Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 22:35:57 UTC

Update Date

2021-09-26 22:54:03 UTC

HMDB ID

HMDB0245536

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2'-Fluoro-2',3'-dideoxyadenosine

Description

2'-Fluoro-2',3'-dideoxyadenosine belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleosides. Purine 2',3'-dideoxyribonucleosides are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at positions 2 and 3. Based on a literature review a small amount of articles have been published on 2'-Fluoro-2',3'-dideoxyadenosine. This compound has been identified in human blood as reported by (PMID: 31557052 ). 2'-fluoro-2',3'-dideoxyadenosine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 2'-Fluoro-2',3'-dideoxyadenosine is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0247792
     RDKit          3D
[(2S,5R)-5-(6-Aminopurin-9-yl)-4-fluorooxolan-2-yl]methanol
 30 32  0  0  0  0  0  0  0  0999 V2000
    4.5619    1.5875   -0.5919 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6768    0.4837   -0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1220   -0.7335   -0.8054 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3084   -1.7884   -0.6839 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0698   -1.5896   -0.2113 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5702   -0.4126    0.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4020    0.6925    0.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6999    1.7373    0.4509 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961    1.3247    0.8138 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3639   -0.0210    0.6462 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7859   -0.8415    0.9248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8626    0.0231    1.1513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3047    0.4807   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8126    0.2136   -0.1581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4931    0.8657    0.8562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6655   -0.3657   -1.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2840   -1.5882   -0.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3542   -2.3671   -0.8870 F   0  0  0  0  0  0  0  0  0  0  0  0
    5.1339    1.6331   -1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6605    2.3433    0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5866   -2.7995   -0.9442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2839    1.9776    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6503   -1.4999    1.7991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1641    1.5598   -0.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9769   -0.8681   -0.1905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1373    0.6951   -1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5514    1.8235    0.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7490    0.1516   -1.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3499   -0.6332   -1.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2264   -2.0846   -0.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 13 16  1  0
 16 17  1  0
 17 18  1  0
  7  2  1  0
 17 11  1  0
 10  6  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  9 22  1  0
 11 23  1  0
 13 24  1  0
 14 25  1  0
 14 26  1  0
 15 27  1  0
 16 28  1  0
 16 29  1  0
 17 30  1  0
M  END


  Mrv1652309112100362D          

 18 20  0  0  0  0            999 V2000
   -1.1831    1.8341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    2.0890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0865    1.4216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.7541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831    1.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8505    0.5241    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6955    3.4867    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  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0245536

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC=NC2=C1N=CN2C1OC(CO)CC1F

> <INCHI_IDENTIFIER>
InChI=1S/C10H12FN5O2/c11-6-1-5(2-17)18-10(6)16-4-15-7-8(12)13-3-14-9(7)16/h3-6,10,17H,1-2H2,(H2,12,13,14)

> <INCHI_KEY>
KBEMFSMODRNJHE-UHFFFAOYSA-N

> <FORMULA>
C10H12FN5O2

> <MOLECULAR_WEIGHT>
253.237

> <EXACT_MASS>
253.097502809

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
23.525983822130247

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[5-(6-amino-9H-purin-9-yl)-4-fluorooxolan-2-yl]methanol

> <ALOGPS_LOGP>
-0.18

> <JCHEM_LOGP>
-0.5095774166666668

> <ALOGPS_LOGS>
-1.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.53524643432034

