MiMeDB: Showing metabocard for 1-Î²-D-Arabinofuranosylcytosine (MMDBc0013654)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:55:55 UTC

Update Date

2022-08-31 06:36:34 UTC

Metabolite ID

MMDBc0013654

Metabolite Identification

Common Name

1-Î²-D-Arabinofuranosylcytosine

Description

Structure

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

HMDB0248553
     RDKit          3D
Arabinofuranosylcytosine
 30 31  0  0  0  0  0  0  0  0999 V2000
    5.1385    0.1823   -0.6252 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8904    0.0234   -0.3406 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5612   -0.8723    0.6567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2196   -1.0213    0.9391 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2953   -0.3165    0.2613 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0894   -0.5038    0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6646    0.7470    0.7631 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0137    0.4693    0.8431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7643    1.7523    0.5572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3579    2.6737    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3064   -0.5968   -0.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0576   -1.5836    0.4450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9009   -1.1087   -0.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539   -2.5021   -0.4162 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6112    0.5574   -0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6297    1.2771   -1.3999 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9182    0.7067   -0.9907 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3720    0.8620   -1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3391   -1.4168    1.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9290   -1.7288    1.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2348   -1.1020    1.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2235    0.1248    1.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8497    1.6305    0.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4405    2.1808   -0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7606    3.5509    1.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7668   -0.2159   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5199   -2.3691    0.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5463   -0.7418   -1.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0717   -2.9377   -1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    2.2790   -1.2107 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  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
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
  5 15  1  0
 15 16  1  0
 15 17  2  0
 17  2  1  0
 13  6  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  0
  6 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 12 27  1  0
 13 28  1  0
 14 29  1  0
 16 30  1  0
M  END


  Mrv1652310061710162D          

 17 18  0  0  0  0            999 V2000
    1.7044   -3.4197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1893   -2.7523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2032   -0.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4186   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8839   -3.3335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0837   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -1.3312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0333   -1.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3990   -4.0009    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5484   -2.5798    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8538   -1.9986    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3748    0.5154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2991   -0.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6977   -1.1587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1637   -1.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  4  3  1  0  0  0  0
  5  1  1  0  0  0  0
  6  4  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
 10  5  2  0  0  0  0
 11  5  1  0  0  0  0
 11  9  2  0  0  0  0
 12  2  1  0  0  0  0
 12  8  1  0  0  0  0
 12  9  1  0  0  0  0
 13  3  1  0  0  0  0
 14  6  1  0  0  0  0
 15  7  1  0  0  0  0
 16  9  1  0  0  0  0
 17  4  1  0  0  0  0
 17  8  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0013654

> <DATABASE_NAME>
MIME

> <SMILES>
OCC1OC(C(O)C1O)N1C=CC(=N)N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)

> <INCHI_KEY>
UHDGCWIWMRVCDJ-UHFFFAOYSA-N

> <FORMULA>
C9H13N3O5

> <MOLECULAR_WEIGHT>
243.2166

> <EXACT_MASS>
243.085520541

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
22.737428489554077

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-amino-1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one

> <ALOGPS_LOGP>
-2.04

> <JCHEM_LOGP>
-2.7975172843333334

> <ALOGPS_LOGS>
-1.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.933688762534231

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.553240841265485

> <JCHEM_PKA_STRONGEST_BASIC>
-0.06234248538184939

> <JCHEM_POLAR_SURFACE_AREA>
128.61

> <JCHEM_REFRACTIVITY>
54.5448

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.80e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
cytidine

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0248553
     RDKit          3D
Arabinofuranosylcytosine
 30 31  0  0  0  0  0  0  0  0999 V2000
    5.1385    0.1823   -0.6252 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8904    0.0234   -0.3406 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5612   -0.8723    0.6567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2196   -1.0213    0.9391 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2953   -0.3165    0.2613 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0894   -0.5038    0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6646    0.7470    0.7631 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0137    0.4693    0.8431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7643    1.7523    0.5572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3579    2.6737    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3064   -0.5968   -0.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0576   -1.5836    0.4450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9009   -1.1087   -0.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539   -2.5021   -0.4162 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6112    0.5574   -0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6297    1.2771   -1.3999 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9182    0.7067   -0.9907 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3720    0.8620   -1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3391   -1.4168    1.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9290   -1.7288    1.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2348   -1.1020    1.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2235    0.1248    1.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8497    1.6305    0.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4405    2.1808   -0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7606    3.5509    1.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7668   -0.2159   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5199   -2.3691    0.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5463   -0.7418   -1.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0717   -2.9377   -1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    2.2790   -1.2107 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  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
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
  5 15  1  0
 15 16  1  0
 15 17  2  0
 17  2  1  0
 13  6  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  0
  6 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 12 27  1  0
 13 28  1  0
 14 29  1  0
 16 30  1  0
M  END

HEADER    PROTEIN                                 06-OCT-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-OCT-17         0                                  
HETATM    1  C   UNK     0       3.182  -6.383   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.087  -5.138   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.846  -0.544   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.381  -1.020   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.650  -6.222   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.136  -0.115   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.890  -1.020   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.366  -2.485   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.929  -3.570   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       0.745  -7.468   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0       1.024  -4.816   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0       3.460  -3.731   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0       8.166   0.962   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       5.136   1.425   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       2.425  -0.544   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.302  -2.163   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       5.906  -2.485   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1   12                                                       
CONECT    3    4   13                                                       
CONECT    4    3    6   17                                                  
CONECT    5    1   10   11                                                  
CONECT    6    4    7   14                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7   12   17                                                  
CONECT    9   11   12   16                                                  
CONECT   10    5                                                            
CONECT   11    5    9                                                       
CONECT   12    2    8    9                                                  
CONECT   13    3                                                            
CONECT   14    6                                                            
CONECT   15    7                                                            
CONECT   16    9                                                            
CONECT   17    4    8                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

COMPND    HMDB0248553
HETATM    1  N1  UNL     1       5.139   0.182  -0.625  1.00  0.00           N  
HETATM    2  C1  UNL     1       3.890   0.023  -0.341  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.561  -0.872   0.657  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.220  -1.021   0.939  1.00  0.00           C  
HETATM    5  N2  UNL     1       1.295  -0.316   0.261  1.00  0.00           N  
HETATM    6  C4  UNL     1      -0.089  -0.504   0.589  1.00  0.00           C  
HETATM    7  O1  UNL     1      -0.665   0.747   0.763  1.00  0.00           O  
HETATM    8  C5  UNL     1      -2.014   0.469   0.843  1.00  0.00           C  
HETATM    9  C6  UNL     1      -2.764   1.752   0.557  1.00  0.00           C  
HETATM   10  O2  UNL     1      -2.358   2.674   1.544  1.00  0.00           O  
HETATM   11  C7  UNL     1      -2.306  -0.597  -0.184  1.00  0.00           C  
HETATM   12  O3  UNL     1      -3.058  -1.584   0.445  1.00  0.00           O  
HETATM   13  C8  UNL     1      -0.901  -1.109  -0.513  1.00  0.00           C  
HETATM   14  O4  UNL     1      -0.854  -2.502  -0.416  1.00  0.00           O  
HETATM   15  C9  UNL     1       1.611   0.557  -0.711  1.00  0.00           C  
HETATM   16  O5  UNL     1       0.630   1.277  -1.400  1.00  0.00           O  
HETATM   17  N3  UNL     1       2.918   0.707  -0.991  1.00  0.00           N  
HETATM   18  H1  UNL     1       5.372   0.862  -1.381  1.00  0.00           H  
HETATM   19  H2  UNL     1       4.339  -1.417   1.174  1.00  0.00           H  
HETATM   20  H3  UNL     1       1.929  -1.729   1.730  1.00  0.00           H  
HETATM   21  H4  UNL     1      -0.235  -1.102   1.511  1.00  0.00           H  
HETATM   22  H5  UNL     1      -2.224   0.125   1.870  1.00  0.00           H  
HETATM   23  H6  UNL     1      -3.850   1.630   0.542  1.00  0.00           H  
HETATM   24  H7  UNL     1      -2.440   2.181  -0.410  1.00  0.00           H  
HETATM   25  H8  UNL     1      -2.761   3.551   1.402  1.00  0.00           H  
HETATM   26  H9  UNL     1      -2.767  -0.216  -1.098  1.00  0.00           H  
HETATM   27  H10 UNL     1      -2.520  -2.369   0.631  1.00  0.00           H  
HETATM   28  H11 UNL     1      -0.546  -0.742  -1.480  1.00  0.00           H  
HETATM   29  H12 UNL     1      -1.072  -2.938  -1.290  1.00  0.00           H  
HETATM   30  H13 UNL     1       0.518   2.279  -1.211  1.00  0.00           H  
CONECT    1    2    2   18
CONECT    2    3   17
CONECT    3    4    4   19
CONECT    4    5   20
CONECT    5    6   15
CONECT    6    7   13   21
CONECT    7    8
CONECT    8    9   11   22
CONECT    9   10   23   24
CONECT   10   25
CONECT   11   12   13   26
CONECT   12   27
CONECT   13   14   28
CONECT   14   29
CONECT   15   16   17   17
CONECT   16   30
END

HMDB0248553
     RDKit          3D
Arabinofuranosylcytosine
 30 31  0  0  0  0  0  0  0  0999 V2000
    5.1385    0.1823   -0.6252 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8904    0.0234   -0.3406 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5612   -0.8723    0.6567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2196   -1.0213    0.9391 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2953   -0.3165    0.2613 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0894   -0.5038    0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6646    0.7470    0.7631 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0137    0.4693    0.8431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7643    1.7523    0.5572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3579    2.6737    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3064   -0.5968   -0.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0576   -1.5836    0.4450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9009   -1.1087   -0.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539   -2.5021   -0.4162 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6112    0.5574   -0.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6297    1.2771   -1.3999 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9182    0.7067   -0.9907 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3720    0.8620   -1.3805 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3391   -1.4168    1.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9290   -1.7288    1.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2348   -1.1020    1.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2235    0.1248    1.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8497    1.6305    0.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4405    2.1808   -0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7606    3.5509    1.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7668   -0.2159   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5199   -2.3691    0.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5463   -0.7418   -1.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0717   -2.9377   -1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    2.2790   -1.2107 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  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
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
  5 15  1  0
 15 16  1  0
 15 17  2  0
 17  2  1  0
 13  6  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  0
  6 21  1  0
  8 22  1  0
  9 23  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 12 27  1  0
 13 28  1  0
 14 29  1  0
 16 30  1  0
M  END

Synonyms

Value	Source
Arabinosylcytosine	MeSH
Aracytidine	MeSH
Cytarabine	MeSH
Cytosar	MeSH
Cytosar-u	MeSH
CytosarU	MeSH
Cytosine arabinoside	MeSH
Hydrochloride, cytarabine	MeSH
beta-Ara C	MeSH
Ara-C	MeSH
Aracytine	MeSH
Cytarabine hydrochloride	MeSH
Cytosar u	MeSH
Arabinofuranosylcytosine	MeSH
Arabinoside, cytosine	MeSH
Cytonal	MeSH

Molecular Formula

C₉H₁₃N₃O₅

Average Mass

243.2166

Monoisotopic Mass

243.085520541

IUPAC Name

4-amino-1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one

Traditional Name

cytidine

CAS Registry Number

Not Available

SMILES

OCC1OC(C(O)C1O)N1C=CC(=N)N=C1O

InChI Identifier

InChI=1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)

InChI Key

UHDGCWIWMRVCDJ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrimidine nucleosides. Pyrimidine nucleosides are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Sub Class

Not Available

Direct Parent

Pyrimidine nucleosides

Alternative Parents

Substituents

Pyrimidine nucleoside
Glycosyl compound
N-glycosyl compound
Pentose monosaccharide
Aminopyrimidine
Pyrimidone
Hydropyrimidine
Monosaccharide
Pyrimidine
Imidolactam
Tetrahydrofuran
Heteroaromatic compound
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Primary alcohol
Organic oxide
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
Organopnictogen compound
Organic oxygen compound
Primary amine
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

a pyrimidine ribonucleoside (CYTIDINE )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	2.8 g/L	ALOGPS
logP	-2	ALOGPS
logP	-2.8	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	12.55	ChemAxon
pKa (Strongest Basic)	-0.062	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	128.61 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	54.54 m³·mol⁻¹	ChemAxon
Polarizability	22.74 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Basidiomycota	4	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB001979

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Cytarabine

METLIN ID

Not Available

PubChem Compound

596

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for 1-Î²-D-Arabinofuranosylcytosine (MMDBc0013654)

MOL for #<Metabolite:0x00007f91f9b86f90>

3D MOL for #<Metabolite:0x00007f91f9b86f90>

3D SDF for #<Metabolite:0x00007f91f9b86f90>

3D-SDF for #<Metabolite:0x00007f91f9b86f90>

PDB for #<Metabolite:0x00007f91f9b86f90>

3D PDB for #<Metabolite:0x00007f91f9b86f90>

SMILES for #<Metabolite:0x00007f91f9b86f90>

INCHI for #<Metabolite:0x00007f91f9b86f90>

Structure for #<Metabolite:0x00007f91f9b86f90>

3D Structure for #<Metabolite:0x00007f91f9b86f90>