3 Polarizability 105.6111 Å3
Polar Surface Area 227.86 Å2 Rotatable Bonds 43 
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
RTECS
FK1000000 expand Show data source
MSDS Link
Download 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
Purity
~95% expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

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PATENTS

PATENTS

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