MiMeDB: Showing metabocard for UDP-2-acetamido-3-amino-2,3-dideoxy-alpha-D-glucuronic acid (MMDBc0056347)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-17 20:23:26 UTC

Update Date

2022-08-12 20:09:41 UTC

Metabolite ID

MMDBc0056347

Metabolite Identification

Common Name

UDP-2-acetamido-3-amino-2,3-dideoxy-alpha-D-glucuronic acid

Description

UDP-2-acetamido-3-amino-2,3-dideoxy-alpha-D-glucuronate, also known as UDP-2-acetamido-3-azaniumyl-2,3-dideoxy-a-D-glucuronic acid(2-) or UDP-glcnac3na(2-), belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group. Based on a literature review a small amount of articles have been published on UDP-2-acetamido-3-amino-2,3-dideoxy-alpha-D-glucuronate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172222232D          

 49 51  0  0  1  0            999 V2000
   10.4754    5.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9912   -3.4197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4761   -2.7523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4901   -0.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0885    5.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7054   -0.5465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1707   -3.3335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3147    3.9561    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5300    3.7011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0380   -0.0616    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.9278    3.4040    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3706   -0.5465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.7562    2.5970    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6255   -1.3312    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3693    2.0450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3585    2.8941    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3201   -1.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4862    4.7630    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.9169    4.2531    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8352   -2.5798    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1406   -1.9986    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.8731    5.3151    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    4.6858   -4.0009    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    7.0380    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7124    3.6590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5859   -0.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1978    1.2380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1539    2.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9845   -1.1587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1913    1.5549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7012   -0.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5954    2.0038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2093    1.6607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6616    0.5154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4505   -1.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9716    2.3421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5739    2.6392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2308    1.0253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4462    0.7703    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   10.4024    1.8322    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    7.8345    0.2683    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7016    4.5081    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7454    3.4462    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3029    0.3129    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5408    2.8520    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7872   -1.1299    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5847    1.7901    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0000   -2.0662    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1431    3.1491    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  5  1  1  4  0  0  0
  6  4  1  1  0  0  0
  7  2  1  0  0  0  0
  9  8  1  0  0  0  0
 10  6  1  0  0  0  0
 11  8  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 13 15  1  1  0  0  0
 16  9  1  0  0  0  0
  8 18  1  1  0  0  0
 19  5  2  0  0  0  0
  9 19  1  6  0  0  0
 20  7  2  0  0  0  0
 20 17  1  0  0  0  0
 21  3  1  0  0  0  0
 14 21  1  1  0  0  0
 21 17  1  0  0  0  0
 22  5  1  0  0  0  0
 23  7  1  0  0  0  0
 10 24  1  6  0  0  0
 11 25  1  6  0  0  0
 12 26  1  6  0  0  0
 27 15  2  0  0  0  0
 28 15  1  0  0  0  0
 29 17  2  0  0  0  0
 34  4  1  0  0  0  0
 35  6  1  0  0  0  0
 35 14  1  0  0  0  0
 36 13  1  0  0  0  0
 36 16  1  0  0  0  0
 16 37  1  1  0  0  0
 39 30  1  0  0  0  0
 39 31  2  0  0  0  0
 39 34  1  0  0  0  0
 39 38  1  0  0  0  0
 40 32  1  0  0  0  0
 40 33  2  0  0  0  0
 40 37  1  0  0  0  0
 40 38  1  0  0  0  0
  6 41  1  6  0  0  0
  8 42  1  6  0  0  0
  9 43  1  1  0  0  0
 10 44  1  1  0  0  0
 11 45  1  1  0  0  0
 12 46  1  1  0  0  0
 13 47  1  6  0  0  0
 14 48  1  6  0  0  0
 16 49  1  1  0  0  0
M  CHG  2  22  -1  23  -1
M  END


  Mrv1652306172222232D          

 49 51  0  0  1  0            999 V2000
   10.4754    5.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9912   -3.4197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4761   -2.7523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4901   -0.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0885    5.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7054   -0.5465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1707   -3.3335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3147    3.9561    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5300    3.7011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0380   -0.0616    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.9278    3.4040    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3706   -0.5465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.7562    2.5970    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6255   -1.3312    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3693    2.0450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3585    2.8941    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3201   -1.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4862    4.7630    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.9169    4.2531    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8352   -2.5798    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1406   -1.9986    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.8731    5.3151    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    4.6858   -4.0009    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    7.0380    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7124    3.6590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5859   -0.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1978    1.2380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1539    2.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9845   -1.1587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1913    1.5549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7012   -0.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5954    2.0038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2093    1.6607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6616    0.5154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4505   -1.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9716    2.3421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5739    2.6392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2308    1.0253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4462    0.7703    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   10.4024    1.8322    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    7.8345    0.2683    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7016    4.5081    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7454    3.4462    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3029    0.3129    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5408    2.8520    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7872   -1.1299    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5847    1.7901    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0000   -2.0662    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1431    3.1491    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  5  1  1  4  0  0  0
  6  4  1  1  0  0  0
  7  2  1  0  0  0  0
  9  8  1  0  0  0  0
 10  6  1  0  0  0  0
 11  8  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 13 15  1  1  0  0  0
 16  9  1  0  0  0  0
  8 18  1  1  0  0  0
 19  5  2  0  0  0  0
  9 19  1  6  0  0  0
 20  7  2  0  0  0  0
 20 17  1  0  0  0  0
 21  3  1  0  0  0  0
 14 21  1  1  0  0  0
 21 17  1  0  0  0  0
 22  5  1  0  0  0  0
 23  7  1  0  0  0  0
 10 24  1  6  0  0  0
 11 25  1  6  0  0  0
 12 26  1  6  0  0  0
 27 15  2  0  0  0  0
 28 15  1  0  0  0  0
 29 17  2  0  0  0  0
 34  4  1  0  0  0  0
 35  6  1  0  0  0  0
 35 14  1  0  0  0  0
 36 13  1  0  0  0  0
 36 16  1  0  0  0  0
 16 37  1  1  0  0  0
 39 30  1  0  0  0  0
 39 31  2  0  0  0  0
 39 34  1  0  0  0  0
 39 38  1  0  0  0  0
 40 32  1  0  0  0  0
 40 33  2  0  0  0  0
 40 37  1  0  0  0  0
 40 38  1  0  0  0  0
  6 41  1  6  0  0  0
  8 42  1  6  0  0  0
  9 43  1  1  0  0  0
 10 44  1  1  0  0  0
 11 45  1  1  0  0  0
 12 46  1  1  0  0  0
 13 47  1  6  0  0  0
 14 48  1  6  0  0  0
 16 49  1  1  0  0  0
M  CHG  2  22  -1  23  -1
M  END
> <DATABASE_ID>
MMDBc0056347

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(COP(O)(=O)OP(O)(=O)O[C@@]2([H])O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(N)[C@@]2([H])N=C(C)[O-])O[C@@]([H])(N2C=CC([O-])=NC2=O)[C@]([H])(O)[C@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C17H26N4O17P2/c1-5(22)19-9-8(18)11(25)13(15(27)28)36-16(9)37-40(32,33)38-39(30,31)34-4-6-10(24)12(26)14(35-6)21-3-2-7(23)20-17(21)29/h2-3,6,8-14,16,24-26H,4,18H2,1H3,(H,19,22)(H,27,28)(H,30,31)(H,32,33)(H,20,23,29)/p-2/t6-,8-,9-,10-,11+,12-,13+,14-,16-/m1/s1

> <INCHI_KEY>
RRAQYLXLCYIZBB-HHKCBAECSA-L

> <FORMULA>
C17H24N4O17P2

> <MOLECULAR_WEIGHT>
618.339

> <EXACT_MASS>
618.062266485

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
50.31593925982732

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
-2

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(2R,3R,4R,5S,6S)-4-amino-6-carboxy-2-({[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxido-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-5-hydroxyoxan-3-yl]ethanecarboximidate

> <JCHEM_LOGP>
-5.134540370954376

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
2.8346885988955157

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7110765484377213

> <JCHEM_PKA_STRONGEST_BASIC>
9.354442911052123

> <JCHEM_POLAR_SURFACE_AREA>
335.91

> <JCHEM_REFRACTIVITY>
141.02599999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-[(2R,3R,4R,5S,6S)-4-amino-6-carboxy-2-[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxido-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-5-hydroxyoxan-3-yl]ethanecarboximidate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-JUN-22         0                                  
HETATM    1  C   UNK     0      19.554  10.476   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.184  -6.383   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.089  -5.138   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.848  -0.544   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.698   9.446   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.383  -1.020   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.652  -6.222   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.987   7.385   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.523   6.909   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.138  -0.115   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      24.132   6.354   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.892  -1.020   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      23.812   4.848   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.368  -2.485   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      24.956   3.817   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.203   5.402   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.931  -3.570   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      23.308   8.891   0.000  0.00  0.00           N+0
HETATM   19  N   UNK     0      20.378   7.939   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0       9.026  -4.816   0.000  0.00  0.00           N+0
HETATM   21  N   UNK     0      11.462  -3.731   0.000  0.00  0.00           N+0
HETATM   22  O   UNK     0      22.163   9.921   0.000  0.00  0.00           O-1
HETATM   23  O   UNK     0       8.747  -7.468   0.000  0.00  0.00           O-1
HETATM   24  O   UNK     0      13.138   1.425   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      25.596   6.830   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      10.427  -0.544   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      24.636   2.311   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      26.421   4.293   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       9.304  -2.163   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      17.157   2.903   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      18.109  -0.027   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      17.911   3.740   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      20.924   3.100   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      16.168   0.962   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      13.908  -2.485   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      22.347   4.372   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      19.738   4.927   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      19.098   1.914   0.000  0.00  0.00           O+0
HETATM   39  P   UNK     0      17.633   1.438   0.000  0.00  0.00           P+0
HETATM   40  P   UNK     0      19.418   3.420   0.000  0.00  0.00           P+0
HETATM   41  H   UNK     0      14.624   0.501   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0      21.843   8.415   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0      20.058   6.433   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0      11.765   0.584   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0      25.276   5.324   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0      10.803  -2.109   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0      23.491   3.341   0.000  0.00  0.00           H+0
HETATM   48  H   UNK     0      13.067  -3.857   0.000  0.00  0.00           H+0
HETATM   49  H   UNK     0      22.667   5.878   0.000  0.00  0.00           H+0
CONECT    1    5                                                            
CONECT    2    3    7                                                       
CONECT    3    2   21                                                       
CONECT    4    6   34                                                       
CONECT    5    1   19   22                                                  
CONECT    6    4   10   35   41                                             
CONECT    7    2   20   23                                                  
CONECT    8    9   11   18   42                                             
CONECT    9    8   16   19   43                                             
CONECT   10    6   12   24   44                                             
CONECT   11    8   13   25   45                                             
CONECT   12   10   14   26   46                                             
CONECT   13   11   15   36   47                                             
CONECT   14   12   21   35   48                                             
CONECT   15   13   27   28                                                  
CONECT   16    9   36   37   49                                             
CONECT   17   20   21   29                                                  
CONECT   18    8                                                            
CONECT   19    5    9                                                       
CONECT   20    7   17                                                       
CONECT   21    3   14   17                                                  
CONECT   22    5                                                            
CONECT   23    7                                                            
CONECT   24   10                                                            
CONECT   25   11                                                            
CONECT   26   12                                                            
CONECT   27   15                                                            
CONECT   28   15                                                            
CONECT   29   17                                                            
CONECT   30   39                                                            
CONECT   31   39                                                            
CONECT   32   40                                                            
CONECT   33   40                                                            
CONECT   34    4   39                                                       
CONECT   35    6   14                                                       
CONECT   36   13   16                                                       
CONECT   37   16   40                                                       
CONECT   38   39   40                                                       
CONECT   39   30   31   34   38                                             
CONECT   40   32   33   37   38                                             
CONECT   41    6                                                            
CONECT   42    8                                                            
CONECT   43    9                                                            
CONECT   44   10                                                            
CONECT   45   11                                                            
CONECT   46   12                                                            
CONECT   47   13                                                            
CONECT   48   14                                                            
CONECT   49   16                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  102    0
END

Synonyms

Value	Source
(2S,3S,4R,5R,6R)-5-(Acetylamino)-4-ammonio-6-({[({[(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methoxy}phosphinato)oxy]phosphinato}oxy)-3-hydroxytetrahydro-2H-pyran-2-carboxylate	ChEBI
UDP-2-Acetamido-3-azaniumyl-2,3-dideoxy-alpha-D-glucuronate(2-)	ChEBI
UDP-GlcNAc3na(2-)	ChEBI
(2S,3S,4R,5R,6R)-5-(Acetylamino)-4-ammonio-6-({[({[(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methoxy}phosphinato)oxy]phosphinato}oxy)-3-hydroxytetrahydro-2H-pyran-2-carboxylic acid	Generator
UDP-2-Acetamido-3-azaniumyl-2,3-dideoxy-a-D-glucuronate(2-)	Generator
UDP-2-Acetamido-3-azaniumyl-2,3-dideoxy-a-D-glucuronic acid(2-)	Generator
UDP-2-Acetamido-3-azaniumyl-2,3-dideoxy-alpha-D-glucuronic acid(2-)	Generator
UDP-2-Acetamido-3-azaniumyl-2,3-dideoxy-α-D-glucuronate(2-)	Generator
UDP-2-Acetamido-3-azaniumyl-2,3-dideoxy-α-D-glucuronic acid(2-)	Generator
UDP-2-Acetamido-3-amino-2,3-dideoxy-a-D-glucuronate	Generator
UDP-2-Acetamido-3-amino-2,3-dideoxy-a-D-glucuronic acid	Generator
UDP-2-Acetamido-3-amino-2,3-dideoxy-alpha-D-glucuronic acid	Generator
UDP-2-Acetamido-3-amino-2,3-dideoxy-α-D-glucuronate	Generator
UDP-2-Acetamido-3-amino-2,3-dideoxy-α-D-glucuronic acid	Generator

Molecular Formula

C₁₇H₂₄N₄O₁₇P₂

Average Mass

618.339

Monoisotopic Mass

618.062266485

IUPAC Name

N-[(2R,3R,4R,5S,6S)-4-amino-6-carboxy-2-({[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxido-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-5-hydroxyoxan-3-yl]ethanecarboximidate

Traditional Name

N-[(2R,3R,4R,5S,6S)-4-amino-6-carboxy-2-[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxido-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-5-hydroxyoxan-3-yl]ethanecarboximidate

CAS Registry Number

Not Available

SMILES

[H][C@]1(COP(O)(=O)OP(O)(=O)O[C@@]2([H])O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(N)[C@@]2([H])N=C(C)[O-])O[C@@]([H])(N2C=CC([O-])=NC2=O)[C@]([H])(O)[C@]1([H])O

InChI Identifier

InChI=1S/C17H26N4O17P2/c1-5(22)19-9-8(18)11(25)13(15(27)28)36-16(9)37-40(32,33)38-39(30,31)34-4-6-10(24)12(26)14(35-6)21-3-2-7(23)20-17(21)29/h2-3,6,8-14,16,24-26H,4,18H2,1H3,(H,19,22)(H,27,28)(H,30,31)(H,32,33)(H,20,23,29)/p-2/t6-,8-,9-,10-,11+,12-,13+,14-,16-/m1/s1

InChI Key

RRAQYLXLCYIZBB-HHKCBAECSA-L

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Sub Class

Pyrimidine nucleotide sugars

Direct Parent

Pyrimidine nucleotide sugars

Alternative Parents

Substituents

Pyrimidine nucleotide sugar
Pyrimidine ribonucleoside diphosphate
Pentose phosphate
Pentose-5-phosphate
Gamma amino acid or derivatives
Glycosyl compound
N-glycosyl compound
Organic pyrophosphate
Monosaccharide phosphate
Pyrimidone
Amino saccharide
Beta-hydroxy acid
Hydroxy acid
Oxane
Alkyl phosphate
Phosphoric acid ester
Monosaccharide
Organic phosphoric acid derivative
Pyran
Pyrimidine
Hydropyrimidine
Tetrahydrofuran
Heteroaromatic compound
Vinylogous amide
Acetamide
Amino acid or derivatives
Carboxamide group
Carboxylic acid salt
1,2-aminoalcohol
Lactam
Urea
Secondary carboxylic acid amide
Secondary alcohol
Amino acid
Azacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid
Organoheterocyclic compound
Primary amine
Organic oxide
Organic salt
Alcohol
Hydrocarbon derivative
Organic nitrogen compound
Amine
Carbonyl group
Primary aliphatic amine
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Organic anion
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

carbohydrate acid derivative anion (CHEBI:62245 )
nucleotide-sugar oxoanion (CHEBI:62245 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	-5.1	ChemAxon
pKa (Strongest Acidic)	1.71	ChemAxon
pKa (Strongest Basic)	9.35	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	335.91 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	141.03 m³·mol⁻¹	ChemAxon
Polarizability	50.32 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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
Bacteria	Proteobacteria	1	Human

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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

26332595

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53262299

PDB ID

Not Available

ChEBI ID

62245

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for UDP-2-acetamido-3-amino-2,3-dideoxy-alpha-D-glucuronic acid (MMDBc0056347)

MOL for #<Metabolite:0x00007fed155905b0>

3D MOL for #<Metabolite:0x00007fed155905b0>

3D SDF for #<Metabolite:0x00007fed155905b0>

3D-SDF for #<Metabolite:0x00007fed155905b0>

PDB for #<Metabolite:0x00007fed155905b0>

3D PDB for #<Metabolite:0x00007fed155905b0>

SMILES for #<Metabolite:0x00007fed155905b0>

INCHI for #<Metabolite:0x00007fed155905b0>

Structure for #<Metabolite:0x00007fed155905b0>

3D Structure for #<Metabolite:0x00007fed155905b0>