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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:13:42 UTC

Update Date

2022-03-07 02:55:58 UTC

HMDB ID

HMDB0038880

Secondary Accession Numbers

HMDB38880

Metabolite Identification

Common Name

5-O-a-L-Arabinofuranosyl-L-arabinose

Description

5-O-a-L-Arabinofuranosyl-L-arabinose, also known as arabinobiose, belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. 5-O-a-L-Arabinofuranosyl-L-arabinose has been detected, but not quantified in, fruits and root vegetables. This could make 5-O-a-L-arabinofuranosyl-L-arabinose a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 5-O-a-L-Arabinofuranosyl-L-arabinose.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0038880
     RDKit          3D
5-O-a-L-Arabinofuranosyl-L-arabinose
 37 38  0  0  0  0  0  0  0  0999 V2000
    4.0019    2.4098   -0.2906 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2327    1.2580   -0.9952 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3130    0.1227   -0.6382 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9863    0.3870   -0.8462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2493   -0.1213    0.2015 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0666   -0.7039   -0.1837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9875   -0.0404    0.4420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3228   -0.6641    0.0351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4124   -0.5326   -1.3446 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7392   -0.2833   -1.6434 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5225   -1.4216   -1.5113 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1459    0.6981   -0.5678 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6713    1.9615   -0.9004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4184    0.1497    0.6390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3098   -0.7204    1.3061 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1512   -1.0892    0.9537 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8159   -1.2149    2.2764 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4968   -0.3820    0.7564 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5503   -1.2804    0.8826 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6328    2.2992    0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1113    1.4219   -2.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2724    0.9170   -0.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5883   -0.7279   -1.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0677    0.7248    0.9086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8843   -0.1113    1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0310    1.0346    0.1908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3343   -1.7248    0.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8035    0.1508   -2.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9999   -2.1471   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2477    0.6799   -0.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4935    2.5026   -0.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0810    0.9325    1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7019   -1.3624    1.7910 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820   -2.0676    0.4728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901   -0.3895    2.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5765    0.4575    1.4740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0217   -1.1231    1.7405 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  5 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18  3  1  0
 14  8  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  6
  5 24  1  1
  7 25  1  0
  7 26  1  0
  8 27  1  6
 10 28  1  6
 11 29  1  0
 12 30  1  1
 13 31  1  0
 14 32  1  1
 15 33  1  0
 16 34  1  6
 17 35  1  0
 18 36  1  1
 19 37  1  0
M  END


  Mrv0541 02011302172D          

 19 20  0  0  0  0            999 V2000
    0.5500   -6.9982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1174   -7.4832    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1375   -8.2677    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9625   -8.2677    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2174   -7.4832    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4474   -8.9352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3474   -8.9352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9021   -7.2282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5151   -7.7803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7944   -5.9383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2752   -6.5795    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7245   -7.2714    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5214   -7.0578    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5646   -6.2340    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2565   -5.7847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1626   -7.5770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4289   -8.0416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4514   -6.5363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0021   -7.2282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5 19  1  1  0  0  0
  4  6  1  6  0  0  0
  3  7  1  1  0  0  0
  2  8  1  6  0  0  0
  8  9  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  1  0  0  0
 13 16  1  6  0  0  0
 12 17  1  1  0  0  0
 11 18  1  6  0  0  0
 18 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038880

> <DATABASE_NAME>
hmdb

> <SMILES>
OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C10H18O9/c11-1-3-5(12)8(15)10(19-3)17-2-4-6(13)7(14)9(16)18-4/h3-16H,1-2H2/t3-,4-,5-,6-,7+,8+,9+,10+/m0/s1

> <INCHI_KEY>
HANDMAIZTZRPTQ-GJAWKPGMSA-N

> <FORMULA>
C10H18O9

> <MOLECULAR_WEIGHT>
282.2445

> <EXACT_MASS>
282.095082174

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_AVERAGE_POLARIZABILITY>
26.19011988405302

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4R,5S)-5-({[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)oxolane-2,3,4-triol

> <ALOGPS_LOGP>
-2.84

> <JCHEM_LOGP>
-3.442704979666666

> <ALOGPS_LOGS>
0.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.228911776483972

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.261828185012591

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981143337099244

> <JCHEM_POLAR_SURFACE_AREA>
149.07

> <JCHEM_REFRACTIVITY>
56.411699999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.64e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4R,5S)-5-({[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)oxolane-2,3,4-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038880
     RDKit          3D
5-O-a-L-Arabinofuranosyl-L-arabinose
 37 38  0  0  0  0  0  0  0  0999 V2000
    4.0019    2.4098   -0.2906 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2327    1.2580   -0.9952 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3130    0.1227   -0.6382 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9863    0.3870   -0.8462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2493   -0.1213    0.2015 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0666   -0.7039   -0.1837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9875   -0.0404    0.4420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3228   -0.6641    0.0351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4124   -0.5326   -1.3446 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7392   -0.2833   -1.6434 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5225   -1.4216   -1.5113 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1459    0.6981   -0.5678 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6713    1.9615   -0.9004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4184    0.1497    0.6390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3098   -0.7204    1.3061 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1512   -1.0892    0.9537 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8159   -1.2149    2.2764 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4968   -0.3820    0.7564 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5503   -1.2804    0.8826 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6328    2.2992    0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1113    1.4219   -2.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2724    0.9170   -0.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5883   -0.7279   -1.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0677    0.7248    0.9086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8843   -0.1113    1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0310    1.0346    0.1908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3343   -1.7248    0.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8035    0.1508   -2.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9999   -2.1471   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2477    0.6799   -0.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4935    2.5026   -0.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0810    0.9325    1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7019   -1.3624    1.7910 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820   -2.0676    0.4728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901   -0.3895    2.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5765    0.4575    1.4740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0217   -1.1231    1.7405 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  5 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18  3  1  0
 14  8  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  6
  5 24  1  1
  7 25  1  0
  7 26  1  0
  8 27  1  6
 10 28  1  6
 11 29  1  0
 12 30  1  1
 13 31  1  0
 14 32  1  1
 15 33  1  0
 16 34  1  6
 17 35  1  0
 18 36  1  1
 19 37  1  0
M  END

HEADER    PROTEIN                                 01-FEB-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-FEB-13         0                                  
HETATM    1  O   UNK     0       1.027 -13.063   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -0.219 -13.969   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.257 -15.433   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.797 -15.433   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.272 -13.969   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.702 -16.679   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -0.648 -16.679   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.684 -13.493   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.828 -14.523   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       7.083 -11.085   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.114 -12.282   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.952 -13.573   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.440 -13.175   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.521 -11.637   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.812 -10.798   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       9.637 -14.144   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.401 -15.011   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.576 -12.201   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.737 -13.493   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    3    8                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    1   19                                                  
CONECT    6    4                                                            
CONECT    7    3                                                            
CONECT    8    2    9                                                       
CONECT    9    8                                                            
CONECT   10   11   14                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   10   15                                                  
CONECT   15   14                                                            
CONECT   16   13                                                            
CONECT   17   12                                                            
CONECT   18   11   19                                                       
CONECT   19    5   18                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   40    0
END

COMPND    HMDB0038880
HETATM    1  O1  UNL     1       4.002   2.410  -0.291  1.00  0.00           O  
HETATM    2  C1  UNL     1       4.233   1.258  -0.995  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.313   0.123  -0.638  1.00  0.00           C  
HETATM    4  O2  UNL     1       1.986   0.387  -0.846  1.00  0.00           O  
HETATM    5  C3  UNL     1       1.249  -0.121   0.201  1.00  0.00           C  
HETATM    6  O3  UNL     1       0.067  -0.704  -0.184  1.00  0.00           O  
HETATM    7  C4  UNL     1      -0.987  -0.040   0.442  1.00  0.00           C  
HETATM    8  C5  UNL     1      -2.323  -0.664   0.035  1.00  0.00           C  
HETATM    9  O4  UNL     1      -2.412  -0.533  -1.345  1.00  0.00           O  
HETATM   10  C6  UNL     1      -3.739  -0.283  -1.643  1.00  0.00           C  
HETATM   11  O5  UNL     1      -4.522  -1.422  -1.511  1.00  0.00           O  
HETATM   12  C7  UNL     1      -4.146   0.698  -0.568  1.00  0.00           C  
HETATM   13  O6  UNL     1      -3.671   1.961  -0.900  1.00  0.00           O  
HETATM   14  C8  UNL     1      -3.418   0.150   0.639  1.00  0.00           C  
HETATM   15  O7  UNL     1      -4.310  -0.720   1.306  1.00  0.00           O  
HETATM   16  C9  UNL     1       2.151  -1.089   0.954  1.00  0.00           C  
HETATM   17  O8  UNL     1       1.816  -1.215   2.276  1.00  0.00           O  
HETATM   18  C10 UNL     1       3.497  -0.382   0.756  1.00  0.00           C  
HETATM   19  O9  UNL     1       4.550  -1.280   0.883  1.00  0.00           O  
HETATM   20  H1  UNL     1       3.633   2.299   0.599  1.00  0.00           H  
HETATM   21  H2  UNL     1       4.111   1.422  -2.104  1.00  0.00           H  
HETATM   22  H3  UNL     1       5.272   0.917  -0.838  1.00  0.00           H  
HETATM   23  H4  UNL     1       3.588  -0.728  -1.328  1.00  0.00           H  
HETATM   24  H5  UNL     1       1.068   0.725   0.909  1.00  0.00           H  
HETATM   25  H6  UNL     1      -0.884  -0.111   1.544  1.00  0.00           H  
HETATM   26  H7  UNL     1      -1.031   1.035   0.191  1.00  0.00           H  
HETATM   27  H8  UNL     1      -2.334  -1.725   0.346  1.00  0.00           H  
HETATM   28  H9  UNL     1      -3.804   0.151  -2.658  1.00  0.00           H  
HETATM   29  H10 UNL     1      -4.000  -2.147  -1.066  1.00  0.00           H  
HETATM   30  H11 UNL     1      -5.248   0.680  -0.433  1.00  0.00           H  
HETATM   31  H12 UNL     1      -3.494   2.503  -0.088  1.00  0.00           H  
HETATM   32  H13 UNL     1      -3.081   0.932   1.333  1.00  0.00           H  
HETATM   33  H14 UNL     1      -3.702  -1.362   1.791  1.00  0.00           H  
HETATM   34  H15 UNL     1       2.182  -2.068   0.473  1.00  0.00           H  
HETATM   35  H16 UNL     1       1.790  -0.389   2.784  1.00  0.00           H  
HETATM   36  H17 UNL     1       3.577   0.458   1.474  1.00  0.00           H  
HETATM   37  H18 UNL     1       5.022  -1.123   1.740  1.00  0.00           H  
CONECT    1    2   20
CONECT    2    3   21   22
CONECT    3    4   18   23
CONECT    4    5
CONECT    5    6   16   24
CONECT    6    7
CONECT    7    8   25   26
CONECT    8    9   14   27
CONECT    9   10
CONECT   10   11   12   28
CONECT   11   29
CONECT   12   13   14   30
CONECT   13   31
CONECT   14   15   32
CONECT   15   33
CONECT   16   17   18   34
CONECT   17   35
CONECT   18   19   36
CONECT   19   37
END

HMDB0038880
     RDKit          3D
5-O-a-L-Arabinofuranosyl-L-arabinose
 37 38  0  0  0  0  0  0  0  0999 V2000
    4.0019    2.4098   -0.2906 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2327    1.2580   -0.9952 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3130    0.1227   -0.6382 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9863    0.3870   -0.8462 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2493   -0.1213    0.2015 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0666   -0.7039   -0.1837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9875   -0.0404    0.4420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3228   -0.6641    0.0351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4124   -0.5326   -1.3446 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7392   -0.2833   -1.6434 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5225   -1.4216   -1.5113 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1459    0.6981   -0.5678 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6713    1.9615   -0.9004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4184    0.1497    0.6390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3098   -0.7204    1.3061 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1512   -1.0892    0.9537 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8159   -1.2149    2.2764 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4968   -0.3820    0.7564 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5503   -1.2804    0.8826 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6328    2.2992    0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1113    1.4219   -2.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2724    0.9170   -0.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5883   -0.7279   -1.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0677    0.7248    0.9086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8843   -0.1113    1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0310    1.0346    0.1908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3343   -1.7248    0.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8035    0.1508   -2.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9999   -2.1471   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2477    0.6799   -0.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4935    2.5026   -0.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0810    0.9325    1.3332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7019   -1.3624    1.7910 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820   -2.0676    0.4728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901   -0.3895    2.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5765    0.4575    1.4740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0217   -1.1231    1.7405 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  5 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18  3  1  0
 14  8  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  6
  5 24  1  1
  7 25  1  0
  7 26  1  0
  8 27  1  6
 10 28  1  6
 11 29  1  0
 12 30  1  1
 13 31  1  0
 14 32  1  1
 15 33  1  0
 16 34  1  6
 17 35  1  0
 18 36  1  1
 19 37  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Arabinobiose	HMDB

Chemical Formula

C₁₀H₁₈O₉

Average Molecular Weight

282.2445

Monoisotopic Molecular Weight

282.095082174

IUPAC Name

(2R,3R,4R,5S)-5-({[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)oxolane-2,3,4-triol

Traditional Name

(2R,3R,4R,5S)-5-({[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)oxolane-2,3,4-triol

CAS Registry Number

Not Available

SMILES

OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C10H18O9/c11-1-3-5(12)8(15)10(19-3)17-2-4-6(13)7(14)9(16)18-4/h3-16H,1-2H2/t3-,4-,5-,6-,7+,8+,9+,10+/m0/s1

InChI Key

HANDMAIZTZRPTQ-GJAWKPGMSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
Disaccharide
Tetrahydrofuran
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Ingestion (HMDB: HMDB0038880)

Source

Exogenous

Food

Food (HMDB: HMDB0038880)

Fruit

Fruits (FooDB: FOOD00871)

Vegetable

Root vegetable

Root vegetables (FooDB: FOOD00873)

Endogenous

Plant

Plant (HMDB: HMDB0038880)

Not Available

Nutrient (HMDB: HMDB0038880)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	564 g/L	ALOGPS
logP	-2.8	ALOGPS
logP	-3.4	ChemAxon
logS	0.3	ALOGPS
pKa (Strongest Acidic)	11.26	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	149.07 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	56.41 m³·mol⁻¹	ChemAxon
Polarizability	26.19 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	165.137	31661259
DarkChem	[M-H]-	162.455	31661259
DeepCCS	[M+H]+	160.692	30932474
DeepCCS	[M-H]-	158.296	30932474
DeepCCS	[M-2H]-	192.175	30932474
DeepCCS	[M+Na]+	166.711	30932474
AllCCS	[M+H]+	165.2	32859911
AllCCS	[M+H-H2O]+	161.8	32859911
AllCCS	[M+NH4]+	168.4	32859911
AllCCS	[M+Na]+	169.3	32859911
AllCCS	[M-H]-	161.4	32859911
AllCCS	[M+Na-2H]-	161.1	32859911
AllCCS	[M+HCOO]-	161.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
5-O-a-L-Arabinofuranosyl-L-arabinose	OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	3802.9	Standard polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose	OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2414.8	Standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose	OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2414.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
5-O-a-L-Arabinofuranosyl-L-arabinose,1TMS,isomer #1	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2430.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2435.9	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)O[C@H]1O	2433.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)O[C@@H](O)[C@@H]1O	2406.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO)O[C@H]1OC[C@@H]1O[C@@H](O)[C@H](O)[C@H]1O	2426.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TMS,isomer #6	C[Si](C)(C)O[C@H]1[C@H](CO)O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2404.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #1	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2450.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C	2426.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@H]1O	2444.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@H]1O	2465.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #13	C[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](O)[C@@H]1O	2421.9	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #14	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO)O[C@H]1OC[C@@H]1O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	2444.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #15	C[Si](C)(C)O[C@H]1[C@H](CO)O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	2410.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #2	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@H]1O	2462.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #3	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2437.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #4	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	2441.9	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #5	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2420.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #6	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@H]1O	2424.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #7	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2444.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #8	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	2416.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TMS,isomer #9	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2422.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #1	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@H]1O	2430.9	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #10	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2414.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2405.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #12	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	2417.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #13	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2413.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #14	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2436.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #15	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2431.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #16	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2396.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #17	C[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C	2436.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #18	C[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](O)[C@@H]1O[Si](C)(C)C	2454.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #19	C[Si](C)(C)O[C@H]1[C@H](CO)O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	2443.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #2	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2432.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #20	C[Si](C)(C)O[C@H]1[C@H](CO)O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2413.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #3	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	2448.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #4	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2425.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #5	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2454.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #6	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	2481.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #7	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2459.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #8	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2455.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TMS,isomer #9	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2431.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #1	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	2416.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #10	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2419.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #11	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2404.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #12	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2400.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #13	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2402.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #14	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2420.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #15	C[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](O)[C@@H]1O[Si](C)(C)C	2434.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #2	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	2440.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #3	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	2426.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #4	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2444.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #5	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2430.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #6	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2394.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #7	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2475.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #8	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2460.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TMS,isomer #9	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2456.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TMS,isomer #1	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	2436.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TMS,isomer #2	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	2427.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TMS,isomer #3	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2408.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TMS,isomer #4	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2413.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TMS,isomer #5	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2447.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TMS,isomer #6	C[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2392.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,6TMS,isomer #1	C[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2424.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2648.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2642.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)O[C@H]1O	2652.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)O[C@@H](O)[C@@H]1O	2630.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO)O[C@H]1OC[C@@H]1O[C@@H](O)[C@H](O)[C@H]1O	2641.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO)O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	2627.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O	2888.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2886.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@H]1O	2893.9	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@H]1O	2912.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](O)[C@@H]1O	2868.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO)O[C@H]1OC[C@@H]1O[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	2888.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO)O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	2872.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O)[C@H]1O	2906.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	2873.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	2884.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	2861.9	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O)[C@H]1O	2881.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	2899.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	2877.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	2885.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O)[C@H]1O	3114.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3092.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3120.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3106.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3117.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3125.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3134.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3100.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3122.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3136.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO)O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	3140.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3106.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO)O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3109.5	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3127.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3106.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3120.9	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3154.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3134.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3114.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3092.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3311.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3312.8	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3320.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3335.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3306.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3324.4	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3346.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3349.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3325.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3336.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3312.6	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3317.7	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3357.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3336.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3353.2	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3506.1	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3488.3	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3503.9	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3487.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@@H](OC[C@@H]2O[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3517.0	Semi standard non polar	33892256
5-O-a-L-Arabinofuranosyl-L-arabinose,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1O[C@@H](CO[C@@H]2O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3491.8	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose GC-MS (Non-derivatized) - 70eV, Positive	splash10-0229-7390000000-8d23580f0bba7820ff6b	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose GC-MS (5 TMS) - 70eV, Positive	splash10-004i-3412149000-16728ef48f4ef09d6b11	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 10V, Positive-QTOF	splash10-00lr-1290000000-4bec79f959b2070aa19e	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 20V, Positive-QTOF	splash10-00lr-1960000000-65ed6267ed91d4c66f3f	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 40V, Positive-QTOF	splash10-00lv-9610000000-3eedf05f3c75fe70240f	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 10V, Negative-QTOF	splash10-001i-2590000000-af60d6adf6f4269d7f7a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 20V, Negative-QTOF	splash10-001i-0920000000-cd0495455804f69be2e6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 40V, Negative-QTOF	splash10-0k9y-8900000000-84824dac989f83e4bd7f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 10V, Negative-QTOF	splash10-01q9-0960000000-7bcbdc535bcf69dfd712	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 20V, Negative-QTOF	splash10-0a5c-9800000000-7d42943895ad2dcb7fe8	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 40V, Negative-QTOF	splash10-0006-9100000000-5a22aed411221a9a2834	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 10V, Positive-QTOF	splash10-001i-0490000000-b3350f85b96ed3cad467	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 20V, Positive-QTOF	splash10-00lr-3920000000-c6fd42fe88fc81dd3f02	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-O-a-L-Arabinofuranosyl-L-arabinose 40V, Positive-QTOF	splash10-066u-9600000000-fcc1855f5e7085008d77	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB018326

KNApSAcK ID

Not Available

Chemspider ID

30777300

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

74539967

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for 5-O-a-L-Arabinofuranosyl-L-arabinose (HMDB0038880)

MOL for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

3D MOL for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

3D SDF for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

3D-SDF for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

PDB for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

3D PDB for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

SMILES for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

INCHI for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

Structure for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

3D Structure for HMDB0038880 (5-O-a-L-Arabinofuranosyl-L-arabinose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra