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6614-35-3 molecular structure
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(4S,5S)-6-({[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxane-2,3,4,5-tetrol

ChemBase ID: 171815
Molecular Formular: C12H22O11
Molecular Mass: 342.29648
Monoisotopic Mass: 342.11621152
SMILES and InChIs

SMILES:
[C@@H]1([C@@H](C([C@H](OC1CO)OCC1[C@H]([C@@H](C(C(O1)O)O)O)O)O)O)O
Canonical SMILES:
OCC1O[C@H](OCC2OC(O)C([C@H]([C@@H]2O)O)O)C([C@H]([C@@H]1O)O)O
InChI:
InChI=1S/C12H22O11/c13-1-3-5(14)8(17)10(19)12(23-3)21-2-4-6(15)7(16)9(18)11(20)22-4/h3-20H,1-2H2/t3?,4?,5-,6-,7+,8+,9?,10?,11?,12+/m1/s1
InChIKey:
DLRVVLDZNNYCBX-KHDAGABXSA-N

Cite this record

CBID:171815 http://www.chembase.cn/molecule-171815.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(4S,5S)-6-({[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxane-2,3,4,5-tetrol
IUPAC Traditional name
(4S,5S)-6-({[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxane-2,3,4,5-tetrol
Synonyms
6-O-α-D-Mannopyranosyl-D-mannopyrannose
6-O-α-Mannobiose
α-(1→6)-Mannobiose
α-D-Man-(1→6)-D-Man
6-O-α-D-Mannopyranosyl-D-mannose
6-O-α-D-Glucopyranosyl-D-glucose
D-Isomaltose
Isomaltose
CAS Number
6614-35-3
499-40-1
PubChem SID
164227725
PubChem CID
46781992

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 46781992 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 11.2481985  H Acceptors 11 
H Donor LogD (pH = 5.5) -4.703376 
LogD (pH = 7.4) -4.7034364  Log P -4.703375 
Molar Refractivity 68.3367 cm3 Polarizability 28.969793 Å3
Polar Surface Area 189.53 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Water expand Show data source
Apperance
White Solid expand Show data source
Yellow Low Melting Solid expand Show data source
Melting Point
>80°C (dec.) expand Show data source
Storage Condition
-20°C Freezer expand Show data source
Hygroscopic, Refrigerator, Under Inert Atmosphere expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
Download expand Show data source

DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - I821250 external link
One of the main product of transformation of maltose into prebiotic isomaltooligosaccharides by novel α-glucosidase from Xantophyllomyces dendrorhous.
Toronto Research Chemicals - M166350 external link
6-O-α-D-Mannopyranosyl-D-mannose is used as an antimicrobial agent against Escherichia coli.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Tzortzis, G., et al.: Appl. Microbiol. Biotechnol., 63, 286 (2003)
  • • Chaen, H., et al.: J. Biosci. Bioeng., 92, 177 (2003)
  • • Ferrer, M., et al.: Biochem. J., 391, 269 (2003)
  • • Hakomori, S., et al.: J. Biochem., 55, 205 (1964)
  • • Nogami, T., et al.: J. Bacteriol., 156, 402 (1964)
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PATENTS

PATENTS

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INTERNET

INTERNET

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