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.667323209018623

> <JCHEM_PKA_STRONGEST_BASIC>
3.9196593627437784

> <JCHEM_POLAR_SURFACE_AREA>
99.08

> <JCHEM_REFRACTIVITY>
60.4064

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.78e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[5-(6-aminopurin-9-yl)-4-fluorooxolan-2-yl]methanol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0247792
     RDKit          3D
[(2S,5R)-5-(6-Aminopurin-9-yl)-4-fluorooxolan-2-yl]methanol
 30 32  0  0  0  0  0  0  0  0999 V2000
    4.5619    1.5875   -0.5919 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6768    0.4837   -0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1220   -0.7335   -0.8054 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3084   -1.7884   -0.6839 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0698   -1.5896   -0.2113 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5702   -0.4126    0.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4020    0.6925    0.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6999    1.7373    0.4509 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961    1.3247    0.8138 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3639   -0.0210    0.6462 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7859   -0.8415    0.9248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8626    0.0231    1.1513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3047    0.4807   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8126    0.2136   -0.1581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4931    0.8657    0.8562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6655   -0.3657   -1.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2840   -1.5882   -0.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3542   -2.3671   -0.8870 F   0  0  0  0  0  0  0  0  0  0  0  0
    5.1339    1.6331   -1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6605    2.3433    0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5866   -2.7995   -0.9442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2839    1.9776    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6503   -1.4999    1.7991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1641    1.5598   -0.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9769   -0.8681   -0.1905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1373    0.6951   -1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5514    1.8235    0.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7490    0.1516   -1.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3499   -0.6332   -1.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2264   -2.0846   -0.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 13 16  1  0
 16 17  1  0
 17 18  1  0
  7  2  1  0
 17 11  1  0
 10  6  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  9 22  1  0
 11 23  1  0
 13 24  1  0
 14 25  1  0
 14 26  1  0
 15 27  1  0
 16 28  1  0
 16 29  1  0
 17 30  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -2.208   3.424   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.744   3.899   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.161   2.654   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -0.744   1.408   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.208   1.884   0.000  0.00  0.00           C+0
HETATM    6  F   UNK     0      -3.454   0.978   0.000  0.00  0.00           F+0
HETATM    7  N   UNK     0      -0.268  -0.057   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -0.268  -2.549   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       2.530   0.237   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       3.864  -0.533   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       3.864  -2.073   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       2.530  -4.383   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -0.268   5.364   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.298   6.509   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5                                                            
CONECT    7    4    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10    7   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10   16                                                  
CONECT   16   15                                                            
CONECT   17    2   18                                                       
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

COMPND    HMDB0245536
HETATM    1  N1  UNL     1      -4.843  -1.030   0.726  1.00  0.00           N  
HETATM    2  C1  UNL     1      -3.684  -0.226   0.779  1.00  0.00           C  
HETATM    3  N2  UNL     1      -3.579   0.855   1.574  1.00  0.00           N  
HETATM    4  C2  UNL     1      -2.462   1.604   1.605  1.00  0.00           C  
HETATM    5  N3  UNL     1      -1.423   1.264   0.820  1.00  0.00           N  
HETATM    6  C3  UNL     1      -1.445   0.213   0.006  1.00  0.00           C  
HETATM    7  C4  UNL     1      -2.592  -0.552  -0.022  1.00  0.00           C  
HETATM    8  N4  UNL     1      -2.339  -1.528  -0.914  1.00  0.00           N  
HETATM    9  C5  UNL     1      -1.096  -1.355  -1.399  1.00  0.00           C  
HETATM   10  N5  UNL     1      -0.522  -0.280  -0.841  1.00  0.00           N  
HETATM   11  C6  UNL     1       0.793   0.173  -1.142  1.00  0.00           C  
HETATM   12  O1  UNL     1       1.696  -0.820  -0.806  1.00  0.00           O  
HETATM   13  C7  UNL     1       2.125  -0.602   0.478  1.00  0.00           C  
HETATM   14  C8  UNL     1       3.634  -0.874   0.500  1.00  0.00           C  
HETATM   15  O2  UNL     1       4.258   0.004  -0.395  1.00  0.00           O  
HETATM   16  C9  UNL     1       1.823   0.806   0.862  1.00  0.00           C  
HETATM   17  C10 UNL     1       1.239   1.376  -0.405  1.00  0.00           C  
HETATM   18  F1  UNL     1       2.271   1.966  -1.152  1.00  0.00           F  
HETATM   19  H1  UNL     1      -5.212  -1.444  -0.153  1.00  0.00           H  
HETATM   20  H2  UNL     1      -5.357  -1.221   1.607  1.00  0.00           H  
HETATM   21  H3  UNL     1      -2.420   2.466   2.260  1.00  0.00           H  
HETATM   22  H4  UNL     1      -0.664  -2.034  -2.147  1.00  0.00           H  
HETATM   23  H5  UNL     1       0.936   0.359  -2.247  1.00  0.00           H  
HETATM   24  H6  UNL     1       1.633  -1.343   1.149  1.00  0.00           H  
HETATM   25  H7  UNL     1       4.039  -0.806   1.515  1.00  0.00           H  
HETATM   26  H8  UNL     1       3.802  -1.902   0.114  1.00  0.00           H  
HETATM   27  H9  UNL     1       4.915   0.529   0.114  1.00  0.00           H  
HETATM   28  H10 UNL     1       1.196   0.920   1.743  1.00  0.00           H  
HETATM   29  H11 UNL     1       2.783   1.320   1.066  1.00  0.00           H  
HETATM   30  H12 UNL     1       0.499   2.160  -0.251  1.00  0.00           H  
CONECT    1    2   19   20
CONECT    2    3    3    7
CONECT    3    4
CONECT    4    5    5   21
CONECT    5    6
CONECT    6    7    7   10
CONECT    7    8
CONECT    8    9    9
CONECT    9   10   22
CONECT   10   11
CONECT   11   12   17   23
CONECT   12   13
CONECT   13   14   16   24
CONECT   14   15   25   26
CONECT   15   27
CONECT   16   17   28   29
CONECT   17   18   30
END

HMDB0247792
     RDKit          3D
[(2S,5R)-5-(6-Aminopurin-9-yl)-4-fluorooxolan-2-yl]methanol
 30 32  0  0  0  0  0  0  0  0999 V2000
    4.5619    1.5875   -0.5919 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6768    0.4837   -0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1220   -0.7335   -0.8054 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3084   -1.7884   -0.6839 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0698   -1.5896   -0.2113 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5702   -0.4126    0.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4020    0.6925    0.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6999    1.7373    0.4509 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961    1.3247    0.8138 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3639   -0.0210    0.6462 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7859   -0.8415    0.9248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8626    0.0231    1.1513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3047    0.4807   -0.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8126    0.2136   -0.1581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4931    0.8657    0.8562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6655   -0.3657   -1.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2840   -1.5882   -0.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3542   -2.3671   -0.8870 F   0  0  0  0  0  0  0  0  0  0  0  0
    5.1339    1.6331   -1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6605    2.3433    0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5866   -2.7995   -0.9442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2839    1.9776    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6503   -1.4999    1.7991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1641    1.5598   -0.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9769   -0.8681   -0.1905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1373    0.6951   -1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5514    1.8235    0.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7490    0.1516   -1.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3499   -0.6332   -1.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2264   -2.0846   -0.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 13 16  1  0
 16 17  1  0
 17 18  1  0
  7  2  1  0
 17 11  1  0
 10  6  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  9 22  1  0
 11 23  1  0
 13 24  1  0
 14 25  1  0
 14 26  1  0
 15 27  1  0
 16 28  1  0
 16 29  1  0
 17 30  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₀H₁₂FN₅O₂

Average Molecular Weight

253.237

Monoisotopic Molecular Weight

253.097502809

IUPAC Name

[5-(6-amino-9H-purin-9-yl)-4-fluorooxolan-2-yl]methanol

Traditional Name

[5-(6-aminopurin-9-yl)-4-fluorooxolan-2-yl]methanol

CAS Registry Number

Not Available

SMILES

NC1=NC=NC2=C1N=CN2C1OC(CO)CC1F

InChI Identifier

InChI=1S/C10H12FN5O2/c11-6-1-5(2-17)18-10(6)16-4-15-7-8(12)13-3-14-9(7)16/h3-6,10,17H,1-2H2,(H2,12,13,14)

InChI Key

KBEMFSMODRNJHE-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleosides. Purine 2',3'-dideoxyribonucleosides are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Sub Class

Purine 2',3'-dideoxyribonucleosides

Direct Parent

Purine 2',3'-dideoxyribonucleosides

Alternative Parents

Substituents

Purine 2',3'-dideoxyribonucleoside
6-aminopurine
Imidazopyrimidine
Purine
Aminopyrimidine
N-substituted imidazole
Imidolactam
Pyrimidine
Azole
Imidazole
Heteroaromatic compound
Tetrahydrofuran
Oxacycle
Azacycle
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Organofluoride
Organohalogen compound
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Amine
Alkyl halide
Primary alcohol
Primary amine
Alkyl fluoride
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

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
logP	-0.18	ALOGPS
logP	-0.51	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	14.67	ChemAxon
pKa (Strongest Basic)	3.92	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	99.08 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	60.41 m³·mol⁻¹	ChemAxon
Polarizability	23.53 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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
DeepCCS	[M+H]+	154.565	30932474
DeepCCS	[M-H]-	152.207	30932474
DeepCCS	[M-2H]-	185.931	30932474
DeepCCS	[M+Na]+	160.907	30932474
AllCCS	[M+H]+	157.6	32859911
AllCCS	[M+H-H2O]+	153.9	32859911
AllCCS	[M+NH4]+	161.1	32859911
AllCCS	[M+Na]+	162.1	32859911
AllCCS	[M-H]-	156.4	32859911
AllCCS	[M+Na-2H]-	156.0	32859911
AllCCS	[M+HCOO]-	155.7	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	9.5603 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.55 minutes	32390414

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2'-Fluoro-2',3'-dideoxyadenosine,1TMS,isomer #1	C[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N)N=CN=C32)O1	2373.2	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TMS,isomer #1	C[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N)N=CN=C32)O1	2317.1	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TMS,isomer #1	C[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N)N=CN=C32)O1	3693.1	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TMS,isomer #2	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO)CC1F	2405.9	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TMS,isomer #2	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO)CC1F	2469.5	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TMS,isomer #2	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO)CC1F	3785.5	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TMS,isomer #1	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C)CC1F	2387.1	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TMS,isomer #1	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C)CC1F	2420.1	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TMS,isomer #1	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C)CC1F	3406.9	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TMS,isomer #2	C[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(CO)CC1F)[Si](C)(C)C	2403.4	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TMS,isomer #2	C[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(CO)CC1F)[Si](C)(C)C	2572.0	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TMS,isomer #2	C[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(CO)CC1F)[Si](C)(C)C	3293.6	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,3TMS,isomer #1	C[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)O1	2406.0	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,3TMS,isomer #1	C[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)O1	2557.7	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,3TMS,isomer #1	C[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)O1	2934.8	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N)N=CN=C32)O1	2625.4	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N)N=CN=C32)O1	2550.9	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N)N=CN=C32)O1	3758.7	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO)CC1F	2587.6	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO)CC1F	2707.1	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO)CC1F	3795.4	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C(C)(C)C)CC1F	2796.2	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C(C)(C)C)CC1F	2861.7	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C(C)(C)C)CC1F	3514.7	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(CO)CC1F)[Si](C)(C)C(C)(C)C	2776.1	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(CO)CC1F)[Si](C)(C)C(C)(C)C	2994.2	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(CO)CC1F)[Si](C)(C)C(C)(C)C	3328.9	Standard polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)O1	2940.3	Semi standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)O1	3174.2	Standard non polar	33892256
2'-Fluoro-2',3'-dideoxyadenosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1CC(F)C(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)O1	3163.2	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine GC-MS (Non-derivatized) - 70eV, Positive	splash10-005a-9230000000-4789b67c32bcb5607e71	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine 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 - 2'-Fluoro-2',3'-dideoxyadenosine 10V, Positive-QTOF	splash10-0udr-0790000000-99654f827ce6e0ff897c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine 20V, Positive-QTOF	splash10-000i-0900000000-c1ee2199364d0258bae1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine 40V, Positive-QTOF	splash10-000i-1900000000-2c3413f14fe2d3deda2d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine 10V, Negative-QTOF	splash10-0ue9-0590000000-9c903bff7a8c8333cbf6	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine 20V, Negative-QTOF	splash10-001i-0900000000-07c214067483fcda99ba	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2'-Fluoro-2',3'-dideoxyadenosine 40V, Negative-QTOF	splash10-053r-1900000000-a70186ca34251fa67a17	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

316716

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

356786

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 2'-Fluoro-2',3'-dideoxyadenosine (HMDB0245536)

MOL for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

3D MOL for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

3D SDF for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

3D-SDF for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

PDB for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

3D PDB for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

SMILES for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

INCHI for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

Structure for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

3D Structure for HMDB0245536 (2'-Fluoro-2',3'-dideoxyadenosine)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra