MiMeDB: Showing metabocard for Uridine (MMDBc0000094)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-10-27 23:30:09 UTC

Update Date

2024-10-10 00:15:15 UTC

Metabolite ID

MMDBc0000094

Metabolite Identification

Common Name

Uridine

Description

Uridine, also known as beta-uridine or 1-beta-D-ribofuranosylpyrimidine-2,4(1H,3H)-dione, is a member of the class of compounds known as pyrimidine nucleosides. Pyrimidine nucleosides are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety. More specifically, uridine is a nucleoside consisting of uracil and D-ribose and a component of RNA. Uridine is soluble (in water) and a very weakly acidic compound (based on its pKa). Uridine can be synthesized from uracil. It is one of the five standard nucleosides which make up nucleic acids, the others being adenosine, thymidine, cytidine and guanosine. The five nucleosides are commonly abbreviated to their one-letter codes U, A, T, C and G respectively. Uridine is also a parent compound for other transformation products, including but not limited to, nikkomycin Z, 3'-(enolpyruvyl)uridine 5'-monophosphate, and 5-aminomethyl-2-thiouridine. Uridine can be found in most biofluids, including urine, breast milk, cerebrospinal fluid (CSF), and blood. Within the cell, uridine is primarily located in the mitochondria, in the nucleus and the lysosome. It can also be found in the extracellular space. As an essential nucleoside, uridine exists in all living species, ranging from bacteria to humans. In humans, uridine is involved in several metabolic disorders, some of which include dhydropyrimidinase deficiency, MNGIE (mitochondrial neurogastrointestinal encephalopathy), and beta-ureidopropionase deficiency. Moreover, uridine is found to be associated with Lesch-Nyhan syndrome, which is an inborn error of metabolism. Uridine is a nucleoside consisting of uracil and D-ribose and a component of RNA. Uridine plays a role in the glycolysis pathway of galactose. In humans there is no catabolic process to metabolize galactose. Therefore, galactose is converted to glucose and metabolized via the normal glucose metabolism pathways. More specifically, consumed galactose is converted into galactose 1-phosphate (Gal-1-P). This molecule is a substrate for the enzyme galactose-1-phosphate uridyl transferase which transfers a UDP molecule to the galactose molecule. The end result is UDP-galactose and glucose-1-phosphate. This process is continued to allow the proper glycolysis of galactose. Uridine is found in many foods (anything containing RNA) but is destroyed in the liver and gastrointestinal tract, and so no food, when consumed, has ever been reliably shown to elevate blood uridine levels. On the other hand, consumption of RNA-rich foods may lead to high levels of purines (adenine and guanosine) in blood. High levels of purines are known to increase uric acid production and may aggravate or lead to conditions such as gout.

Structure

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

HMDB0000296
     RDKit          3D
Uridine
 29 30  0  0  0  0  0  0  0  0999 V2000
    5.4528   -0.1646   -0.5518 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2120   -0.1635   -0.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6593    0.4277    0.7081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025    0.4143    0.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4700   -0.1577   -0.0541 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0766   -0.1078    0.2036 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6830   -1.0635   -0.4136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9724   -0.6966   -0.0001 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0343   -1.3987   -0.8142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2709   -0.9718   -0.3319 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0554    0.8003   -0.1185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4537    1.3579    1.1004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790    1.1840   -0.2854 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2267    2.2216    0.5490 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411   -0.7283   -1.1270 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2511   -1.2604   -1.9661 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3751   -0.7289   -1.2907 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2741    0.9060    1.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8871    0.8881    1.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1455   -0.1454    1.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0346   -0.9755    1.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9060   -1.2308   -1.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9574   -2.4912   -0.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2502   -0.8541    0.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6675    1.1341   -0.9584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2495    0.7100    1.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3744    1.3628   -1.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9402    2.9056    0.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7992   -1.1736   -2.1243 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  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  2  0
 15 17  1  0
 17  2  1  0
 13  6  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  1
  8 21  1  1
  9 22  1  0
  9 23  1  0
 10 24  1  0
 11 25  1  6
 12 26  1  0
 13 27  1  6
 14 28  1  0
 17 29  1  0
M  END


  Mrv1652309042000002D          

 17 18  0  0  1  0            999 V2000
    0.0000   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674   -1.3099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6675   -1.3099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.0945    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4125   -2.0945    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4521   -1.0550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2374    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4290    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8975   -2.7620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8974   -2.7620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5618   -3.5157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  1  0  0  0
  1  3  1  0  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  4  8  1  0  0  0  0
  4  9  1  6  0  0  0
  5 10  1  0  0  0  0
  5 11  2  0  0  0  0
  6 12  2  0  0  0  0
  7 15  1  1  0  0  0
  8 13  1  6  0  0  0
 10 14  1  0  0  0  0
 14 17  2  0  0  0  0
  7  8  1  0  0  0  0
 12 14  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000094

> <DATABASE_NAME>
MIME

> <SMILES>
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C9H12N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h1-2,4,6-8,12,14-15H,3H2,(H,10,13,16)/t4-,6-,7-,8-/m1/s1

> <INCHI_KEY>
DRTQHJPVMGBUCF-XVFCMESISA-N

> <FORMULA>
C9H12N2O6

> <MOLECULAR_WEIGHT>
244.2014

> <EXACT_MASS>
244.069536126

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
29

> <JCHEM_AVERAGE_POLARIZABILITY>
21.809000940587058

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione

> <ALOGPS_LOGP>
-1.84

> <JCHEM_LOGP>
-2.415242141666667

> <ALOGPS_LOGS>
-0.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.620123384629313

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.700740441527786

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9802996389517045

> <JCHEM_POLAR_SURFACE_AREA>
119.32999999999998

> <JCHEM_REFRACTIVITY>
52.56559999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.35e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
uridine

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000296
     RDKit          3D
Uridine
 29 30  0  0  0  0  0  0  0  0999 V2000
    5.4528   -0.1646   -0.5518 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2120   -0.1635   -0.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6593    0.4277    0.7081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025    0.4143    0.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4700   -0.1577   -0.0541 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0766   -0.1078    0.2036 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6830   -1.0635   -0.4136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9724   -0.6966   -0.0001 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0343   -1.3987   -0.8142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2709   -0.9718   -0.3319 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0554    0.8003   -0.1185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4537    1.3579    1.1004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790    1.1840   -0.2854 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2267    2.2216    0.5490 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411   -0.7283   -1.1270 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2511   -1.2604   -1.9661 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3751   -0.7289   -1.2907 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2741    0.9060    1.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8871    0.8881    1.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1455   -0.1454    1.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0346   -0.9755    1.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9060   -1.2308   -1.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9574   -2.4912   -0.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2502   -0.8541    0.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6675    1.1341   -0.9584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2495    0.7100    1.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3744    1.3628   -1.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9402    2.9056    0.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7992   -1.1736   -2.1243 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  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  2  0
 15 17  1  0
 17  2  1  0
 13  6  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  1
  8 21  1  1
  9 22  1  0
  9 23  1  0
 10 24  1  0
 11 25  1  6
 12 26  1  0
 13 27  1  6
 14 28  1  0
 17 29  1  0
M  END

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM    3  O   UNK     0      -1.246  -2.445   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       1.246  -2.445   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.770  -3.910   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.770  -3.910   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.711  -1.969   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       1.334   2.310   0.000  0.00  0.00           N+0
HETATM   11  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.675  -5.156   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.675  -5.156   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.049  -6.563   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7                                                       
CONECT    4    1    8    9                                                  
CONECT    5    2   10   11                                                  
CONECT    6    2   12                                                       
CONECT    7    3   15    8                                                  
CONECT    8    4   13    7                                                  
CONECT    9    4                                                            
CONECT   10    5   14                                                       
CONECT   11    5                                                            
CONECT   12    6   14                                                       
CONECT   13    8                                                            
CONECT   14   10   17   12                                                  
CONECT   15    7   16                                                       
CONECT   16   15                                                            
CONECT   17   14                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

COMPND    HMDB0000296
HETATM    1  O1  UNL     1       5.453  -0.165  -0.552  1.00  0.00           O  
HETATM    2  C1  UNL     1       4.212  -0.164  -0.399  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.659   0.428   0.708  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.302   0.414   0.850  1.00  0.00           C  
HETATM    5  N1  UNL     1       1.470  -0.158  -0.054  1.00  0.00           N  
HETATM    6  C4  UNL     1       0.077  -0.108   0.204  1.00  0.00           C  
HETATM    7  O2  UNL     1      -0.683  -1.063  -0.414  1.00  0.00           O  
HETATM    8  C5  UNL     1      -1.972  -0.697  -0.000  1.00  0.00           C  
HETATM    9  C6  UNL     1      -3.034  -1.399  -0.814  1.00  0.00           C  
HETATM   10  O3  UNL     1      -4.271  -0.972  -0.332  1.00  0.00           O  
HETATM   11  C7  UNL     1      -2.055   0.800  -0.118  1.00  0.00           C  
HETATM   12  O4  UNL     1      -2.454   1.358   1.100  1.00  0.00           O  
HETATM   13  C8  UNL     1      -0.579   1.184  -0.285  1.00  0.00           C  
HETATM   14  O5  UNL     1      -0.227   2.222   0.549  1.00  0.00           O  
HETATM   15  C9  UNL     1       2.041  -0.728  -1.127  1.00  0.00           C  
HETATM   16  O6  UNL     1       1.251  -1.260  -1.966  1.00  0.00           O  
HETATM   17  N2  UNL     1       3.375  -0.729  -1.291  1.00  0.00           N  
HETATM   18  H1  UNL     1       4.274   0.906   1.474  1.00  0.00           H  
HETATM   19  H2  UNL     1       1.887   0.888   1.734  1.00  0.00           H  
HETATM   20  H3  UNL     1      -0.146  -0.145   1.303  1.00  0.00           H  
HETATM   21  H4  UNL     1      -2.035  -0.975   1.071  1.00  0.00           H  
HETATM   22  H5  UNL     1      -2.906  -1.231  -1.888  1.00  0.00           H  
HETATM   23  H6  UNL     1      -2.957  -2.491  -0.542  1.00  0.00           H  
HETATM   24  H7  UNL     1      -4.250  -0.854   0.634  1.00  0.00           H  
HETATM   25  H8  UNL     1      -2.668   1.134  -0.958  1.00  0.00           H  
HETATM   26  H9  UNL     1      -2.249   0.710   1.833  1.00  0.00           H  
HETATM   27  H10 UNL     1      -0.374   1.363  -1.352  1.00  0.00           H  
HETATM   28  H11 UNL     1      -0.940   2.906   0.648  1.00  0.00           H  
HETATM   29  H12 UNL     1       3.799  -1.174  -2.124  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   17
CONECT    3    4    4   18
CONECT    4    5   19
CONECT    5    6   15
CONECT    6    7   13   20
CONECT    7    8
CONECT    8    9   11   21
CONECT    9   10   22   23
CONECT   10   24
CONECT   11   12   13   25
CONECT   12   26
CONECT   13   14   27
CONECT   14   28
CONECT   15   16   16   17
CONECT   17   29
END

HMDB0000296
     RDKit          3D
Uridine
 29 30  0  0  0  0  0  0  0  0999 V2000
    5.4528   -0.1646   -0.5518 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2120   -0.1635   -0.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6593    0.4277    0.7081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025    0.4143    0.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4700   -0.1577   -0.0541 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0766   -0.1078    0.2036 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6830   -1.0635   -0.4136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9724   -0.6966   -0.0001 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0343   -1.3987   -0.8142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2709   -0.9718   -0.3319 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0554    0.8003   -0.1185 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4537    1.3579    1.1004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5790    1.1840   -0.2854 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2267    2.2216    0.5490 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411   -0.7283   -1.1270 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2511   -1.2604   -1.9661 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3751   -0.7289   -1.2907 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2741    0.9060    1.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8871    0.8881    1.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1455   -0.1454    1.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0346   -0.9755    1.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9060   -1.2308   -1.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9574   -2.4912   -0.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2502   -0.8541    0.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6675    1.1341   -0.9584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2495    0.7100    1.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3744    1.3628   -1.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9402    2.9056    0.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7992   -1.1736   -2.1243 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  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  2  0
 15 17  1  0
 17  2  1  0
 13  6  1  0
  3 18  1  0
  4 19  1  0
  6 20  1  1
  8 21  1  1
  9 22  1  0
  9 23  1  0
 10 24  1  0
 11 25  1  6
 12 26  1  0
 13 27  1  6
 14 28  1  0
 17 29  1  0
M  END

Synonyms

Value	Source
1-beta-D-Ribofuranosylpyrimidine-2,4(1H,3H)-dione	ChEBI
1-beta-D-Ribofuranosyluracil	ChEBI
beta-Uridine	ChEBI
u	ChEBI
Urd	ChEBI
Uridin	ChEBI
1-b-D-Ribofuranosylpyrimidine-2,4(1H,3H)-dione	Generator
1-Β-D-ribofuranosylpyrimidine-2,4(1H,3H)-dione	Generator
1-b-D-Ribofuranosyluracil	Generator
1-Β-D-ribofuranosyluracil	Generator
b-Uridine	Generator
Β-uridine	Generator
1-b-D-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione	HMDB
1-beta-delta-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione	HMDB
1-beta-delta-Ribofuranosyluracil	HMDB
b-D-Ribofuranoside 2,4(1H,3H)-pyrimidinedione-1	HMDB
beta-delta-Ribofuranoside 2,4(1H,3H)-pyrimidinedione-1	HMDB
Allo uridine	HMDB
Allo-uridine	HMDB
Allouridine	HMDB

Molecular Formula

C₉H₁₂N₂O₆

Average Mass

244.2014

Monoisotopic Mass

244.069536126

IUPAC Name

1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione

Traditional Name

uridine

CAS Registry Number

58-96-8

SMILES

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=O

InChI Identifier

InChI=1S/C9H12N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h1-2,4,6-8,12,14-15H,3H2,(H,10,13,16)/t4-,6-,7-,8-/m1/s1

InChI Key

DRTQHJPVMGBUCF-XVFCMESISA-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
Pyrimidone
Hydropyrimidine
Monosaccharide
Pyrimidine
Vinylogous amide
Tetrahydrofuran
Heteroaromatic compound
Urea
Secondary alcohol
Lactam
Organoheterocyclic compound
Oxacycle
Azacycle
Hydrocarbon derivative
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Primary alcohol
Alcohol
Organic oxygen compound
Organic oxide
Organic nitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

uridines (CHEBI:16704 )
Ribonucleosides (C00299 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	135 g/L	ALOGPS
logP	-1.8	ALOGPS
logP	-2.4	ChemAxon
logS	-0.26	ALOGPS
pKa (Strongest Acidic)	9.7	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	119.33 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	52.57 m³·mol⁻¹	ChemAxon
Polarizability	21.81 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

Spectrum Type	Description	Splash Key	Deposition Date	View
GC-MS	GC-MS Spectrum - GC-EI-TOF (Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies) (3 TMS)	splash10-00kb-1970000000-d1bfa838a4e9fa77c862	2014-06-16	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies) (Non-derivatized)	splash10-00kb-1960000000-a8283468b762a8520102	2014-06-16	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies) (Non-derivatized)	splash10-014i-1950000000-70fdf4785544d0968f70	2014-06-16	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies) (3 TMS)	splash10-00di-9520000000-591c0bcf8f956d710367	2014-06-16	View Spectrum
GC-MS	GC-MS Spectrum - GC-MS (4 TMS)	splash10-066s-2970000000-36fbef6f6b10c2895df4	2014-06-16	View Spectrum
GC-MS	GC-MS Spectrum - GC-MS (3 TMS)	splash10-014i-1890000000-dd0569d4351a64c566c9	2014-06-16	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Non-derivatized)	splash10-00kb-1970000000-d1bfa838a4e9fa77c862	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Non-derivatized)	splash10-00kb-1960000000-a8283468b762a8520102	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Non-derivatized)	splash10-014i-1950000000-70fdf4785544d0968f70	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Non-derivatized)	splash10-00di-9520000000-591c0bcf8f956d710367	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-MS (Non-derivatized)	splash10-066s-2970000000-36fbef6f6b10c2895df4	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-MS (Non-derivatized)	splash10-014i-1890000000-dd0569d4351a64c566c9	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Non-derivatized)	splash10-014j-1940000000-8b7a5ce66afa9b9bf939	2017-09-12	View Spectrum
GC-MS	GC-MS Spectrum - GC-EI-TOF (Non-derivatized)	splash10-00kb-1950000000-00519445de22f955367d	2017-09-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-056u-9530000000-e83d5f042dbda82911cf	2016-09-22	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (3 TMS) - 70eV, Positive	splash10-0g30-5935200000-88c9a24e13b0f41cbc83	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - Quattro_QQQ 10V, Positive (Annotated)	splash10-03di-0900000000-7010b37007f5c3d9ce1f	2012-07-24	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - Quattro_QQQ 25V, Positive (Annotated)	splash10-03di-3900000000-b4639c8c89eac6158da6	2012-07-24	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - Quattro_QQQ 40V, Positive (Annotated)	splash10-022a-9200000000-f8472930d09b32f54790	2012-07-24	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive	splash10-014i-0291000000-aebaa77a411473acb859	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive	splash10-014j-9000000000-205562662b564ebdca28	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive	splash10-03di-0900000000-776595fd1c19f6ec51cd	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive	splash10-000i-0900000000-10358e53c56bcb50ed4c	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive	splash10-0002-0971000000-f989283d2dec564a3af0	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive	splash10-00kf-9000000000-c11e7bfdec0b5c7bf450	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive	splash10-000i-9000000000-104e62fbffc4110779ef	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive	splash10-03di-0900000000-eaf6ff9ac3971d6f045f	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative	splash10-052f-0697120000-c9fd5b8d641165d84e92	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative	splash10-0006-9000000000-995de18be458c48a8d2d	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative	splash10-0udi-0590000000-4d1d6aba25697dd11da8	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative	splash10-0uki-0190000000-3aea11527d0520158d77	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative	splash10-004l-0291010000-c8f22405e9290fccc011	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative	splash10-0udi-0490000000-1a2f990a874bb1868249	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative	splash10-0006-0090000000-c8efbe58f0df63698b2c	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative	splash10-0006-0090000000-7495d9b948a8e3b7b83b	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 10V, Positive	splash10-03dj-3960000000-3466ccfdf88139ddf140	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 20V, Positive	splash10-03di-3900000000-0d08e4a7d4b8aacee6e6	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 30V, Positive	splash10-03di-4900000000-d942ee27b3ca1d6ef94d	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 40V, Positive	splash10-03di-9700000000-594c7bb6dc6de848ff11	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 50V, Positive	splash10-022d-9100000000-2826c4eb794745ec3148	2012-08-31	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-IT (LC/MSD Trap XCT, Agilent Technologies) , Positive	splash10-03di-0910000000-617b4ec6cf749942c0cd	2012-08-31	View Spectrum
MS	Mass Spectrum (Electron Ionization)	splash10-08mi-9400000000-bafe048989f1a5c86d2d	2018-05-25	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, H₂O, experimental)		2012-12-04	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, experimental)		2012-12-04	View Spectrum
1D NMR	¹H NMR Spectrum (1D, D₂O, experimental)		2016-10-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, experimental)		2021-10-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, experimental)		2021-10-10	View Spectrum
2D NMR	[¹H, ¹H]-TOCSY. Unexported temporarily by An Chi on Oct 15, 2021 until json or nmrML file is generated. 2D NMR Spectrum (experimental)		2012-12-04	View Spectrum
2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, H₂O, experimental)		2012-12-05	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Lysosome
Mitochondria
Nucleus

Biospecimen Locations

Blood
Breast Milk
Cerebrospinal Fluid (CSF)
Feces
Placenta
Urine

Tissue Locations

Placenta

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species
MMDBp0191677	5'-nucleotidase	Unknown	P21589	Homo sapiens
MMDBp0191680	Cytosolic 5'-nucleotidase 1B	Unknown	Q96P26	Homo sapiens
MMDBp0191681	Cytosolic 5'-nucleotidase 1A	Unknown	Q9BXI3	Homo sapiens
MMDBp0191682	5'(3')-deoxyribonucleotidase, cytosolic type	Unknown	Q8TCD5	Homo sapiens
MMDBp0191684	5'(3')-deoxyribonucleotidase, mitochondrial	Unknown	Q9NPB1	Homo sapiens
MMDBp0191778	Uridine-cytidine kinase 1	Unknown	Q9HA47	Homo sapiens
MMDBp0192704	tRNA pseudouridine synthase A, mitochondrial	Enzyme	Q9Y606	Homo sapiens
MMDBp0193196	H/ACA ribonucleoprotein complex subunit 4	Enzyme	O60832	Homo sapiens
MMDBp0193590	Uridine-cytidine kinase 2	Unknown	Q9BZX2	Homo sapiens
MMDBp0193783	AID	Enzyme	Q546Y9	Homo sapiens
MMDBp0193860	Cytosolic 5'-nucleotidase 3	Enzyme	Q9H0P0	Homo sapiens
MMDBp0193932	Cytosolic purine 5'-nucleotidase	Unknown	P49902	Homo sapiens
MMDBp0194012	Cytidine deaminase	Unknown	P32320	Homo sapiens
MMDBp0194034	Uridine phosphorylase 1	Enzyme	Q16831	Homo sapiens
MMDBp0194035	Uridine phosphorylase 2	Enzyme	O95045	Homo sapiens
MMDBp0194185	Uridine-cytidine kinase-like 1	Enzyme	Q9NWZ5	Homo sapiens
MMDBp0195902	Putative tRNA pseudouridine synthase Pus10	Enzyme	Q3MIT2	Homo sapiens
MMDBp0195903	tRNA pseudouridine synthase 3	Enzyme	Q9BZE2	Homo sapiens
MMDBp0196233	tRNA pseudouridine synthase-like 1	Enzyme	Q8N0Z8	Homo sapiens
MMDBp0196270	DNA dC->dU-editing enzyme APOBEC-3H	Enzyme	Q6NTF7	Homo sapiens
MMDBp0196667	Probable DNA dC->dU-editing enzyme APOBEC-3A	Unknown	P31941
MMDBp0196668	Probable DNA dC->dU-editing enzyme APOBEC-3B	Unknown	Q9UH17
MMDBp0196669	Probable DNA dC->dU-editing enzyme APOBEC-3C	Unknown	Q9NRW3
MMDBp0196670	Probable DNA dC->dU-editing enzyme APOBEC-3D	Unknown	Q96AK3
MMDBp0196671	DNA dC->dU-editing enzyme APOBEC-3F	Unknown	Q8IUX4
MMDBp0196681	Activation-induced cytidine deaminase	Unknown	Q9GZX7

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Data Source	Reference
MMDBr0000574	Cytidine	Uridine	Not Available	VMH; KEGG	14744791 15087440 7923172 8001985 8422236
MMDBr0000577	Cytidine	Uridine	activation-induced cytidine deaminase	VMH; KEGG	15087440
MMDBr0001786	Uridine 5'-monophosphate	Uridine	5'-nucleotidase, ecto (CD73)	VMH; KEGG	30371894
MMDBr0001787	Uridine 5'-monophosphate	Uridine	acid phosphatase 2, lysosomal	VMH; KEGG	30371894
MMDBr0001788	Uridine 5'-monophosphate	Uridine	5',3'-nucleotidase, mitochondrial	VMH	10899995
MMDBr0002045	Uridine	Ribose-1-phosphate	Not Available	VMH; KEGG	30371894
MMDBr0002361	Uridine	Uridine 5'-monophosphate	Not Available	VMH; KEGG	30371894
MMDBr0002867	Deoxyuridine triphosphate	dUDP	uridine-cytidine kinase 1	VMH	11306702 11494055 64250 9923963
MMDBr0006748	Inosine triphosphate	IDP	Not Available	VMH; KEGG	30371894
MMDBr0007637	Uridine 5'-monophosphate	Uridine	Not Available	VMH; KEGG	30371894
MMDBr0008002	Guanosine triphosphate	Guanosine diphosphate	Not Available	VMH; KEGG	30371894
MMDBr0008003	Uridine	Uridine 5'-diphosphate	Not Available	VMH	30371894
MMDBr0008004	dCTP	dCDP	Not Available	VMH	30371894
MMDBr0008005	Deoxyuridine triphosphate	dUDP	Not Available	VMH	30371894
MMDBr0008006	Deoxyadenosine triphosphate	Uridine 5'-monophosphate	Not Available	VMH	30371894
MMDBr0008007	dGTP	Uridine 5'-monophosphate	Not Available	VMH	30371894
MMDBr0008008	Thymidine 5'-triphosphate	dTDP	Not Available	VMH	30371894
MMDBr0010321	Guanosine triphosphate	Guanosine diphosphate	uridine-cytidine kinase 1	VMH	30371894

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference
Argininemia		Association	Human Urine	HMDB	6796772
Canavan disease	Slight Increase	Association	Human Blood	HMDB	16139832
Degenerative disc disease		Association	Human Cerebrospinal Fluid (CSF)	HMDB	6656991
Lesch-nyhan syndrome	Increased	Association	Human Blood	HMDB	3148065
Uremia		Association	Human Blood	HMDB	12675874

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota	Parabasalia	1		Microbial culture
Bacteria	Firmicutes	658	Human feces; Human ; Human stool; Human urine; Human sputum; Human pleural fluid plaque; Pig ; Human subgingival plaque; Human saliva; Human mucosa; Human supragingival plaque; Cattle ; Catfish	Microbial culture; Indirect association between microbiota composition and metabolites measured in host biospecimen; Metabolic reconstruction
Bacteria	Bacteroidetes	243	Human ; Human urine; Human feces; Human appendix biopsy; Human stool; Human saliva; Human gastric fluid; Human subgingival plaque; Human supragingival plaque	Microbial culture; Indirect association between microbiota composition and metabolites measured in host biospecimen; Metabolic reconstruction
Bacteria	Verrucomicrobia	3	Human feces; Human stool; Human ; Human urine	Indirect association between microbiota composition and metabolites measured in host biospecimen; Metabolic reconstruction
Bacteria	Proteobacteria	479	Human feces; Human stool; Human ; Human feces; pleural fluid plaque; bal; Human sputum; Human unknown; Pig ; Human pleural fluid plaque; Human dental plaque; Human nasal swab; Cattle ; River trout ; Chicken ; Human subgingival plaque	Indirect association between microbiota composition and metabolites measured in host biospecimen; Metabolic reconstruction
Bacteria	Actinobacteria	179	Human feces; Human sputum; Human bronchial brush; Human nasopharyngeal swab; Human pleural fluid plaque; Human dental plaque; Human ; Human supragingival plaque; Human mucosa; Human subgingival plaque; Human saliva	Metabolic reconstruction
Bacteria	Synergistetes	5	Human feces	Metabolic reconstruction
Bacteria	Spirochaetes	14	Human feces; Human ; Relapsing fever tick	Metabolic reconstruction
Archaea	Thaumarchaeota	1		Metabolic reconstruction
Bacteria	Fusobacteria	25	Human feces; Human	Metabolic reconstruction
Archaea	Euryarchaeota	8		Metabolic reconstruction
Bacteria	Candidatus melainabacteria	2	Human feces	Metabolic reconstruction
Bacteria	Tenericutes	10	Human feces; Human	Metabolic reconstruction
Bacteria	Planctomycetes	3	Human feces	Metabolic reconstruction
Archaea	Crenarchaeota	1		Metabolic reconstruction
Eukaryota/Fungi	Ascomycota	3	Human feces; Human saliva	Unknown
Bacteria	Chloroflexi	3
Bacteria	Chlamydiae	1	Human
Bacteria	Deinococcus-thermus	4
Archaea/Archaea	Euryarchaeota	1		Metabolic reconstruction
Bacteria	Chlorobi	1

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified									HMDB
Human Urine	Detected and Quantified	67.836		18.0896	125.497	umol/mmol creatinine	Children (1-13 years old)	Not Specified	Arginase Deficiency	HMDB	6796772
Human Blood	Detected and Quantified	4.23	1.92			uM	Adult (>18 years old)	Both	Canavan disease	HMDB	16139832
Human Cerebrospinal fluid (csf)	Detected and Quantified	2.30		1.90	2.70	uM	Adult (>18 years old)	Both	Degenerative disc disease	HMDB	6656991
Human Blood	Detected and Quantified	7.7	0.9			uM	Adult (>18 years old)	Both	Lesch-Nyhan syndrome	HMDB	3148065
Human Blood	Detected and Quantified	40.164	46.721			uM	Adult (>18 years old)	Both	Uremia	HMDB	12675874
Human Urine	Detected and Quantified			0	15	umol/mmol creatinine	Newborn (0-30 days old)	Both	Normal	HMDB	31506554
Human Urine	Detected and Quantified	0.21	0.08			umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	9129323
Human Urine	Detected and Quantified	0.21	0.09			umol/mmol creatinine	Adult (>18 years old)	Female	Normal	HMDB	9129323
Human Urine	Detected and Quantified	0.22	0.07			umol/mmol creatinine	Adult (>18 years old)	Male	Normal	HMDB	9129323
Human Urine	Detected and Quantified	0.994		0.637	1.351	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	15116424
Human Feces	Detected and Quantified	1296.744		668.847	1924.641	nmol/g wet feces	Infant (0-1 year old)	Not Specified	Normal	HMDB	22435727
Human Blood	Detected and Quantified	3.10		2.90	3.30	uM	Adult (>18 years old)	Both	Normal	HMDB	6656991
Human Blood	Detected and Quantified	3.12	1.31			uM	Adult (>18 years old)	Both	Normal	HMDB	16139832
Human Breast milk	Detected and Quantified	4.17	4.75			uM	Adult (>18 years old)	Female	Normal	HMDB	7702711
Human Feces	Detected and Quantified	559.647		259.349	859.946	nmol/g wet feces	Infant (0-1 year old)	Not Specified	Normal	HMDB	22435727
Human Blood	Detected and Quantified	6.148	5.328			uM	Adult (>18 years old)	Both	Normal	HMDB	12675874
Human Breast milk	Detected and Quantified	7.1	3.7			uM	Adult (>18 years old)	Female	Normal	HMDB	24027187
Human Feces	Detected and Quantified	982.795		600.597	1364.994	nmol/g wet feces	Infant (0-1 year old)	Not Specified	Normal	HMDB	22435727
Human Urine	Detected and Quantified			0	9	umol/mmol creatinine	Children (1 - 18 years old)	Both	Normal	HMDB	BC Children's Hospital Biochemical Genetics Lab
Human Blood	Detected and Quantified	21.1	8.4			uM	Adult (>18 years old)	Not Specified	Normal	HMDB	Geigy Scientific Tables, 8th Rev edition, pp. 130. Edited by C. Lentner, West Cadwell, N.J.: Medical education Div., Ciba-Geigy Corp. Basel, Switzerland c1981-1992.
Human Placenta	Detected but not Quantified						Not Specified	Not Specified	Normal	HMDB	34986597
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	21761941
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	24029555
Human Blood	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	19678709
Human Feces	Detected but not Quantified						Infant (0-1 year old)	NULL	Normal	HMDB	24628373
Human Feces	Detected but not Quantified						Infant (0-1 year old)	Not Specified	Normal	HMDB	24628373
Human Feces	Detected but not Quantified						Infant (0-1 year old)	Not Specified	Normal	HMDB	24628373
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	27543620
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	25037050
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	29808030
Human Urine	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	32966057
Human Blood	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	32966057

External Links

HMDB ID

HMDB0000296

DrugBank ID

DB02745

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Wikipedia Link

METLIN ID

PubChem Compound

6029

PDB ID

Not Available

ChEBI ID

16704

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Lee SH, Jung BH, Kim SY, Chung BC: A rapid and sensitive method for quantitation of nucleosides in human urine using liquid chromatography/mass spectrometry with direct urine injection. Rapid Commun Mass Spectrom. 2004;18(9):973-7. doi: 10.1002/rcm.1400. [PubMed:15116424 ]
Eells JT, Spector R: Purine and pyrimidine base and nucleoside concentrations in human cerebrospinal fluid and plasma. Neurochem Res. 1983 Nov;8(11):1451-7. doi: 10.1007/BF00965000. [PubMed:6656991 ]
Elshenawy S, Pinney SE, Stuart T, Doulias PT, Zura G, Parry S, Elovitz MA, Bennett MJ, Bansal A, Strauss JF 3rd, Ischiropoulos H, Simmons RA: The Metabolomic Signature of the Placenta in Spontaneous Preterm Birth. Int J Mol Sci. 2020 Feb 4;21(3). pii: ijms21031043. doi: 10.3390/ijms21031043. [PubMed:32033212 ]

Showing metabocard for Uridine (MMDBc0000094)

MOL for #<Metabolite:0x00007f46cc6223b0>

3D MOL for #<Metabolite:0x00007f46cc6223b0>

3D SDF for #<Metabolite:0x00007f46cc6223b0>

3D-SDF for #<Metabolite:0x00007f46cc6223b0>

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Structure for #<Metabolite:0x00007f46cc6223b0>

3D Structure for #<Metabolite:0x00007f46cc6223b0>